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L Yamamoto

Showing results (141-150 of 161) with videos related to

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American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|October 31, 2020
Phenotype-genotype analysis of 242 individuals with RASopathies: 18-year experience of a tertiary center in BrazilDébora R Bertola, Matheus A A Castro, Guilherme L Yamamoto, et al.
Journal of Cachexia, Sarcopenia and Muscle|October 25, 2019
Myopalladin promotes muscle growth through modulation of the serum response factor pathwayMaria Carmela Filomena, Daniel L Yamamoto, Marco Caremani, et al.
Scientific Reports|June 9, 2018
Characterization of a novel MYO3A missense mutation associated with a dominant form of late onset hearing lossVitor G L Dantas, Manmeet H Raval, Angela Ballesteros, et al.
Cancer Research|July 18, 2013
Intestinal bacteria modify lymphoma incidence and latency by affecting systemic inflammatory state, oxidative stress, and leukocyte genotoxicityMitsuko L Yamamoto, Irene Maier, Angeline Tilly Dang, et al.
The Journal of Clinical Endocrinology and Metabolism|November 21, 2017
IHH Gene Mutations Causing Short Stature With Nonspecific Skeletal Abnormalities and Response to Growth Hormone TherapyGabriela A Vasques, Mariana F A Funari, Frederico M Ferreira, et al.
Disease Models & Mechanisms|December 13, 2019
Altered <i>in vitro</i> muscle differentiation in X-linked myopathy with excessive autophagyStephanie A Fernandes, Camila F Almeida, Lucas S Souza, et al.
Journal of Cell Science|September 19, 2013
The nebulin SH3 domain is dispensable for normal skeletal muscle structure but is required for effective active load bearing in mouseDaniel L Yamamoto, Carmen Vitiello, Jianlin Zhang, et al.
Elife|September 24, 2021
Myopalladin knockout mice develop cardiac dilation and show a maladaptive response to mechanical pressure overloadMaria Carmela Filomena, Daniel L Yamamoto, Pierluigi Carullo, et al.
Genetics and Molecular Biology|July 26, 2018
Development of a comprehensive noninvasive prenatal testCarolina Malcher, Guilherme L Yamamoto, Philip Burnham, et al.
Bone|January 2, 2019
Novel fibronectin mutations and expansion of the phenotype in spondylometaphyseal dysplasia with "corner fractures"Alice Costantini, Helena Valta, Nissan Vida Baratang, et al.
Pageof 17

Showing results (141-150 of 161) with videos related to

Sort By:
Pageof 17
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|October 31, 2020
Phenotype-genotype analysis of 242 individuals with RASopathies: 18-year experience of a tertiary center in BrazilDébora R Bertola, Matheus A A Castro, Guilherme L Yamamoto, et al.
Journal of Cachexia, Sarcopenia and Muscle|October 25, 2019
Myopalladin promotes muscle growth through modulation of the serum response factor pathwayMaria Carmela Filomena, Daniel L Yamamoto, Marco Caremani, et al.
Scientific Reports|June 9, 2018
Characterization of a novel MYO3A missense mutation associated with a dominant form of late onset hearing lossVitor G L Dantas, Manmeet H Raval, Angela Ballesteros, et al.
Cancer Research|July 18, 2013
Intestinal bacteria modify lymphoma incidence and latency by affecting systemic inflammatory state, oxidative stress, and leukocyte genotoxicityMitsuko L Yamamoto, Irene Maier, Angeline Tilly Dang, et al.
The Journal of Clinical Endocrinology and Metabolism|November 21, 2017
IHH Gene Mutations Causing Short Stature With Nonspecific Skeletal Abnormalities and Response to Growth Hormone TherapyGabriela A Vasques, Mariana F A Funari, Frederico M Ferreira, et al.
Disease Models & Mechanisms|December 13, 2019
Altered <i>in vitro</i> muscle differentiation in X-linked myopathy with excessive autophagyStephanie A Fernandes, Camila F Almeida, Lucas S Souza, et al.
Journal of Cell Science|September 19, 2013
The nebulin SH3 domain is dispensable for normal skeletal muscle structure but is required for effective active load bearing in mouseDaniel L Yamamoto, Carmen Vitiello, Jianlin Zhang, et al.
Elife|September 24, 2021
Myopalladin knockout mice develop cardiac dilation and show a maladaptive response to mechanical pressure overloadMaria Carmela Filomena, Daniel L Yamamoto, Pierluigi Carullo, et al.
Genetics and Molecular Biology|July 26, 2018
Development of a comprehensive noninvasive prenatal testCarolina Malcher, Guilherme L Yamamoto, Philip Burnham, et al.
Bone|January 2, 2019
Novel fibronectin mutations and expansion of the phenotype in spondylometaphyseal dysplasia with "corner fractures"Alice Costantini, Helena Valta, Nissan Vida Baratang, et al.
Pageof 17