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Y Matsubara

Showing results (171-180 of 367) with videos related to

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Prenatal Diagnosis|January 1, 1992
Prenatal exclusion of medium-chain acyl-CoA dehydrogenase (MCAD) deficiency by direct detection of the mutation with PCRJ Hendrickx, P Van Osta, F Eyskens, et al.
Journal of Comparative Pathology|April 1, 1995
Granulomatous lesions caused by Pseudomonas aeruginosa in the ostrich (Struthio camelus)E Momotani, M Kiryu, M Ohshiro, et al.
Journal of Reproduction and Fertility|May 1, 1996
Penetration by field vole spermatozoa of mouse and hamster zonae pellucidae without acrosome reactionT Wakayama, A Ogura, J Suto, et al.
Animal Genetics|December 12, 2001
Cloning of porcine IGF1 receptor cDNA and detection of sequence polymorphisms using RT-PCRT Harumi, K Maruyama, H Kagami, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|November 8, 2001
GJB2 (connexin 26) mutations and childhood deafness in ThailandT Kudo, K Ikeda, T Oshima, et al.
Digestive Diseases and Sciences|September 1, 1992
Intestinal fatty acid-binding protein as a sensitive marker of intestinal ischemiaT Kanda, Y Nakatomi, H Ishikawa, et al.
The Thoracic and Cardiovascular Surgeon|June 7, 2006
Clinical impact of interstitial pneumonia following surgery for lung cancerS Takeda, H Maeda, N Sawabata, et al.
Journal of the Neurological Sciences|October 1, 1994
Familial amyotrophic lateral sclerosis (ALS) in Japan associated with H46R mutation in Cu/Zn superoxide dismutase gene: a possible new subtype of familial ALSM Aoki, M Ogasawara, Y Matsubara, et al.
Masui. the Japanese Journal of Anesthesiology|October 1, 1987
[The effect of epidural anesthesia on arrhythmia during funnel chest operation]K Tsuda, M Oda, M Tadokoro, et al.
Journal of Human Genetics|September 25, 1999
Molecular analysis of Japanese patients with steroid 21-hydroxylase deficiencyA Asanuma, T Ohura, E Ogawa, et al.
Pageof 37

Showing results (171-180 of 367) with videos related to

Sort By:
Pageof 37
Prenatal Diagnosis|January 1, 1992
Prenatal exclusion of medium-chain acyl-CoA dehydrogenase (MCAD) deficiency by direct detection of the mutation with PCRJ Hendrickx, P Van Osta, F Eyskens, et al.
Journal of Comparative Pathology|April 1, 1995
Granulomatous lesions caused by Pseudomonas aeruginosa in the ostrich (Struthio camelus)E Momotani, M Kiryu, M Ohshiro, et al.
Journal of Reproduction and Fertility|May 1, 1996
Penetration by field vole spermatozoa of mouse and hamster zonae pellucidae without acrosome reactionT Wakayama, A Ogura, J Suto, et al.
Animal Genetics|December 12, 2001
Cloning of porcine IGF1 receptor cDNA and detection of sequence polymorphisms using RT-PCRT Harumi, K Maruyama, H Kagami, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|November 8, 2001
GJB2 (connexin 26) mutations and childhood deafness in ThailandT Kudo, K Ikeda, T Oshima, et al.
Digestive Diseases and Sciences|September 1, 1992
Intestinal fatty acid-binding protein as a sensitive marker of intestinal ischemiaT Kanda, Y Nakatomi, H Ishikawa, et al.
The Thoracic and Cardiovascular Surgeon|June 7, 2006
Clinical impact of interstitial pneumonia following surgery for lung cancerS Takeda, H Maeda, N Sawabata, et al.
Journal of the Neurological Sciences|October 1, 1994
Familial amyotrophic lateral sclerosis (ALS) in Japan associated with H46R mutation in Cu/Zn superoxide dismutase gene: a possible new subtype of familial ALSM Aoki, M Ogasawara, Y Matsubara, et al.
Masui. the Japanese Journal of Anesthesiology|October 1, 1987
[The effect of epidural anesthesia on arrhythmia during funnel chest operation]K Tsuda, M Oda, M Tadokoro, et al.
Journal of Human Genetics|September 25, 1999
Molecular analysis of Japanese patients with steroid 21-hydroxylase deficiencyA Asanuma, T Ohura, E Ogawa, et al.
Pageof 37