46 research outputs found
CUT-PCR: CRISPR-mediated, ultrasensitive detection of target DNA using PCR
- Author
- A Narayan
- AE Friedland
- AM Newman
- B Vogelstein
- B Zetsche
- BP Kleinstiver
- C Alix-Panabieres
- C Anders
- C Bettegowda
- C Song
- D Kim
- D Y Park
- E Heitzer
- FF Cheng
- G-H Hwang
- H Kim
- H Nishimasu
- H S Kim
- H Schwarzenbach
- I Kinde
- J Park
- J Park
- J Yu
- J-S Kim
- JM Kim
- JT Park
- JY Park
- K Baek
- K Kim
- KC Chan
- KM Kruglyak
- L De Mattos-Arruda
- L Sorber
- LD Wood
- M Jinek
- M Li
- MB Freidin
- N Chang
- PD Hsu
- S Bae
- S Chang-Hao Tsao
- S H Lee
- S Kim
- S Ye
- SA Forbes
- SH Lee
- SJ Dawson
- SW Cho
- SW Cho
- T Forshew
- T Yamano
- X Xu
- Y Wu
- Y Zhang
- Y-K Cho
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/12/2017
- Field of study
Circulating tumor DNA (ctDNA) has emerged as a tumor-specific biomarker for the early detection of various cancers. To date, several techniques have been devised to enrich the extremely small amounts of ctDNA present in plasma, but they are still insufficient for cancer diagnosis, especially at the early stage. Here, we developed a novel method, CUT (CRISPR-mediated, Ultrasensitive detection of Target DNA)-PCR, which uses CRISPR endonucleases to enrich and detect the extremely small amounts of tumor DNA fragments among the much more abundant wild-type DNA fragments by specifically eliminating the wild-type sequences. We computed that by using various orthologonal CRISPR endonucleases such as SpCas9 and FnCpf1, the CUT-PCR method would be applicable to 80% of known cancer-linked substitution mutations registered in the COSMIC database. We further verified that CUT-PCR together with targeted deep sequencing enables detection of a broad range of oncogenes with high sensitivity (<0.01%) and accuracy, which is superior to conventional targeted deep sequencing. In the end, we successfully applied CUT-PCR to detect sequences with oncogenic mutations in the ctDNA of colorectal cancer patients' blood, suggesting that our technique could be adopted for diagnosing various types of cancer at early stages
Epstein-Barr Virus-Encoded LMP1 Interacts with FGD4 to Activate Cdc42 and Thereby Promote Migration of Nasopharyngeal Carcinoma Cells
- Author
- A Dovas
- A Kaykas
- A Luna
- A Musch
- A Puls
- A Schmidt
- AG Eliopoulos
- AG Eliopoulos
- AW Oliver
- Bill Sugden
- C Kintscher
- C Stendel
- CD White
- Chia-Chun Chen
- Chih-Ching Wu
- CT Lin
- CT Lin
- CW Dawson
- D Wang
- E Haddad
- G Niedobitek
- H Houlden
- H Nakanishi
- H Obaishi
- H Wu
- Hao-Ping Liu
- HP Li
- HP Liu
- HP Liu
- I Ayala
- J Yang
- JM Vallat
- JW Erickson
- Kai-Ping Chang
- KL Rossman
- KP Harris
- L Estrada
- M Higuchi
- MA Lemmon
- MJ Hart
- MJ Rebecchi
- MM Hsu
- MV Egorov
- N Lam
- N Lam
- N Osmani
- NA Sallee
- NG Pasteris
- NG Pasteris
- O Devergne
- O Gires
- O Gires
- P Kreis
- P Vandenabeele
- PH Anborgh
- R Fahraeus
- S Etienne-Manneville
- S Gruenheid
- S Rauch
- S Rothenberger
- S Sinha
- Shu-Chen Liu
- SW Tsao
- SW Tsao
- T Takenawa
- T Yasui
- V Delague
- V Ravn
- VR Baichwal
- W Ikeda
- WF Coffin 3rd
- XM Chen
- Y Kawasaki
- Y Kim
- Y Ono
- Y Zheng
- Yi-Chuan Huang
- Ying Liang
- Yu-Sun Chang
- Publication venue
- Public Library of Science
- Publication date
- 10/05/2012
- Field of study
Epstein-Barr virus (EBV) is closely associated with nasopharyngeal carcinoma (NPC), a human malignancy notorious for its highly metastatic nature. Among EBV-encoded genes, latent membrane protein 1 (LMP1) is expressed in most NPC tissues and exerts oncogenicity by engaging multiple signaling pathways in a ligand-independent manner. LMP1 expression also results in actin cytoskeleton reorganization, which modulates cell morphology and cell motility— cellular process regulated by RhoGTPases, such as Cdc42. Despite the prominent association of Cdc42 activation with tumorigenesis, the molecular basis of Cdc42 activation by LMP1 in NPC cells remains to be elucidated. Here using GST-CBD (active Cdc42-binding domain) as bait in GST pull-down assays to precipitate active Cdc42 from cell lysates, we demonstrated that LMP1 acts through its transmembrane domains to preferentially induce Cdc42 activation in various types of epithelial cells, including NPC cells. Using RNA interference combined with re-introduction experiments, we identified FGD4 (FYVE, RhoGEF and PH domain containing 4) as the GEF (guanine nucleotide exchange factor) responsible for the activation of Cdc42 by LMP1. Serial deletion experiments and co-immunoprecipitation assays further revealed that ectopically expressed FGD4 modulated LMP1-mediated Cdc42 activation by interacting with LMP1. Moreover, LMP1, through its transmembrane