TMEM67 protein (human) - STRING interaction network
MKS3/TMEM67 mutations in patients with nephronophthisis (NPHP) and... | Download Scientific Diagram
Functional validation of novel MKS3/TMEM67 mutations in COACH syndrome | Scientific Reports
Anti-TMEM67 Polyclonal Antibody, CSB-PA689243LA01HU | ARP American Research Products, Inc.
TMEM67 Gene - GeneCards | MKS3 Protein | MKS3 Antibody
TMEM67 Fusion Protein Ag5009 | Proteintech
Meckel syndrome | Polycystic Kidney Disease: from Bench to Bedside
TMEM67 Polyclonal Antibody | EpigenTek
Hydrocephalus in a rat model of Meckel Gruber syndrome with a TMEM67 mutation | Scientific Reports
Anti-TMEM67 항체의, FITC (PACO36180)
Characterization of the TMEM67 genotype in the Wpk rat. (a) Design of... | Download Scientific Diagram
TMEM67 Antibody (ABIN2856740)
![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
MKS3 antibody (13975-1-AP) | Proteintech
TMEM67, TMEM237, and Embigin in Complex With Monocarboxylate Transporter MCT1 Are Unique Components of the Photoreceptor Outer Segment Plasma Membrane - ScienceDirect
TMEM67 antibody | Biorbyt
Treatment of hydrocephalic Tmem67 -/-rats with TRPV4 agonist... | Download Scientific Diagram
Meckelin (TMEM67) Antibody | Abbexa Ltd
JCI Insight - TRPV4 antagonists ameliorate ventriculomegaly in a rat model of hydrocephalus
The ciliary Frizzled-like receptor Tmem67 regulates canonical Wnt/β-catenin signalling in the developing cerebellum via Hoxb5 | Scientific Reports
Genes | Free Full-Text | Prenatal Versus Postnatal Diagnosis of Meckel–Gruber and Joubert Syndrome in Patients with TMEM67 Mutations
Characterizing the morbid genome of ciliopathies | Genome Biology | Full Text
TMEM67 Polyclonal Antibody, Invitrogen 100 μL; Unconjugated:Antibodies, | Fisher Scientific
MKS3 (NPHP11 or Meckelin or TMEM67) (Xenopus) antibody - BiCell Scientific®
Hypomorphic mutations in meckelin (MKS3/TMEM67) cause nephronophthisis with liver fibrosis (NPHP11) | Journal of Medical Genetics
TMEM67 Polyclonal Antibody | EpigenTek
