Results 51 to 60 of about 3,124 (186)
Differential role of planar cell polarity gene Vangl2 in embryonic and adult mammalian kidneys.
Planar cell polarity (PCP) pathway is crucial for tissue morphogenesis. Mutations in PCP genes cause multi-organ anomalies including dysplastic kidneys.
Ida Derish +10 more
doaj +1 more source
(A) Immunoprecipitation (IP) of EGFP-Vangl1 or EGFP-Vangl2 using an antibody against GFP pulls down 3XHA-tagged Vangl2 when co-expressed in MDCK cells demonstrating the formation of an oligomeric complex.
Lisa V. Goodrich (182668) +3 more
core +1 more source
Van Gogh-like 2 (Vangl2), a core planar cell polarity component, plays an important role in polarized cellular and tissue morphology induction, growth development, and cancer. However, its role in regulating inflammatory responses remains elusive.
Jiansen Lu +16 more
doaj +1 more source
Betydelsen av VANGL2 i lymfangiogenes
The lymphatic system is a network of vessels that permeate a substantial part of the whole body. It plays an essential role in fluid homeostasis by the drainage of interstitial fluid from the blood capillaries, after which the fluid, now called lymph, is
Jakobsson, Emma
core
VANGL2 en situation de stress hématologique et en cancérologie [PDF]
PARTIE I Les voies de signalisation WNT sont essentielles pour plusieurs fonctions des cellules souches hématopoïétiques et progénitrices (HSPC) lors de l’hématopoïèse. Une des voies de signalisation Wnt permet la polarisation planaire des cellules (PCP)
Gauthier, Roxanne A
core +2 more sources
Abstract Background Endocytosis constitutes a fundamental cellular process governing development through coordinated regulation of plasma membrane remodeling and ciliogenesis, processes essential for cell shape changes and tissue development. Although Twist1 null embryos display complete cranial neural tube (NT) closure defects and conditional knockout
Derrick Thomas +8 more
wiley +1 more source
Muscle‐Specific Kinase Signaling and Its Therapeutic Potential
ABSTRACT The function of the neuromuscular junction (NMJ) is compromised in many neuromuscular diseases (NMDs) such as autoimmune or congenital myasthenia gravis (MG), amyotrophic lateral sclerosis (ALS), spinal muscular atrophy (SMA), and muscular dystrophies.
Stine Marie Jensen +2 more
wiley +1 more source
(A) CHO–N10 cells were transfected with HA-Fzd4, and the formation of a Fzd4-NHERF1 complex was determined by coimmunoprecipitation of the HA-tag followed by Western blotting with specific anti-NHERF1 antibodies.
Donna B. Stolz (270230) +5 more
core +1 more source
Functional analysis of germline VANGL2 variants using rescue assays of vangl2 knockout zebrafish [PDF]
\ua9 The Author(s) 2023. Published by Oxford University Press. Developmental studies have shown that the evolutionarily conserved Wnt Planar Cell Polarity (PCP) pathway is essential for the development of a diverse range of tissues and organs including ...
Chaudhry B +20 more
core +4 more sources
Prenatal exome sequencing significantly improves diagnostic yield over chromosomal microarray analysis for fetal CNS abnormalities, with a diagnostic yield of 16% in our cohort and 27% in the meta‐analysis. Diagnostic yields vary across different phenotypes. Abstract Introduction Fetal central nervous system (CNS) abnormalities have diverse etiologies,
Jia Yao +5 more
wiley +1 more source