domains, directly bound FGD4 and enhanced FGD4 activity toward Cdc42, leading to actin cytoskeleton rearrangement and increased motility of NPC cells. Depletion of FGD4 or Cdc42 significantly reduced (∼50%) the LMP1-stimulated cell motility, an effect that was partially reversed by expression of a constitutively active mutant of Cdc42. Finally, quantitative RT-PCR and immunohistochemistry analyses showed that FGD4 and LMP1 were expressed in NPC tissues, supporting the potential physiologically relevance of this mechanism in NPC. Collectively, our results not only uncover a novel mechanism underlying LMP1-mediated Cdc42 activation, namely LMP1 interaction with FGD4, but also functionally link FGD4 to NPC tumorigenesis
Aqueous extracts from dietary supplements influence the production of inflammatory cytokines in immortalized and primary T lymphocytes
- Author
- A Bose
- A Corthay
- BH Garcia
- BJ Moynihan
- BT Metzger
- C Wang
- Chris Scholl
- David M Barnes
- E Gigi
- F Chamian
- G Bouma
- GS Firestein
- H Barth
- H Lu
- HJ Jeong
- HK Ziegler
- HY Shin
- I Lampronti
- J Nakagawa
- J Pene
- JS Lee
- L Borish
- L Guo
- M Kawamura
- Melissa G Robbins
- MW Pfaffl
- NL Nisly
- P Alvarez
- P Anderson
- P Devan
- P Morazzoni
- P Scott
- Paul R Hanlon
- PS Haddad
- QT Gao
- RK Katial
- RS Schulof
- S Clement-Kruzelweka
- S Hao
- S Kaminogawa
- S Matsuba
- SL Chang
- SY Lyu
- TB Schwartz
- TP Tsao
- U Lindequist
- WP Zeng
- Y Xi Bao
- Y-K Yim
- YN Zhang
- Publication venue
- BioMed Central
- Publication date
- 01/01/2009
- Field of study
<p>Abstract</p> <p>Background</p> <p>Congaplex<sup>® </sup>and Immuplex<sup>® </sup>are dietary supplements that have been traditionally used to support immune system function. The purpose of these experiments was to determine whether Congaplex<sup>® </sup>and Immuplex<sup>® </sup>affect immune function using primary and immortalized T lymphocytes.</p> <p>Methods</p> <p>Immortalized CEM and Jurkat T lymphocytes and primary peripheral mononuclear blood cells (PBMCs) were treated with the aqueous extracts from Congaplex<sup>® </sup>and Immuplex<sup>® </sup>to determine the effects of these products on cytokine production in activated T lymphocytes.</p> <p>Results</p> <p>Congaplex<sup>® </sup>enhanced phytohemagglutinin/phorbol 12-myristate 13-acetate (PHA/PMA) stimulation of both CEM and Jurkat cells as measured by the production of cytokines, while Immuplex<sup>® </sup>suppressed PHA/PMA-induced production of cytokines, with the exception of interleukin (IL)-8 which was enhanced by Immuplex<sup>®</sup>. <it>In vitro </it>treatment of PBMCs from 10 healthy donors with Congaplex<sup>® </sup>or Immuplex<sup>® </sup>decreased PHA-stimulated production of interferon (IFN)-γ but increased the production of IL-13.</p> <p>Conclusions</p> <p>While the effects of Congaplex<sup>® </sup>and Immuplex<sup>® </sup>differed in these two models, these data demonstrate that the aqueous extracts from these two dietary supplements can affect the inflammatory response of T lymphocytes.</p
An ultra-deep sequencing strategy to detect sub-clonal TP53 mutations in presentation chronic lymphocytic leukemia cases using multiple polymerases
- Author
- A Jethwa
- A Petitjean
- A Rawstron
- A Schuh
- A Varghese
- AC Joerger
- AC Joerger
- AG Knudson Jr
- AM Goh
- AP Grollman
- D Gonzalez
- D J Newton
- D Rossi
- DA Landau
- DR Bentley
- E Stieglitz
- E Wawrzyniak
- EE Balint
- F Dicker
- G Lozanski
- H Dohner
- H Li
- H Li
- I Gravanis
- J Delgado
- J Malcikova
- J Mohr
- J Ojha
- JA Woyach
- JF Huggett
- JJ van Dongen
- K Tian
- L Hazelwood
- L Worrillow
- M A Care
- M Greaves
- M Hallek
- M Olivier
- MB Stocks
- NL Komarova
- P A Evans
- P Baskaran
- P Hillmen
- P McInerney
- PJ Campbell
- R M Tooze
- RK Saiki
- RR Furman
- S Chang-Hao Tsao
- S J O'Connor
- S Nakamura
- S Stilgenbauer
- SM Huse
- T Forshew
- T Munir
- T Zenz
- T Zenz
- T Zenz
- TN Wong
- Y Benjamini
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/10/2016
- Field of study
Chronic lymphocytic leukaemia (CLL) is the most common clonal B-cell disorder characterized by clonal diversity, a relapsing and remitting course, and in its aggressive forms remains largely incurable. Current front-line regimes include agents such as fludarabine, which act primarily via the DNA damage response pathway. Key to this is the transcription factor p53. Mutations in the TP53 gene, altering p53 functionality, are associated with genetic instability, and are present in aggressive CLL. Furthermore, the emergence of clonal TP53 mutations in relapsed CLL, refractory to DNA-damaging therapy, suggests that accurate detection of sub-clonal TP53 mutations prior to and during treatment may be indicative of early relapse. In this study, we describe a novel deep sequencing workflow using multiple polymerases to generate sequencing libraries (MuPol-Seq), facilitating accurate detection of TP53 mutations at a frequency as low as 0.3%, in presentation CLL cases tested. As these mutations were mostly clustered within the regions of TP53 encoding DNA-binding domains, essential for DNA contact and structural architecture, they are likely to be of prognostic relevance in disease progression. The workflow described here has the potential to be implemented routinely to identify rare mutations across a range of diseases
