A
Allan Bradley
Researcher at Wellcome Trust Sanger Institute
Publications - 385
Citations - 81969
Allan Bradley is an academic researcher from Wellcome Trust Sanger Institute. The author has contributed to research in topics: Gene & Genome. The author has an hindex of 127, co-authored 379 publications receiving 77492 citations. Previous affiliations of Allan Bradley include Howard Hughes Medical Institute & University of Texas MD Anderson Cancer Center.
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Journal ArticleDOI
Butyrate Greatly Enhances Derivation of Human Induced Pluripotent Stem Cells by Promoting Epigenetic Remodeling and the Expression of Pluripotency-Associated Genes
Prashant Mali,Bin Kuan Chou,Jonathan Yen,Zhaohui Ye,Jizhong Zou,Sarah N. Dowey,Robert A. Brodsky,Joyce E. Ohm,Wayne Yu,Stephen B. Baylin,Kosuke Yusa,Allan Bradley,David J. Meyers,Chandrani Mukherjee,Philip A. Cole,Linzhao Cheng +15 more
TL;DR: It is reported here that butyrate, a naturally occurring fatty acid commonly used as a nutritional supplement and differentiation agent, greatly enhances the efficiency of induced pluripotent stem (iPS) cell derivation from human adult or fetal fibroblasts and provides an efficient method for reprograming various human adult somatic cells, including cells from patients that are more refractory to reprogramming.
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Abnormal behavior in a chromosome-engineered mouse model for human 15q11-13 duplication seen in autism
Jin Nakatani,Kota Tamada,Kota Tamada,Fumiyuki Hatanaka,Fumiyuki Hatanaka,Satoko Ise,Hisashi Ohta,Kiyoshi Inoue,Shozo Tomonaga,Yasuhito Watanabe,Yasuhito Watanabe,Yeun Jun Chung,Ruby Banerjee,Kazuya Iwamoto,Tadafumi Kato,Makoto Okazawa,Kenta Yamauchi,Koichi Tanda,Keizo Takao,Keizo Takao,Tsuyoshi Miyakawa,Tsuyoshi Miyakawa,Allan Bradley,Toru Takumi,Toru Takumi,Toru Takumi +25 more
TL;DR: This chromosome-engineered mouse model for autism seems to replicate various aspects of human autistic phenotypes and validates the relevance of the human chromosome abnormality.
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Disruption of mRad50 causes embryonic stem cell lethality, abnormal embryonic development, and sensitivity to ionizing radiation
Guangbin Luo,Michelle S. Yao,Carla F. Bender,Michael Mills,Anthony R. Bladl,Allan Bradley,John H.J. Petrini +6 more
TL;DR: The null mrad50 mutation is lethal in cultured embryonic stem cells and in early developing embryos, indicating that the mammalian Mre11/Rad50 protein complex mediates functions in normally growing cells that are essential for viability.
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Ulcerative colitis and adenocarcinoma of the colon in G alpha i2-deficient mice
Uwe Rudolph,Milton J. Finegold,Susan Solliday Rich,Gregory R. Harriman,Yogambal Srinivasan,Philippe Brabet,Philippe Brabet,Guylain Boulay,Guylain Boulay,Allan Bradley,Lutz Birnbaumer +10 more
TL;DR: Gαi2–deficient mice display growth retardation and develop a lethal diffuse colitis with clinical and histopathological features closely resembling ulcerative colitis in humans, including the development of adenocarcinoma of the colon.
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Congenital heart disease in mice deficient for the DiGeorge syndrome region
Elizabeth A. Lindsay,Annalisa Botta,Vesna Jurecic,Sandra Carattini-Rivera,Yin Chai Cheah,Howard M. Rosenblatt,Allan Bradley,Antonio Baldini +7 more
TL;DR: The Df1/+ mouse model reveals the pathogenic basis of the most clinically severe aspect of DiGeorge syndrome and uncovers a new mechanism leading to aortic arch abnormalities.