10 research outputs found
DNA methylation signatures of chronic low-grade inflammation are associated with complex diseases.
- Author
- Absher Devin M
- Agha Golareh
- Arnett Donna K
- Aslibekyan Stella
- Assimes Themistocles L
- Baccarelli Andrea A
- Bakulski Kelly
- Bandinelli Stefania
- Benjamin Emelia J
- Binder Elisabeth B
- Bis Joshua C
- Boerwinkle Eric
- Bressler Jan
- Brody Jennifer A
- CHARGE epigenetics of Coronary Heart Disease
- Chen Brian H
- Chen Yii-Der Ida
- Chu Audrey Y
- Colicino Elena
- Conneely Karen N
- Deary Ian J
- Dehghan Abbas
- Demerath Ellen W
- Dupuis Josée
- Elks Cathy
- Fallin Daniele
- Feinberg Andrew P
- Ferrucci Luigi
- Fiorito Giovanni
- Fornage Myriam
- Franco Oscar H
- Grallert Harald
- Guan Weihua
- Guarrera Simonetta
- Herder Christian
- Hernandez Dena G
- Hofman Albert
- Horvath Steve
- Huan Tianxiao
- Jhun Min A
- Joehanes Roby
- Just Allan C
- Kardia Sharon LR
- Koenig Wolfgang
- Levy Daniel
- Ligthart Symen
- Lin Honghuang
- Liu Chunyu
- Marioni Riccardo
- Marzi Carola
- Matullo Giuseppe
- McRae Allan F
- Melzer David
- Mendelson Michael M
- Michopoulos Vasiliki J
- Murabito Joanne M
- Ong Ken K
- Pankow James S
- Peters Annette
- Peters Marjolein J
- Pilling Luke C
- Prokisch Holger
- Ressler Kerry J
- Salfati Elias L
- Schramm Katharina
- Schwartz Joel D
- Sha Jin
- Shah Sonia
- Singleton Andrew B
- Smith Alicia K
- Smith Jennifer A
- Sotoodehnia Nona
- Starr John M
- Tanaka Toshiko
- Tsao Phil S
- Turner Stephen T
- Uitterlinden André G
- van Meurs Joyce BJ
- Visscher Peter M
- Vokonas Pantel
- Wahl Simone
- Waite Lindsay L
- Waldenberger Melanie
- Ward-Caviness Cavin K
- Wareham Nicholas J
- WHI-EMPC Investigators
- Wiggins Kerri L
- Yao Chen
- Zhao Wei
- Publication venue
- Genome Biol
- Publication date
- 01/01/2016
- Field of study
BACKGROUND: Chronic low-grade inflammation reflects a subclinical immune response implicated in the pathogenesis of complex diseases. Identifying genetic loci where DNA methylation is associated with chronic low-grade inflammation may reveal novel pathways or therapeutic targets for inflammation. RESULTS: We performed a meta-analysis of epigenome-wide association studies (EWAS) of serum C-reactive protein (CRP), which is a sensitive marker of low-grade inflammation, in a large European population (n = 8863) and trans-ethnic replication in African Americans (n = 4111). We found differential methylation at 218 CpG sites to be associated with CRP (P < 1.15 × 10-7) in the discovery panel of European ancestry and replicated (P < 2.29 × 10-4) 58 CpG sites (45 unique loci) among African Americans. To further characterize the molecular and clinical relevance of the findings, we examined the association with gene expression, genetic sequence variants, and clinical outcomes. DNA methylation at nine (16%) CpG sites was associated with whole blood gene expression in cis (P < 8.47 × 10-5), ten (17%) CpG sites were associated with a nearby genetic variant (P < 2.50 × 10-3), and 51 (88%) were also associated with at least one related cardiometabolic entity (P < 9.58 × 10-5). An additive weighted score of replicated CpG sites accounted for up to 6% inter-individual variation (R2) of age-adjusted and sex-adjusted CRP, independent of known CRP-related genetic variants. CONCLUSION: We have completed an EWAS of chronic low-grade inflammation and identified many novel genetic loci underlying inflammation that may serve as targets for the development of novel therapeutic interventions for inflammation
Ductal pancreatic cancer modeling and drug screening using human pluripotent stem cell- and patient-derived tumor organoids
- Author
- Arrowsmith Cheryl
- Begora Michael
- Cleary Sean
- Connor Ashton A.
- Crawford Howard C.
- Gallinger Steven
- Holtzinger Audrey
- Huang Ling
- Jagan Ishaan
- Kalloger Steve E.
- Keller Gordon
- Lohse Ines
- Muthuswamy Lakshmi B.
- Muthuswamy Senthil K.
- Ngai Nicholas
- Nostro Cristina
- Renouf Daniel J.
- Roehrl Michael
- Schaeffer David F.
- Tsao Ming Sound
- Wang Rennian
- Publication venue
- Scholarship@Western
- Publication date
- 01/11/2015
- Field of study
There are few in vitro models of exocrine pancreas development and primary human pancreatic adenocarcinoma (PDAC). We establish three-dimensional culture conditions to induce the differentiation of human pluripotent stem cells into exocrine progenitor organoids that form ductal and acinar structures in culture and in vivo. Expression of mutant KRAS or TP53 in progenitor organoids induces mutation-specific phenotypes in culture and in vivo. Expression of TP53 R175H induces cytosolic SOX9 localization. In patient tumors bearing TP53 mutations, SOX9 was cytoplasmic and associated with mortality. We also define culture conditions for clonal generation of tumor organoids from freshly resected PDAC. Tumor organoids maintain the differentiation status, histoarchitecture and phenotypic heterogeneity of the primary tumor and retain patient-specific physiological changes, including hypoxia, oxygen consumption, epigenetic marks and differences in sensitivity to inhibition of the histone methyltransferase EZH2. Thus, pancreatic progenitor organoids and tumor organoids can be used to model PDAC and for drug screening to identify precision therapy strategies
Resection arthroplasty for failed patellar components
- Author
- A Slupik
- AD Hanssen
- AG Rosenberg
- AJ Smith
- Audrey K. Tsao
- BE Chalidis
- Carlos J. Lavernia
- D Musil
- David S. Hungerford
- EM Keating
- GA Paletta Jr
- HC Hsu
- HJ Kooijman
- I Günal
- IS Oh
- J Parvizi
- JD Reuben
- JH Lonner
- Jose C. Alcerro
- KA Chun
