Results 131 to 140 of about 4,652 (175)

Decoding congenital heart disease: a multi-omic framework for cardiac lineage and regulatory dysfunction. [PDF]

Front Cell Dev Biol
Lv H, Sun F, Chen Y.
europepmc   +1 more source

High-intensity intermittent training promotes adipose tissue browning via the IL-27/p38 MAPK-PGC-1α signaling pathway in diet-induced obese rats. [PDF]

Front Physiol
Wang C, Hu Y, Chen J, Wu Y.
europepmc   +1 more source

Genetics of Congenital Heart Disease: A Narrative Review of Challenges and Strategies in Identifying Novel Genes. [PDF]

Cureus
Rao E, Annavarapu S.
europepmc   +1 more source

Correlation between 22q11.2 deletion syndrome phenotype and deletion location: a meta-analysis. [PDF]

Arch Gynecol Obstet
Li J, Wang R, Liu L, Zhao J, Zhao Y, Liu F, Zhu M, Feng C, Zhao Y.   +8 more
europepmc   +1 more source

Hypercalcemia and co-occurring TBX1 mutation in Glycogen Storage Disease Type Ib: case report. [PDF]

BMC Med Genomics
Kasmi Z, Ain El Hayat I, Aadam Z, Errami A, Benhsaien I, El Bakkouri J, Ben Sabbahia D, Atrassi M, Bousfiha AA, Ailal F.   +9 more
europepmc   +1 more source

Highly demarcated structural alterations in the brain and impaired social incentive learning in Tbx1 heterozygous mice. [PDF]

Mol Psychiatry
Hiramoto T, Sumiyoshi A, Kato R, Yamauchi T, Takano T, Kang G, Esparza M, Matsumura B, Stevens LJ, Hiroi YJ, Tanifuji T, Ryoke R, Nonaka H, Machida A, Nomoto K, Mogi K, Kikusui T, Kawashima R, Hiroi N.   +18 more
europepmc   +1 more source

Logic-based modeling of biological networks with Netflux. [PDF]

PLoS Comput Biol
Clark AP, Chowkwale M, Paap A, Dang S, Saucerman JJ.   +4 more
europepmc   +1 more source

Case Report: From imaging to genetics: a case of congenital restrictive strabismus with SEOM expands the 22q11.2 duplication syndrome phenotype. [PDF]

Front Med (Lausanne)
Wei X, Gao R, Xie R.
europepmc   +1 more source

Spectrum of Copy Number Variants in Fetal Congenital Heart Disease and Their Clinical Implications: A Retrospective Study from a Tertiary Care Center. [PDF]

Diagnostics (Basel)
Cai M, Lin N, Fu M, Que Y, Zheng M, Xu L, Huang H.   +6 more
europepmc   +1 more source

Diagnostic value of karyotyping, CMA/CNV-seq, and WES in fetuses with thickened nuchal translucency: perinatal and two-year follow-up outcomes. [PDF]

BMC Med Genomics
Wang M, Ji Y, Xu Y, Sun S, Yang X, Sun L, Wu Q.   +6 more
europepmc   +1 more source