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Kristian Gray

Showing results (1-10 of 18) with videos related to

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Nucleic Acids Research|November 25, 2025
Genenames.org: the HGNC and PGNC resources in 2026Ruth L Seal, Bryony Braschi, Kristian Gray, et al.
Nucleic Acids Research|October 11, 2018
Genenames.org: the HGNC and VGNC resources in 2019Bryony Braschi, Paul Denny, Kristian Gray, et al.
Genome Biology|May 12, 2023
The VGNC: expanding standardized vertebrate gene nomenclatureTamsin E M Jones, Bethan Yates, Bryony Braschi, et al.
Nucleic Acids Research|November 5, 2020
Genenames.org: the HGNC and VGNC resources in 2021Susan Tweedie, Bryony Braschi, Kristian Gray, et al.
Nucleic Acids Research|October 16, 2022
Genenames.org: the HGNC resources in 2023Ruth L Seal, Bryony Braschi, Kristian Gray, et al.
American Journal of Human Genetics|April 17, 2007
Mutations in ZDHHC9, which encodes a palmitoyltransferase of NRAS and HRAS, cause X-linked mental retardation associated with a Marfanoid habitusF Lucy Raymond, Patrick S Tarpey, Sarah Edkins, et al.
Molecular Cancer Therapeutics|November 8, 2006
Mutation analysis of 24 known cancer genes in the NCI-60 cell line setOgechi N Ikediobi, Helen Davies, Graham Bignell, et al.
American Journal of Human Genetics|August 2, 2007
Mutations in the BRWD3 gene cause X-linked mental retardation associated with macrocephalyMichael Field, Patrick S Tarpey, Raffaella Smith, et al.
American Journal of Human Genetics|December 23, 2006
Mutations in the gene encoding the Sigma 2 subunit of the adaptor protein 1 complex, AP1S2, cause X-linked mental retardationPatrick S Tarpey, Claire Stevens, Jon Teague, et al.
American Journal of Human Genetics|January 20, 2007
Mutations in CUL4B, which encodes a ubiquitin E3 ligase subunit, cause an X-linked mental retardation syndrome associated with aggressive outbursts, seizures, relative macrocephaly, central obesity, hypogonadism, pes cavus, and tremorPatrick S Tarpey, F Lucy Raymond, Sarah O'Meara, et al.
Pageof 2

Showing results (1-10 of 18) with videos related to

Sort By:
Pageof 2
Nucleic Acids Research|November 25, 2025
Genenames.org: the HGNC and PGNC resources in 2026Ruth L Seal, Bryony Braschi, Kristian Gray, et al.
Nucleic Acids Research|October 11, 2018
Genenames.org: the HGNC and VGNC resources in 2019Bryony Braschi, Paul Denny, Kristian Gray, et al.
Genome Biology|May 12, 2023
The VGNC: expanding standardized vertebrate gene nomenclatureTamsin E M Jones, Bethan Yates, Bryony Braschi, et al.
Nucleic Acids Research|November 5, 2020
Genenames.org: the HGNC and VGNC resources in 2021Susan Tweedie, Bryony Braschi, Kristian Gray, et al.
Nucleic Acids Research|October 16, 2022
Genenames.org: the HGNC resources in 2023Ruth L Seal, Bryony Braschi, Kristian Gray, et al.
American Journal of Human Genetics|April 17, 2007
Mutations in ZDHHC9, which encodes a palmitoyltransferase of NRAS and HRAS, cause X-linked mental retardation associated with a Marfanoid habitusF Lucy Raymond, Patrick S Tarpey, Sarah Edkins, et al.
Molecular Cancer Therapeutics|November 8, 2006
Mutation analysis of 24 known cancer genes in the NCI-60 cell line setOgechi N Ikediobi, Helen Davies, Graham Bignell, et al.
American Journal of Human Genetics|August 2, 2007
Mutations in the BRWD3 gene cause X-linked mental retardation associated with macrocephalyMichael Field, Patrick S Tarpey, Raffaella Smith, et al.
American Journal of Human Genetics|December 23, 2006
Mutations in the gene encoding the Sigma 2 subunit of the adaptor protein 1 complex, AP1S2, cause X-linked mental retardationPatrick S Tarpey, Claire Stevens, Jon Teague, et al.
American Journal of Human Genetics|January 20, 2007
Mutations in CUL4B, which encodes a ubiquitin E3 ligase subunit, cause an X-linked mental retardation syndrome associated with aggressive outbursts, seizures, relative macrocephaly, central obesity, hypogonadism, pes cavus, and tremorPatrick S Tarpey, F Lucy Raymond, Sarah O'Meara, et al.
Pageof 2