- Kenneth A. Krackow
- MA Rousseau
- MH Gonzalez
- Michael K. Drakeford
- MJ Kraay
- P Aglietti
- PF Sharkey
- RL Worland
- RM Meneghini
- SD Martin
- W Wulff
- WV Burke
- YH Kim
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- Field of study
Circulating Tumor DNA Measurement by Picoliter Droplet-Based Digital PCR and Vemurafenib Plasma Concentrations in Patients with Advanced BRAF-Mutated Melanoma
- Author
- A Diaz-Lagares
- A Puszkiel
- A Ribas
- AC Knol
- Alicja Puszkiel
- Audrey Thomas-Schoemann
- Benoit Blanchet
- BJ Hindson
- CA Milbury
- E Funck-Brentano
- E Hartsough
- Fanny Garlan
- Gaelle Noe
- H Davies
- JA Sosman
- Jean-Louis Golmard
- K Trunzer
- M Atefi
- M Schreuer
- MF Sanmamed
- Michel Vidal
- MR Gray
- MS Carlino
- N Kramkimel
- Nicolas Dupin
- Nora Kramkimel
- PB Chapman
- Pierre Laurent-Puig
- SC Tsao
- V Taly
- Valerie Taly
- Y Zhen
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- Field of study
Ductal pancreatic cancer modeling and drug screening using human pluripotent stem cell– and patient-derived tumor organoids
- Author
- A Marusyk
- A Rezania
- A Viale
- A Vincent
- AB Johnson
- AC Hick
- Ashton A Connor
- Audrey Holtzinger
- B Xiang
- BM Lyttle
- C Agbunag
- Cheryl Arrowsmith
- Cristina Nostro
- Daniel J Renouf
- David F Schaeffer
- DK Chang
- FC Pan
- FW Pagliuca
- G Chakravarty
- G Chakravarty
- Gordon Keller
- HC Outzen
- Howard C Crawford
- Ines Lohse
- Ishaan Jagan
- JV Schiesser
- KW McCracken
- Lakshmi B Muthuswamy
- Ling Huang
- M Huch
- M Laitio
- MC Nostro
- MC Nostro
- ME Ritchie
- Michael BeGora
- Michael Roehrl
- Ming-Sound Tsao
- MJ Riedel
- N Waddell
- Nicholas Ngai
- P Ghaneh
- RE Jennings
- Rennian Wang
- Sean Cleary
- Senthil K Muthuswamy
- SF Boj
- SK Nielsen
- Steve E Kalloger
- Steven Gallinger
- T Kolodecik
- T van den Beucken
- X Li
- ZS Kanji
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/11/2015
- Field of study
There are few in vitro models of exocrine pancreas development and primary human pancreatic adenocarcinoma (PDAC). We establish three-dimensional culture conditions to induce the differentiation of human pluripotent stem cells (PSCs) into exocrine progenitor organoids that form ductal and acinar structures in culture and in vivo. Expression of mutant KRAS or TP53 in progenitor organoids induces mutation-specific phenotypes in culture and in vivo. Expression of TP53(R175H) induced cytosolic SOX9 localization. In patient tumors bearing TP53 mutations, SOX9 was cytoplasmic and associated with mortality. Culture conditions are also defined for clonal generation of tumor organoids from freshly resected PDAC. Tumor organoids maintain the differentiation status, histoarchitecture, phenotypic heterogeneity of the primary tumor, and retain patient-specific physiologic changes including hypoxia, oxygen consumption, epigenetic marks, and differential sensitivity to EZH2 inhibition. Thus, pancreatic progenitor organoids and tumor organoids can be used to model PDAC and for drug screening to identify precision therapy strategies
Antiviral Activity of Gold/Copper Sulfide Core/Shell Nanoparticles against Human Norovirus Virus-Like Particles
- Author
- A Citkowicz
- A Hale
- A Ingle
- A Vimont
- AJ Hall
- AP Ingle
- Audrey F. Adcock
- AW Jensen
- BI Escudero-Abarca
- Brittny Alston
- BV Prasad
- Chang Yang
- CS Manuel
- DH D'Souza
- DH D'Souza
- DH D’Souza
- DH Kingsley
- DP Zheng
- DR Macinga
- E Addae
- E Duizer
- F Lou
- GW Park
- H Bozkurt
- HL Kirking
- HL Koo
- I Bertrand
- IM El-Nahhal
- J Bae
- J Yap
- JE Lee
- Jessica Jenkins Broglie
- JJ Broglie
- JL Cannon
- JL Cuellar
- K Feng
- K Kornylo
- K Seo
- KR Wigginton
- KY Green
- Liju Yang
- LK Pattenden
- Lun Ma
- M Girard
- M Herbst-Kralovetz
- M Wadl
- ME Hardy
- MM Patel
- N Shionoiri
- N Tsao
- P Gajjar
- P Liu
- P Liu
- P Pumpens
- PF Teunis
- R Ganapathy
- R Huang
- RA Colvin
- RJ Narayan
- S Kang
- S Morter
- S Park
- SA Thornton
- SB Lakshmanan
- SF Grove
- SK Manna
- SL Warnes
- SL Warnes
- SL Warnes
- T Cromeans
- T Mashino
- Wei Chen
- WR Li
- X Li
- X Su
- Y-N Chang
- YJ Tang
- Yongchang Cao
- Publication venue
- 'Public Library of Science (PLoS)'
- Publication date
- Field of study
Whole-genome sequencing reveals host factors underlying critical COVID-19
- Author
- Abd Elghafar Mohamed S.
- Abdel-Aziz Mahmoud
- Abdelrazik Marwa
- Abdollahi Hamed
- Abdullah T.
- Abecasis Goncalo
- Abedalthagafi M.
- Abel Lynn
- Abernathy C.
- Abraheem Azmeralde
- Abul-Husn Noura S.
- Acquilini D.
- Adams C.
- Adams Emma L.
- Adams K.
- Adamsara Alireza
- Adanini Olurenke
- Adeleye O.
- Adra D.
- Afilalo J.
- Afilalo M.
- Afolabi D.
- Afrasiabi Z.
- Agasou A.
- Agrawal Shruti
- Agüero D.
- Ahmad N.
- Ahmadi Saeideh
- Ahmed A.
- Ahmed Cecilia
- Akeroyd L.
- Akhtar M.N.
- Akinkugbe O.
- Aksentijevich Alexandra
- Al-Afghani H.
- Al-Awdah L.
- Alaamery M.
- Alahmadey Z.Z.
- Alaverdian D.
- Alavere H.
- Albader A.
- Albaiceta G.M.
- Albakri J.K.
- AlBardis H.
- Albeladi M.
- Albesher N.
- Albrich W.
- AlDhawi N.
- Aldridge J.
- Aleagha Afshar Etemadi
- Alexander Peter.
- Alfonso J.
- Alghamdi B.
- Alghamdi J.
- Ali A.
- Ali Altaf
- Ali I.A.M.
- Ali Syamlan
- Aliannejad Rasoul
- Aljawini N.
- AlJohani S.
- Alkwai S.
- Allan A.
- Allan E.
- Allan J.
- Alldis Zoe
- Allen L.
- Allen Meryem
- Allen Schvearn
- Allibone S.
- Allison K.S.
- Allos R.
- Ally S.M.
- AlMalik A.
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- Almohammed I.
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- Altabaibeh A.
- Alvaro A.
- AlZahrani D.
- Amin V.
- Amirsavadkouhi Ali
- Amitrano Sara
- Anastasescu E.
- Anderson F.
