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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
TMEM67 Polyclonal Antibody (PA5-99981)
TMEM67 Antikörper (ABIN7270970)
Differential expression analysis of the Tmem67 −/− post-natal... | Download Scientific Diagram
Functional validation of novel MKS3/TMEM67 mutations in COACH syndrome | Scientific Reports
Treatment of hydrocephalic Tmem67 -/-rats with TRPV4 agonist... | Download Scientific Diagram
What is TMEM67 Gene Meckel syndrome type 3 NGS Genetic DNA Test ?
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
Interpreting TMEM67 missense variants of uncertain significance (VUS) in an animal model | bioRxiv
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
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