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American Journal of Human Genetics
|
February 1, 1989
Assignment of autosomal dominant spinocerebellar ataxia (SCA1) centromeric to the HLA region on the short arm of chromosome 6, using multilocus linkage analysis
H Y Zoghbi, L A Sandkuyl, J Ott, et al.
Journal of Immunology (Baltimore, Md. : 1950)
|
August 1, 1993
Gene targeting yields a CD18-mutant mouse for study of inflammation
R W Wilson, C M Ballantyne, C W Smith, et al.
American Journal of Medical Genetics
|
June 1, 1989
Prenatal diagnosis of cystic fibrosis by using linked DNA markers in 138 pregnancies at 1-in-4 risk
G L Feldman, N Lewiston, S D Fernbach, et al.
The Journal of Pediatrics
|
April 1, 1989
Prenatal diagnosis and heterozygote detection by DNA analysis in ornithine transcarbamylase deficiency
J E Spence, A Maddalena, W E O'Brien, et al.
The Journal of Experimental Medicine
|
October 23, 1997
Neutrophil emigration in the skin, lungs, and peritoneum: different requirements for CD11/CD18 revealed by CD18-deficient mice
J P Mizgerd, H Kubo, G J Kutkoski, et al.
Journal of Neurochemistry
|
May 9, 2000
Mice homozygous for the L250T mutation in the alpha7 nicotinic acetylcholine receptor show increased neuronal apoptosis and die within 1 day of birth
A Orr-Urtreger, R S Broide, M R Kasten, et al.
Molecular Medicine (Cambridge, Mass.)
|
August 31, 2000
Toxicity associated with repeated administration of first-generation adenovirus vectors does not occur with a helper-dependent vector
W K O'Neal, H Zhou, N Morral, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
September 15, 1993
Inflammatory and immune responses are impaired in mice deficient in intercellular adhesion molecule 1
J E Sligh, C M Ballantyne, S S Rich, et al.
Blood
|
July 27, 2001
Dermal and pulmonary inflammatory disease in E-selectin and P-selectin double-null mice is reduced in triple-selectin-null mice
R G Collins, U Jung, M Ramirez, et al.
American Journal of Medical Genetics
|
December 2, 1996
Validation studies of SNRPN methylation as a diagnostic test for Prader-Willi syndrome
T Kubota, J S Sutcliffe, S Aradhya, et al.
Page
of 24
Search research articles
Search
Showing results (171-180 of 233) with videos related to
Sort By:
Page
of 24
American Journal of Human Genetics
|
February 1, 1989
Assignment of autosomal dominant spinocerebellar ataxia (SCA1) centromeric to the HLA region on the short arm of chromosome 6, using multilocus linkage analysis
H Y Zoghbi, L A Sandkuyl, J Ott, et al.
Journal of Immunology (Baltimore, Md. : 1950)
|
August 1, 1993
Gene targeting yields a CD18-mutant mouse for study of inflammation
R W Wilson, C M Ballantyne, C W Smith, et al.
American Journal of Medical Genetics
|
June 1, 1989
Prenatal diagnosis of cystic fibrosis by using linked DNA markers in 138 pregnancies at 1-in-4 risk
G L Feldman, N Lewiston, S D Fernbach, et al.
The Journal of Pediatrics
|
April 1, 1989
Prenatal diagnosis and heterozygote detection by DNA analysis in ornithine transcarbamylase deficiency
J E Spence, A Maddalena, W E O'Brien, et al.
The Journal of Experimental Medicine
|
October 23, 1997
Neutrophil emigration in the skin, lungs, and peritoneum: different requirements for CD11/CD18 revealed by CD18-deficient mice
J P Mizgerd, H Kubo, G J Kutkoski, et al.
Journal of Neurochemistry
|
May 9, 2000
Mice homozygous for the L250T mutation in the alpha7 nicotinic acetylcholine receptor show increased neuronal apoptosis and die within 1 day of birth
A Orr-Urtreger, R S Broide, M R Kasten, et al.
Molecular Medicine (Cambridge, Mass.)
|
August 31, 2000
Toxicity associated with repeated administration of first-generation adenovirus vectors does not occur with a helper-dependent vector
W K O'Neal, H Zhou, N Morral, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
September 15, 1993
Inflammatory and immune responses are impaired in mice deficient in intercellular adhesion molecule 1
J E Sligh, C M Ballantyne, S S Rich, et al.
Blood
|
July 27, 2001
Dermal and pulmonary inflammatory disease in E-selectin and P-selectin double-null mice is reduced in triple-selectin-null mice
R G Collins, U Jung, M Ramirez, et al.
American Journal of Medical Genetics
|
December 2, 1996
Validation studies of SNRPN methylation as a diagnostic test for Prader-Willi syndrome
T Kubota, J S Sutcliffe, S Aradhya, et al.
Page
of 24