- Anderson J.
- Anderson Madeleine
- Anderson Peter
- Anderson S.
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- Anderson T.
- Andolfo I.
- Andretta F.
- Andreucci E.
- Andrew Angela
- Andrew B.
- Andrew Gratrix
- Andrews E.
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- Anedda F.
- Anemoli V.
- Annis A.
- Antcliffe David
- Antinori Andrea
- Antoni M.D.
- Anumakonda V.
- Apetri E.
- Aquino Maia
- Arabi Y.M.
- Aravindan Latha
- Arbane Gill
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- Arden T.
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- Armstrong Jacob
- Armstrong Lisa
- Armstrong Ruth
- Arning N.
- Arnold Sophie
- Arranz María Jesús
- Arribas E.
- Artuso R.
- Arumugam Prabhu
- Ascolillo Steven
- Ashraf Saima
- Ashton L.
- Aslibekyan S.
- Astin-Chamberlain Raine
- Atkinson E.G.
- Attwood B.
- Aucella F.
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- Austin Karen
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- Baillie John Kenneth
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- de Gordoa Laura Ortiz-Ruiz
- de la Cal-Sabater P.
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- Dearden Joy
- Death Y.
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- Zhao J.H.
- Zheng Chenqing
- Zhou W.
- Zitter L.
- Zlatopolsky Menachem
- Zongo Olivier
- Zucchi P.
- Zyndorf Marissa
- Zöllner S.
- Åsvold Bjørn Olav
- Publication venue
- Publication date
- 01/01/2022
- Field of study
Altres ajuts: Department of Health and Social Care (DHSC); Illumina; LifeArc; Medical Research Council (MRC); UKRI; Sepsis Research (the Fiona Elizabeth Agnew Trust); the Intensive Care Society, Wellcome Trust Senior Research Fellowship (223164/Z/21/Z); BBSRC Institute Program Support Grant to the Roslin Institute (BBS/E/D/20002172, BBS/E/D/10002070, BBS/E/D/30002275); UKRI grants (MC_PC_20004, MC_PC_19025, MC_PC_1905, MRNO2995X/1); UK Research and Innovation (MC_PC_20029); the Wellcome PhD training fellowship for clinicians (204979/Z/16/Z); the Edinburgh Clinical Academic Track (ECAT) programme; the National Institute for Health Research, the Wellcome Trust; the MRC; Cancer Research UK; the DHSC; NHS England; the Smilow family; the National Center for Advancing Translational Sciences of the National Institutes of Health (CTSA award number UL1TR001878); the Perelman School of Medicine at the University of Pennsylvania; National Institute on Aging (NIA U01AG009740); the National Institute on Aging (RC2 AG036495, RC4 AG039029); the Common Fund of the Office of the Director of the National Institutes of Health; NCI; NHGRI; NHLBI; NIDA; NIMH; NINDS.Critical COVID-19 is caused by immune-mediated inflammatory lung injury. Host genetic variation influences the development of illness requiring critical care or hospitalization after infection with SARS-CoV-2. The GenOMICC (Genetics of Mortality in Critical Care) study enables the comparison of genomes from individuals who are critically ill with those of population controls to find underlying disease mechanisms. Here we use whole-genome sequencing in 7,491 critically ill individuals compared with 48,400 controls to discover and replicate 23 independent variants that significantly predispose to critical COVID-19. We identify 16 new independent associations, including variants within genes that are involved in interferon signalling (IL10RB and PLSCR1), leucocyte differentiation (BCL11A) and blood-type antigen secretor status (FUT2). Using transcriptome-wide association and colocalization to infer the effect of gene expression on disease severity, we find evidence that implicates multiple genes-including reduced expression of a membrane flippase (ATP11A), and increased expression of a mucin (MUC1)-in critical disease. Mendelian randomization provides evidence in support of causal roles for myeloid cell adhesion molecules (SELE, ICAM5 and CD209) and the coagulation factor F8, all of which are potentially druggable targets. Our results are broadly consistent with a multi-component model of COVID-19 pathophysiology, in which at least two distinct mechanisms can predispose to life-threatening disease: failure to control viral replication; or an enhanced tendency towards pulmonary inflammation and intravascular coagulation. We show that comparison between cases of critical illness and population controls is highly efficient for the detection of therapeutically relevant mechanisms of disease
Exome-wide association study of plasma lipids in >300,000 individuals.
- Author
- A Albrechtsen
- A Mehta
- A Mullally
- Adam S Butterworth
- AE Locke
- AF Schmidt
- Alan R Tall
- Alanna C Morrison
- Albert V Smith
- Alex P Reiner
- Alexessander Couto Alves
- Aliki-Eleni Farmaki
- Alisa K Manning
- Allan Linneberg
- Amit V Khera
- Anders Malarstig
- Andrea Maschio
- Andres Metspalu
- Andrew P Morris
- Anette Varbo
- Ani Manichaikul
- Aniruddh P Patel
- Anna Dominiczak
- Anne Langsted
- Anne Tybjaerg-Hansen
- Anne U Jackson
- Annette Peters
- Antonella Mulas
- Anubha Mahajan
- AP Morris
- Asif Rasheed
- Audrey Y Chu
- BA Ference
- BF Voight
- Blair H Smith
- BM Neale
- Bruce M Psaty
- Børge G Nordestgaard
- C Fuchsberger
- C James
- C Sidore
- CA Galloway
- Caroline Hayward
- Chad A Cowan
- Charles Kooperberg
- Charlotta Pisinger
- Christian Gieger
- Christian M Shaffer
- Christie M Ballantyne
- Christoper J O'Donnell
- CJ Willer
- Claudia Langenberg
- Cliona M Molony
- Colin N A Palmer
- Connor Emdin
