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Christopher D Brown

Showing results (61-70 of 104) with videos related to

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The Journal of Clinical Endocrinology and Metabolism|November 1, 2014
A novel mechanism of inherited TBG deficiency: mutation in a liver-specific enhancerAlfonso Massimiliano Ferrara, Theodora Pappa, Jiao Fu, et al.
Plos Genetics|January 20, 2010
A comprehensive map of insulator elements for the Drosophila genomeNicolas Nègre, Christopher D Brown, Parantu K Shah, et al.
Oral Oncology|September 27, 2014
Rare occurrence of EGFRvIII deletion in head and neck squamous cell carcinomaArun Khattri, Zhixiang Zuo, Johannes Brägelmann, et al.
Nature Communications|February 5, 2015
Coordinated regulatory variation associated with gestational hyperglycaemia regulates expression of the novel hexokinase HKDC1Cong Guo, Anton E Ludvik, Michelle E Arlotto, et al.
Journal of Alzheimer'S Disease : JAD|September 29, 2019
Inferring the Molecular Mechanisms of Noncoding Alzheimer's Disease-Associated Genetic VariantsAlexandre Amlie-Wolf, Mitchell Tang, Jessica Way, et al.
American Journal of Human Genetics|October 24, 2017
A Dementia-Associated Risk Variant near TMEM106B Alters Chromatin Architecture and Gene ExpressionMichael D Gallagher, Marijan Posavi, Peng Huang, et al.
Human Molecular Genetics|September 25, 2012
A conserved eEF2 coding variant in SCA26 leads to loss of translational fidelity and increased susceptibility to proteostatic insultKatherine E Hekman, Guo-Yun Yu, Christopher D Brown, et al.
The Journal of Clinical Investigation|May 17, 2021
Transcriptome-wide association analysis identifies DACH1 as a kidney disease risk gene that contributes to fibrosisTomohito Doke, Shizheng Huang, Chengxiang Qiu, et al.
American Journal of Human Genetics|August 5, 2014
Identification and validation of genetic variants that influence transcription factor and cell signaling protein levelsRonald J Hause, Amy L Stark, Nirav N Antao, et al.
Blood|December 6, 2012
CUX1 is a haploinsufficient tumor suppressor gene on chromosome 7 frequently inactivated in acute myeloid leukemiaMegan E McNerney, Christopher D Brown, Xiaoyue Wang, et al.
Pageof 11

Showing results (61-70 of 104) with videos related to

Sort By:
Pageof 11
The Journal of Clinical Endocrinology and Metabolism|November 1, 2014
A novel mechanism of inherited TBG deficiency: mutation in a liver-specific enhancerAlfonso Massimiliano Ferrara, Theodora Pappa, Jiao Fu, et al.
Plos Genetics|January 20, 2010
A comprehensive map of insulator elements for the Drosophila genomeNicolas Nègre, Christopher D Brown, Parantu K Shah, et al.
Oral Oncology|September 27, 2014
Rare occurrence of EGFRvIII deletion in head and neck squamous cell carcinomaArun Khattri, Zhixiang Zuo, Johannes Brägelmann, et al.
Nature Communications|February 5, 2015
Coordinated regulatory variation associated with gestational hyperglycaemia regulates expression of the novel hexokinase HKDC1Cong Guo, Anton E Ludvik, Michelle E Arlotto, et al.
Journal of Alzheimer'S Disease : JAD|September 29, 2019
Inferring the Molecular Mechanisms of Noncoding Alzheimer's Disease-Associated Genetic VariantsAlexandre Amlie-Wolf, Mitchell Tang, Jessica Way, et al.
American Journal of Human Genetics|October 24, 2017
A Dementia-Associated Risk Variant near TMEM106B Alters Chromatin Architecture and Gene ExpressionMichael D Gallagher, Marijan Posavi, Peng Huang, et al.
Human Molecular Genetics|September 25, 2012
A conserved eEF2 coding variant in SCA26 leads to loss of translational fidelity and increased susceptibility to proteostatic insultKatherine E Hekman, Guo-Yun Yu, Christopher D Brown, et al.
The Journal of Clinical Investigation|May 17, 2021
Transcriptome-wide association analysis identifies DACH1 as a kidney disease risk gene that contributes to fibrosisTomohito Doke, Shizheng Huang, Chengxiang Qiu, et al.
American Journal of Human Genetics|August 5, 2014
Identification and validation of genetic variants that influence transcription factor and cell signaling protein levelsRonald J Hause, Amy L Stark, Nirav N Antao, et al.
Blood|December 6, 2012
CUX1 is a haploinsufficient tumor suppressor gene on chromosome 7 frequently inactivated in acute myeloid leukemiaMegan E McNerney, Christopher D Brown, Xiaoyue Wang, et al.
Pageof 11