MKS3 (NPHP11 or Meckelin or TMEM67) antibody - BiCell Scientific®
Meckel syndrome | Polycystic Kidney Disease: from Bench to Bedside
MKS3 antibody (13975-1-AP) | Proteintech
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
Hydrocephalus in a rat model of Meckel Gruber syndrome with a TMEM67 mutation | Scientific Reports
Anti-TMEM67 Polyclonal Antibody, CSB-PA689243LA01HU | ARP American Research Products, Inc.
TMEM67 Polyclonal Antibody | EpigenTek
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 MGI Mouse Gene Detail - MGI:1923928 - transmembrane protein 67
TMEM67 Polyclonal Antibody | EpigenTek
TMEM67 Antibody (ABIN2856740)
TMEM67 Antikörper (ABIN6263272)
JCI Insight - TRPV4 antagonists ameliorate ventriculomegaly in a rat model of hydrocephalus
TMEM67 Gene - GeneCards | MKS3 Protein | MKS3 Antibody
TMEM67 Polyclonal Antibody (PA5-141155)
Hemorrhage at birth and neonatal ventriculomegaly. (a) Hemorrhage in... | Download Scientific Diagram
TMEM67 Antikörper (ABIN6263272)
Functional validation of novel MKS3/TMEM67 mutations in COACH syndrome | Scientific Reports
Hypomorphic mutations in meckelin (MKS3/TMEM67) cause nephronophthisis with liver fibrosis (NPHP11) | Journal of Medical Genetics
Treatment of hydrocephalic Tmem67 -/-rats with TRPV4 agonist... | Download Scientific Diagram
TMEM67 antibody | Biorbyt
TMEM67 Gene - GeneCards | MKS3 Protein | MKS3 Antibody