Platelet counts modulate the quantitative relationship between hepatitis B viral DNA and surface antigen concentrations: a cross-sectional study of hematological, histological and viral factors
- Author
- A Vallet-Pichard
- ASF Lok
- C Wai
- C-M Chu
- Chao-Wei Hsu
- Chau-Ting Yeh
- Chih-Lang Lin
- D Ganem
- D Lavanchy
- EASL Clinical Practice Guidelines
- F Poordad
- G Garcia–Tsao
- H-I Yang
- HJ Yim
- HL-Y Chan
- HM Elgouhari
- J Bruix
- K Ishak
- KH Liang
- KR Machlus
- Kung-Hao Liang
- M Bernardi
- M Zobeiri
- MR Yeaman
- P Marcellin
- P Marcellin
- S Ocana
- S Pol
- T Kodama
- T-T Chang
- Tong-Hong Wang
- W-K Seto
- Y-F Liaw
- Y-F Liaw
- Y-F Liaw
- Y-F Liaw
- YF Liaw
- ZNA Said
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- Field of study
Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)
- Author
- A. -G. Wu
- A. C. Ma
- A. K. Au
- Abdel-Aziz A. K.
- Abdelfatah S.
- Abdellatif M.
- Abdoli A.
- Abel S.
- Abeliovich H.
- Abildgaard M. H.
- Abudu Y. P.
- Acevedo-Arozena A.
- Adamopoulos I. E.
- Adeli K.
- Adolph T. E.
- Adornetto A.
- Aflaki E.
- Agam G.
- Agarwal A.
- Aggarwal B. B.
- Agnello M.
- Agostinis P.
- Agrewala J. N.
- Agrotis A.
- Aguilar P. V.
- Ahmad S. T.
- Ahmed Z. M.
- Ahumada-Castro U.
- Aits S.
- Aizawa S.
- Akkoc Y.
- Akoumianaki T.
- Akpinar H. A.
- Al-Abd A. M.
- Al-Akra L.
- Al-Gharaibeh A.
- Alaoui-Jamali M. A.
- Alberti S.
- Alcocer-Gomez E.
- Alessandri C.
- Ali M.
- Alim Al-Bari M. A.
- Aliwaini S.
- Alizadeh J.
- Almacellas E.
- Almasan A.
- Alonso A.
- Alonso G. D.
- Altan-Bonnet N.
- Altieri D. C.
- Alvarez E. M. C.
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- Publication venue
- 'Informa UK Limited'
- Publication date
- 01/01/2021
- Field of study
Antiinflammatory Therapy with Canakinumab for Atherosclerotic Disease
- Author
- A Abbate
- A Abhyankar
- A Adams
- A Agafina
- A Akyea-Djamson
- A Alan
- A Alfieri
- A Alfrey
- A Alvarisqueta
- A Amos
- A Anadiotis
- A Anneveldt
- A Antolick
- A Arthur
- A Aslam
- Abaci F
- Abdullakutty J
- Abhaichand R
- Abib E Jr
- Aboufakher R
- Abrantes J
- Abreu M
- Abulencia K
- Acampora D
- Acampora M
- Accini Mendoza Jl
- Aceto L
- Acevedo B
- Acevedo L
- Acheatel R
- Actis Mv
- Adams M
- Adjic Nc
- Affaki Gs
- Agarwal Dk
- Aggarwal Rk
- Agosta Gf
- Aguilar M
- Aguilar M
- Ahire N
- Ahmad I
- Ahmed Sh
- Ahn Y
- Aish B
- Aiub F
- Aiub J
- Ajax K
- Ajioka M
- Akai Y
- Akatova E
- Akrap B
- Al Joundi T
- Al-Khalili F
- Albisu J
- Alcalde Jm
- Alcide P
- Alfonso T
- Allen J
- Alllison Dc
- Almaliky T
- Amerena J
- Andersen K
- Andor M
- Angelova I
- Angiolillo D
- Anita S
- Anker Sd
- Antalik L
- Antonicelli R
- Aparicio Cv
- Apel T
- Apostolovic S
- Ara M
- Aragorn L
- Arango Jl
- Araujo Fonseca M
- Ardissino D
- Arenas Leon Jl
- Arevalo S
- Argiolas G
- Arif I
- Armas E
- Aron G
- Arora S
- Asafu-Adjaye N
- Ashcom T
- Ashford M
- Ashino K
- Asim Oktay Ao
- Assarsson E
- Ata B
- Ather N
- Atieh M
- Aull L
- Avalos V
- Avdonina N
- Awasthi Ak
- Axthelm C
- Ayala M
- Ayasse D
- Ayasse M
- Azizad M
- Azize Gm
- B Becker
- Baar M
- Babu R
- Backer T
- Badea C
- Baden M
- Baehl S
- Baek C
- Baeumer A
- Bagi Es
- Bai A
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- Bakhai A
- Bakker H
- Baksi A
- Baldin Mg
- Bali Hk
- Ballantyne C
- Ballmajo M
- Balode A
- Balukova E
- Bang Sa
- Banker D
- Banker K
- Baquero A
- Barbarash Ol
- Barbato E
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- Barnett S
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- Barreto M
- Barroso A
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- Chhabra A
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- D Dash
- D Dattani
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- Donaubauer T
- Dong X
- Dormidontova G
- Dorogova I
- Dos Santos A
- Dos Santos F
- Dos Santos P
- Doughty A
- Doughty L
- Dovgalevskiy Y
- Dovgolis S
- Dragutksy B
- Dreese M
- Drost I
- Drouin K
- Duchesne L
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- E Eleuteri
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- Zielinski M
- Zieve F
- Zineldine A.
