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T Ikeuchi

Showing results (231-240 of 303) with videos related to

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Nature|January 21, 1988
Loss of constitutional heterozygosity in colon carcinoma from patients with familial polyposis coliM Okamoto, M Sasaki, K Sugio, et al.
Acta Neuropathologica|November 26, 1998
Dentatorubropallidoluysian atrophy: clinicopathological study of dementia and involvement of the nucleus basalis of Meynert in seven autopsy casesK Tsuchiya, S Oyanagi, K Arima, et al.
Uchu Seibutsu Kagaku|January 21, 2003
[The change of human sperm motility in parabolic flight]T Ikeuchi, S Sasaki, Y Kubota, et al.
Hinyokika Kiyo. Acta Urologica Japonica|April 1, 1991
[Clinical evaluation of the bladder tumor marker "Tu-MARK-BTA"]S Yogi, T Ikeuchi, H Yoshikawa, et al.
American Journal of Human Genetics|April 1, 1996
Non-Mendelian transmission in dentatorubral-pallidoluysian atrophy and Machado-Joseph disease: the mutant allele is preferentially transmitted in male meiosisT Ikeuchi, S Igarashi, Y Takiyama, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|October 30, 1998
Famotidine-induced acute interstitial nephritisK Hirayama, K Hanatsuka, T Ikeuchi, et al.
Biochemical and Biophysical Research Communications|October 23, 1997
cDNA cloning of a short type of multidrug resistance protein homologue, SMRP, from a human lung cancer cell lineT Suzuki, K Nishio, H Sasaki, et al.
Genes, Chromosomes & Cancer|May 25, 1999
Severe phenotype of neurofibromatosis type 2 in a patient with a 7.4-MB constitutional deletion on chromosome 22: possible localization of a neurofibromatosis type 2 modifier gene?C E Bruder, K Ichimura, E Blennow, et al.
Japanese Journal of Cancer Research : Gann|August 1, 1991
Chromosome changes in desmoid tumors developed in patients with familial adenomatous polyposisM A Yoshida, T Ikeuchi, T Iwama, et al.
Jinrui Idengaku Zasshi. the Japanese Journal of Human Genetics|March 1, 1984
A case of mosaic trisomy 14 due to an isochromosome, i(14q)N Ozawa, Z D Xu, K Soh, et al.
Pageof 31

Showing results (231-240 of 303) with videos related to

Sort By:
Pageof 31
Nature|January 21, 1988
Loss of constitutional heterozygosity in colon carcinoma from patients with familial polyposis coliM Okamoto, M Sasaki, K Sugio, et al.
Acta Neuropathologica|November 26, 1998
Dentatorubropallidoluysian atrophy: clinicopathological study of dementia and involvement of the nucleus basalis of Meynert in seven autopsy casesK Tsuchiya, S Oyanagi, K Arima, et al.
Uchu Seibutsu Kagaku|January 21, 2003
[The change of human sperm motility in parabolic flight]T Ikeuchi, S Sasaki, Y Kubota, et al.
Hinyokika Kiyo. Acta Urologica Japonica|April 1, 1991
[Clinical evaluation of the bladder tumor marker "Tu-MARK-BTA"]S Yogi, T Ikeuchi, H Yoshikawa, et al.
American Journal of Human Genetics|April 1, 1996
Non-Mendelian transmission in dentatorubral-pallidoluysian atrophy and Machado-Joseph disease: the mutant allele is preferentially transmitted in male meiosisT Ikeuchi, S Igarashi, Y Takiyama, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|October 30, 1998
Famotidine-induced acute interstitial nephritisK Hirayama, K Hanatsuka, T Ikeuchi, et al.
Biochemical and Biophysical Research Communications|October 23, 1997
cDNA cloning of a short type of multidrug resistance protein homologue, SMRP, from a human lung cancer cell lineT Suzuki, K Nishio, H Sasaki, et al.
Genes, Chromosomes & Cancer|May 25, 1999
Severe phenotype of neurofibromatosis type 2 in a patient with a 7.4-MB constitutional deletion on chromosome 22: possible localization of a neurofibromatosis type 2 modifier gene?C E Bruder, K Ichimura, E Blennow, et al.
Japanese Journal of Cancer Research : Gann|August 1, 1991
Chromosome changes in desmoid tumors developed in patients with familial adenomatous polyposisM A Yoshida, T Ikeuchi, T Iwama, et al.
Jinrui Idengaku Zasshi. the Japanese Journal of Human Genetics|March 1, 1984
A case of mosaic trisomy 14 due to an isochromosome, i(14q)N Ozawa, Z D Xu, K Soh, et al.
Pageof 31