- Cramer Christensen
- Cristen J Willer
- CS Tang
- CY Cheng
- Dajiang J Liu
- Dan M Roden
- Daniel I Chasman
- Daniel J Rader
- Danish Saleheen
- David C M Liewald
- Derek Klarin
- Dermot F Reilly
- Dewan Alam
- DJ Liu
- Dominique Arveiler
- Dorota Pasko
- Eirini Marouli
- EJ Baxter
- EK Speliotes
- Eleftheria Zeggini
- Elizabeth K Speliotes
- Ellen M Schmidt
- Emanuele Di Angelantonio
- Eric Boerwinkle
- Erwin P Bottinger
- Fabio Busonero
- Francesco Cucca
- Franco Giulianini
- Frank Kee
- Fredrik Karpe
- Frida Renström
- FW Asselbergs
- Gail Davies
- George Dedoussis
- Gina M Peloso
- Giorgio Pistis
- GM Peloso
- Goncalo Abecasis
- Gorm B Jensen
- Gudny Eiriksdottir
- H Lellek
- Hanieh Yaghootkar
- Haojie Yu
- Harald Grallert
- Hayato Tada
- He Zhang
- Heather M Stringham
- Heikki A Koistinen
- Helen R Warren
- Hua Tang
- I Surakka
- Ian Ford
- Ian J Deary
- Igor Rudan
- Ivan Brandslund
- J Wouter Jukema
- JA Tennessen
- Jaakko Tuomilehto
- James B Meigs
- James G Wilson
- Jarmo Virtamo
- Jaspal S Kooner
- Jean Ferrieres
- Jean-Claude Tardif
- Jennifer Huffman
- Jennifer Wessel
- Jerome I Rotter
- Jette Bork-Jensen
- JI Goldstein
- Joanna M M Howson
- Joel N Hirschhorn
- Johanna Jakobsdottir
- Johanna Kuusisto
- Johanne M Justesen
- John C Chambers
- John D Rioux
- John Danesh
- John M Connell
- John M Starr
- Jonas B Nielsen
- Jose M Ordovas
- Joshua C Bis
- Joshua C Denny
- Joshua Weinstock
- K Musunuru
- Kari Kuulasmaa
- Kathleen E Stirrups
- Kent D Taylor
- Kerrin S Small
- Kiran Musunuru
- KJ Gaulton
- Konstantin Strauch
- Kristian Hveem
- L Adrienne Cupples
- LA Lotta
- Lars G Fritsche
- Leif Groop
- Lenore J Launer
- LG Fritsche
- Li An Lin
- Lia E Bang
- Lorraine Southam
- Magdalena Zoledziewska
- Marco Ferrario
- Marianne Benn
- Marie-Pierre Dubé
- Marit E Jørgensen
- Marjo-Riitta Jarvelin
- Marju Orho-Melander
- Mark I McCarthy
- Mark J Caulfield
- Mark O Goodarzi
- Markku Laakso
- Markus Perola
- Martina Müller-Nurasyid
- Mary F Feitosa
- Matt J Neville
- Megan L Grove
- Melanie Waldenberger
- Melissa E Garcia
- Michael Boehnke
- Ming Xu
- ML Grove
- Morris Brown
- Myriam Fornage
- Nan Wang
- Natalie R van Zuydam
- Nathan Stitziel
- Naveed Sattar
- Neil Poulter
- Neil R Robertson
- Neil S Zheng
- Nicholas G D Masca
- Nick J Wareham
- Niels Grarup
- Nilesh J Samani
- Oddgeir L Holmen
- OL Holmen
- Olle Melander
- Oluf Pedersen
- Ozren Polasek
- P Fessas
- Panos Deloukas
- Patricia B Munroe
- Paul L Auer
- Paul M Ridker
- Paul W Franks
- Pekka Mäntyselkä
- Peter E Weeke
- Peter Sever
- Peter W F Wilson
- Philip S Tsao
- Philippe Amouyel
- Philippe Frossard
- Pia R Kamstrup
- Pieter Muntendam
- Praveen Surendran
- R Burkhardt
- R Do
- R Galanello
- R Kralovics
- Rainer Rauramaa
- Rajiv Chowdhury
- Raquel S Sevilla
- Reedik Mägi
- RL Levine
- Robert A Scott
- Robin Young
- Roxana Mehran
- Ruth Frikke-Schmidt
- Ruth J F Loos
- S Feng
- S Jaiswal
- S Jaiswal
- Sandosh Padmanabhan
- Sangeetha Somayajula
- Santhi K Ganesh
- Scott M Damrauer
- Sehrish Jabeen
- Sekar Kathiresan
- Serena Sanna
- Stavroula Kanoni
- Stella Trompet
- Stephen S Rich
- Sune F Nielsen
- Suthesh Sivapalaratnam
- Tamara B Harris
- Tapani Ebeling
- Themistocles L Assimes
- Tibor V Varga
- Timo Lakka
- Timothy D Spector
- Timothy M Frayling
- TM Teslovich
- Torben Hansen
- Torsten Lauritzen
- Tõnu Esko
- U Baber
- Usman Baber
- Valentin Fuster
- Veikko Salomaa
- Vilmundur Gudnason
- W Chen
- Wei Gao
- Wei Zhou
- Weihua Zhang
- X Shen
- X Zhan
- Xiangfeng Lu
- Xiao Wang
- Xueling Sim
- Y Eugene Chen
- Y Momozawa
- Yan Zhang
- Yanhua Zhou
- YF Wang
- Yii-Der Ida Chen
- Yingchang Lu
- Yong Huo
- Publication venue
- Nat Genet
- Publication date
- 01/01/2017
- Field of study
We screened variants on an exome-focused genotyping array in >300,000 participants (replication in >280,000 participants) and identified 444 independent variants in 250 loci significantly associated with total cholesterol (TC), high-density-lipoprotein cholesterol (HDL-C), low-density-lipoprotein cholesterol (LDL-C), and/or triglycerides (TG). At two loci (JAK2 and A1CF), experimental analysis in mice showed lipid changes consistent with the human data. We also found that: (i) beta-thalassemia trait carriers displayed lower TC and were protected from coronary artery disease (CAD); (ii) excluding the CETP locus, there was not a predictable relationship between plasma HDL-C and risk for age-related macular degeneration; (iii) only some mechanisms of lowering LDL-C appeared to increase risk for type 2 diabetes (T2D); and (iv) TG-lowering alleles involved in hepatic production of TG-rich lipoproteins (TM6SF2 and PNPLA3) tracked with higher liver fat, higher risk for T2D, and lower risk for CAD, whereas TG-lowering alleles involved in peripheral lipolysis (LPL and ANGPTL4) had no effect on liver fat but decreased risks for both T2D and CAD
Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)
- Author
- Abdel-Aziz Amal Kamal
- Abdelfatah Sara
- Abdellatif Mahmoud
- Abdoli Asghar
- Abel Steffen
- Abeliovich Hagai
- Abildgaard Marie H
- Abudu Yakubu Princely
- Acevedo-Arozena Abraham
- Adamopoulos Iannis E
- Adeli Khosrow
- Adolph Timon E
- Adornetto Annagrazia
- Aflaki Elma
- Afshar Elham Ghasemipour
- Agam Galila
- Agarwal Anupam
- Aggarwal Bharat B
- Agnello Maria
- Agostinis Patrizia
- Agrewala Javed N
- Agrotis Alexander
- Aguilar Patricia V
- Ahmad S Tariq
- Ahmed Zubair M
- Ahumada-Castro Ulises
- Aits Sonja
