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M Fukami

Showing results (51-60 of 65) with videos related to

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Arzneimittel-Forschung|November 1, 1991
Antiarrhythmic and cardiovascular profiles of the fused indole compound (3aR,12R,12aR,12bS)-12-amino-2,3,3a,4,11,12,12a,12b-octahydro-10-hydrox yisoquino [2,1,8-lma]carbazol-5(1H)-one hydrochloride 1.5 hydrateR Yorikane, H Mizuno, Y Itoh, et al.
DNA Research : an International Journal for Rapid Publication of Reports on Genes and Genomes|March 21, 1998
A fine physical map of Arabidopsis thaliana chromosome 5: construction of a sequence-ready contig mapH Kotani, S Sato, M Fukami, et al.
Animal Genetics|September 12, 2015
Copy number variations in the amylase gene (AMY2B) in Japanese native dog breedsA Tonoike, Y Hori, M Inoue-Murayama, et al.
Human Genetics|August 1, 1997
FISH-deletion mapping defines a 270-kb short stature critical interval in the pseudoautosomal region PAR1 on human sex chromosomesE Rao, B Weiss, M Fukami, et al.
European Journal of Human Genetics : EJHG|March 14, 2000
Phenotypic variation and genetic heterogeneity in Léri-Weill syndromeS Schiller, S Spranger, B Schechinger, et al.
Diabetic Medicine : a Journal of the British Diabetic Association|December 25, 2019
Low prevalence of maternal microchimerism in peripheral blood of Japanese children with type 1 diabetesK Ushijima, M Okuno, T Ayabe, et al.
The Journal of Biological Chemistry|January 16, 2004
The hippocampal cholinergic neurostimulating peptide, the N-terminal fragment of the secreted phosphatidylethanolamine-binding protein, possesses a new biological activity on cardiac physiologyYannick Goumon, Tommaso Angelone, Françoise Schoentgen, et al.
American Journal of Human Genetics|July 25, 2000
A member of a gene family on Xp22.3, VCX-A, is deleted in patients with X-linked nonspecific mental retardationM Fukami, S Kirsch, S Schiller, et al.
Andrology|July 19, 2017
Next-generation sequencing for patients with non-obstructive azoospermia: implications for significant roles of monogenic/oligogenic mutationsS Nakamura, M Miyado, K Saito, et al.
Nature Genetics|May 1, 1997
Pseudoautosomal deletions encompassing a novel homeobox gene cause growth failure in idiopathic short stature and Turner syndromeE Rao, B Weiss, M Fukami, et al.
Pageof 7

Showing results (51-60 of 65) with videos related to

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Pageof 7
Arzneimittel-Forschung|November 1, 1991
Antiarrhythmic and cardiovascular profiles of the fused indole compound (3aR,12R,12aR,12bS)-12-amino-2,3,3a,4,11,12,12a,12b-octahydro-10-hydrox yisoquino [2,1,8-lma]carbazol-5(1H)-one hydrochloride 1.5 hydrateR Yorikane, H Mizuno, Y Itoh, et al.
DNA Research : an International Journal for Rapid Publication of Reports on Genes and Genomes|March 21, 1998
A fine physical map of Arabidopsis thaliana chromosome 5: construction of a sequence-ready contig mapH Kotani, S Sato, M Fukami, et al.
Animal Genetics|September 12, 2015
Copy number variations in the amylase gene (AMY2B) in Japanese native dog breedsA Tonoike, Y Hori, M Inoue-Murayama, et al.
Human Genetics|August 1, 1997
FISH-deletion mapping defines a 270-kb short stature critical interval in the pseudoautosomal region PAR1 on human sex chromosomesE Rao, B Weiss, M Fukami, et al.
European Journal of Human Genetics : EJHG|March 14, 2000
Phenotypic variation and genetic heterogeneity in Léri-Weill syndromeS Schiller, S Spranger, B Schechinger, et al.
Diabetic Medicine : a Journal of the British Diabetic Association|December 25, 2019
Low prevalence of maternal microchimerism in peripheral blood of Japanese children with type 1 diabetesK Ushijima, M Okuno, T Ayabe, et al.
The Journal of Biological Chemistry|January 16, 2004
The hippocampal cholinergic neurostimulating peptide, the N-terminal fragment of the secreted phosphatidylethanolamine-binding protein, possesses a new biological activity on cardiac physiologyYannick Goumon, Tommaso Angelone, Françoise Schoentgen, et al.
American Journal of Human Genetics|July 25, 2000
A member of a gene family on Xp22.3, VCX-A, is deleted in patients with X-linked nonspecific mental retardationM Fukami, S Kirsch, S Schiller, et al.
Andrology|July 19, 2017
Next-generation sequencing for patients with non-obstructive azoospermia: implications for significant roles of monogenic/oligogenic mutationsS Nakamura, M Miyado, K Saito, et al.
Nature Genetics|May 1, 1997
Pseudoautosomal deletions encompassing a novel homeobox gene cause growth failure in idiopathic short stature and Turner syndromeE Rao, B Weiss, M Fukami, et al.
Pageof 7