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B Friedman

Showing results (921-930 of 968) with videos related to

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Cell|June 1, 2010
Actin-bundling protein TRIOBP forms resilient rootlets of hair cell stereocilia essential for hearingShin-ichiro Kitajiri, Takeshi Sakamoto, Inna A Belyantseva, et al.
Journal of the Endocrine Society|April 3, 2026
Insulin receptor expression and its association with hyperinsulinemia in triple negative breast cancerAlexis J Engel, Krupa Samuel, Ilana R Bass, et al.
The Journal of Clinical Investigation|December 22, 2012
Iron deficiency accelerates Helicobacter pylori-induced carcinogenesis in rodents and humansJennifer M Noto, Jennifer A Gaddy, Josephine Y Lee, et al.
Implementation Science Communications|July 14, 2023
Implementing shared decision making for early-stage breast cancer treatment using a coproduction learning collaborative: the SHAIR Collaborative protocolDanielle Schubbe, Renata W Yen, Hannah Leavitt, et al.
Cancer Control : Journal of the Moffitt Cancer Center|November 9, 2021
Acral Lentiginous Melanoma: A United States Multi-Center Substage Survival AnalysisAvani M Kolla, Gerardo A Vitiello, Erica B Friedman, et al.
Plos One|February 26, 2013
Intravenous glial growth factor 2 (GGF2) isoform of neuregulin-1β improves left ventricular function, gene and protein expression in rats after myocardial infarctionMichael F Hill, Amish V Patel, Abigail Murphy, et al.
Human Genetics|July 8, 1998
Correlation between Waardenburg syndrome phenotype and genotype in a population of individuals with identified PAX3 mutationsA L DeStefano, L A Cupples, K S Arnos, et al.
Human Mutation|July 15, 2021
Variants of human CLDN9 cause mild to profound hearing lossMemoona Ramzan, Christophe Philippe, Inna A Belyantseva, et al.
American Journal of Human Genetics|February 9, 2010
Mutations in Grxcr1 are the basis for inner ear dysfunction in the pirouette mouseHana Odeh, Kristina L Hunker, Inna A Belyantseva, et al.
Human Molecular Genetics|January 3, 2019
The phenotypic landscape of a Tbc1d24 mutant mouse includes convulsive seizures resembling human early infantile epileptic encephalopathyRisa Tona, Wenqian Chen, Yoko Nakano, et al.
Pageof 97

Showing results (921-930 of 968) with videos related to

Sort By:
Pageof 97
Cell|June 1, 2010
Actin-bundling protein TRIOBP forms resilient rootlets of hair cell stereocilia essential for hearingShin-ichiro Kitajiri, Takeshi Sakamoto, Inna A Belyantseva, et al.
Journal of the Endocrine Society|April 3, 2026
Insulin receptor expression and its association with hyperinsulinemia in triple negative breast cancerAlexis J Engel, Krupa Samuel, Ilana R Bass, et al.
The Journal of Clinical Investigation|December 22, 2012
Iron deficiency accelerates Helicobacter pylori-induced carcinogenesis in rodents and humansJennifer M Noto, Jennifer A Gaddy, Josephine Y Lee, et al.
Implementation Science Communications|July 14, 2023
Implementing shared decision making for early-stage breast cancer treatment using a coproduction learning collaborative: the SHAIR Collaborative protocolDanielle Schubbe, Renata W Yen, Hannah Leavitt, et al.
Cancer Control : Journal of the Moffitt Cancer Center|November 9, 2021
Acral Lentiginous Melanoma: A United States Multi-Center Substage Survival AnalysisAvani M Kolla, Gerardo A Vitiello, Erica B Friedman, et al.
Plos One|February 26, 2013
Intravenous glial growth factor 2 (GGF2) isoform of neuregulin-1β improves left ventricular function, gene and protein expression in rats after myocardial infarctionMichael F Hill, Amish V Patel, Abigail Murphy, et al.
Human Genetics|July 8, 1998
Correlation between Waardenburg syndrome phenotype and genotype in a population of individuals with identified PAX3 mutationsA L DeStefano, L A Cupples, K S Arnos, et al.
Human Mutation|July 15, 2021
Variants of human CLDN9 cause mild to profound hearing lossMemoona Ramzan, Christophe Philippe, Inna A Belyantseva, et al.
American Journal of Human Genetics|February 9, 2010
Mutations in Grxcr1 are the basis for inner ear dysfunction in the pirouette mouseHana Odeh, Kristina L Hunker, Inna A Belyantseva, et al.
Human Molecular Genetics|January 3, 2019
The phenotypic landscape of a Tbc1d24 mutant mouse includes convulsive seizures resembling human early infantile epileptic encephalopathyRisa Tona, Wenqian Chen, Yoko Nakano, et al.
Pageof 97