Differential expression analysis of the Tmem67 −/− post-natal... | Download Scientific Diagram
TMEM67 Fusion Protein Ag5174 | Proteintech
Meckel syndrome | Polycystic Kidney Disease: from Bench to Bedside
TMEM67 Polyclonal Antibody, Invitrogen 100 μL; Unconjugated:Antibodies, | Fisher Scientific
TMEM67 Gene - GeneCards | MKS3 Protein | MKS3 Antibody
TMEM67 Polyclonal Antibody | EpigenTek
Hydrocephalus in a rat model of Meckel Gruber syndrome with a TMEM67 mutation | Scientific Reports
Treatment of hydrocephalic Tmem67 -/-rats with TRPV4 agonist... | Download Scientific Diagram
JCI Insight - TRPV4 antagonists ameliorate ventriculomegaly in a rat model of hydrocephalus
![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/3-Figure1-1.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")
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
Joubert syndrome: congenital cerebellar ataxia with the molar tooth - The Lancet Neurology
TMEM67, TMEM237, and Embigin in Complex With Monocarboxylate Transporter MCT1 Are Unique Components of the Photoreceptor Outer Segment Plasma Membrane - ScienceDirect
Interpreting TMEM67 missense variants of uncertain significance (VUS) in an animal model | bioRxiv
Functional validation of novel MKS3/TMEM67 mutations in COACH syndrome | Scientific Reports
Novel compound heterozygous TMEM67 variants in a Vietnamese family with Joubert syndrome: a case report | BMC Medical Genetics | Full Text
Identification of two missense mutations in TMEM67. (a) Sequence... | Download Scientific Diagram
Characterizing the morbid genome of ciliopathies | Genome Biology | Full Text
The ciliary Frizzled-like receptor Tmem67 regulates canonical Wnt/β-catenin signalling in the developing cerebellum via Hoxb5 | Scientific Reports
What is TMEM67 Gene Joubert syndrome type 6 NGS Genetic DNA Test ?
Current models of protein localization in the transition zone. a... | Download Scientific Diagram
Hypomorphic mutations in meckelin (MKS3/TMEM67) cause nephronophthisis with liver fibrosis (NPHP11) | Journal of Medical Genetics
TMEM67 Polyclonal Antibody (PA5-141155)
The ciliary Frizzled-like receptor Tmem67 regulates canonical Wnt/β-catenin signalling in the developing cerebellum via Hoxb5 | Scientific Reports
