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F Endo

Showing results (111-120 of 197) with videos related to

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Spinal Cord|June 7, 2014
Myelopathy due to lumbar disc herniation in the presence of a tethered cordF Endo, H Iizuka, Y Iizuka, et al.
The Journal of Clinical Investigation|April 1, 1991
Molecular defect in siblings with prolidase deficiency and absence or presence of clinical symptoms. A 0.8-kb deletion with breakpoints at the short, direct repeat in the PEPD gene and synthesis of abnormal messenger RNA and inactive polypeptideA Tanoue, F Endo, I Akaboshi, et al.
Journal of Inherited Metabolic Disease|January 1, 1989
Biochemical nature of pyruvate dehydrogenase complex in the patient with primary lactic acidaemiaA Kitano, F Endo, Y Kuroda, et al.
Kidney International|November 1, 1993
Identification of a single base insertion in the COL4A5 gene in Alport syndromeH Nakazato, S Hattori, T Matsuura, et al.
Journal of Human Genetics|March 18, 2000
A novel nonsense mutation of the PEPD gene in a Japanese patient with prolidase deficiencyS Kikuchi, A Tanoue, F Endo, et al.
Pediatric Neurology|March 1, 1986
Carnitine prevents Reye-like syndrome in atypical carnitine deficiencyT Matsubasa, Y Ohtani, T Miike, et al.
Blood|July 4, 2001
Improved superoxide-generating ability by interferon gamma due to splicing pattern change of transcripts in neutrophils from patients with a splice site mutation in CYBB geneF Ishibashi, T Mizukami, S Kanegasaki, et al.
Journal of Inherited Metabolic Disease|January 1, 1994
Measurement of blood holoceruloplasmin by EIA using a mouse monoclonal antibody directed to holoceruloplasmin. Implication for mass screening of Wilson diseaseF Endo, K Taketa, K Nakamura, et al.
Kidney International|January 20, 1999
Chloride channel CLCN5 mutations in Japanese children with familial idiopathic low molecular weight proteinuriaH Nakazato, J Yoshimuta, S Karashima, et al.
Biochemistry|February 6, 1990
Isolation and characterization of a complementary DNA clone coding for the E1 beta subunit of the bovine branched-chain alpha-ketoacid dehydrogenase complex: complete amino acid sequence of the precursor protein and its proteolytic processingY Nobukuni, H Mitsubuchi, F Endo, et al.
Pageof 20

Showing results (111-120 of 197) with videos related to

Sort By:
Pageof 20
Spinal Cord|June 7, 2014
Myelopathy due to lumbar disc herniation in the presence of a tethered cordF Endo, H Iizuka, Y Iizuka, et al.
The Journal of Clinical Investigation|April 1, 1991
Molecular defect in siblings with prolidase deficiency and absence or presence of clinical symptoms. A 0.8-kb deletion with breakpoints at the short, direct repeat in the PEPD gene and synthesis of abnormal messenger RNA and inactive polypeptideA Tanoue, F Endo, I Akaboshi, et al.
Journal of Inherited Metabolic Disease|January 1, 1989
Biochemical nature of pyruvate dehydrogenase complex in the patient with primary lactic acidaemiaA Kitano, F Endo, Y Kuroda, et al.
Kidney International|November 1, 1993
Identification of a single base insertion in the COL4A5 gene in Alport syndromeH Nakazato, S Hattori, T Matsuura, et al.
Journal of Human Genetics|March 18, 2000
A novel nonsense mutation of the PEPD gene in a Japanese patient with prolidase deficiencyS Kikuchi, A Tanoue, F Endo, et al.
Pediatric Neurology|March 1, 1986
Carnitine prevents Reye-like syndrome in atypical carnitine deficiencyT Matsubasa, Y Ohtani, T Miike, et al.
Blood|July 4, 2001
Improved superoxide-generating ability by interferon gamma due to splicing pattern change of transcripts in neutrophils from patients with a splice site mutation in CYBB geneF Ishibashi, T Mizukami, S Kanegasaki, et al.
Journal of Inherited Metabolic Disease|January 1, 1994
Measurement of blood holoceruloplasmin by EIA using a mouse monoclonal antibody directed to holoceruloplasmin. Implication for mass screening of Wilson diseaseF Endo, K Taketa, K Nakamura, et al.
Kidney International|January 20, 1999
Chloride channel CLCN5 mutations in Japanese children with familial idiopathic low molecular weight proteinuriaH Nakazato, J Yoshimuta, S Karashima, et al.
Biochemistry|February 6, 1990
Isolation and characterization of a complementary DNA clone coding for the E1 beta subunit of the bovine branched-chain alpha-ketoacid dehydrogenase complex: complete amino acid sequence of the precursor protein and its proteolytic processingY Nobukuni, H Mitsubuchi, F Endo, et al.
Pageof 20