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R Stratton

Showing results (401-410 of 525) with videos related to

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American Journal of Human Genetics|March 18, 2008
SLC9A6 mutations cause X-linked mental retardation, microcephaly, epilepsy, and ataxia, a phenotype mimicking Angelman syndromeGregor D Gilfillan, Kaja K Selmer, Ingrid Roxrud, et al.
Nature Genetics|February 2, 2000
Localization to Xq27 of a susceptibility gene for testicular germ-cell tumoursE A Rapley, G P Crockford, D Teare, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|March 31, 2000
The pathology of familial breast cancer: histological features of cancers in families not attributable to mutations in BRCA1 or BRCA2S R Lakhani, B A Gusterson, J Jacquemier, et al.
Oncogene|March 3, 2015
SETD2 loss-of-function promotes renal cancer branched evolution through replication stress and impaired DNA repairN Kanu, E Grönroos, P Martinez, et al.
Nature Communications|May 17, 2022
Mutational landscape of normal epithelial cells in Lynch Syndrome patientsBernard C H Lee, Philip S Robinson, Tim H H Coorens, et al.
Nature|October 29, 2010
The patterns and dynamics of genomic instability in metastatic pancreatic cancerPeter J Campbell, Shinichi Yachida, Laura J Mudie, et al.
Nature|May 1, 2020
The mutational landscape of normal human endometrial epitheliumLuiza Moore, Daniel Leongamornlert, Tim H H Coorens, et al.
Journal of Medical Genetics|January 27, 2011
DICER1 syndrome: clarifying the diagnosis, clinical features and management implications of a pleiotropic tumour predisposition syndromeIngrid Slade, Chiara Bacchelli, Helen Davies, et al.
Nature Genetics|October 29, 2013
Distinct H3F3A and H3F3B driver mutations define chondroblastoma and giant cell tumor of boneSam Behjati, Patrick S Tarpey, Nadège Presneau, et al.
Nature|January 15, 2025
Prolonged persistence of mutagenic DNA lesions in somatic cellsMichael Spencer Chapman, Emily Mitchell, Kenichi Yoshida, et al.
Pageof 53

Showing results (401-410 of 525) with videos related to

Sort By:
Pageof 53
American Journal of Human Genetics|March 18, 2008
SLC9A6 mutations cause X-linked mental retardation, microcephaly, epilepsy, and ataxia, a phenotype mimicking Angelman syndromeGregor D Gilfillan, Kaja K Selmer, Ingrid Roxrud, et al.
Nature Genetics|February 2, 2000
Localization to Xq27 of a susceptibility gene for testicular germ-cell tumoursE A Rapley, G P Crockford, D Teare, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|March 31, 2000
The pathology of familial breast cancer: histological features of cancers in families not attributable to mutations in BRCA1 or BRCA2S R Lakhani, B A Gusterson, J Jacquemier, et al.
Oncogene|March 3, 2015
SETD2 loss-of-function promotes renal cancer branched evolution through replication stress and impaired DNA repairN Kanu, E Grönroos, P Martinez, et al.
Nature Communications|May 17, 2022
Mutational landscape of normal epithelial cells in Lynch Syndrome patientsBernard C H Lee, Philip S Robinson, Tim H H Coorens, et al.
Nature|October 29, 2010
The patterns and dynamics of genomic instability in metastatic pancreatic cancerPeter J Campbell, Shinichi Yachida, Laura J Mudie, et al.
Nature|May 1, 2020
The mutational landscape of normal human endometrial epitheliumLuiza Moore, Daniel Leongamornlert, Tim H H Coorens, et al.
Journal of Medical Genetics|January 27, 2011
DICER1 syndrome: clarifying the diagnosis, clinical features and management implications of a pleiotropic tumour predisposition syndromeIngrid Slade, Chiara Bacchelli, Helen Davies, et al.
Nature Genetics|October 29, 2013
Distinct H3F3A and H3F3B driver mutations define chondroblastoma and giant cell tumor of boneSam Behjati, Patrick S Tarpey, Nadège Presneau, et al.
Nature|January 15, 2025
Prolonged persistence of mutagenic DNA lesions in somatic cellsMichael Spencer Chapman, Emily Mitchell, Kenichi Yoshida, et al.
Pageof 53