- Aizawa Shu
- Akkoc Yunus
- Akoumianaki Tonia
- Akpinar Hafize Aysin
- Al-Abd Ahmed M
- Al-Akra Lina
- Al-Bari M Abdul Alim
- Al-Gharaibeh Abeer
- Alaoui-Jamali Moulay A
- Alberti Simon
- Alcocer-Gomez Elisabet
- Alcon Soledad Porte
- Alessandri Cristiano
- Ali Muhammad
- Aliwaini Saeb
- Alizadeh Javad
- Almacellas Eugenia
- Almasan Alexandru
- Alonso Alicia
- Alonso Guillermo D
- Altan-Bonnet Nihal
- Altieri Dario C
- Alvarez Elida MC
- Alves Sara
- Alzaharna Mazen M
- Amadio Marialaura
- Amantini Consuelo
- Amaral Cristina
- Ambrosio Susanna
- Amer Amal O
- Ammanathan Veena
- An Zhenyi
- Andersen Stig U
- Andrabi Shaida A
- Andrade-Silva Magaiver
- Andres Allen M
- Angelini Sabrina
- Ann David
- Anozie Uche C
- Ansari Mohammad Y
- Antas Pedro
- Antebi Adam
- Anton Zurine
- Anwar Tahira
- Apetoh Lionel
- Apostolova Nadezda
- Araki Toshiyuki
- Araki Yasuhiro
- Arasaki Kohei
- Araujo Thais Fenz
- Araujo Wagner L
- Araya Jun
- Arden Catherine
- Arevalo Maria-Angeles
- Arguelles Sandro
- Arias Esperanza
- Arikkath Jyothi
- Arimoto Hirokazu
- Ariosa Aileen R
- Armstrong-James Darius
- Arnaune-Pelloquin Laetitia
- Aroca Angeles
- Arroyo Daniela S
- Arsov Ivica
- Artero Ruben
- Asaro Dalia Maria Lucia
- Aschner Michael
- Ashrafizadeh Milad
- Ashur-Fabian Osnat
- Atanasov Atanas G
- Au Alicia K
- Auberger Patrick
- Auner Holger W
- Aurelian Laure
- Autelli Riccardo
- Avagliano Laura
- Avalos Yenniffer
- Aveic Sanja
- Aveleira Celia Alexandra
- AvinWittenberg Tamar
- Aydin Yucel
- Ayton Scott
- Ayyadevara Srinivas
- Azzopardi Maria
- Baba Misuzu
- Backer Jonathan M
- Backues Steven K
- Bae Dong-Hun
- Bae Ok-Nam
- Bae Soo Han
- Baehrecke Eric H
- Baek Ahruem
- Baek Seung-Hoon
- Baek Sung Hee
- Bagetta Giacinto
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- Liang Chengyu
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- Shen Weili
- Shen Zheni
- Sheng Rui
- Sheng Zhi
- Sheng Zu-Hang
- Shi Jianjian
- Shi Xiaobing
- Shi Ying-Hong
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- Susztak Katalin
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- Tagaya Mitsuo
- Tai Haoran
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- Takahashi Yoshinori
- Takats Szabolcs
- Talwar Priti
- Tam Chit
- Tam Shing Yau
- Tampellini Davide
- Tamura Atsushi
- Tan Chong Teik
- Tan Eng-King
- Tan Ya-Qin
- Tanaka Masaki
- Tanaka Motomasa
- Tang Daolin
- Tang Jingfeng
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- Thirumalaikumar VP
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- Vega-Rubin-de-Celis Silvia
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- Velasco Guillermo
- Velazquez Ariadna P
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- Verdier Mireille
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- Wang Dong
- Wang Fangyang
- Wang Feng
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- Wang Guansong
- Wang Han
- Wang Hao
- Wang Hexiang
- Wang Hong-Gang
- Wang Jianrong
- Wang Jigang
- Wang Jiou
- Wang Jundong
- Wang Kui
- Wang Lianrong
- Wang Liming
- Wang Maggie Haitian
- Wang Meiqing
- Wang Nanbu
- Wang Peipei
- Wang Pengwei
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- Wang Wen-Tao
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- Wang Yan
- Wang Yanchang
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- Wang Yipeng
- Wang Yu
- Wang Yuqi
- Wang Zhe
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- Xiao Hong-tao
- Xiao Jian
- Xiao Lan
- Xiao Shi
- Xiao Yin
- Xie Baoming
- Xie Chuan-Ming
- Xie Min
- Xie Yuxiang
- Xie Zhiping
- Xie Zhonglin
- Xilouri Maria
- Xu Congfeng
- Xu En
- Xu Haoxing
- Xu Jing
- Xu JinRong
- Xu Liang
- Xu Wen Wen
- Xu Xiulong
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- Yakhine-Diop Sokhna MS
- Yamaguchi Masamitsu
- Yamaguchi Osamu
- Yamamoto Ai
- Yamashina Shunhei
- Yan Shengmin
- Yan Shian-Jang
- Yan Zhen
- Yanagi Yasuo
- Yang Chuanbin
- Yang Dun-Sheng
- Yang Huan
- Yang Huang-Tian
- Yang Hui
- Yang Jin-Ming
- Yang Jing
- Yang Jingyu
- Yang Ling
- Yang Liu
- Yang Ming
- Yang Pei-Ming
- Yang Qian
- Yang Seungwon
- Yang Shu
- Yang Shun-Fa
- Yang Wannian
- Yang Wei Yuan
- Yang Xiaoyong
- Yang Xuesong
- Yang Yi
- Yang Ying
- Yao Honghong
- Yao Shenggen
- Yao Xiaoqiang
- Yao Yong-Gang
- Yao Yong-Ming
- Yasui Takahiro
- Yazdankhah Meysam
- Yen Paul M
- Yi Cong
- Yin Xiao-Ming
- Yin Yanhai
- Yin Zhangyuan
- Yin Ziyi
- Ying Meidan
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- Yiu Stephanie Pei Tung
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- Yoshida Kiyotsugu
- Yoshii Saori R
- Yoshimori Tamotsu
- Yousefi Bahman
- Yu Boxuan
- Yu Haiyang
- Yu Jun
- Yu Jun
- Yu Li
- Yu Ming-Lung
- Yu Seong-Woon
- Yu Victor C
- Yu W Haung
- Yu Zhengping
- Yu Zhou
- Yuan Junying
- Yuan Ling-Qing
- Yuan Shilin
- Yuan Shyng-Shiou F
- Yuan Yanggang
- Yuan Zengqiang
- Yue Jianbo
- Yue Zhenyu
- Yun Jeanho
- Yung Raymond L
- Zacks David N
- Zaffagnini Gabriele
- Zambelli Vanessa O
- Zanella Isabella
- Zang Qun S
- Zanivan Sara
- Zappavigna Silvia
- Zaragoza Pilar
- Zarbalis Konstantinos S
- Zarebkohan Amir
- Zarrouk Amira
- Zeitlin Scott O
- Zeng Jialiu
- Zeng Ju-deng
- Zerovnik Eva
- Zhan Lixuan
- Zhang Bin
- Zhang Donna D
- Zhang Hanlin
- Zhang Hong
- Zhang Hong
- Zhang Honghe
- Zhang Huafeng
- Zhang Huaye
- Zhang Hui
- Zhang Hui-Ling
- Zhang Jianbin
- Zhang Jianhua
- Zhang Jing-Pu
- Zhang Kalin YB
- Zhang Leshuai W
- Zhang Lin
- Zhang Lisheng
- Zhang Lu
- Zhang Luoying
- Zhang Menghuan
