Pages that link to "Q28302896"

The following pages link to Filamin B mutations cause chondrocyte defects in skeletal development (Q28302896):

Displaying 44 items.

• Maternal genes and facial clefts in offspring: a comprehensive search for genetic associations in two population-based cleft studies from Scandinavia (Q21091121) (← links)
• Phenotypic and imaging features of FLNA-negative patients with bilateral periventricular nodular heterotopia and epilepsy. (Q30356209) (← links)
• Filamin B plays a key role in vascular endothelial growth factor-induced endothelial cell motility through its interaction with Rac-1 and Vav-2. (Q30494138) (← links)
• Temperature alters solute transport in growth plate cartilage measured by in vivo multiphoton microscopy (Q33431104) (← links)
• The ECM-cell interaction of cartilage extracellular matrix on chondrocytes. (Q33736114) (← links)
• Filamins in mechanosensing and signaling (Q33900830) (← links)
• Formin 1 and filamin B physically interact to coordinate chondrocyte proliferation and differentiation in the growth plate (Q33991787) (← links)
• Disease-associated mutations in the actin-binding domain of filamin B cause cytoplasmic focal accumulations correlating with disease severity (Q34108318) (← links)
• Targeting filamin B induces tumor growth and metastasis via enhanced activity of matrix metalloproteinase-9 and secretion of VEGF-A. (Q34284310) (← links)
• Systematic analysis of somatic mutations in phosphorylation signaling predicts novel cancer drivers (Q34323801) (← links)
• Diverse functions for the semaphorin receptor PlexinD1 in development and disease. (Q34361068) (← links)
• Conditional testing of multiple variants associated with bone mineral density in the FLNB gene region suggests that they represent a single association signal (Q35029582) (← links)
• Filamin B regulates chondrocyte proliferation and differentiation through Cdk1 signaling (Q35097777) (← links)
• The E3 ubiquitin ligase specificity subunit ASB2α targets filamins for proteasomal degradation by interacting with the filamin actin-binding domain (Q35112298) (← links)
• Phenotype and genotype in patients with Larsen syndrome: clinical homogeneity and allelic heterogeneity in seven patients (Q35980440) (← links)
• Whole-genome sequencing reveals small genomic regions of introgression in an introduced crater lake population of threespine stickleback (Q36662133) (← links)
• ASB2 targets filamins A and B to proteasomal degradation (Q37003539) (← links)
• Genome-wide association study identifies two novel loci containing FLNB and SBF2 genes underlying stature variation (Q37154259) (← links)
• Leucine restriction inhibits chondrocyte proliferation and differentiation through mechanisms both dependent and independent of mTOR signaling (Q37216757) (← links)
• ASB2α, an E3 ubiquitin ligase specificity subunit, regulates cell spreading and triggers proteasomal degradation of filamins by targeting the filamin calponin homology 1 domain (Q37272236) (← links)
• Upregulation of neurovascular communication through filamin abrogation promotes ectopic periventricular neurogenesis (Q37309763) (← links)
• Rapamycin regulates autophagy and cell adhesion in induced pluripotent stem cells. (Q37414577) (← links)
• Genetics of osteoporosis: accelerating pace in gene identification and validation (Q37681343) (← links)
• Specific entities affecting the craniocervical region: syndromes affecting the craniocervical junction (Q40109959) (← links)
• Refilins are short-lived Actin-bundling proteins that regulate lamellipodium protrusion dynamics. (Q41627580) (← links)
• Comparison of long noncoding RNA and mRNA expression profiles in mesenchymal stem cells derived from human periodontal ligament and bone marrow (Q41790458) (← links)
• Joint aging and chondrocyte cell death (Q41877821) (← links)
• Filamin A- and formin 2-dependent endocytosis regulates proliferation via the canonical Wnt pathway. (Q41921880) (← links)
• Characterization of two ENU-induced mutations affecting mouse skeletal morphology (Q42958302) (← links)
• Isoform divergence of the filamin family of proteins (Q43266833) (← links)
• Differential expression of the Toll-like receptor pathway and related genes of chicken bursa after experimental infection with infectious bursa disease virus (Q45355961) (← links)
• Atelosteogenesis Type I: Autopsy Findings (Q46690915) (← links)
• FilaminA and Formin2 regulate skeletal, muscular, and intestinal formation through mesenchymal progenitor proliferation. (Q47103216) (← links)
• Varicose and cheerio collaborate with pebble to mediate semaphorin-1a reverse signaling in Drosophila (Q47820441) (← links)
• Structural Analysis of G1691S Variant in the Human Filamin B Gene Responsible for Larsen Syndrome: A Comparative Computational Approach. (Q48290136) (← links)
• Opposing FlnA and FlnB interactions regulate RhoA activation in guiding dynamic actin stress fiber formation and cell spreading. (Q50456908) (← links)
• FilaminB is required for the directed localization of cell-cell adhesion molecules in embryonic epithelial development. (Q50530478) (← links)
• Genetic association of ARHGAP21 gene variant with mandibular prognathism (Q50957863) (← links)
• Filamin B Loss-of-Function Mutation in Dimerization Domain Causes Autosomal-Recessive Spondylocarpotarsal Synostosis Syndrome with Rib Anomalies (Q51158820) (← links)
• Three novel missense mutations in the filamin B gene are associated with isolated congenital talipes equinovarus (Q51652863) (← links)
• Comparative analysis of the two extremes of FLNB-mutated autosomal dominant disease spectrum: from clinical phenotypes to cellular and molecular findings. (Q55413613) (← links)
• Prune belly syndrome in surviving males can be caused by Hemizygous missense mutations in the X-linked Filamin A gene (Q89835791) (← links)
• Novel in-frame FLNB deletion causes Larsen syndrome in a three-generation pedigree (Q91971611) (← links)
• Filamin B extensively regulates transcription and alternative splicing, and is associated with apoptosis in HeLa cells (Q93173832) (← links)