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J Vacha

Showing results (1-10 of 5) with videos related to

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Developmental Biology|July 26, 2005
Connexin43 deficiency causes dysregulation of coronary vasculogenesisDiana L Walker, Scott J Vacha, Margaret L Kirby, et al.
Clinical Genetics|January 5, 2001
Sudden death caused by pulmonary thromboembolism in Proteus syndromeA M Slavotinek, S J Vacha, K F Peters, et al.
Journal of Clinical Periodontology|July 20, 2004
Genetic variations in the matrix metalloproteinase-1 promoter and risk of susceptibility and/or severity of chronic periodontitis in the Czech populationL Izakovicová Hollá, M Jurajda, A Fassmann, et al.
Developmental Genetics|January 1, 1997
Identification of a growth arrest specific (gas 5) gene by differential display as a candidate gene for determining susceptibility to hyperthermia-induced exencephaly in miceS J Vacha, G D Bennett, S A Mackler, et al.
Tissue Antigens|February 17, 2005
Association of tumour necrosis factor-alpha, lymphotoxin-alpha and HLA-DRB1 gene polymorphisms with Löfgren's syndrome in Czech patients with sarcoidosisF Mrazek, L I Holla, B Hutyrova, et al.
Pageof 1

Showing results (1-10 of 5) with videos related to

Sort By:
Pageof 1
Developmental Biology|July 26, 2005
Connexin43 deficiency causes dysregulation of coronary vasculogenesisDiana L Walker, Scott J Vacha, Margaret L Kirby, et al.
Clinical Genetics|January 5, 2001
Sudden death caused by pulmonary thromboembolism in Proteus syndromeA M Slavotinek, S J Vacha, K F Peters, et al.
Journal of Clinical Periodontology|July 20, 2004
Genetic variations in the matrix metalloproteinase-1 promoter and risk of susceptibility and/or severity of chronic periodontitis in the Czech populationL Izakovicová Hollá, M Jurajda, A Fassmann, et al.
Developmental Genetics|January 1, 1997
Identification of a growth arrest specific (gas 5) gene by differential display as a candidate gene for determining susceptibility to hyperthermia-induced exencephaly in miceS J Vacha, G D Bennett, S A Mackler, et al.
Tissue Antigens|February 17, 2005
Association of tumour necrosis factor-alpha, lymphotoxin-alpha and HLA-DRB1 gene polymorphisms with Löfgren's syndrome in Czech patients with sarcoidosisF Mrazek, L I Holla, B Hutyrova, et al.
Pageof 1