- Zhang Peng
- Zhang Sheng
- Zhang Wei
- Zhang Xiangnan
- Zhang Xiao-Wei
- Zhang Xiaolei
- Zhang Xiaoyan
- Zhang Xin
- Zhang Xinxin
- Zhang Xu Dong
- Zhang Yang
- Zhang Yanjin
- Zhang Yi
- Zhang Ying-Dong
- Zhang Yingmei
- Zhang Yuan-Yuan
- Zhang Yuchen
- Zhang Zhe
- Zhang Zhengguang
- Zhang Zhibing
- Zhang Zhihai
- Zhang Zhiyong
- Zhang Zili
- Zhao Haobin
- Zhao Lei
- Zhao Shuang
- Zhao Tongbiao
- Zhao Xiao-Fan
- Zhao Ying
- Zhao Yongchao
- Zhao Yongliang
- Zhao Yuting
- Zheng Guoping
- Zheng Kai
- Zheng Ling
- Zheng Shizhong
- Zheng Xi-Long
- Zheng Yi
- Zheng Zu-Guo
- Zhivotovsky Boris
- Zhong Qing
- Zhou Ao
- Zhou Ben
- Zhou Cefan
- Zhou Gang
- Zhou Hao
- Zhou Hong
- Zhou Hongbo
- Zhou Jie
- Zhou Jing
- Zhou Jing
- Zhou Jiyong
- Zhou Kailiang
- Zhou Rongjia
- Zhou Xu-Jie
- Zhou Yanshuang
- Zhou Yinghong
- Zhou Yubin
- Zhou Zheng-Yu
- Zhou Zhou
- Zhu Binglin
- Zhu Changlian
- Zhu Guo-Qing
- Zhu Haining
- Zhu Hongxin
- Zhu Hua
- Zhu WeiGuo
- Zhu Yanping
- Zhu Yushan
- Zhuang Haixia
- Zhuang Xiaohong
- Zientara-Rytter Katarzyna
- Zimmermann Christine M
- Ziviani Elena
- Zoladek Teresa
- Zong Wei-Xing
- Zorov Dmitry B
- Zorzano Antonio
- Zou Weiping
- Zou Zhen
- Zou Zhengzhi
- Zuryn Steven
- Zwerschke Werner
- Publication venue
- 'Informa UK Limited'
- Publication date
- 01/01/2021
- Field of study
In 2008, we published the first set of guidelines for standardizing research in autophagy. Since then, this topic has received increasing attention, and many scientists have entered the field. Our knowledge base and relevant new technologies have also been expanding. Thus, it is important to formulate on a regular basis updated guidelines for monitoring autophagy in different organisms. Despite numerous reviews, there continues to be confusion regarding acceptable methods to evaluate autophagy, especially in multicellular eukaryotes. Here, we present a set of guidelines for investigators to select and interpret methods to examine autophagy and related processes, and for reviewers to provide realistic and reasonable critiques of reports that are focused on these processes. These guidelines are not meant to be a dogmatic set of rules, because the appropriateness of any assay largely depends on the question being asked and the system being used. Moreover, no individual assay is perfect for every situation, calling for the use of multiple techniques to properly monitor autophagy in each experimental setting. Finally, several core components of the autophagy machinery have been implicated in distinct autophagic processes (canonical and noncanonical autophagy), implying that genetic approaches to block autophagy should rely on targeting two or more autophagy-related genes that ideally participate in distinct steps of the pathway. Along similar lines, because multiple proteins involved in autophagy also regulate other cellular pathways including apoptosis, not all of them can be used as a specific marker for bona fide autophagic responses. Here, we critically discuss current methods of assessing autophagy and the information they can, or cannot, provide. Our ultimate goal is to encourage intellectual and technical innovation in the field
Westem Language Publications on Religions in China, 1990-1994
- Author
- Addiss Stephen
- Aldridge A. Owen
- Allan Sarah
- Allanic Bernard
- Allinson Robert E
- Alt Wayne
- An Jingfu
- Anderson Poul
- Ang John Kwang-Ming
- App Urs
- App Urs
- App Urs
- App Urs
- Arbuckle Gary
- Arbuckle Gary
- Arbuckle Gary
- Asia Watch Committee (U.S.)
- Asia Watch Committee (U.S.)
- Asia Watch Committee (U.S.)
- Asim Ina
- Aubert-Chen Ruey-Yuch Cecilia
- Aubin Françoise
- Baker Janet
- Baldrian-Hussein Farzeen
- Baldwin Michelle
- Banks Michael
- Bannon David
- Baptandier-Berthier Brigitte
- Barbier-Kontler Christine
- Barrett T. H
- Barrett T. H.
- Barrett T. H.
- Barrett T. H.
- Barrett T. H.
- Barrett T. H.
- Barrett T. H.
- Bartholomew Terese Tse
- Bary De
- Bays Daniel H.
- Becker Carl B
- Bell Catherine
- Bell Catherine
- Benn Charles D
- Berger Kenneth J. E.
- Berkowitz Alan J.
- Berkowitz Alan J.
- Berling Judith A.
- Berling Judith A.
- Billeter Jean François
- Birrell Anne
- Birrell Anne
- Blum Mark L.
- Bokenkamp Stephen
- Bokenkamp Stephen
- Bokenkamp Stephen
- Bonnefoy Yves
- Borgen Robert
- Boschi Giulia
- Bower Virginia L.
- Bowring Richard
- Brandauer Frederick P.
- Breton Roland J. L.
- Brook Timothy
- Brook Timothy
- Brooks E. Bruce
- Brownell Susan E.
- Cadonna Alfredo
- Cahill Suzanne E
- Cahill Suzanne E.
- Cahill Suzanne E.
- Campany Robert F.
- Campany Robert F.
- Campany Robert F.
- Cao Zuoya
- Carmody Denise Lardner
- Cedzich Angelika
- Center
- Chamberlain Franc
- Chamberlayne John H
- Chan Alan K. L
- Chan Alan K. L.
- Chan Hon S.
- Chan Kim-Kwong
- Chan Kim-Kwong
- Chan Kim-Kwong
- Chan Leo Tak-Hung
- Chan Leo Tak-Hung
- Chan Leo Tak-Hung
- Chan Sau Y.
- Chan Sin-wai
- Chang Cornelius
- Chang Sheng-Tai
- Chang Winnie
- Chapman Cynthia R.
- Charbonnier Jean
- Chard Robert L.
- Chaves Jonathan
- Chen David H. H.
- Chen Hong
- Chen Jingsong
- Chen Min-sun
- Chen Robert Cheng-hsiung
- Chen Robert Shanmu
- Chen Rui-lin
- Chen Yen-huei
- Chen-Hua
- Cheng Chung-ying
- Chew Phyllis Ghim Lian
- ChIao Wei
- Chien Cheng
- Childs-Johnson Elizabeth
- Ching Julia
- Choi Chi Cheung
- Choi Kwei-Hang
- Chongqing Huangpu
- Chow Kai-wing
- Chu Kun-liang
- Chun Allen
- Ch’iu Huan-hsing
- Clart Philip
- Clart Philip
- Cleary J. C.
