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Human Molecular Genetics
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January 3, 2018
Myostatin inhibition using mRK35 produces skeletal muscle growth and tubular aggregate formation in wild type and TgACTA1D286G nemaline myopathy mice
Jennifer A Tinklenberg, Emily M Siebers, Margaret J Beatka, et al.
Expert Review of Vaccines
|
November 16, 2018
Development of a measure to assess vaccine confidence among men who have sex with men
Paula M Frew, Ian W Holloway, Cameron Goldbeck, et al.
Genome Research
|
February 21, 1998
Contig maps and genomic sequencing identify candidate genes in the usher 1C locus
M J Higgins, C D Day, N J Smilinich, et al.
Genomics
|
August 1, 1997
A 1-Mb physical map and PAC contig of the imprinted domain in 11p15.5 that contains TAPA1 and the BWSCR1/WT2 region
L H Reid, C Davies, P R Cooper, et al.
Plos One
|
February 9, 2017
Identification of a vacuolar proton channel that triggers the bioluminescent flash in dinoflagellates
Juan D Rodriguez, Saddef Haq, Tsvetan Bachvaroff, et al.
Clinical and Translational Gastroenterology
|
November 3, 2018
Clinical Heterogeneity of Immune Dysregulation, Polyendocrinopathy, Enteropathy, X-Linked Syndrome: A French Multicenter Retrospective Study
R Duclaux-Loras, F Charbit-Henrion, B Neven, et al.
Archives of Otolaryngology--Head & Neck Surgery
|
May 23, 2007
Comparative genomic instabilities of thyroid and colon cancers
Daniel L Stoler, Norma J Nowak, Sei-ichi Matsui, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
November 17, 2020
Thymus-derived B cell clones persist in the circulation after thymectomy in myasthenia gravis
Ruoyi Jiang, Kenneth B Hoehn, Casey S Lee, et al.
Neuromuscular Disorders : NMD
|
September 2, 2006
Severe nemaline myopathy caused by mutations of the stop codon of the skeletal muscle alpha actin gene (ACTA1)
William Wallefeld, Sabine Krause, Kristen J Nowak, et al.
Cancer Research
|
September 23, 2003
Genome-wide array CGH analysis of murine neuroblastoma reveals distinct genomic aberrations which parallel those in human tumors
Christopher S Hackett, J Graeme Hodgson, Mark E Law, et al.
Page
of 81
Search research articles
Search
Showing results (701-710 of 807) with videos related to
Sort By:
Page
of 81
Human Molecular Genetics
|
January 3, 2018
Myostatin inhibition using mRK35 produces skeletal muscle growth and tubular aggregate formation in wild type and TgACTA1D286G nemaline myopathy mice
Jennifer A Tinklenberg, Emily M Siebers, Margaret J Beatka, et al.
Expert Review of Vaccines
|
November 16, 2018
Development of a measure to assess vaccine confidence among men who have sex with men
Paula M Frew, Ian W Holloway, Cameron Goldbeck, et al.
Genome Research
|
February 21, 1998
Contig maps and genomic sequencing identify candidate genes in the usher 1C locus
M J Higgins, C D Day, N J Smilinich, et al.
Genomics
|
August 1, 1997
A 1-Mb physical map and PAC contig of the imprinted domain in 11p15.5 that contains TAPA1 and the BWSCR1/WT2 region
L H Reid, C Davies, P R Cooper, et al.
Plos One
|
February 9, 2017
Identification of a vacuolar proton channel that triggers the bioluminescent flash in dinoflagellates
Juan D Rodriguez, Saddef Haq, Tsvetan Bachvaroff, et al.
Clinical and Translational Gastroenterology
|
November 3, 2018
Clinical Heterogeneity of Immune Dysregulation, Polyendocrinopathy, Enteropathy, X-Linked Syndrome: A French Multicenter Retrospective Study
R Duclaux-Loras, F Charbit-Henrion, B Neven, et al.
Archives of Otolaryngology--Head & Neck Surgery
|
May 23, 2007
Comparative genomic instabilities of thyroid and colon cancers
Daniel L Stoler, Norma J Nowak, Sei-ichi Matsui, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
November 17, 2020
Thymus-derived B cell clones persist in the circulation after thymectomy in myasthenia gravis
Ruoyi Jiang, Kenneth B Hoehn, Casey S Lee, et al.
Neuromuscular Disorders : NMD
|
September 2, 2006
Severe nemaline myopathy caused by mutations of the stop codon of the skeletal muscle alpha actin gene (ACTA1)
William Wallefeld, Sabine Krause, Kristen J Nowak, et al.
Cancer Research
|
September 23, 2003
Genome-wide array CGH analysis of murine neuroblastoma reveals distinct genomic aberrations which parallel those in human tumors
Christopher S Hackett, J Graeme Hodgson, Mark E Law, et al.
Page
of 81