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C Inoue

Showing results (71-80 of 91) with videos related to

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American Journal of Medical Genetics|September 12, 2000
Rapid screening method to detect mutations in CYP21, the gene for 21-hydroxylaseY Yokoyama, M Teraoka, K Tsuji, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|February 1, 1996
Functional neuroanatomy of visual object naming: a PET studyM Kiyosawa, C Inoue, T Kawasaki, et al.
Annals of the New York Academy of Sciences|January 1, 1988
Complete nucleotide sequence of human vasoactive intestinal peptide/PHM-27 gene and its inducible promoterT Yamagami, K Ohsawa, M Nishizawa, et al.
The Journal of Biological Chemistry|June 5, 1992
Molecular cloning of the gene encoding Thiobacillus ferrooxidans Fe(II) oxidase. High homology of the gene product with HiPIPT Kusano, T Takeshima, K Sugawara, et al.
Nihon Naika Gakkai Zasshi. the Journal of the Japanese Society of Internal Medicine|May 26, 1999
[Case of post-Chlamydia perihepatitis adhesion (Fitz-Hugh-Curtis syndrome) with effective peritoneoscopic diagnosis]H Goto, S Miyafuku, H Ezaki, et al.
Thrombosis and Haemostasis|August 6, 2000
Homozygous Pro74-->Arg mutation in the platelet glycoprotein Ibbeta gene associated with Bernard-Soulier syndromeS Kunishima, Y Tomiyama, S Honda, et al.
[Rinsho Ketsueki] the Japanese Journal of Clinical Hematology|July 1, 1989
[Growth inhibition of erythroid colonies by autologous sera and the clinical effect of erythropoietin in chronic renal disease]J Y Wang, T Hotta, T Murate, et al.
The Veterinary Record|September 20, 2005
Acute monocytic leukaemia in a catN Nagashima, R Kano, A Hirai, et al.
Clinical Genetics|November 15, 2000
A novel mutation (296 del G) of the SOX90 gene in a patient with campomelic syndrome and sex reversalS Ninomiya, Y Yokoyama, M Teraoka, et al.
Nihon Rinsho. Japanese Journal of Clinical Medicine|February 1, 1991
[Structure and expression of rig]K Shiga, M Unno, S Takasawa, et al.
Pageof 10

Showing results (71-80 of 91) with videos related to

Sort By:
Pageof 10
American Journal of Medical Genetics|September 12, 2000
Rapid screening method to detect mutations in CYP21, the gene for 21-hydroxylaseY Yokoyama, M Teraoka, K Tsuji, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|February 1, 1996
Functional neuroanatomy of visual object naming: a PET studyM Kiyosawa, C Inoue, T Kawasaki, et al.
Annals of the New York Academy of Sciences|January 1, 1988
Complete nucleotide sequence of human vasoactive intestinal peptide/PHM-27 gene and its inducible promoterT Yamagami, K Ohsawa, M Nishizawa, et al.
The Journal of Biological Chemistry|June 5, 1992
Molecular cloning of the gene encoding Thiobacillus ferrooxidans Fe(II) oxidase. High homology of the gene product with HiPIPT Kusano, T Takeshima, K Sugawara, et al.
Nihon Naika Gakkai Zasshi. the Journal of the Japanese Society of Internal Medicine|May 26, 1999
[Case of post-Chlamydia perihepatitis adhesion (Fitz-Hugh-Curtis syndrome) with effective peritoneoscopic diagnosis]H Goto, S Miyafuku, H Ezaki, et al.
Thrombosis and Haemostasis|August 6, 2000
Homozygous Pro74-->Arg mutation in the platelet glycoprotein Ibbeta gene associated with Bernard-Soulier syndromeS Kunishima, Y Tomiyama, S Honda, et al.
[Rinsho Ketsueki] the Japanese Journal of Clinical Hematology|July 1, 1989
[Growth inhibition of erythroid colonies by autologous sera and the clinical effect of erythropoietin in chronic renal disease]J Y Wang, T Hotta, T Murate, et al.
The Veterinary Record|September 20, 2005
Acute monocytic leukaemia in a catN Nagashima, R Kano, A Hirai, et al.
Clinical Genetics|November 15, 2000
A novel mutation (296 del G) of the SOX90 gene in a patient with campomelic syndrome and sex reversalS Ninomiya, Y Yokoyama, M Teraoka, et al.
Nihon Rinsho. Japanese Journal of Clinical Medicine|February 1, 1991
[Structure and expression of rig]K Shiga, M Unno, S Takasawa, et al.
Pageof 10