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Muscular Dystrophy, Hemizygous Lethal Type

 
National Institutes of Health

Papers overview

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2012
2012
While oxidative stress has been linked to Alzheimer's disease, the underlying pathophysiological relationship is unclear. To… Expand
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2012
2012
Studies of striatal physiology and motor control have increasingly relied on the use of bacterial artificial chromosome (BAC… Expand
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Highly Cited
2011
Highly Cited
2011
The development of BAC transgenic mice expressing promoter-specific fluorescent reporter proteins has been a great asset for… Expand
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Review
2011
Review
2011
Whereas glutamate dehydrogenase in most mammals (hGDH1 in the human) is encoded by a single functional GLUD1 gene expressed… Expand
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Highly Cited
2010
Highly Cited
2010
Aims To develop a fluorescence in-situ hybridisation (FISH) assay for detecting p16/CDKN2A deletion on paraffin tissue sections… Expand
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Highly Cited
2001
Highly Cited
2001
The genes at the INK4A/ARF locus at 9p21 are frequently involved in human cancer. Virtually all p16(INK4A) exon 2 (henceforth… Expand
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Highly Cited
2000
Highly Cited
2000
Ornithine transcarbamylase (OTC) deficiency, a partially dominant X-linked disorder, is the most common inherited defect of the… Expand
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1998
1998
Insulin-like growth factor I (IGF-I) has been postulated to function as a smooth muscle cell (SMC) mitogen and to play a role in… Expand
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1993
1993
Enucleated mouse oocytes were successfully fertilized in vitro, and the resultant androgenetic eggs developed to the blastocyst… Expand
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Highly Cited
1991
Highly Cited
1991
Scurfy (sf) is a spontaneous, sex-linked, recessive mutation that maps to the extreme proximal portion of the X chromosome, about… Expand
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