- Cleary Thomas
- Cleary Thomas
- Cleary Thomas
- Cleary Thomas
- Cleary Thomas
- Coblin W. South
- Cohen Alvin P
- Cohen Alvin P.
- Cohen Alvin P.
- Cohen Myron L.
- Collins Roy
- Constable Nicole
- Cook Constance A.
- Cook Constance A.
- Covell Ralph R.
- Crump J.
- Cui Dahua
- Cummins J. S
- Dars Jacques
- Dawson Raymond
- Dean Kenneth
- Dean Kenneth
- Dean Kenneth
- Dean Kenneth
- DeBernardi Jean
- Debon Günter
- DeMarco Michael A.
- Desjardins Marc
- Despeux Catherine
- Despeux Catherine
- DeWoskin Kenneth
- Dixon Paul W.
- Doezema William R.
- Donner Neal
- Duan Wenjie
- Dudbridge Glen
- Durt Hubert
- Duteil Jean-Pierre
- Dwight Alan
- Eber Irene
- Eber Irene
- Eber Irene
- Ebrey Patricia Buckley
- Ebrey Patricia Buckley
- Ebrey Patricia Buckley
- Emerson John
- Emmons Charles F.
- Entenmann Robert
- Erickson Susan N.
- Erickson Susan N.
- Eschenbach Silvia Freiin Ebner von
- Eskildsen Steve
- Esposito Monica
- Ess Hans van
- Falkenhausen Lothar von
- Falkenhausen Lothar von
- Fan Carol C.
- Fan Jinshi
- Fang Litian
- Faulkes Brittani
- Faure Bernard
- Faure Bernard
- Faure Bernard
- Faure David
- Faure David
- Feng Lide
- Feuchtwang Stephan
- Field Stephen
- Fong Mary H.
- Fong Mary H.
- Fontein Jan
- Forte Antonio
- Foulk T. Griffith
- Foulk T. Griffith
- Fox Allan
- Franke Herbert
- Franke Herbert
- Franke Herbert
- Franke Herbert
- Franz Rainer von
- Fukui Fumimasa
- Furth Charlotte
- Fyler Jennifer
- Gagan Rosemary R
- Galik Jozef Marian
- Galik Jozef Marian
- Ganza Kenneth
- Gard Richard A.
- Garrett Valery M.
- Gewurtz Margo S.
- Gimello Robert M.
- Gimm Martin
- Girardot Norman J.
- Gladney Dru C.
- Glahn Richard Von
- Goodman Howard L.
- Goodrich Anne S
- Granoff Phyllis
- Grant Beata
- Green Jean M.
- Gregory Peter N
- Gregory Peter N.
- Gridley Marilyn Leidig
- Grieszler Margareta T. J
- Grieszler Margareta T. J.
- Grobe-Hagel Karl
- Grønvald Elisabeth
- Gu Zhizhong
- Gyss-Vermande Caroline
- Haar Barend J
- Halén Harry
- Hammond Charles E.
- Hammond Charles E.
- Hammond Charles E.
- Hammond Charles E.
- Hansen Chad
- Hara Wing-han
- Hardy Grant
- Harper Donald
- Harrison Paul
- Hartz Paul R
- Hawes Colin
- Hayashi Minao
- Hayes James W.
- Hayes James W.
- Heddra Martin
- Hendrischke Barbara
- Hendrischke Barbara
- Hershock Peter D.
- Hevia James Louis
- Ho Kin-chung
- Ho Peng Yoke
- Holm David L.
- Holm David L.
- Holm David L.
- Holzman Donald
- Honey David B.
- Hoobler Thomas
- Hooker Floyd B.
- Howard Angela F
- Howard Angela F.
- Hrdlickova Vena
- Hsia H. J
- Hsieh Ding-Hwa Evelyn
- Hsu C. Y.
- Hu Jun
- Hu William Chao-Chung
- Huang Du
- Huang Shaorong
- Huang Shu-min
- Huang Yi-long
- Hubbard Jamie
- Hunter Alan
- Hunter Alan
- Hunter Alan
- Hunter Alan
- Hunter Alan
- Hunter Alan
- Hunter Alan
- Huntington Rania
- Hwang Jim
- Hyers Conrad
- Ichimura Shohei
- Israeli Raphael
- Ivanhoe Philip J
- Ivanhoe Philip J.
- Ivanhoe Philip J.
- Iwasaki Tsutomu
- Jang Scarlett
- Jankowiak William R
- Jing Anning
- Jl Xianlin
- Jochim Christian
- Johnson David
- Jones Stephen
- Jones Stephen
- Jong De
- Kanno Hiroshi
- Kao Karl S. Y.
- Karetzky Patricia Eichenbaum
- Karetzky Patricia Eichenbaum
- Karetzky Patricia Eichenbaum
- Karetzky Patricia Eichenbaum
- Karetzky Patricia Eichenbaum
- Katz Paul R.
- Katz Paul R.
- Katz Paul R.
- Katz Paul R.
- Keenan John P
- Keller Andrea
- Kern Iso
- Kesner Ladislav
- Kheridian David
- Kimura Kiyotaka
- King Gail
- Kinney Anne Behnke
- Kirkland Russell
- Kirkland Russell
- Kirkland Russell
- Kirkland Russell
- Kitagawa Joseph M.
- Kleeman Terry F
- Kleeman Terry F.
- Kleeman Terry F.
- Kobayashi Masayoshi
- Kohn Livia
- Kohn Livia
- Kohn Livia
- Kohn Livia
- Kohn Livia
- Kohn Livia
- Kohn Livia
- Kohn Livia
- Kohn Livia
- Kohn Livia
- Kohn Livia
- Kohn Livia
- Kohn Livia
- Kravtsova Marina
- Kuhn Dieter
- Kuschel Brigitte
- Kwok Pui-lan
- Kühner Hans
- Lachman Charles
- Lachman Charles
- LaFargue Michael
- LaFargue Michael
- Lagerwey John
- Lagerwey John
- Lagerwey John
- Lagerwey John
- Lai Whalen
- Lai Whalen
- Lai Whalen
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- Lai Whalen
- Lai Yonghai
- Lambert Tony
- Lancaster Lewis
- Lancaster Lewis
- Lang Graeme
- Larre Claude
- Larson John
- Lauwaert Francoise
- Lee Agnes Chwen Jiuan
- Lee Agnes Chwen Jiuan
- Lee Jung Young
- Lee Junghee
- Lee Peter K. H.
- Lee Peter K. H.
- Lee Peter K. H.
- Lee Peter K. H.
- Lee Richard C. Y.
- Lee Schu-chi
- Lee Sherman E.
- Lee Yü-min
- Lefeuvre Jean A.
