TMEM67 Antikörper (ABIN6263272)
Meckelin (TMEM67) Antibody | Abbexa Ltd
Anti-TMEM67 항체의, FITC (PACO36180)
CILIA: before and after | Cilia | Full Text
TMEM67, TMEM237, and Embigin in Complex With Monocarboxylate Transporter MCT1 Are Unique Components of the Photoreceptor Outer Segment Plasma Membrane - ScienceDirect
TMEM67, TMEM237, and Embigin in Complex With Monocarboxylate Transporter MCT1 Are Unique Components of the Photoreceptor Outer Segment Plasma Membrane - ScienceDirect
Hypomorphic mutations in meckelin (MKS3/TMEM67) cause nephronophthisis with liver fibrosis (NPHP11) | Journal of Medical Genetics
Characterizing the morbid genome of ciliopathies | Genome Biology | Full Text
Identification of two missense mutations in TMEM67. (a) Sequence... | Download Scientific Diagram
Treatment of hydrocephalic Tmem67 -/-rats with TRPV4 agonist... | Download Scientific Diagram
TMEM67 Polyclonal Antibody | EpigenTek
TMEM67 protein (human) - STRING interaction network
The ciliary Frizzled-like receptor Tmem67 regulates canonical Wnt/β-catenin signalling in the developing cerebellum via Hoxb5 | Scientific Reports
TMEM67 Polyclonal Antibody, Invitrogen 100 μL; Unconjugated:Antibodies, | Fisher Scientific
Genes | Free Full-Text | Prenatal Versus Postnatal Diagnosis of Meckel–Gruber and Joubert Syndrome in Patients with TMEM67 Mutations
TMEM67 Antikörper (ABIN6263272)
Joubert syndrome: congenital cerebellar ataxia with the molar tooth - The Lancet Neurology
TMEM67 Gene - GeneCards | MKS3 Protein | MKS3 Antibody
TMEM67 Polyclonal Antibody, Invitrogen 100 μL; Unconjugated:Antibodies, | Fisher Scientific
MKS3 (NPHP11 or Meckelin or TMEM67) antibody - BiCell Scientific®
TMEM67 Antibody (ABIN2856740)
TMEM67 Polyclonal Antibody | EpigenTek
Tmem67 MGI Mouse Gene Detail - MGI:1923928 - transmembrane protein 67
Interpreting TMEM67 missense variants of uncertain significance (VUS) in an animal model | bioRxiv
Meckel syndrome | Polycystic Kidney Disease: from Bench to Bedside