- Zirlik A
- Zucchetti C
- Publication venue
- 'Massachusetts Medical Society'
- Publication date
- 01/01/2017
- Field of study
Background: Experimental and clinical data suggest that reducing inflammation without affecting lipid levels may reduce the risk of cardiovascular disease. Yet, the inflammatory hypothesis of atherothrombosis has remained unproved. Methods: We conducted a randomized, double-blind trial of canakinumab, a therapeutic monoclonal antibody targeting interleukin-1β, involving 10,061 patients with previous myocardial infarction and a high-sensitivity C-reactive protein level of 2 mg or more per liter. The trial compared three doses of canakinumab (50 mg, 150 mg, and 300 mg, administered subcutaneously every 3 months) with placebo. The primary efficacy end point was nonfatal myocardial infarction, nonfatal stroke, or cardiovascular death. RESULTS: At 48 months, the median reduction from baseline in the high-sensitivity C-reactive protein level was 26 percentage points greater in the group that received the 50-mg dose of canakinumab, 37 percentage points greater in the 150-mg group, and 41 percentage points greater in the 300-mg group than in the placebo group. Canakinumab did not reduce lipid levels from baseline. At a median follow-up of 3.7 years, the incidence rate for the primary end point was 4.50 events per 100 person-years in the placebo group, 4.11 events per 100 person-years in the 50-mg group, 3.86 events per 100 person-years in the 150-mg group, and 3.90 events per 100 person-years in the 300-mg group. The hazard ratios as compared with placebo were as follows: in the 50-mg group, 0.93 (95% confidence interval [CI], 0.80 to 1.07; P = 0.30); in the 150-mg group, 0.85 (95% CI, 0.74 to 0.98; P = 0.021); and in the 300-mg group, 0.86 (95% CI, 0.75 to 0.99; P = 0.031). The 150-mg dose, but not the other doses, met the prespecified multiplicity-adjusted threshold for statistical significance for the primary end point and the secondary end point that additionally included hospitalization for unstable angina that led to urgent revascularization (hazard ratio vs. placebo, 0.83; 95% CI, 0.73 to 0.95; P = 0.005). Canakinumab was associated with a higher incidence of fatal infection than was placebo. There was no significant difference in all-cause mortality (hazard ratio for all canakinumab doses vs. placebo, 0.94; 95% CI, 0.83 to 1.06; P = 0.31). Conclusions: Antiinflammatory therapy targeting the interleukin-1β innate immunity pathway with canakinumab at a dose of 150 mg every 3 months led to a significantly lower rate of recurrent cardiovascular events than placebo, independent of lipid-level lowering. (Funded by Novartis; CANTOS ClinicalTrials.gov number, NCT01327846.
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- Abdelfatah S
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- Sargeant TJ
- Sarin A
- Sarkar C
- Sarkar S
- Sarkar S
- Sarmah DT
- Sarparanta J
- Sarrias M-R
- Sathyanarayan A
- Sathyanarayanan R
- Scaglione KM
- Scatozza F
- Schaefer L
- Schafer ZT
- Schaible UE
- Schapira AHV
- Scharl M
- Schatzl HM
- Schein CH
- Scheper W
- Scheuring D
- Schiaffino MV
- Schiappacassi M
- Schindl R
- Schlattner U
- Schmidt O
- Schmidt SD
- Schmitt R
- Schmitz I
- Schmukler E
- Schneider A
- Schneider BE
- Schober R
- Schoijet AC
- Schott MB
- Schramm M
- Schröder B
- Schuh K
- Schulze RJ
- Schwamborn JC
- Schwarten M
- Schüller C
- Schürmanns L
- Scialo F
- Sciarretta S
- Scott MJ
- Scotto KW
- Scovassi AI
- Scrima A
- Scrivo A
- Sebastian D
- Sebti S
- Sedej S
- Segatori L
- Segev N
- Seglen PO
- Seiliez I
- Seki E
- Selleck SB
- Sellke FW
- Selsby JT
- Sendtner M
- Senturk S
- Seranova E
