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KHDRBS3 protein, human

Known as: Sam68-like phosphotyrosine protein, T-STAR, human, T-STAR protein, human, KH domain containing, RNA binding, signal transduction associated 3 protein, human 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

1964-2016
01219642016

Related topics

Related topics

2 relations
KHDRBS3 gene

Broader (1)

RNA-Binding Proteins

Related mentions per year

Related mentions per year

1964-2018
1960198020002020
KHDRBS3 protein, human
RNA-Binding Proteins
KHDRBS3 gene

Papers overview

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2016
2016
Drug resistance and tropism as markers of the dynamics of HIV-1 DNA quasispecies in blood cells of heavily pretreated patients who achieved sustained virological suppression.
OBJECTIVES The objective of this study was to address the dynamics of archived resistant quasispecies in cell-associated HIV-1… (More)
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2012
2012
Hypophosphatasia - pathophysiology and treatment.
Hypophosphatasia (HPP) is the inborn-error-of-metabolism caused by loss-of-function mutation(s) in the gene that encodes the… (More)
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2011
2011
Enzyme replacement therapy prevents dental defects in a model of hypophosphatasia.
Hypophosphatasia (HPP) occurs from loss-of-function mutation in the tissue-non-specific alkaline phosphatase (TNALP) gene… (More)
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2011
2011
Dose response of bone-targeted enzyme replacement for murine hypophosphatasia.
Hypophosphatasia (HPP) features rickets or osteomalacia from tissue-nonspecific alkaline phosphatase (TNSALP) deficiency due to… (More)
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Highly Cited
2008
Highly Cited
2008
Enzyme replacement therapy for murine hypophosphatasia.
INTRODUCTION Hypophosphatasia (HPP) is the inborn error of metabolism that features rickets or osteomalacia caused by loss-of… (More)
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1964
1964
[traditions of H Opital Salp Etri'ere (paris)].
 
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