Endothelial BMAL1 decline during aging leads to bone loss by destabilizing extracellular fibrillin-1. [PDF]
Yin Y +12 more
europepmc +1 more source
Fibrillin-1 gene mutations in a Chinese cohort with congenital ectopia lentis: spectrum and genotype-phenotype analysis. [PDF]
Chen Z +7 more
europepmc +1 more source
Dinucleotide composition representation -based deep learning to predict scoliosis-associated Fibrillin-1 genotypes. [PDF]
Zhang S +8 more
europepmc +1 more source
A novel variant in fibrillin-1 is responsible for early-onset familial thoracic aortic aneurysms in Marfan patients. [PDF]
Duan Y, Chang H, Ling J, Liu S, Zhong Y.
europepmc +1 more source
Novel fibrillin-1 mutation with variable presentation as a thoracic aortic aneurysm and intramural hematoma. [PDF]
Brahmandam A, Vallabhajosyula P.
europepmc +1 more source
A felszálló aorta megbetegedései Marfan-szindrómában-molekuláris biológiai háttér és szívsebészeti megoldások [PDF]
Benke, Kálmán
core +1 more source
Fibrillin-1 Gene Variant p.Gly1754Ser Associated With Weill-Marchesani Syndrome Type 2: A Case Report. [PDF]
Tamhankar PM +3 more
europepmc +1 more source
Assembly assay identifies a critical region of human fibrillin-1 required for 10-12 nm diameter microfibril biogenesis. [PDF]
Jensen SA, Atwa O, Handford PA.
europepmc +1 more source
Neonatal Marfan syndrome: a case report of a novel fibrillin 1 mutation, with genotype-phenotype correlation and brief review of the literature. [PDF]
Pugnaloni F +8 more
europepmc +1 more source
Knockdown of fibrillin-1 suppresses retina-blood barrier dysfunction by inhibiting vascular endothelial apoptosis under diabetic conditions. [PDF]
Zhang Y +10 more
europepmc +1 more source