- Sergi C
- Serra-Moreno R
- Sesaki H
- Settembre C
- Setty SRG
- Sgarbi G
- Sha O
- Shacka JJ
- Shah JA
- Shang D
- Shao C
- Shao F
- Sharbati S
- Sharkey LM
- Sharma D
- Sharma G
- Sharma K
- Sharma P
- Sharma S
- Shen H
- Shen H-M
- Shen J
- Shen M
- Shen W
- Shen Z
- Sheng R
- Sheng Z
- Sheng Z-H
- Shi J
- Shi X
- Shi Y-H
- Shiba-Fukushima K
- Shieh J-J
- Shimada Y
- Shimizu S
- Shimozawa M
- Shintani T
- Shoemaker CJ
- Shojaei S
- Shoji I
- Shravage BV
- Shridhar V
- Shu C-W
- Shu H-B
- Shui K
- Shukla AK
- Shutt TE
- Sica V
- Siddiqui A
- Sierra A
- Sierra-Torre V
- Signorelli S
- Sil P
- Silva BJDA
- Silva JD
- Silva-Pavez E
- Silvente-Poirot S
- Simmonds RE
- Simon AK
- Simon H-U
- Simons M
- Singh A
- Singh LP
- Singh R
- Singh S
- Singh SB
- Singh SK
- Singh SP
- Singh SV
- Sinha D
- Sinha RA
- Sinha S
- Sirko A
- Sirohi K
- Sivridis EL
- Skendros P
- Skirycz A
- Slaninová I
- Sluimer JC
- Smaili SS
- Smertenko A
- Smith MD
- Soenen SJ
- Sohn EJ
- Sok SPM
- Solaini G
- Soldati T
- Soleimanpour SA
- Soler RM
- Solovchenko A
- Somarelli JA
- Sonawane A
- Song F
- Song HK
- Song J-X
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- Song Z
- Soria LR
- Sorice M
- Soukas AA
- Soukup S-F
- Sousa D
- Sousa N
- Spagnuolo PA
- Spector SA
- Srinivas Bharath MM
- St Clair D
- Stagni V
- Staiano L
- Stallings CL
- Stalnecker CA
- Stankov MV
- Stathopulos PB
- Stefan K
- Stefan SM
- Stefanis L
- Steffan JS
- Steinkasserer A
- Stenmark H
- Sterneckert J
- Stevens C
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- Storch S
- Stork B
- Strappazzon F
- Strohecker AM
- Stupack DG
- Su H
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- Subauste CS
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- Subirada PV
- Sudhandiran G
- Sue CM
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- Symons JD
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- Szewczyk NJ
- Tabolacci C
- Tabęcka-Łonczynska A
- Tacke F
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- Tagaya M
- Tai H
- Tait SWG
- Takahashi Y
- Takats S
- Talwar P
- Tam C
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- Tamura A
- Tan CT
- Tan E-K
- Tan Y-Q
- Tanaka M
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- Tang D
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- Tanida I
- Tao Z
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- Tavernarakis N
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- Taylor JM
- Tchetina E
- Tee AR
- Tegeder I
- Teis D
- Teixeira N
- Teixeira-Clerc F
- Tekirdag KA
- Tencomnao T
- Tenreiro S
- Tepikin AV
- Testillano PS
- Tettamanti G
- Tharaux P-L
- Thedieck K
- Thekkinghat AA
- Thellung S
- Thinwa JW
- Thirumalaikumar VP
- Thomas SM
- Thomes PG
- Thorburn A
- Thukral L
- Thum T
- Thumm M
- Tian L
- Tichy A
- Till A
- Timmerman V
- Titorenko VI
- Todi SV
- Todorova K
- Toivonen JM
- Tomaipitinca L
- Tomar D
- Tomas-Zapico C
- Tomić S
- Tong BC-K
- Tong C
- Tong C-K
- Tong X
- Tooze SA
- Torgersen ML
- Torii S
- Torres-López L
- Torriglia A
- Towers CG
- Towns R
- Toyokuni S
- Trajkovic V
- Tramontano D
- Tran Q-G
- Travassos LH
- Trelford CB
- Tremel S
- Trougakos IP
- Tsao BP
- Tschan MP
- Tse H-F
- Tse TF
- Tsugawa H
- Tsvetkov AS
- Tumbarello DA
- Tumtas Y
- Turcotte S
- Turk B
- Turk V
- Turner BJ
- Tuxworth RI
- Tuñón MJ
- Tyler JK
- Tyutereva EV
- Uchiyama Y
- Ugun-Klusek A
- Uhlig HH
- Ulasov IV
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- Urbe S
- Uribe-Carretero E
- Uversky VN
- Ułamek-Kozioł M
- Vaccari T
- Vaccaro MI
- Vahsen BF
- Vakifahmetoglu-Norberg H
- Valdor R
- Valente MJ
- Valko A
- Vallee RB
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- van der Veen S
