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Journal of Immunology (Baltimore, Md. : 1950)
|
March 21, 2006
Rapid demethylation of the IFN-gamma gene occurs in memory but not naive CD8 T cells
Ellen N Kersh, David R Fitzpatrick, Kaja Murali-Krishna, et al.
Wellcome Open Research
|
March 21, 2017
Returning genome sequences to research participants: Policy and practice
Caroline F Wright, Anna Middleton, Jeffrey C Barrett, et al.
Genome Research
|
August 21, 2021
Mutational bias in spermatogonia impacts the anatomy of regulatory sites in the human genome
Vera B Kaiser, Lana Talmane, Yatendra Kumar, et al.
Nature Communications
|
May 26, 2021
Cornelia de Lange syndrome-associated mutations cause a DNA damage signalling and repair defect
Gabrielle Olley, Madapura M Pradeepa, Graeme R Grimes, et al.
Open Biology
|
June 12, 2015
Warburg Micro syndrome is caused by RAB18 deficiency or dysregulation
Mark T Handley, Sarah M Carpanini, Girish R Mali, et al.
American Journal of Medical Genetics. Part A
|
May 18, 2007
Cornelia de Lange syndrome: clinical review, diagnostic and scoring systems, and anticipatory guidance
Antonie D Kline, Ian D Krantz, Annemarie Sommer, et al.
American Journal of Medical Genetics. Part A
|
April 21, 2017
Genotype-phenotype correlations in Cornelia de Lange syndrome: Behavioral characteristics and changes with age
Joanna Moss, Jessica Penhallow, Morad Ansari, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
February 26, 2003
Single-cell perforin and granzyme expression reveals the anatomical localization of effector CD8+ T cells in influenza virus-infected mice
Barbara J Johnson, Elaine O Costelloe, David R Fitzpatrick, et al.
The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association
|
December 21, 2016
Genetic Interactions in Nonsyndromic Orofacial Clefts in Europe-EUROCRAN Study
Peter A Mossey, Julian Little, Regine Steegers-Theunissen, et al.
Molecular Systems Biology
|
June 7, 2024
Deep mutational scanning quantifies DNA binding and predicts clinical outcomes of PAX6 variants
Alexander F McDonnell, Marcin Plech, Benjamin J Livesey, et al.
Page
of 15
Search research articles
Search
Showing results (31-40 of 144) with videos related to
Sort By:
Page
of 15
Journal of Immunology (Baltimore, Md. : 1950)
|
March 21, 2006
Rapid demethylation of the IFN-gamma gene occurs in memory but not naive CD8 T cells
Ellen N Kersh, David R Fitzpatrick, Kaja Murali-Krishna, et al.
Wellcome Open Research
|
March 21, 2017
Returning genome sequences to research participants: Policy and practice
Caroline F Wright, Anna Middleton, Jeffrey C Barrett, et al.
Genome Research
|
August 21, 2021
Mutational bias in spermatogonia impacts the anatomy of regulatory sites in the human genome
Vera B Kaiser, Lana Talmane, Yatendra Kumar, et al.
Nature Communications
|
May 26, 2021
Cornelia de Lange syndrome-associated mutations cause a DNA damage signalling and repair defect
Gabrielle Olley, Madapura M Pradeepa, Graeme R Grimes, et al.
Open Biology
|
June 12, 2015
Warburg Micro syndrome is caused by RAB18 deficiency or dysregulation
Mark T Handley, Sarah M Carpanini, Girish R Mali, et al.
American Journal of Medical Genetics. Part A
|
May 18, 2007
Cornelia de Lange syndrome: clinical review, diagnostic and scoring systems, and anticipatory guidance
Antonie D Kline, Ian D Krantz, Annemarie Sommer, et al.
American Journal of Medical Genetics. Part A
|
April 21, 2017
Genotype-phenotype correlations in Cornelia de Lange syndrome: Behavioral characteristics and changes with age
Joanna Moss, Jessica Penhallow, Morad Ansari, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
February 26, 2003
Single-cell perforin and granzyme expression reveals the anatomical localization of effector CD8+ T cells in influenza virus-infected mice
Barbara J Johnson, Elaine O Costelloe, David R Fitzpatrick, et al.
The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association
|
December 21, 2016
Genetic Interactions in Nonsyndromic Orofacial Clefts in Europe-EUROCRAN Study
Peter A Mossey, Julian Little, Regine Steegers-Theunissen, et al.
Molecular Systems Biology
|
June 7, 2024
Deep mutational scanning quantifies DNA binding and predicts clinical outcomes of PAX6 variants
Alexander F McDonnell, Marcin Plech, Benjamin J Livesey, et al.
Page
of 15