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UnknownPlasma MMP and TIMP evaluation in patients with deep venous thrombosis: could they have a predictive role in the development of post-thrombotic syndrome?
Not available
S-EPMC7949807 | biostudies-literature
GenomicsCopy Number Variation in Congenital Kidney Malformations

We report a study of large rare, copy number variants (CNVs) in 192 patients with renal hypodysplasia (RHD). Congenital malformations of the kidney and urinary tract are present in 3 to 7 per 1,000 births, accounting for 16% of birth defects. These malformations account for 40-50% of pediatric an...

phs000565.v1.p1 | EGA
GenomicsTranscription Factor TLX1 Controls Retinoic Acid Signaling to Ensure Spleen Development [ChIP-Seq]
The molecular mechanisms that underlie spleen development and congenital asplenia, a condition linked to increased risk of overwhelming infections, remain largely unknown. The transcription factor TLX1 controls cell fate specification and organ expansion during spleen development, and Tlx1 deletion ...
ORGANISM(S): Mus musculus 
2016-07-01 | E-GEOD-81660 | biostudies-arrayexpress
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