- Van Kaer L
- van Loosdregt J
- van Wijk SJL
- Vandenberghe W
- Vanhorebeek I
- Vannier-Santos MA
- Vannini N
- Vanrell MC
- Vantaggiato C
- Varano G
- Varela-Nieto I
- Varga M
- Vasconcelos MH
- Vats S
- Vavvas DG
- Vega-Naredo I
- Vega-Rubin-de-Celis S
- Velasco G
- Vellai T
- Vellenga E
- Velotti F
- Velázquez AP
- Verdier M
- Verginis P
- Vergne I
- Verkade P
- Verma M
- Verstreken P
- Vervliet T
- Vervoorts J
- Vessoni AT
- Victor VM
- Vidal M
- Vidoni C
- Vieira OV
- Vierstra RD
- Viganó S
- Vihinen H
- Vijayan V
- Vila M
- Vilar M
- Villalba JM
- Villalobo A
- Villarejo-Zori B
- Villarroya F
- Villarroya J
- Vincent O
- Vindis C
- Viret C
- Viscomi MT
- Visnjic D
- Vitale I
- Vocadlo DJ
- Voitsekhovskaja OV
- Volonté C
- Volta M
- Vomero M
- Von Haefen C
- Vooijs MA
- Voos W
- Vucicevic L
- Wade-Martins R
- Waguri S
- Waite KA
- Wakatsuki S
- Walker DW
- Walker MJ
- Walker SA
- Walter J
- Wandosell FG
- Wang B
- Wang C
- Wang C
- Wang C
- Wang C-Y
- Wang C-Y
- Wang D
- Wang F
- Wang F
- Wang F
- Wang G
- Wang H
- Wang H
- Wang H
- Wang H-G
- Wang J
- Wang J
- Wang J
- Wang J
- Wang K
- Wang L
- Wang L
- Wang M
- Wang MH
- Wang N
- Wang P
- Wang P
- Wang P
- Wang P
- Wang Q
- Wang QA
- Wang QJ
- Wang QK
- Wang W
- Wang W-T
- Wang X
- Wang X
- Wang Y
- Wang Y
- Wang Y
- Wang Y
- Wang Y
- Wang Y
- Wang Y
- Wang Y-Y
- Wang Z
- Wang Z
- Wang Z
- Warnes G
- Warnsmann V
- Watada H
- Watanabe E
- Watchon M
- Wawrzyńska A
- Weaver TE
- Wegrzyn G
- Wehman AM
- Wei H
- Wei L
- Wei T
- Wei Y
- Weiergräber OH
- Weihl CC
- Weindl G
- Weiskirchen R
- Wells A
- Wen RH
- Wen X
- Werner A
- Weykopf B
- Wheatley SP
- Whitton JL
- Whitworth AJ
- Wiktorska K
- Wildenberg ME
- Wileman T
- Wilkinson S
- Willbold D
- Williams B
- Williams RL
- Williams RSB
- Williamson PR
- Wilson RA
- Winner B
- Winsor NJ
- Witkin SS
- Wodrich H
- Woehlbier U
- Wollert T
- Wong E
- Wong JH
- Wong RW
- Wong VKW
- Wong WW-L
- Wu A-G
- Wu C
- Wu J
- Wu J
- Wu KK
- Wu M
- Wu S
- Wu S
- Wu S-Y
- Wu S-Y
- Wu WKK
- Wu X
- Wu X
- Wu Y
- Wu Y-W
- Xavier RJ
- Xia H
- Xia L
- Xia Z
- Xiang G
- Xiang J
- Xiang M
- Xiang W
- Xiao B
- Xiao G
- Xiao H
- Xiao H-T
- Xiao J
- Xiao L
- Xiao S
- Xiao Y
- Xie B
- Xie C-M
- Xie M
- Xie Y
- Xie Z
- Xie Z
- Xilouri M
- Xu C
- Xu E
- Xu H
- Xu J
- Xu J
- Xu L
- Xu WW
- Xu X
- Xue Y
- Yakhine-Diop SMS
- Yamaguchi M
- Yamaguchi O
- Yamamoto A
- Yamashina S
- Yan S
- Yan S-J
- Yan Z
- Yanagi Y
- Yang C
- Yang D-S
- Yang H
- Yang H
- Yang H-T
- Yang J
- Yang J
- Yang J-M
- Yang L
- Yang L
- Yang M
- Yang P-M
- Yang Q
- Yang S
- Yang S
- Yang S-F
- Yang W
- Yang WY
- Yang X
- Yang X
- Yang Y
- Yang Y
- Yao H
- Yao S
- Yao X
- Yao Y-G
- Yao Y-M
- Yasui T
- Yazdankhah M
- Yen PM
- Yi C
- Yi-Ren Hong C-WH
- Yin X-M
- Yin Y
- Yin Z
- Yin Z
- Ying M
- Ying Z
- Yip CK
- Yiu SPT
- Yoo YH
- Yoshida K
- Yoshii SR
- Yoshimori T
- Yousefi B
- Yu B
- Yu H
- Yu J
- Yu J
- Yu L
- Yu M-L
- Yu S-W
- Yu VC
- Yu WH
- Yu Z
- Yu Z
- Yuan J
- Yuan L-Q
- Yuan S
- Yuan S-SF
- Yuan Y
- Yuan Z
- Yue J
- Yue Z
- Yun J
- Yung RL
- Zacks DN
- Zaffagnini G
- Zambelli VO
- Zanella I
- Zang QS
- Zanivan S
- Zappavigna S
- Zaragoza P
- Zarbalis KS
- Zarebkohan A
- Zarrouk A
- Zeitlin SO
- Zeng J
- Zeng J-D
- Zhan L
- Zhang B
- Zhang DD
- Zhang H
- Zhang H
- Zhang H
- Zhang H
- Zhang H
- Zhang H
- Zhang H
- Zhang H-L
- Zhang J
- Zhang J
- Zhang J-P
- Zhang KYB
- Zhang L
- Zhang L
- Zhang L
- Zhang L
- Zhang LW
- Zhang M
- Zhang P
- Zhang S
- Zhang W
- Zhang X
- Zhang X
- Zhang X
- Zhang X
- Zhang X
- Zhang X-W
- Zhang XD
- Zhang Y
- Zhang Y
- Zhang Y
- Zhang Y
- Zhang Y
- Zhang Y-D
- Zhang Y-Y
- Zhang Z
- Zhang Z
- Zhang Z
- Zhang Z
- Zhang Z
- Zhang Z
- Zhao H
- Zhao L
