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Human Genetics
|
March 1, 1996
Angelman syndrome in an inbred family
J Beuten, R C Hennekam, B Van Roy, et al.
Nature Medicine
|
September 23, 2003
Differential requirement for CD18 in T-helper effector homing
Seung-Hyo Lee, Joseph E Prince, Muhammad Rais, et al.
Genomics
|
December 1, 1993
A complete YAC contig of the Prader-Willi/Angelman chromosome region (15q11-q13) and refined localization of the SNRPN gene
A Mutirangura, A Jayakumar, J S Sutcliffe, et al.
Human Gene Therapy
|
April 14, 2006
Improved hepatic transduction, reduced systemic vector dissemination, and long-term transgene expression by delivering helper-dependent adenoviral vectors into the surgically isolated liver of nonhuman primates
Nicola Brunetti-Pierri, Thomas Ng, David A Iannitti, et al.
American Journal of Perinatology
|
August 18, 2016
Universal Prenatal Chromosomal Microarray Analysis: Additive Value and Clinical Dilemmas in Fetuses with a Normal Karyotype
Eran Bornstein, Sharon Berger, Sau W Cheung, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
October 26, 1999
Multiorgan autonomic dysfunction in mice lacking the beta2 and the beta4 subunits of neuronal nicotinic acetylcholine receptors
W Xu, A Orr-Urtreger, F Nigro, et al.
European Journal of Human Genetics : EJHG
|
May 25, 2007
Identification of novel deletions of 15q11q13 in Angelman syndrome by array-CGH: molecular characterization and genotype-phenotype correlations
Trilochan Sahoo, Carlos A Bacino, Jennifer R German, et al.
Experimental Cell Research
|
March 17, 2004
Synergistic control of keratinocyte adhesion through muscarinic and nicotinic acetylcholine receptor subtypes
Vu Thuong Nguyen, Alexander I Chernyavsky, Juan Arredondo, et al.
Somatic Cell and Molecular Genetics
|
May 1, 1995
Severe phenotype in mice with termination mutation in exon 2 of cystic fibrosis gene
P Hasty, W K O'Neal, K Q Liu, et al.
Clinical Chemistry
|
February 1, 1990
3-Hydroxy-3-methylglutaryl-CoA lyase deficiency as detected by radiochemical assay in cell extracts by thin-layer chromatography, and identification of three new cases
K M Gibson, C F Lee, V Kamali, et al.
Page
of 46
Search research articles
Search
Showing results (331-340 of 456) with videos related to
Sort By:
Page
of 46
Human Genetics
|
March 1, 1996
Angelman syndrome in an inbred family
J Beuten, R C Hennekam, B Van Roy, et al.
Nature Medicine
|
September 23, 2003
Differential requirement for CD18 in T-helper effector homing
Seung-Hyo Lee, Joseph E Prince, Muhammad Rais, et al.
Genomics
|
December 1, 1993
A complete YAC contig of the Prader-Willi/Angelman chromosome region (15q11-q13) and refined localization of the SNRPN gene
A Mutirangura, A Jayakumar, J S Sutcliffe, et al.
Human Gene Therapy
|
April 14, 2006
Improved hepatic transduction, reduced systemic vector dissemination, and long-term transgene expression by delivering helper-dependent adenoviral vectors into the surgically isolated liver of nonhuman primates
Nicola Brunetti-Pierri, Thomas Ng, David A Iannitti, et al.
American Journal of Perinatology
|
August 18, 2016
Universal Prenatal Chromosomal Microarray Analysis: Additive Value and Clinical Dilemmas in Fetuses with a Normal Karyotype
Eran Bornstein, Sharon Berger, Sau W Cheung, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
October 26, 1999
Multiorgan autonomic dysfunction in mice lacking the beta2 and the beta4 subunits of neuronal nicotinic acetylcholine receptors
W Xu, A Orr-Urtreger, F Nigro, et al.
European Journal of Human Genetics : EJHG
|
May 25, 2007
Identification of novel deletions of 15q11q13 in Angelman syndrome by array-CGH: molecular characterization and genotype-phenotype correlations
Trilochan Sahoo, Carlos A Bacino, Jennifer R German, et al.
Experimental Cell Research
|
March 17, 2004
Synergistic control of keratinocyte adhesion through muscarinic and nicotinic acetylcholine receptor subtypes
Vu Thuong Nguyen, Alexander I Chernyavsky, Juan Arredondo, et al.
Somatic Cell and Molecular Genetics
|
May 1, 1995
Severe phenotype in mice with termination mutation in exon 2 of cystic fibrosis gene
P Hasty, W K O'Neal, K Q Liu, et al.
Clinical Chemistry
|
February 1, 1990
3-Hydroxy-3-methylglutaryl-CoA lyase deficiency as detected by radiochemical assay in cell extracts by thin-layer chromatography, and identification of three new cases
K M Gibson, C F Lee, V Kamali, et al.
Page
of 46