5 research outputs found
De novo malignant melanoma occurred in renal allograft: DNA typing to determine the origin of the tumour
- Author
- Bein G.
- Bunce M.
- Heynemann H.
- Hollenbeak C.S.
- Kasiske B.L.
- Kaufmann H.M.
- Kaufmann H.M.
- Kaufmann H.M.
- Keresztury L.
- Kim J.K.
- Laing M.E.
- Langer R.M.
- LeMire L.
- Mackie R.M.
- Miller S.A.
- Milton C.A.
- Montegnino G.
- Morris-Stiff G.
- Nemes B.
- Nemes B.
- Olerup O.
- Penn I.
- Penn I.
- Sandrini S.
- Schmidt R.
- Schmitt C.
- Stephens J.K.
- Suranyi M.G.
- Thaunat O.
- Vajdic C.M.
- Végső G.
- Werner W.
- Wilson L.J.
- Wimmer C.D.
- Publication venue
- 'Akademiai Kiado Zrt.'
- Publication date
- Field of study
Mitochondrial cytochrome c oxidase and succinate dehydrogenase complexes contain plant specific subunits
- Author
- A.C. Eriksson
- A.G. Rasmusson
- A.G. Rasmusson
- A.H. Millar
- A.H. Millar
- A.J. Hiatt
- A.U. Igamberdiev
- A.Y. Gracey
- B. Combettes
- B. Hamasur
- B. Kadenbach
- B.L. Lemire
- C. Dagsgaard
- C.S. Moore
- G. Burger
- G.C. Vanlerberghe
- H. Eubel
- H. Eubel
- H. Schägger
- H. Schägger
- H.P. Braun
- H.P. Braun
- H.P. Braun
- H.P. Braun
- I.M. Fearnley
- I.M. Moller
- J. Heinemeyer
- J.A. Heazlewood
- J.J. Burke
- J.L. Heazlewood
- J.L. Heazlewood
- J.M. Gualberto
- K. Kadowaki
- L. Jänsch
- M. Maeshima
- M. Matsuoka
- M. Sabar
- M. Unseld
- M.J. Hawkesford
- M.K. Smith
- O.M.H Richter
- P. Figueroa
- P. Figueroa
- P.G. Issac
- P.S. Covello
- R. Hiesel
- R. Hiesel
- R.A. Capaldi
- S. Leterme
- T. Hattori
- T. Nakagawa
- T. Nakagawa
- T.D. Fox
- U. Herz
- V. Kruft
- V. Neuhoff
- V. Neuhoff
- V. Yankovskaya
- W. Werhahn
- W.E. Pfeiffer
- Y.K. Sharma
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- Field of study
Discovery of common and rare genetic risk variants for colorectal cancer
- Publication venue
- Publication date
- 01/01/2019
- Field of study
To further dissect the genetic architecture of colorectal cancer (CRC), we performed whole-genome sequencing of 1,439 cases and 720 controls, imputed discovered sequence variants and Haplotype Reference Consortium panel variants into genome-wide association study data, and tested for association in 34,869 cases and 29,051 controls. Findings were followed up in an additional 23,262 cases and 38,296 controls. We discovered a strongly protective 0.3% frequency variant signal at CHD1. In a combined meta-analysis of 125,478 individuals, we identified 40 new independent signals at P < 5 × 10 −8 , bringing the number of known independent signals for CRC to ~100. New signals implicate lower-frequency variants, Krüppel-like factors, Hedgehog signaling, Hippo-YAP signaling, long noncoding RNAs and somatic drivers, and support a role for immune function. Heritability analyses suggest that CRC risk is highly polygenic, and larger, more comprehensive studies enabling rare variant analysis will improve understanding of biology underlying this risk and influence personalized screening strategies and drug development. © 2018, This is a U.S. government work and not under copyright protection in the U.S.; foreign copyright protection may apply
Bibliography of the living coelacanth Latimeria chalumnae, with comments on publication trends
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- A. Ricgles de
- A. Roberto
- A. Witkowski
- A.C. Bruggen Van
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- A.L. Gaski
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- C. Munnion
- C. Newman
- C. Poplin
- C.A. Toit Du
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- C.L. Smith
- C.P. Idyll
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From feast to famine; adaptation to nutrient availability in yeast
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- R. Fernandez
- R. Jiang
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- R. Needleman
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- R.E. Baker
- R.J. Bram
- R.J. Rolfes
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- S. Özcan
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- S. Özcan
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- S.L. Forsburg
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- S.M. Jazwinski
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- S.M. Schork
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- T Powers
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- T. Beck
- T. Didion
- T. Doorenbosch
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- T. Ito
- T. Kataoka
- T. Kishi
- T. Lodi
- T. Munder
- T. Petit
- T. Schmelzle
- T. Soto
- T. Soto
- T. Soto
- T. Soto
- T. Toda
- T. Toda
- T. Toda
- T. Toda
- T.A. Hardy
- T.A. Hardy
- T.E. Ellenberger
- T.G. Cooper
- T.H. Brondijk
- T.M. Kriegel
- T.R. Bürglin
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