- Zhao S
- Zhao T
- Zhao X-F
- Zhao Y
- Zhao Y
- Zhao Y
- Zhao Y
- Zheng G
- Zheng K
- Zheng L
- Zheng S
- Zheng X-L
- Zheng Y
- Zheng Z-G
- Zhivotovsky B
- Zhong Q
- Zhou A
- Zhou B
- Zhou C
- Zhou G
- Zhou H
- Zhou H
- Zhou H
- Zhou J
- Zhou J
- Zhou J
- Zhou J
- Zhou K
- Zhou R
- Zhou X-J
- Zhou Y
- Zhou Y
- Zhou Y
- Zhou Z
- Zhou Z-Y
- Zhu B
- Zhu C
- Zhu G-Q
- Zhu H
- Zhu H
- Zhu H
- Zhu W-G
- Zhu Y
- Zhu Y
- Zhuang H
- Zhuang X
- Zientara-Rytter K
- Zimmermann CM
- Ziviani E
- Zoladek T
- Zong W-X
- Zorov DB
- Zorzano A
- Zou W
- Zou Z
- Zou Z
- Zuryn S
- Zwerschke W
- Álvarez ÉMC
- Ávalos Y
- Önal G
- Üstün S
- Čolić M
- Đokić J
- Žerovnik E
- 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
withdrawn 2017 hrs ehra ecas aphrs solaece expert consensus statement on catheter and surgical ablation of atrial fibrillation
- Author
- Abdulla
- Abecasis
- Abed
- Abed
- Abhishek
- Abreu Filho
- Ad
- Ad
- Ad
- Adragao
- Ahmed
- Ailawadi
- Aizer
- Ajaj
- Akoum
- Akpinar
- Al Chekakie
- Al Halabi
- Al-Hijji
- Aldhoon
- Allan
- Allessie
- Allessie
- Allessie
- Allison
- Alonso
- Andersen
- Anderson
- Anderson
- Andrade
- Andrade
- Andrade
- Andrade
- Andrade
- Andrade
- Andrade
- Andrade
- Andrade
- Andrea Natale
- André d’Avila
- Angelo A V De Paola
- Anne
- Anne B Curtis
- Anousheh
- Anter
- Anter
- Anter
- Antonio Raviele
- Arbelo
- Arentz
- Arentz
- Arentz
- Armbruster
- Armour
- Arnar
- Aronsson
- Arora
- Arruda
- Arruda
- Arya
- Arya
- Aryana
- Aryana
- Asbach
- Assasi
- Atienza
- Atienza
- Atienza
- Atul Verma
- Avitall
- Badhwar
- Bai
- Bai
- Bai
- Bai
- Bakris
- Balk
- Baman
- Baman
- Bansch
- Baran
- Barbhaiya
- Barnett
- Bartus
- Bassiouny
- Bassiouny
- Basso
- Bauer
- Beck
- Belden
- Ben Amar
- Bendszus
- Benharash
- Benito
- Benjamin
- Benjamin
- Berenfeld
- Berkowitsch
- Berntsen
- Berruezo
- Bertaglia
- Bertaglia
- Bertaglia
- Bertaglia
- Bettoni
- Beyer
- Bharat
- Bian
- Bin Abdulhak
- Bisleri
- Bisleri
- Bitter
- Black-Maier
- Blackshear
- Blomstrom-Lundqvist
- Boersma
- Boersma
- Boersma
- Bogachev-Prokophiev
- Bogachev-Prokophiev
- Boldt
- Borchert
- Bordignon
- Bordignon
- Bordignon
- Boriani
- Bourier
- Bradfield
- Briceno
- Brooks
- Bruce
- Bruce
- Bruce D Lindsay
- Buber
- Bubien
- Buch
- Budera
- Bulava
- Bulava
- Bunch
- Bunch
- Bunch
- Bunch
- Bunch
- Bunch
- Bunch
- Bunch
- Bunch
- Bunch
- Byrd
- Byrne
- Caballero
- Cabrera
- Calkins
- Calkins
- Calkins
- Calkins
- Calkins
- Calkins
- Calkins
- Callans
- Calvo
- Camm
- Camm
- Canpolat
- Caponi
- Cappato
- Cappato
- Cappato
- Cappato
- Cappato
- Carina Blomström-Lundqvist
- Carlsson
- Carroll
- Cauchemez
- Cazavet
- Cha
- Chae
- Chalfoun
- Chan
- Chang
- Chang
- Chao
- Charitos
- Chavez
- Cheema
- Chen
- Chen
- Chen
- Chen
- Chen
- Chen
- Chen
- Chen
- Chen
- Chen
- Cheng
- Cheng
- Cherniavsky
- Chevalier
- Chevalier
- Chiang
- Chiappini
- Chilukuri
- Chilukuri
- Chilukuri
- Chilukuri
- Chiou
- Choi
- Choi
- Choi
- Choi
- Chopra
- Chrispin
- Christ
- Christophersen
- Chugh
- Chugh
- Chugh
- Chugh
- Chugh
- Chugh
- Chun
- Chun
- Chung
- Ciconte
- Ciconte
- Ciconte
- Civello
- Claudio Tondo
- Cochet
- Cochet
- Colilla
- Conen
- Connolly
- Connolly
- Contreras-Valdes
- Corradi
- Corrado
- Cosedis Nielsen
- Coulombe
- Cox
- Cox
- Cox
- Cristiano F Pisani
- Cuculich
- Cummings
- Cummings
- Cummings
- Cutler
- D Wyn Davies
- D'Ascenzo
- Dagres
- Dagres
- Dagres
- Dagres
- Dagres
- Dallaglio
- Damiano
- Damiano
- Damiano
- Daoud
- Das
- Datino
- Datino
- David E Haines
- David J Wilber
- Davidenko
- de Bakker
- de Bakker
- de Boer
- De Greef
- De Greef
- de Groot
- De Groot
- de Oliveira
- De Ponti
- De Ponti
- De Potter
- De Potter
- de Vos
- Deftereos
- Deftereos
