Why is "Fibrillin" trending?

Search Interest Perspective

• Angiotensin II Induces Abdominal Aortic Branch Aneurysms in Fibrillin-1 - American Heart Association Journals
• Fibrillin microfibril structure identifies long-range effects of inherited pathogenic mutations affecting a key regulatory latent TGFβ-binding site - Nature
• Determination of the molecular basis of Marfan syndrome: a growth industry - National Institutes of Health (NIH) | (.gov)
• How sugars shape Marfan syndrome - American Society for Biochemistry and Molecular Biology
• Mutations in Fibrillin-1 Cause Congenital Scleroderma: Stiff Skin Syndrome - Science | AAAS
• Endothelial BMAL1 decline during aging leads to bone loss by destabilizing extracellular fibrillin-1 - JCI.org
• Increased extracellular deposition of fibrillin-containing fibrils in pseudoexfoliation syndrome. - ARVO Journals
• Pathogenetic sequence for aneurysm revealed in mice underexpressing fibrillin-1 - PNAS
• Aqueous humor TGFβ and fibrillin-1 in Tsk mice reveal clues to POAG pathogenesis - Nature
• Fibrillin-1–enriched microenvironment drives endothelial injury and vascular rarefaction in chronic kidney disease - Science | AAAS
• Intravitreal injection of fibrillin 2 (Fbn2) recombinant protein for therapy of retinopathy in a retina-specific Fbn2 knock-down mouse model - Nature
• DNA methylation ambiguity in the Fibrillin-1 FBN1 ) CpG island shore possibly involved in Marfan syndrome - Nature
• Fibrillin-1 mutant mouse captures defining features of human primary open glaucoma including anomalous aqueous humor TGF beta-2 - Nature
• Generation of heterozygous fibrillin-1 mutant cloned pigs from genome-edited foetal fibroblasts | Scientific Reports - Nature
• In vivo phenotypic vascular dysfunction extends beyond the aorta in a mouse model for fibrillin-1 ( Fbn1 ) mutation - Nature
• Fibrillin-1 expression in normal and fibrotic rat liver and in cultured hepatic fibroblastic cells: modulation by mechanical stress and role in cell adhesion - Nature
• Correction: Intravitreal injection of fibrillin 2 (Fbn2) recombinant protein for therapy of retinopathy in a retina-specific Fbn2 knock-down mouse model - Nature
• Gremlin-1 associates with fibrillin microfibrils in vivo and regulates mesothelioma cell survival through transcription factor slug - Nature
• Rare and common variants in extracellular matrix gene fibrillin 2 (FBN2) are associated with inherited and age-related macular degeneration, respectively | IOVS | ARVO Journals - ARVO Journals
• Disrupted Cellularity in Partial Tendon Enthesis Injury of Fibrillin-1 Deficient Mice - Stanford Medicine
• Fibulin-4 deposition requires EMILIN-1 in the extracellular matrix of osteoblasts - Nature
• Marfanoid–progeroid–lipodystrophy syndrome: a newly recognized fibrillinopathy - Nature
• Marfan syndrome in the third Millennium - European Journal of Human Genetics - Nature
• Meet Your Gene: An Introduction to the Marfan Gene and Current Research - Marfan Foundation
• The Fibrillin-1/VEGFR2/STAT2 signaling axis promotes chemoresistance via modulating glycolysis and angiogenesis in ovarian cancer organoids and cells - Wiley Online Library
• Hand and fibrillin-1 deposition abnormalities in Loeys–Dietz syndrome—expanding the clinical spectrum - Wiley Online Library
• Latent TGF-β binding protein 4 promotes elastic fiber assembly by interacting with fibulin-5 - PNAS
• New insights into the structural role of EMILINs within the human skin microenvironment - Nature
• Co-expression of FBN1 with mesenchyme-specific genes in mouse cell lines: implications for phenotypic variability in Marfan syndrome - Nature
• Latent TGF-β binding protein 2 and 4 have essential overlapping functions in microfibril development - Nature
• New research on Marfan syndrome focuses on eyes | Newswise - newswise.com
• Severe scoliosis linked to rare mutations - EurekAlert!
• Fibrillin-1 microfibril deposition is dependent on fibronectin assembly - The Company of Biologists
• A Molecular Approach to the Stratification of Cardiovascular Risk in Families with Marfan's Syndrome - The New England Journal of Medicine
• ADAMTS-10 and -6 differentially regulate cell-cell junctions and focal adhesions | Scientific Reports - Nature
• Genotype-phenotype correlations of marfan syndrome and related fibrillinopathies: Phenomenon and molecular relevance - Frontiers
• New clues in aortic dissection: Endothelial dysfunction meets immune infiltration - Medical Xpress
• Possible break-down of redox homeostasis in Beals-Hecht syndrome - Nature
• Hopkins doctor makes breakthrough discovery on cause of Marfan syndrome - Johns Hopkins University
• Recent progress in genetics of Marfan syndrome and Marfan-associated disorders - Nature
• Analysis of the tight skin ( Tsk1/+ ) mouse as a model for testing antifibrotic agents - Nature
• Reversion-inducing cysteine-rich protein with Kazal motifs and MT1-MMP promote the formation of robust fibrillin fibers - Wiley Online Library
• Building Strength to Survive With Marfan Syndrome - Froedtert & MCW
• 2 THE FIBRILLINOPATHIES: A SPECTRUM OF DISORDERS WITH OPPOSING PHENOTYPES - Wiley Online Library
• Microspherophakia: Genetics, Diagnosis, and Management - American Academy of Ophthalmology
• Johns Hopkins Researcher Elected To National Academy of Sciences | Newswise - newswise.com
• Gene affects the height of Peruvians - Revista Pesquisa Fapesp
• World-first ‘super peptide’ technology bio-hacks the skin’s natural repair process - The University of Manchester
• 'Proof' face creams beat wrinkles - BBC
• Secret new Boots No7 skincare being called 'game changer' as waiting list opens - Birmingham Live
• Marfan Syndrome: The Connective Tissue Disorder Hidden in Tall, Thin Bodies - Observer Voice