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The Journal of Pediatrics
|
October 1, 1981
A new malformation syndrome of long palpebral fissures, large ears, depressed nasal tip, and skeletal anomalies associated with postnatal dwarfism and mental retardation
Y Kuroki, Y Suzuki, H Chyo, et al.
Rinsho Hoshasen. Clinical Radiography
|
February 1, 1982
[Diagnostic value of arteriography of the primary hepatic tumor in infants and children (author's transl)]
Y Morita, M Shinohara, A Hata, et al.
Genes & Development
|
April 15, 1997
The TGF-beta family mediator Smad1 is phosphorylated directly and activated functionally by the BMP receptor kinase
M Kretzschmar, F Liu, A Hata, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1989
Deduced amino acid sequence of human prolidase and molecular analyses of prolidase deficiency
F Endo, A Tanoue, A Hata, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
December 15, 1989
Structure of the ornithine transcarbamylase (OTC) gene and DNA diagnosis of OTC deficiency
I Matsuda, A Hata, T Matsuura, et al.
FEBS Letters
|
July 31, 1989
Direct evidence that the kinase activity of protein kinase C is involved in transcriptional activation through a TPA-responsive element
A Hata, Y Akita, Y Konno, et al.
Journal of the American Society of Echocardiography : Official Publication of the American Society of Echocardiography
|
February 15, 2001
Simple method for estimating regurgitant volume with use of a single radius for measuring proximal isovelocity surface area: an in vitro study of simulated mitral regurgitation
T Tokushima, C L Reid, A Hata, et al.
Human Genetics
|
June 1, 1995
Recurrence of osteogenesis imperfecta because of paternal mosaicism: Gly862-->Ser substitution in a type I collagen gene (COL1A1)
C Namikawa, K Suzumori, Y Fukushima, et al.
Kansenshogaku Zasshi. the Journal of the Japanese Association for Infectious Diseases
|
June 1, 1970
[Hemagglutination and hemagglutination inhibition tests of rubella virus]
H Yoshikawa, K Oashi, A Hata, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1987
Immunochemical analysis of prolidase deficiency and molecular cloning of cDNA for prolidase of human liver
F Endo, A Hata, Y Indo, et al.
Page
of 19
Search research articles
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Showing results (41-50 of 183) with videos related to
Sort By:
Page
of 19
The Journal of Pediatrics
|
October 1, 1981
A new malformation syndrome of long palpebral fissures, large ears, depressed nasal tip, and skeletal anomalies associated with postnatal dwarfism and mental retardation
Y Kuroki, Y Suzuki, H Chyo, et al.
Rinsho Hoshasen. Clinical Radiography
|
February 1, 1982
[Diagnostic value of arteriography of the primary hepatic tumor in infants and children (author's transl)]
Y Morita, M Shinohara, A Hata, et al.
Genes & Development
|
April 15, 1997
The TGF-beta family mediator Smad1 is phosphorylated directly and activated functionally by the BMP receptor kinase
M Kretzschmar, F Liu, A Hata, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1989
Deduced amino acid sequence of human prolidase and molecular analyses of prolidase deficiency
F Endo, A Tanoue, A Hata, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
December 15, 1989
Structure of the ornithine transcarbamylase (OTC) gene and DNA diagnosis of OTC deficiency
I Matsuda, A Hata, T Matsuura, et al.
FEBS Letters
|
July 31, 1989
Direct evidence that the kinase activity of protein kinase C is involved in transcriptional activation through a TPA-responsive element
A Hata, Y Akita, Y Konno, et al.
Journal of the American Society of Echocardiography : Official Publication of the American Society of Echocardiography
|
February 15, 2001
Simple method for estimating regurgitant volume with use of a single radius for measuring proximal isovelocity surface area: an in vitro study of simulated mitral regurgitation
T Tokushima, C L Reid, A Hata, et al.
Human Genetics
|
June 1, 1995
Recurrence of osteogenesis imperfecta because of paternal mosaicism: Gly862-->Ser substitution in a type I collagen gene (COL1A1)
C Namikawa, K Suzumori, Y Fukushima, et al.
Kansenshogaku Zasshi. the Journal of the Japanese Association for Infectious Diseases
|
June 1, 1970
[Hemagglutination and hemagglutination inhibition tests of rubella virus]
H Yoshikawa, K Oashi, A Hata, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1987
Immunochemical analysis of prolidase deficiency and molecular cloning of cDNA for prolidase of human liver
F Endo, A Hata, Y Indo, et al.
Page
of 19