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Biology
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September 17, 2013
The role of nuclear bodies in gene expression and disease
Marie Morimoto, Cornelius F Boerkoel
Disease Models & Mechanisms
|
January 10, 2012
The NIH Undiagnosed Diseases Program: bonding scientists and clinicians
William A Gahl, Cornelius F Boerkoel, Manfred Boehm
Nucleus (Austin, Tex.)
|
February 18, 2011
SMARCAL1 and replication stress: an explanation for SIOD?
Carol E Bansbach, Cornelius F Boerkoel, David Cortez
Current Neurology and Neuroscience Reports
|
March 20, 2002
The genetic convergence of Charcot-Marie-Tooth disease types 1 and 2 and the role of genetics in sporadic neuropathy
Cornelius F Boerkoel, Hiroshi Takashima, James R Lupski
Current Opinion in Genetics & Development
|
June 6, 2003
Chromatin remodeling and human disease
Cheng Huang, Emily A Sloan, Cornelius F Boerkoel
American Journal of Medical Genetics. Part A
|
October 31, 2014
4q12-4q21.21 deletion genotype-phenotype correlation and the absence of piebaldism in presence of KIT haploinsufficiency
Parisa Hemati, Christèle du Souich, Cornelius F Boerkoel
Current Opinion in Genetics & Development
|
June 3, 2004
Advances in chromatin remodeling and human disease
Kyoung Sang Cho, Leah I Elizondo, Cornelius F Boerkoel
European Journal of Medical Genetics
|
January 17, 2012
Hypothesis: SLC12A3 Polymorphism modifies thiazide hypersensitivity of antenatal Bartter syndrome to thiazide resistance
Cherry Mammen, Rosemarie Rupps, Peter Trnka, et al.
Nucleus (Austin, Tex.)
|
November 5, 2016
Chromatin changes in SMARCAL1 deficiency: A hypothesis for the gene expression alterations of Schimke immuno-osseous dysplasia
Marie Morimoto, Kunho Choi, Cornelius F Boerkoel, et al.
Journal of Cellular and Molecular Medicine
|
November 16, 2019
Pan-cancer RNA-seq data stratifies tumours by some hallmarks of cancer
F Graeme Frost, Praveen F Cherukuri, Samuel Milanovich, et al.
Page
of 14
Search research articles
Search
Showing results (1-10 of 134) with videos related to
Sort By:
Page
of 14
Biology
|
September 17, 2013
The role of nuclear bodies in gene expression and disease
Marie Morimoto, Cornelius F Boerkoel
Disease Models & Mechanisms
|
January 10, 2012
The NIH Undiagnosed Diseases Program: bonding scientists and clinicians
William A Gahl, Cornelius F Boerkoel, Manfred Boehm
Nucleus (Austin, Tex.)
|
February 18, 2011
SMARCAL1 and replication stress: an explanation for SIOD?
Carol E Bansbach, Cornelius F Boerkoel, David Cortez
Current Neurology and Neuroscience Reports
|
March 20, 2002
The genetic convergence of Charcot-Marie-Tooth disease types 1 and 2 and the role of genetics in sporadic neuropathy
Cornelius F Boerkoel, Hiroshi Takashima, James R Lupski
Current Opinion in Genetics & Development
|
June 6, 2003
Chromatin remodeling and human disease
Cheng Huang, Emily A Sloan, Cornelius F Boerkoel
American Journal of Medical Genetics. Part A
|
October 31, 2014
4q12-4q21.21 deletion genotype-phenotype correlation and the absence of piebaldism in presence of KIT haploinsufficiency
Parisa Hemati, Christèle du Souich, Cornelius F Boerkoel
Current Opinion in Genetics & Development
|
June 3, 2004
Advances in chromatin remodeling and human disease
Kyoung Sang Cho, Leah I Elizondo, Cornelius F Boerkoel
European Journal of Medical Genetics
|
January 17, 2012
Hypothesis: SLC12A3 Polymorphism modifies thiazide hypersensitivity of antenatal Bartter syndrome to thiazide resistance
Cherry Mammen, Rosemarie Rupps, Peter Trnka, et al.
Nucleus (Austin, Tex.)
|
November 5, 2016
Chromatin changes in SMARCAL1 deficiency: A hypothesis for the gene expression alterations of Schimke immuno-osseous dysplasia
Marie Morimoto, Kunho Choi, Cornelius F Boerkoel, et al.
Journal of Cellular and Molecular Medicine
|
November 16, 2019
Pan-cancer RNA-seq data stratifies tumours by some hallmarks of cancer
F Graeme Frost, Praveen F Cherukuri, Samuel Milanovich, et al.
Page
of 14