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Y Jinno

Showing results (81-90 of 130) with videos related to

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Nature Genetics|March 1, 1994
Mosaic and polymorphic imprinting of the WT1 gene in humansY Jinno, K Yun, K Nishiwaki, et al.
The Japanese Journal of Human Genetics|June 1, 1997
The growth hormone receptor gene mutation of a Japanese patient with Laron syndromeT Otsuka, N Iwatani, M Kodama, et al.
Lancet (London, England)|February 8, 1992
Familial Angelman syndrome caused by imprinted submicroscopic deletion encompassing GABAA receptor beta 3-subunit geneS Saitoh, T Kubota, T Ohta, et al.
Journal of Oral Rehabilitation|November 6, 2009
Simvastatin enhances bone formation around titanium implants in rat tibiaeY Ayukawa, Y Ogino, Y Moriyama, et al.
British Journal of Pharmacology|July 1, 1993
Vasorelaxant mechanism of KRN2391 and nicorandil in porcine coronary arteries of different sizesA Miwa, S Kaneta, K Motoki, et al.
Gene|December 15, 1992
Characterization of the gene encoding human pituitary-specific transcription factor, Pit-1K Ohta, Y Nobukuni, H Mitsubuchi, et al.
Genome Research|May 16, 2000
Comparative genomic sequencing identifies novel tissue-specific enhancers and sequence elements for methylation-sensitive factors implicated in Igf2/H19 imprintingK Ishihara, N Hatano, H Furuumi, et al.
Human Genetics|August 1, 1993
The origin of cytologically unidentifiable chromosome abnormalities: six cases ascertained by targeted chromosome-band paintingT Ohta, T Tohma, H Soejima, et al.
The Journal of Biological Chemistry|September 25, 1989
Domain II mutants of Pseudomonas exotoxin deficient in translocationY Jinno, M Ogata, V K Chaudhary, et al.
Jinrui Idengaku Zasshi. the Japanese Journal of Human Genetics|September 1, 1986
Localization of the human prealbumin gene to 18p11.1-q12.3 by gene dose effect study of Southern blot hybridizationY Jinno, T Matsumoto, T Kamel, et al.
Pageof 13

Showing results (81-90 of 130) with videos related to

Sort By:
Pageof 13
Nature Genetics|March 1, 1994
Mosaic and polymorphic imprinting of the WT1 gene in humansY Jinno, K Yun, K Nishiwaki, et al.
The Japanese Journal of Human Genetics|June 1, 1997
The growth hormone receptor gene mutation of a Japanese patient with Laron syndromeT Otsuka, N Iwatani, M Kodama, et al.
Lancet (London, England)|February 8, 1992
Familial Angelman syndrome caused by imprinted submicroscopic deletion encompassing GABAA receptor beta 3-subunit geneS Saitoh, T Kubota, T Ohta, et al.
Journal of Oral Rehabilitation|November 6, 2009
Simvastatin enhances bone formation around titanium implants in rat tibiaeY Ayukawa, Y Ogino, Y Moriyama, et al.
British Journal of Pharmacology|July 1, 1993
Vasorelaxant mechanism of KRN2391 and nicorandil in porcine coronary arteries of different sizesA Miwa, S Kaneta, K Motoki, et al.
Gene|December 15, 1992
Characterization of the gene encoding human pituitary-specific transcription factor, Pit-1K Ohta, Y Nobukuni, H Mitsubuchi, et al.
Genome Research|May 16, 2000
Comparative genomic sequencing identifies novel tissue-specific enhancers and sequence elements for methylation-sensitive factors implicated in Igf2/H19 imprintingK Ishihara, N Hatano, H Furuumi, et al.
Human Genetics|August 1, 1993
The origin of cytologically unidentifiable chromosome abnormalities: six cases ascertained by targeted chromosome-band paintingT Ohta, T Tohma, H Soejima, et al.
The Journal of Biological Chemistry|September 25, 1989
Domain II mutants of Pseudomonas exotoxin deficient in translocationY Jinno, M Ogata, V K Chaudhary, et al.
Jinrui Idengaku Zasshi. the Japanese Journal of Human Genetics|September 1, 1986
Localization of the human prealbumin gene to 18p11.1-q12.3 by gene dose effect study of Southern blot hybridizationY Jinno, T Matsumoto, T Kamel, et al.
Pageof 13