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ADAMTS19 gene

Known as: A DISINTEGRIN-LIKE AND METALLOPROTEINASE WITH THROMBOSPONDIN TYPE 1 MOTIF, 19, ADAM metallopeptidase with thrombospondin type 1 motif 19, ADAMTS19 
 
National Institutes of Health

Papers overview

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2020
2020
Recently, ADAMTS19 was identified as a novel causative gene for autosomal recessive heart valve disease (HVD), affecting mainly… Expand
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Review
2020
Review
2020
Secreted a disintegrin-like and metalloprotease with thrombospondin type 1 motif (ADAMTS) proteases play crucial roles in tissue… Expand
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2019
2019
Valvular heart disease is observed in approximately 2% of the general population 1 . Although the initial observation is often… Expand
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2015
2015
BackgroundADAMTS19 encodes a member of the ADAMTS (a disintegrin and metalloproteinase domain with thrombospondin motifs) protein… Expand
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2015
2015
ObjectiveThis study investigated whether epistasis between single nucleotide polymorphisms (SNPs) within ACVR2B (activin A… Expand
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2015
2015
OBJECTIVE To identify new molecular actors involved in nonsyndromic premature ovarian failure (POF) etiology. DESIGN This is a… Expand
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2015
2015
OBJECTIVE To Investigate the biological effects of miR-144 in rats' pulmanory injury induced by nanosized SiO₂preliminarily… Expand
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2010
2010
Premature ovarian failure (POF) is defined as an amenorrhea for more than 4months, associated with elevated gonadotropins… Expand
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Highly Cited
2009
Highly Cited
2009
BACKGROUND Spontaneous premature ovarian failure (POF) occurs in 1% of women and has major implications for their fertility and… Expand
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