Results 211 to 220 of about 115,582 (346)
Pathogenesis of biliary atresia: defining biology to understand clinical phenotypes
A. Asai, A. Miethke, J. Bezerra
semanticscholar +1 more source
Our study demonstrated the downregulation of GPD1L and its mediated glycerophospholipid metabolism dysfunction in patients with diminished ovarian reserve. Moreover, we verified that GPD1L knockdown leads to increased cell apoptosis and mitochondrial dysfunction of KGN cells, as well as impaired oocyte quality.
Jiaqi Wu+8 more
wiley +1 more source
Unrecognized constellation of multiple congenital anomalies in a newborn: a rare case report. [PDF]
Jaber M+6 more
europepmc +1 more source
Chromatin machinery influences how DNA is ‘wrapped’ around histones in the nucleosome of immune and brain cells. Plain language summary: https://onlinelibrary.wiley.com/doi/10.1111/dmcn.16299 Abstract We report eight children with de novo pathogenic DNA variants in chromatin‐related genes: MORC2, CHD7, KANSL1, KMT2D, ZMYND11, HIST1HIE, EP300, and KMT2B.
Russell C. Dale+14 more
wiley +1 more source
Routine 36-week scan: diagnosis of fetal abnormalities. [PDF]
Syngelaki A+5 more
europepmc +1 more source
A narrative review of metformin in pregnancy: Navigating benefit and uncertainty
Abstract Metformin is well‐established as a treatment for type 2 diabetes in non‐pregnant individuals. The low cost, acceptability and broad tolerability of metformin have also made it an attractive option for research into the treatment of other conditions associated with insulin resistance.
Robert P. McEvoy+3 more
wiley +1 more source
Long-Gap Esophageal Atresia Gross Type C and D: A Retrospective Study of Surgical Management and Postoperative Complications Within the First Year of Life in the Nordic Countries. [PDF]
Olsen ACW+14 more
europepmc +1 more source