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Experimental and Clinical Endocrinology
|
March 1, 1987
Influence of microinjection of glucagon into ventromedial hypothalamus on acetate metabolism in liver slices of rabbit
K Seto, H Saito, H Kaba, et al.
Biochemical and Biophysical Research Communications
|
October 3, 1996
Japanese cases of type 1 thanatophoric dysplasia exclusively carry a C to T transition at nucleotide 742 of the fibroblast growth factor receptor 3 gene
R K Pokharel, H Alimsardjono, Y Takeshima, et al.
American Journal of Human Genetics
|
January 1, 1994
A novel point mutation (G-1 to T) in a 5' splice donor site of intron 13 of the dystrophin gene results in exon skipping and is responsible for Becker muscular dystrophy
Y Hagiwara, H Nishio, Y Kitoh, et al.
Neurology
|
September 1, 1994
Amino-terminal deletion of 53% of dystrophin results in an intermediate Duchenne-Becker muscular dystrophy phenotype
Y Takeshima, H Nishio, N Narita, et al.
Neuroscience Research
|
February 1, 1997
Odorant evoked magnetic fields in humans
K Sakuma, R Kakigi, Y Kaneoke, et al.
Endocrinologia Japonica
|
February 1, 1991
Intranasal administration of His-D-Trp-Ala-Trp-D-Phe-LysNH2 (growth hormone releasing peptide) increased plasma growth hormone and insulin-like growth factor-I levels in normal men
S Hayashi, Y Okimura, H Yagi, et al.
Journal of Neurology
|
February 13, 1999
High incidence of a survival motor neuron gene/cBCD541 gene ratio of 2 in Japanese parents of spinal muscular atrophy patients: a characteristic background of spinal muscular atrophy in Japan?
H Nishio, Y Ishikawa, M J Lee, et al.
Ryumachi. [Rheumatism]
|
October 1, 1992
[An autopsied case of progressive systemic sclerosis with anti Wa antibody who showed a rapid progression]
T Abe, A Yachi, Y Ishii, et al.
The Journal of Clinical Investigation
|
September 1, 1994
Identification of a novel first exon in the human dystrophin gene and of a new promoter located more than 500 kb upstream of the nearest known promoter
H Nishio, Y Takeshima, N Narita, et al.
Lancet (London, England)
|
December 18, 1993
p53 mutations in lung cancers from non-smoking atomic-bomb survivors
Y Takeshima, T Seyama, W P Bennett, et al.
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of 8
Search research articles
Search
Showing results (61-70 of 79) with videos related to
Sort By:
Page
of 8
Experimental and Clinical Endocrinology
|
March 1, 1987
Influence of microinjection of glucagon into ventromedial hypothalamus on acetate metabolism in liver slices of rabbit
K Seto, H Saito, H Kaba, et al.
Biochemical and Biophysical Research Communications
|
October 3, 1996
Japanese cases of type 1 thanatophoric dysplasia exclusively carry a C to T transition at nucleotide 742 of the fibroblast growth factor receptor 3 gene
R K Pokharel, H Alimsardjono, Y Takeshima, et al.
American Journal of Human Genetics
|
January 1, 1994
A novel point mutation (G-1 to T) in a 5' splice donor site of intron 13 of the dystrophin gene results in exon skipping and is responsible for Becker muscular dystrophy
Y Hagiwara, H Nishio, Y Kitoh, et al.
Neurology
|
September 1, 1994
Amino-terminal deletion of 53% of dystrophin results in an intermediate Duchenne-Becker muscular dystrophy phenotype
Y Takeshima, H Nishio, N Narita, et al.
Neuroscience Research
|
February 1, 1997
Odorant evoked magnetic fields in humans
K Sakuma, R Kakigi, Y Kaneoke, et al.
Endocrinologia Japonica
|
February 1, 1991
Intranasal administration of His-D-Trp-Ala-Trp-D-Phe-LysNH2 (growth hormone releasing peptide) increased plasma growth hormone and insulin-like growth factor-I levels in normal men
S Hayashi, Y Okimura, H Yagi, et al.
Journal of Neurology
|
February 13, 1999
High incidence of a survival motor neuron gene/cBCD541 gene ratio of 2 in Japanese parents of spinal muscular atrophy patients: a characteristic background of spinal muscular atrophy in Japan?
H Nishio, Y Ishikawa, M J Lee, et al.
Ryumachi. [Rheumatism]
|
October 1, 1992
[An autopsied case of progressive systemic sclerosis with anti Wa antibody who showed a rapid progression]
T Abe, A Yachi, Y Ishii, et al.
The Journal of Clinical Investigation
|
September 1, 1994
Identification of a novel first exon in the human dystrophin gene and of a new promoter located more than 500 kb upstream of the nearest known promoter
H Nishio, Y Takeshima, N Narita, et al.
Lancet (London, England)
|
December 18, 1993
p53 mutations in lung cancers from non-smoking atomic-bomb survivors
Y Takeshima, T Seyama, W P Bennett, et al.
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of 8