Comandant Revizuire comandant de vas tmem67 conform Circulaţie Energize
Hydrocephalus in a rat model of Meckel Gruber syndrome with a TMEM67 mutation | Scientific Reports
JCI Insight - TRPV4 antagonists ameliorate ventriculomegaly in a rat model of hydrocephalus
MKS3 (NPHP11 or Meckelin or TMEM67) (Xenopus) antibody - BiCell Scientific®
Association of novel TMEM67 variants with mild phenotypes of high gamma-glutamyl transpeptidase cholestasis and congenital hepatic fibrosis,Journal of Cellular Physiology - X-MOL
TMEM67 Fusion Protein Ag5174 | Proteintech
PDF] The Meckel-Gruber syndrome protein TMEM67 controls basal body positioning and epithelial branching morphogenesis in mice via the non-canonical Wnt pathway | Semantic Scholar
Functional validation of novel MKS3/TMEM67 mutations in COACH syndrome | Scientific Reports
PDF] The Meckel-Gruber syndrome protein TMEM67 controls basal body positioning and epithelial branching morphogenesis in mice via the non-canonical Wnt pathway | Semantic Scholar
PDF] The Meckel-Gruber syndrome protein TMEM67 controls basal body positioning and epithelial branching morphogenesis in mice via the non-canonical Wnt pathway | Semantic Scholar
TMEM67 Polyclonal Antibody (PA5-99981)
TMEM67 Antikörper (ABIN6263272)
MKS3 antibody (13975-1-AP) | Proteintech
Defects in Purkinje cell morphology, ciliogenesis and Shh signalling in... | Download Scientific Diagram
The ciliary Frizzled-like receptor Tmem67 regulates canonical Wnt/β-catenin signalling in the developing cerebellum via Hoxb5 | Scientific Reports
Hypomorphic mutations in meckelin (MKS3/TMEM67) cause nephronophthisis with liver fibrosis (NPHP11) | Journal of Medical Genetics
MKS3/TMEM67 mutations in patients with nephronophthisis (NPHP) and... | Download Scientific Diagram
TMEM67, TMEM237, and Embigin in Complex With Monocarboxylate Transporter MCT1 Are Unique Components of the Photoreceptor Outer Segment Plasma Membrane - ScienceDirect
What is TMEM67 Gene Meckel syndrome type 3 NGS Genetic DNA Test ?
TMEM67 Gene - GeneCards | MKS3 Protein | MKS3 Antibody
MKS3 (NPHP11 or Meckelin or TMEM67) antibody - BiCell Scientific®
Differential expression analysis of the Tmem67 −/− post-natal... | Download Scientific Diagram
TMEM67 is required for the gating function of the transition zone that controls entry of membrane-associated proteins ARL13B and INPP5E into primary cilia - ScienceDirect
Genes | Free Full-Text | Prenatal Versus Postnatal Diagnosis of Meckel–Gruber and Joubert Syndrome in Patients with TMEM67 Mutations
TMEM67 Gene - GeneCards | MKS3 Protein | MKS3 Antibody