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UnknownProbiotic Supplementation in Preterm: Feeding Intolerance and Hospital Cost.
Not available
S-EPMC5622725 | biostudies-literature
UnknownEspin gene (ESPN) mutations associated with autosomal dominant hearing loss cause defects in microvillar elongation or organisation.
Not available
S-EPMC2564636 | biostudies-literature
UnknownClinical characterization of a novel RAB39B nonstop mutation in a family with ASD and severe ID causing RAB39B downregulation and study of a Rab39b knock down mouse model.
Not available
S-EPMC9071400 | biostudies-literature
UnknownNANOG Plays a Hierarchical Role in the Transcription Network Regulating the Pluripotency and Plasticity of Adipose Tissue-Derived Stem Cells.
Not available
S-EPMC5485931 | biostudies-literature
UnknownCombinatorial effects on gene expression at the Lbx1/Fgf8 locus resolve split-hand/foot malformation type 3.
Not available
S-EPMC10020157 | biostudies-literature
UnknownCytogenetic and Array-CGH Characterization of a Simple Case of Reciprocal t(3;10) Translocation Reveals a Hidden Deletion at 5q12.
Not available
S-EPMC8226940 | biostudies-literature
UnknownEzetimibe Enhances Lipid Droplet and Mitochondria Contact Formation, Improving Fatty Acid Transfer and Reducing Lipotoxicity in Alport Syndrome Podocytes.
Not available
S-EPMC11642288 | biostudies-literature
UnknownCorrection of intermittent hypoxia reduces inflammation in obese subjects with obstructive sleep apnea.
Not available
S-EPMC5621882 | biostudies-literature
UnknownA functional study of plasma-membrane calcium-pump isoform 2 mutants causing digenic deafness.
Not available
S-EPMC1785272 | biostudies-literature
UnknownNonmuscle myosin heavy-chain gene MYH14 is expressed in cochlea and mutated in patients affected by autosomal dominant hearing impairment (DFNA4).
Not available
S-EPMC1181955 | biostudies-literature
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