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David N Cooper

Showing results (241-250 of 398) with videos related to

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Cell Cycle (Georgetown, Tex.)|November 16, 2017
DNA polymerase η mutational signatures are found in a variety of different types of cancerIgor B Rogozin, Alexander Goncearenco, Artem G Lada, et al.
Human Genetics|January 25, 2003
Human genetic disease caused by de novo mitochondrial-nuclear DNA transferClesson Turner, Christina Killoran, Nick S T Thomas, et al.
Medecine Sciences : M/S|May 12, 2006
[Gains of glycosylation mutations]Guillaume Vogt, Ariane Chapgier, Nadia Chuzhanova, et al.
Biorxiv : the Preprint Server for Biology|February 27, 2026
Ancestry-specific performance of variant effect predictors in clinical variant classificationRachel Hoffing, Daniel Zeiberg, Sarah L Stenton, et al.
Human Mutation|May 20, 2021
Common polymorphic OTC variants can act as genetic modifiers of enzymatic activityMónica Lopes-Marques, Ana Rita Pacheco, Maria João Peixoto, et al.
Frontiers in Genetics|January 8, 2021
<i>EXT1</i> and <i>EXT2</i> Variants in 22 Chinese Families With Multiple Osteochondromas: Seven New Variants and Potentiation of Preimplantation Genetic Testing and Prenatal DiagnosisYe Wang, Liangying Zhong, Yan Xu, et al.
European Journal of Human Genetics : EJHG|May 26, 2011
Assessing the pathological relevance of SPINK1 promoter variantsArnaud Boulling, Heiko Witt, Giriraj Ratan Chandak, et al.
The Journal of Biological Chemistry|February 3, 2011
Non-B DNA-forming sequences and WRN deficiency independently increase the frequency of base substitution in human cellsAlbino Bacolla, Guliang Wang, Aklank Jain, et al.
Human Mutation|December 23, 2011
Tissue-specific differences in the proportion of mosaic large NF1 deletions are suggestive of a selective growth advantage of hematopoietic del(+/-) stem cellsAngelika C Roehl, Tanja Mussotter, David N Cooper, et al.
Transfusion|August 7, 2020
Pathogenic and likely pathogenic variants in at least five genes account for approximately 3% of mild isolated nonsyndromic thrombocytopeniaPaul Guéguen, Arnaud Dupuis, Jean-Yves Py, et al.
Pageof 40

Showing results (241-250 of 398) with videos related to

Sort By:
Pageof 40
Cell Cycle (Georgetown, Tex.)|November 16, 2017
DNA polymerase η mutational signatures are found in a variety of different types of cancerIgor B Rogozin, Alexander Goncearenco, Artem G Lada, et al.
Human Genetics|January 25, 2003
Human genetic disease caused by de novo mitochondrial-nuclear DNA transferClesson Turner, Christina Killoran, Nick S T Thomas, et al.
Medecine Sciences : M/S|May 12, 2006
[Gains of glycosylation mutations]Guillaume Vogt, Ariane Chapgier, Nadia Chuzhanova, et al.
Biorxiv : the Preprint Server for Biology|February 27, 2026
Ancestry-specific performance of variant effect predictors in clinical variant classificationRachel Hoffing, Daniel Zeiberg, Sarah L Stenton, et al.
Human Mutation|May 20, 2021
Common polymorphic OTC variants can act as genetic modifiers of enzymatic activityMónica Lopes-Marques, Ana Rita Pacheco, Maria João Peixoto, et al.
Frontiers in Genetics|January 8, 2021
<i>EXT1</i> and <i>EXT2</i> Variants in 22 Chinese Families With Multiple Osteochondromas: Seven New Variants and Potentiation of Preimplantation Genetic Testing and Prenatal DiagnosisYe Wang, Liangying Zhong, Yan Xu, et al.
European Journal of Human Genetics : EJHG|May 26, 2011
Assessing the pathological relevance of SPINK1 promoter variantsArnaud Boulling, Heiko Witt, Giriraj Ratan Chandak, et al.
The Journal of Biological Chemistry|February 3, 2011
Non-B DNA-forming sequences and WRN deficiency independently increase the frequency of base substitution in human cellsAlbino Bacolla, Guliang Wang, Aklank Jain, et al.
Human Mutation|December 23, 2011
Tissue-specific differences in the proportion of mosaic large NF1 deletions are suggestive of a selective growth advantage of hematopoietic del(+/-) stem cellsAngelika C Roehl, Tanja Mussotter, David N Cooper, et al.
Transfusion|August 7, 2020
Pathogenic and likely pathogenic variants in at least five genes account for approximately 3% of mild isolated nonsyndromic thrombocytopeniaPaul Guéguen, Arnaud Dupuis, Jean-Yves Py, et al.
Pageof 40