- Deisenhofer
- Della Bella
- Dello Russo
- Demaria
- Deneke
- Deneke
- Deneke
- Deneke
- Deneke
- Deshmukh
- Deshmukh
- Desimone
- Dewire
- Di Biase
- Di Biase
- Di Biase
- Di Biase
- Di Biase
- Di Biase
- Di Biase
- Di Biase
- Di Biase
- Di Biase
- Di Giovanni
- Dimitri
- Dixit
- Doll
- Doll
- Donal
- Dong
- Dong
- Dong
- Dorian
- Dorwarth
- Douglas Packer
- Doukas
- Dragusin
- Driessen
- Driessen
- Dublin
- Dukkipati
- Dukkipati
- Dukkipati
- Dukkipati
- Dumonceau
- Earley
- Eckard
- Ector
- Ector
- Edgerton
- Edgerton
- Edgerton
- Edgerton
- Edgerton
- Edgerton
- Edgerton
- Eduardo B Saad
- Eduardo B Saad
- Edward P Gerstenfeld
- EHRA Scientific Committee Task Force
- EHRA Scientific Committee Task Force
- Ehrlich
- Eick
- Eijsvogels
- Eitel
- Eitel
- Eitel
- Ejima
- Elaine Hylek
- Elayi
- Elayi
- Elkassabany
- Ellinor
- Ellinor
- Ellis
- Emmert
- Engelman
- Engelmann
- Ernst
- Errahmouni
- Estner
- Ettinger
- European Heart Rhythm
- Everett
- Everett
- Evgeny Pokushalov
- Evonich
- Faddis
- Farina
- Fast
- Fayad
- Fein
- Feinberg
- Fender
- Fender
- Fenelon
- Ferguson
- Fichtner
- Filgueiras-Rama
- Filgueiras-Rama
- Finta
- Fisher
- Fjeldsoe
- Fletcher
- Forleo
- Forleo
- Forleo
- Fox
- Franceschi
- Francis E Marchlinski
- Franzen
- Friberg
- Furlanello
- Furnkranz
- Furnkranz
- Furnkranz
- Furnkranz
- Fynn
- Gaita
- Gaita
- Gaita
- Gaita
- Gal
- Gami
- Gammie
- Gammie
- Ganesan
- Ganesan
- Garrey
- Gay-Jordi
- Gaynor
- Gaztanaga
- Gehi
- Geidel
- Geidel
- Gentlesk
- Gerhard Hindricks
- Gersak
- Gersak
- Gerstenfeld
- Gerstenfeld
- Gerstenfeld
- Gerstenfeld
- Gerstenfeld
- Gerstenfeld
- Ghanbari
- Ghia
- Ghias
- Gianni
- Gibson
- Gilcrease
- Gillinov
- Gillinov
- Gillinov
- Gittenberger-de Groot
- Giugliano
- Glotzer
- Go
- Goette
- Goette
- Good
- Gopinath
- Gottlieb
- Granger
- Gray
- Greenberg
- Gregory F Michaud
- Gregory Y H Lip
- Greiser
- Greiser
- Grothoff
- Grove
- Grubman
- Grundvold
- Gudbjartsson
- Gudbjartsson
- Guhl
- Guilherme Fenelon
- Guillem
- Guillem
- Guiot
- Guiot
- Gula
- Gunes
- Gupta
- Gurbuz
- Gussak
- Hadid
- Haemers
- Haines
- Haines
- Haines
- Haissaguerre
- Haissaguerre
- Haissaguerre
- Haissaguerre
- Haissaguerre
- Haissaguerre
- Haissaguerre
- Haissaguerre
- Haissaguerre
- Hakalahti
- Hakalahti
- Haldar
- Halm
- Halperin
- Han
- Hanazawa
- Hanke
- Hans Kottkamp
- Hansen
- Hao
- Harada
- Hauser
- Hazell
- He
- He
- Healey
- Healey
- Healey
- Heeger
- Heidbuchel
- Heijman
- Heist
- Helps
- Henn
- Herrera
- Hilbert
- Hilbert
- Hindricks
- Hindricks
- Hiroshi Nakagawa
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- Ullah
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- Yagishita
- Yaksh
- Yamada
- Yamaguchi
- Yamaguchi
- Yamamoto
- Yamane
- Yamashita
- Yang
- Yokoyama
- Yokoyama
- Yong Ji
- Yoo
- Young-Hoon Kim
- Yousuf
- Zado
- Zaman
- Zeljko
- Zellerhoff
- Zellerhoff
- Zellerhoff
- Zellerhoff
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- Zeng
- Zhang
- Zhang
- Zhang
- Zhao
- Zhao
- Zhao
- Zhou
- Zhou
- Ziegler
- Zipes
- Zuern
- Publication venue
- Publication date
- 01/01/2017
- Field of study
n/
Sensitivity of plasma BRAF mutant
- Author
- Anna Pavlick
- Balch
- Benesova
- Bettegowda
- Chang-Hao Tsao
- Chapman
- Cindy Spittle
- Das Thakur
- David Polsky
- Dawne N. Shelton
- Dawson
- Diehl
- Diehl
- Egberts
- Eric Robinson
- Flaherty
- Forbes
- George Karlin-Neumann
- Gregory A. Chang
- Hodi
- Hodis
- Hwu
- Iman Osman
- Jyothirmayee S. Tadepalli
- Lipson
- Lo
- Long
- Manohar Furtado
- Oxnard
- Robert
- Sanmamed
- Sarah Weiss
- Sosman
- Topalian
- Wolchok
- Wolchok
- Yilong Zhang
- Yongzhao Shao
- Publication venue
- 'Elsevier BV'
- Publication date
- Field of study