B Beatty - JoVE Visualize

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Genomics|May 15, 1997

Mapping of the gene encoding the integrin-linked kinase, ILK, to human chromosome 11p15.5-p15.4G E Hannigan, J Bayani, R Weksberg, et al.

Biochemical and Biophysical Research Communications|July 2, 1998

Structural characterization and mapping of the normal epithelial cell-specific 1 geneL Luo, J A Herbrick, S W Scherer, et al.

Genomics|November 5, 1997

Chromosomal mapping of the human and murine orphan receptors ERRalpha (ESRRA) and ERRbeta (ESRRB) and identification of a novel human ERRalpha-related pseudogeneR Sladek, B Beatty, J Squire, et al.

Mammalian Genome : Official Journal of the International Mammalian Genome Society|January 1, 1997

Human and murine PTX1/Ptx1 gene maps to the region for Treacher Collins syndromeM J Crawford, C Lanctôt, J J Tremblay, et al.

Oncogene|June 17, 1998

Down-regulation of T1A12/mac25, a novel insulin-like growth factor binding protein related gene, is associated with disease progression in breast carcinomasA M Burger, X Zhang, H Li, et al.

Obstetrical & Gynecological Survey|November 17, 2023

Optimizing Surgical Wound Care in Obstetrics and GynecologyJulia R Salinaro, Penny S Jones, Amelia B Beatty, et al.

Human Molecular Genetics|April 18, 1998

Detection of a homozygous four base pair deletion in the protein X gene in a case of pyruvate dehydrogenase complex deficiencyM Ling, G McEachern, A Seyda, et al.

Health Education & Behavior : the Official Publication of the Society for Public Health Education|April 18, 2000

The North Carolina Black Churches United for Better Health Project: intervention and process evaluationM K Campbell, B M Motsinger, A Ingram, et al.

Gene Therapy|September 7, 1999

Metabolic instability of plasmid DNA in the cytosol: a potential barrier to gene transferD Lechardeur, K J Sohn, M Haardt, et al.

Genomics|February 12, 1998

Characterization of the gene encoding human sarcolipin (SLN), a proteolipid associated with SERCA1: absence of structural mutations in five patients with Brody diseaseA Odermatt, P E Taschner, S W Scherer, et al.

Pageof 3

Showing results (11-20 of 23) with videos related to

Sort By:

Pageof 3

Genomics|May 15, 1997

Mapping of the gene encoding the integrin-linked kinase, ILK, to human chromosome 11p15.5-p15.4G E Hannigan, J Bayani, R Weksberg, et al.

Biochemical and Biophysical Research Communications|July 2, 1998

Structural characterization and mapping of the normal epithelial cell-specific 1 geneL Luo, J A Herbrick, S W Scherer, et al.

Genomics|November 5, 1997

Chromosomal mapping of the human and murine orphan receptors ERRalpha (ESRRA) and ERRbeta (ESRRB) and identification of a novel human ERRalpha-related pseudogeneR Sladek, B Beatty, J Squire, et al.

Mammalian Genome : Official Journal of the International Mammalian Genome Society|January 1, 1997

Human and murine PTX1/Ptx1 gene maps to the region for Treacher Collins syndromeM J Crawford, C Lanctôt, J J Tremblay, et al.

Oncogene|June 17, 1998

Down-regulation of T1A12/mac25, a novel insulin-like growth factor binding protein related gene, is associated with disease progression in breast carcinomasA M Burger, X Zhang, H Li, et al.

Obstetrical & Gynecological Survey|November 17, 2023

Optimizing Surgical Wound Care in Obstetrics and GynecologyJulia R Salinaro, Penny S Jones, Amelia B Beatty, et al.

Human Molecular Genetics|April 18, 1998

Detection of a homozygous four base pair deletion in the protein X gene in a case of pyruvate dehydrogenase complex deficiencyM Ling, G McEachern, A Seyda, et al.

Health Education & Behavior : the Official Publication of the Society for Public Health Education|April 18, 2000

The North Carolina Black Churches United for Better Health Project: intervention and process evaluationM K Campbell, B M Motsinger, A Ingram, et al.

Gene Therapy|September 7, 1999

Metabolic instability of plasmid DNA in the cytosol: a potential barrier to gene transferD Lechardeur, K J Sohn, M Haardt, et al.

Genomics|February 12, 1998

Characterization of the gene encoding human sarcolipin (SLN), a proteolipid associated with SERCA1: absence of structural mutations in five patients with Brody diseaseA Odermatt, P E Taschner, S W Scherer, et al.

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