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Showing results (271-280 of 299) with videos related to

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Proceedings of the National Academy of Sciences of the United States of America|April 30, 2008
Inhibition of neural crest migration underlies craniofacial dysmorphology and Hirschsprung's disease in Bardet-Biedl syndromeJonathan L Tobin, Matt Di Franco, Erica Eichers, et al.
Blood|May 23, 2007
Mutations in the cofilin partner Aip1/Wdr1 cause autoinflammatory disease and macrothrombocytopeniaBenjamin T Kile, Athanasia D Panopoulos, Roslynn A Stirzaker, et al.
Nature Genetics|July 1, 1996
Identification of the murine beige gene by YAC complementation and positional cloningC M Perou, K J Moore, D L Nagle, et al.
Stem Cells (Dayton, Ohio)|October 21, 2014
Human adipose-derived stem cells ameliorate cigarette smoke-induced murine myelosuppression via secretion of TSG-6Jie Xie, Hal E Broxmeyer, Dongni Feng, et al.
Plos One|April 12, 2014
Comparative analyses of lung transcriptomes in patients with alveolar capillary dysplasia with misalignment of pulmonary veins and in foxf1 heterozygous knockout micePartha Sen, Avinash V Dharmadhikari, Tadeusz Majewski, et al.
Hormones and Behavior|March 1, 2026
Sex differences in corticotropin-releasing factor receptor-2α expressing neurons in acutely stressed miceJennifer J Lafrican, Katherine E Parra, Krystyna A Rybka, et al.
Human Molecular Genetics|February 5, 2020
Deficiency of FRAS1-related extracellular matrix 1 (FREM1) causes congenital diaphragmatic hernia in humans and miceTyler F Beck, Danielle Veenma, Oleg A Shchelochkov, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|March 18, 2021
Dissociable Roles of Pallidal Neuron Subtypes in Regulating Motor PatternsQiaoling Cui, Arin Pamukcu, Suraj Cherian, et al.
Human Molecular Genetics|December 11, 2012
Deficiency of FRAS1-related extracellular matrix 1 (FREM1) causes congenital diaphragmatic hernia in humans and miceTyler F Beck, Danielle Veenma, Oleg A Shchelochkov, et al.
Plos Genetics|June 16, 2010
Mice with alopecia, osteoporosis, and systemic amyloidosis due to mutation in Zdhhc13, a gene coding for palmitoyl acyltransferaseAmir N Saleem, Yen-Hui Chen, Hwa Jin Baek, et al.
Pageof 30

Showing results (271-280 of 299) with videos related to

Sort By:
Pageof 30
Proceedings of the National Academy of Sciences of the United States of America|April 30, 2008
Inhibition of neural crest migration underlies craniofacial dysmorphology and Hirschsprung's disease in Bardet-Biedl syndromeJonathan L Tobin, Matt Di Franco, Erica Eichers, et al.
Blood|May 23, 2007
Mutations in the cofilin partner Aip1/Wdr1 cause autoinflammatory disease and macrothrombocytopeniaBenjamin T Kile, Athanasia D Panopoulos, Roslynn A Stirzaker, et al.
Nature Genetics|July 1, 1996
Identification of the murine beige gene by YAC complementation and positional cloningC M Perou, K J Moore, D L Nagle, et al.
Stem Cells (Dayton, Ohio)|October 21, 2014
Human adipose-derived stem cells ameliorate cigarette smoke-induced murine myelosuppression via secretion of TSG-6Jie Xie, Hal E Broxmeyer, Dongni Feng, et al.
Plos One|April 12, 2014
Comparative analyses of lung transcriptomes in patients with alveolar capillary dysplasia with misalignment of pulmonary veins and in foxf1 heterozygous knockout micePartha Sen, Avinash V Dharmadhikari, Tadeusz Majewski, et al.
Hormones and Behavior|March 1, 2026
Sex differences in corticotropin-releasing factor receptor-2α expressing neurons in acutely stressed miceJennifer J Lafrican, Katherine E Parra, Krystyna A Rybka, et al.
Human Molecular Genetics|February 5, 2020
Deficiency of FRAS1-related extracellular matrix 1 (FREM1) causes congenital diaphragmatic hernia in humans and miceTyler F Beck, Danielle Veenma, Oleg A Shchelochkov, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|March 18, 2021
Dissociable Roles of Pallidal Neuron Subtypes in Regulating Motor PatternsQiaoling Cui, Arin Pamukcu, Suraj Cherian, et al.
Human Molecular Genetics|December 11, 2012
Deficiency of FRAS1-related extracellular matrix 1 (FREM1) causes congenital diaphragmatic hernia in humans and miceTyler F Beck, Danielle Veenma, Oleg A Shchelochkov, et al.
Plos Genetics|June 16, 2010
Mice with alopecia, osteoporosis, and systemic amyloidosis due to mutation in Zdhhc13, a gene coding for palmitoyl acyltransferaseAmir N Saleem, Yen-Hui Chen, Hwa Jin Baek, et al.
Pageof 30