Results 131 to 140 of about 2,722 (177)

Identification of basement membrane-associated genes as biomarkers for atrial fibrillation. [PDF]

Medicine (Baltimore)
Huang L, Huang M, Li H, Shi J.
europepmc   +1 more source

Multi-omics and causal inference reveal lactylation-based osteoblast regulatory networks and drug candidates. [PDF]

iScience
Chen R, Ge S, Chang F, Chen M, Li Y, Li Y, You D, Tang P, Yin P.   +8 more
europepmc   +1 more source

Genetic heterogeneity and homogeneity among orofacial cleft subtypes: genome-wide association studies in the cleft collective. [PDF]

Hum Mol Genet
Dack K, Ludwig KU, Stergiakouli E, Sandy J, Aryee S, Davey Smith G, Davies A, Wren Y, Sharp GC, Humphries K, Mangold E, Goudswaard L, Ho K, Dudding T, Lewis SJ.   +14 more
europepmc   +1 more source

An Integrated Multi-Omics Analysis Identifies Oxeiptosis-Related Biomarkers in Diabetic Retinopathy. [PDF]

Biomedicines
Deng J, Ge P, Gao Y, Li HY, Lin Y, Lu Y, Xie H, Xu D, Xie P, Hu Z.   +9 more
europepmc   +1 more source

Whole genome sequencing in adolescent idiopathic scoliosis cohort implicates multiple biological pathways. [PDF]

NPJ Genom Med
Tuncay IO, Lee EK, Gustafson A, Lee Y, Jung D, Koh JY, Lee W, Lee S, Shazand K.   +8 more
europepmc   +1 more source

Get the ball rolling: update and perspective on the role of chloroplast plastoglobule-associated proteins under abiotic stress. [PDF]

J Exp Bot
Ying S.
europepmc   +1 more source

Extracellular matrix deposition precedes muscle-tendon integration during murine forelimb morphogenesis. [PDF]

Commun Biol
Leng Y, Lipp SN, Bu Y, Larson H, Jacobson KR, Colling HA, Calve S.   +6 more
europepmc   +1 more source

Relation between the FBN2 haplotype and phenotypical hip dysplasia

, 2012
Broeckx, Bart, Coopman, Frank, Verhoeven, Geert, Bosmans, Tim, Criel, Ann CC, Gielen, Ingrid, Saunders, Jimmy, Soetaert, Sandra, van Bree, Henri, Van Haeringen, Wim, Van Nieuwerburgh, Filip, Van Ryssen, Bernadette, Deforce, Dieter   +12 more
openaire   +1 more source

Exome sequencing uncovers promising candidate genes for foetal structural malformations. [PDF]

Indian J Med Res
Sudhakar DV, Joseph S, Bansal V, Gangurde A, Nitin Minde N, Gawde H, Pande SS.   +6 more
europepmc   +1 more source

Marfan syndrome variation of the POGLUT2 and POGLUT3 consensus sequence can produce aberrant fibrillin-1 O-glucosylation. [PDF]

J Biol Chem
Kegley NR, Ito A, Williamson DB, McArdle CC, Haltiwanger RS.   +4 more
europepmc   +1 more source