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Nature Genetics
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February 16, 2005
Integrated transcriptional profiling and linkage analysis for identification of genes underlying disease
Norbert Hubner, Caroline A Wallace, Heike Zimdahl, et al.
American Journal of Human Genetics
|
December 25, 2012
Genomic pathology of SLE-associated copy-number variation at the FCGR2C/FCGR3B/FCGR2B locus
Michael Mueller, Paula Barros, Abigail S Witherden, et al.
Journal of Medical Genetics
|
October 9, 2023
Genetic complexity of diagnostically unresolved Ehlers-Danlos syndrome
Anthony M Vandersteen, Ruwan A Weerakkody, David A Parry, et al.
Nature
|
August 11, 2015
The zinc transporter ZIP12 regulates the pulmonary vascular response to chronic hypoxia
Lan Zhao, Eduardo Oliver, Klio Maratou, et al.
Journal of Neurology
|
December 14, 2022
Genotype-phenotype characterisation of long survivors with motor neuron disease in Scotland
Danielle J Leighton, Morad Ansari, Judith Newton, et al.
Scientific Reports
|
April 23, 2020
Impulsivity is a heritable trait in rodents and associated with a novel quantitative trait locus on chromosome 1
Bianca Jupp, Silvia Pitzoi, Enrico Petretto, et al.
Nature
|
February 17, 2006
Copy number polymorphism in Fcgr3 predisposes to glomerulonephritis in rats and humans
Timothy J Aitman, Rong Dong, Timothy J Vyse, et al.
Nature Genetics
|
May 29, 2007
FCGR3B copy number variation is associated with susceptibility to systemic, but not organ-specific, autoimmunity
Manuela Fanciulli, Penny J Norsworthy, Enrico Petretto, et al.
Genome Research
|
May 1, 2010
The genome sequence of the spontaneously hypertensive rat: Analysis and functional significance
Santosh S Atanur, Inanç Birol, Victor Guryev, et al.
Nature Genetics
|
April 30, 2008
Integrated genomic approaches implicate osteoglycin (Ogn) in the regulation of left ventricular mass
Enrico Petretto, Rizwan Sarwar, Ian Grieve, et al.
Page
of 11
Search research articles
Search
Showing results (81-90 of 103) with videos related to
Sort By:
Page
of 11
Nature Genetics
|
February 16, 2005
Integrated transcriptional profiling and linkage analysis for identification of genes underlying disease
Norbert Hubner, Caroline A Wallace, Heike Zimdahl, et al.
American Journal of Human Genetics
|
December 25, 2012
Genomic pathology of SLE-associated copy-number variation at the FCGR2C/FCGR3B/FCGR2B locus
Michael Mueller, Paula Barros, Abigail S Witherden, et al.
Journal of Medical Genetics
|
October 9, 2023
Genetic complexity of diagnostically unresolved Ehlers-Danlos syndrome
Anthony M Vandersteen, Ruwan A Weerakkody, David A Parry, et al.
Nature
|
August 11, 2015
The zinc transporter ZIP12 regulates the pulmonary vascular response to chronic hypoxia
Lan Zhao, Eduardo Oliver, Klio Maratou, et al.
Journal of Neurology
|
December 14, 2022
Genotype-phenotype characterisation of long survivors with motor neuron disease in Scotland
Danielle J Leighton, Morad Ansari, Judith Newton, et al.
Scientific Reports
|
April 23, 2020
Impulsivity is a heritable trait in rodents and associated with a novel quantitative trait locus on chromosome 1
Bianca Jupp, Silvia Pitzoi, Enrico Petretto, et al.
Nature
|
February 17, 2006
Copy number polymorphism in Fcgr3 predisposes to glomerulonephritis in rats and humans
Timothy J Aitman, Rong Dong, Timothy J Vyse, et al.
Nature Genetics
|
May 29, 2007
FCGR3B copy number variation is associated with susceptibility to systemic, but not organ-specific, autoimmunity
Manuela Fanciulli, Penny J Norsworthy, Enrico Petretto, et al.
Genome Research
|
May 1, 2010
The genome sequence of the spontaneously hypertensive rat: Analysis and functional significance
Santosh S Atanur, Inanç Birol, Victor Guryev, et al.
Nature Genetics
|
April 30, 2008
Integrated genomic approaches implicate osteoglycin (Ogn) in the regulation of left ventricular mass
Enrico Petretto, Rizwan Sarwar, Ian Grieve, et al.
Page
of 11