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
MKS3 (NPHP11 or Meckelin or TMEM67) (Xenopus) antibody - BiCell Scientific®
TMEM67, TMEM237, and Embigin in Complex With Monocarboxylate Transporter MCT1 Are Unique Components of the Photoreceptor Outer Segment Plasma Membrane - ScienceDirect
Characterizing the morbid genome of ciliopathies | Genome Biology | Full Text
Hypomorphic mutations in meckelin (MKS3/TMEM67) cause nephronophthisis with liver fibrosis (NPHP11) | Journal of Medical Genetics
TMEM67 Antibody (ABIN2856740)
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
Orientation defects in stereociliary hair bundles with uncoupling from... | Download Scientific Diagram
TMEM67, TMEM237, and Embigin in Complex With Monocarboxylate Transporter MCT1 Are Unique Components of the Photoreceptor Outer Segment Plasma Membrane - ScienceDirect
MKS3 antibody (13975-1-AP) | Proteintech
MKS3 (NPHP11 or Meckelin or TMEM67) antibody - BiCell Scientific®
TMEM67 Polyclonal Antibody | EpigenTek
TMEM67 Polyclonal Antibody (PA5-141155)
Genes | Free Full-Text | Prenatal Versus Postnatal Diagnosis of Meckel–Gruber and Joubert Syndrome in Patients with TMEM67 Mutations
Novel compound heterozygous TMEM67 variants in a Vietnamese family with Joubert syndrome: a case report | BMC Medical Genetics | Full Text