- Leung Beatrice
- Leung Man-Kam
- Leung Yuen-Sang
- Li Hong
- Li Hong
- Li Houbo
- Li Ling
- Li Ling
- Li Qiqian
- Li Shuang
- Li Shujiang
- Li Xixing
- Li Yuanguo
- Li Yuhang
- Lieu Samuel N. C
- Lin Chang-kuan
- Lin Chang-kuan
- Lin Sen-shou
- Lin Shuen-fu
- Lin Shuen-fu
- Linrothe Robert N.
- Liscák Vladimír
- Little Stephen
- Liu Cary Y.
- Liu Jiahe
- Liu Ming-Wood
- Liu Shu-hsien
- Liu Shu-hsien
- Liu Shu-hsien
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- Liu Xiaogan
- Liu Xiaogan
- Liu Xiaogan
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- Loewe Michael
- Loewe Michael
- Loon Piet van der
- Lowe Scott
- Lowry Kathryn
- Lu Chui-Kuan
- Luo Zhewen
- Lurao Mark D.
- Lutz Albert
- Lynn Richard John
- Machle Edward J
- Machle Edward J.
- MacInnis Donald E
- Mair Victor H
- Mair Victor H
- Mair Victor H
- Mair Victor H.
- Mair Victor H.
- Major John S
- Major John S.
- Malatesta Edward J.
- Masson Michel
- Mather Richard B.
- Mathieu Rémi
- Mathieu Rémi
- Mathieu Rémi
- Mayer Alexander Leonhard
- Mayer Alexander Leonhard
- McBain Audrey
- McClenon James
- McFarlane Stewart
- McLaughlin Michael C.
- McNair Amy
- McRae John R.
- McRae John R.
- Meyer Jeffrey F
- Meyer Jeffrey F
- Meyer Jeffrey F
- Meyer Jeffrey F.
- Miranda Marina
- Mitchell Elsie P
- Mittag Achim
- Morgan Carole
- Munakata Kiyohiko
- Mungello D. E
- Murray Dian
- Müller Gotelind
- Müller Gotelind
- Nadeau Randall L.
- Nadeau Randall L.
- Naquin Susan
- Nattier Jan
- Nemeth David J.
- Ng On-cho
- Ng Yu-Kwan
- Nickerson Peter
- Nielsen Bent
- Nienhauser William H.
- Ning Chen
- Ning Qiang
- Nylan Michael
- Nylan Michael
- Okada Takehiko
- Overmyer Daniel L
- Pachow W
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- Paludan Ann
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- Pan An-yi
- Paolillo Maurizio
- Paper Jordan
- Paper Jordan
- Pas Julian F.
- Peerenboom R. P
- Peerenboom R. P
- Pennarz Johanna
- Peterson Jens O.
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- Pfister Lauren
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- Picard François
- Po Sung-nien
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- Potman Don A.
- Powers John
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- Rainey Lee
- Raphals Lisa
- Rawson Jessica
- Rea Kenneth W.
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- Reis-Habito Maria
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- Reiter Florian C
- Reiter Florian C
- Reiter Florian C
- Reiter Florian C
- Reiter Florian C.
- Reiter Florian C.
- Reiter Florian C.
- Riley Josephine
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- Rosner Erhard
- Ross Andrew C
- Roth Harold D
- Roth Harold D.
- Roth Harold D.
- Roth Harold D.
- Roth Harold D.
- Roth Harold D.
- Rubinstein Murray A
- Russell Terrence
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- Röhrborn Klaus
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- Sakade Yoshinobu
- Samosyuk K. F.
- Sangren P. Steven
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- Schafer Phyllis Brooks
- Schipper Kristofer
- Schipper Kristofer
- Schipper Kristofer
- Schmid D. Neil
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- Seaman Gary
- Seidel Anna
- Seidel Anna
- Seiwert Hubert
- Seiwert Hubert
- Shahar Meir
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- Sharf Robert H.
- Sharf Robert H.
- Shaughnessy Edward L.
- She Shusheng
- Shen Ching-sung
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- Sheng-Yen
- Shi Mingfei
- Shi Pingting
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- Shih Heng-ching
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- Shimbo Tora
- Shinohara Koichi
- Shinohara Koichi
- Shinohara Koichi
- Shinohara Koichi
- Sissaouri Vladislav
- Sivin Nathan
- Smith Richard J
- Smith Richard J
- Smith Richard J.
- Smith Thomas E.
- Smyth Bernard T
- So Francis K. H.
- Song Arthur
- Sorgenfrei Carol Fisher
- Spiro Audrey
- Spiro Audrey
- Spring Madeline K
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- Standaert Nicolas
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- Steinhardt Nancy Shatzman
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- Stevens Keith G.
- Stevens Keith G.
- Stevens Keith G.
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- Stevens Keith G.
- Stevenson Frank W.
- Stockwell Foster
- Storch Tanya
- Strickmann Michel
- Stuart Kevin
- Stuart Kevin
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- Stuart Kevin
- Sturman Peter C.
- Swan James A.
- Swanson Paul L.
- Sørensen Henrik H.
- Sørensen Henrik H.
- Sørensen Henrik H.
- Tajadod Nahal
- Takasaki Jikido
- Takehiro Teri
- Tanaka Kenneth K.
- Tang Jian
- Taylor Rodney L.
- Teiser Stephen F
- Teiser Stephen F.
- Teiser Stephen F.
- Teng Ch’i-yao
- Teng Shu-p’ing
- Teo Geok Lian
- Thompson Kirill Ole
- Thompson Laurence G
- Thompson Laurence G.
- Thompson Laurence G.
- Thoraval Joël
- Thote Alain
- Till Barry
- Tillman Hoyt C.
- Tjandra Lukas
- Tournier Maurice Louis
- Towery Britt
- Tsai Kathryn Ann
- Tsang Ka Bo
- Tsang Ka Bo
- Tsao Pen-yeh
- Tsui Bartholomew P. M
- Tsui Bartholomew P. M.
- Tu Weiming
- Tuohy Sue
- Tzen Peifeng
- T’ang I-chieh
- T’ien Ju-K’ang
- Underwood Laurie
- Unschuld Paul U.
- Vandermeersch Léon
- Vandermeersch Léon
- Verellen Franciscus
- Vermeer Eduard B
- Vervoorn Aat
- Vitiello Giovanni
- Waley-Cohen Joanna
- Walf Knut
- Walf Knut
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- Wawrytko Sandra A.
- Webb Richard
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- Wong Dorothy C.
- Wong Eva
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- Wong Timothy C.
- Wong Timothy Man Kong
- Wright Dale S.
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- Wu Emma
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- Wu Hung
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- Wu Hung
- Wu Jing-nuan
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- Wu Kuang-ming
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- Wädow Gerd
- Yan Shoucheng
- Yanaka Shin’ichi
- Yang Lianfen
- Yates Robin D. S.
- Yeo Khiok-Khng
- Yeoh Brenda S. A.
- Yu David C.
- Yu Kuang-hong
- Yun Eugenia
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- Zeitlin Judith T
- Zhang Dainian
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