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Genome Research
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August 7, 2007
Architectures of somatic genomic rearrangement in human cancer amplicons at sequence-level resolution
Graham R Bignell, Thomas Santarius, Jessica C M Pole, et al.
Molecular Cancer Therapeutics
|
October 26, 2019
Targeting the Somatostatin Receptor 2 with the Miniaturized Drug Conjugate, PEN-221: A Potent and Novel Therapeutic for the Treatment of Small Cell Lung Cancer
Kerry A Whalen, Brian H White, James M Quinn, et al.
Breast Cancer Research : BCR
|
July 3, 2016
Genome co-amplification upregulates a mitotic gene network activity that predicts outcome and response to mitotic protein inhibitors in breast cancer
Zhi Hu, Jian-Hua Mao, Christina Curtis, et al.
Breast Cancer Research : BCR
|
February 11, 2017
Erratum to: Genome co-amplification upregulates a mitotic gene network activity that predicts outcome and response to mitotic protein inhibitors in breast cancer
Zhi Hu, Jian-Hua Mao, Christina Curtis, et al.
American Journal of Human Genetics
|
June 9, 2004
Mutations in the DLG3 gene cause nonsyndromic X-linked mental retardation
Patrick Tarpey, Josep Parnau, Matthew Blow, 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 habitus
F 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 set
Ogechi 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 macrocephaly
Michael Field, Patrick S Tarpey, Raffaella Smith, et al.
Nature Genetics
|
October 3, 2006
Mutations in FRMD7, a newly identified member of the FERM family, cause X-linked idiopathic congenital nystagmus
Patrick Tarpey, Shery Thomas, Nagini Sarvananthan, 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 retardation
Patrick S Tarpey, Claire Stevens, Jon Teague, et al.
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of 7
Search research articles
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Showing results (41-50 of 61) with videos related to
Sort By:
Page
of 7
Genome Research
|
August 7, 2007
Architectures of somatic genomic rearrangement in human cancer amplicons at sequence-level resolution
Graham R Bignell, Thomas Santarius, Jessica C M Pole, et al.
Molecular Cancer Therapeutics
|
October 26, 2019
Targeting the Somatostatin Receptor 2 with the Miniaturized Drug Conjugate, PEN-221: A Potent and Novel Therapeutic for the Treatment of Small Cell Lung Cancer
Kerry A Whalen, Brian H White, James M Quinn, et al.
Breast Cancer Research : BCR
|
July 3, 2016
Genome co-amplification upregulates a mitotic gene network activity that predicts outcome and response to mitotic protein inhibitors in breast cancer
Zhi Hu, Jian-Hua Mao, Christina Curtis, et al.
Breast Cancer Research : BCR
|
February 11, 2017
Erratum to: Genome co-amplification upregulates a mitotic gene network activity that predicts outcome and response to mitotic protein inhibitors in breast cancer
Zhi Hu, Jian-Hua Mao, Christina Curtis, et al.
American Journal of Human Genetics
|
June 9, 2004
Mutations in the DLG3 gene cause nonsyndromic X-linked mental retardation
Patrick Tarpey, Josep Parnau, Matthew Blow, 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 habitus
F 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 set
Ogechi 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 macrocephaly
Michael Field, Patrick S Tarpey, Raffaella Smith, et al.
Nature Genetics
|
October 3, 2006
Mutations in FRMD7, a newly identified member of the FERM family, cause X-linked idiopathic congenital nystagmus
Patrick Tarpey, Shery Thomas, Nagini Sarvananthan, 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 retardation
Patrick S Tarpey, Claire Stevens, Jon Teague, et al.
Page
of 7