TMEM67, TMEM237, and Embigin in Complex With Monocarboxylate Transporter MCT1 Are Unique Components of the Photoreceptor Outer Segment Plasma Membrane - ScienceDirect
The ciliary Frizzled-like receptor Tmem67 regulates canonical Wnt/β-catenin signalling in the developing cerebellum via Hoxb5 | Scientific Reports
TMEM67 Polyclonal Antibody (PA5-22095)
The ciliary Frizzled-like receptor Tmem67 regulates canonical Wnt/β-catenin signalling in the developing cerebellum via Hoxb5 | Scientific Reports
Characterization of the TMEM67 genotype in the Wpk rat. (a) Design of... | Download Scientific Diagram
Hypomorphic mutations in meckelin (MKS3/TMEM67) cause nephronophthisis with liver fibrosis (NPHP11) | Journal of Medical Genetics
Treatment of hydrocephalic Tmem67 -/-rats with TRPV4 agonist... | Download Scientific Diagram
MKS3 (NPHP11 or Meckelin or TMEM67) (Xenopus) antibody - BiCell Scientific®
TMEM67 Gene - GeneCards | MKS3 Protein | MKS3 Antibody
Association of novel TMEM67 variants with mild phenotypes of high gamma-glutamyl transpeptidase cholestasis and congenital hepatic fibrosis,Journal of Cellular Physiology - X-MOL
JCI Insight - TRPV4 antagonists ameliorate ventriculomegaly in a rat model of hydrocephalus
Characterizing the morbid genome of ciliopathies | Genome Biology | Full Text
anti-TMEM67 antibody | anti-Human, Mouse Meckelin Polyclonal Antibody-NP_001135773.1
CILIA: before and after | Cilia | Full Text
Defects in Purkinje cell morphology, ciliogenesis and Shh signalling in... | Download Scientific Diagram
Hydrocephalus in a rat model of Meckel Gruber syndrome with a TMEM67 mutation | Scientific Reports
MKS3/TMEM67 mutations in patients with nephronophthisis (NPHP) and... | Download Scientific Diagram
Identification of two missense mutations in TMEM67. (a) Sequence... | Download Scientific Diagram
MKS3 antibody (13975-1-AP) | Proteintech
What is TMEM67 Gene Meckel syndrome type 3 NGS Genetic DNA Test ?
TMEM67 Fusion Protein Ag5174 | Proteintech
TMEM67 Antikörper (ABIN7270970)
TMEM67 Antikörper (ABIN6263272)
Functional validation of novel MKS3/TMEM67 mutations in COACH syndrome | Scientific Reports
Joubert syndrome: congenital cerebellar ataxia with the molar tooth - The Lancet Neurology
![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](https://d3i71xaburhd42.cloudfront.net/3b59f3f90ace79b035acd9b92330325268517b4f/11-Figure7-1.png "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")