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MKS3/TMEM67 mutations in patients with nephronophthisis (NPHP) and... |  Download Scientific Diagram
MKS3/TMEM67 mutations in patients with nephronophthisis (NPHP) and... | Download Scientific Diagram

Genes | Free Full-Text | Prenatal Versus Postnatal Diagnosis of  Meckel–Gruber and Joubert Syndrome in Patients with TMEM67 Mutations
Genes | Free Full-Text | Prenatal Versus Postnatal Diagnosis of Meckel–Gruber and Joubert Syndrome in Patients with TMEM67 Mutations

Identification of two missense mutations in TMEM67. (a) Sequence... |  Download Scientific Diagram
Identification of two missense mutations in TMEM67. (a) Sequence... | Download Scientific Diagram

MKS3 (NPHP11 or Meckelin or TMEM67) (Xenopus) antibody - BiCell Scientific®
MKS3 (NPHP11 or Meckelin or TMEM67) (Xenopus) antibody - BiCell Scientific®

TMEM67 Polyclonal Antibody, Invitrogen 100 μL; Unconjugated:Antibodies, |  Fisher Scientific
TMEM67 Polyclonal Antibody, Invitrogen 100 μL; Unconjugated:Antibodies, | Fisher Scientific

Differential expression analysis of the Tmem67 −/− post-natal... | Download  Scientific Diagram
Differential expression analysis of the Tmem67 −/− post-natal... | Download Scientific Diagram

Functional validation of novel MKS3/TMEM67 mutations in COACH syndrome |  Scientific Reports
Functional validation of novel MKS3/TMEM67 mutations in COACH syndrome | Scientific Reports

TMEM67 Gene - GeneCards | MKS3 Protein | MKS3 Antibody
TMEM67 Gene - GeneCards | MKS3 Protein | MKS3 Antibody

Joubert syndrome: congenital cerebellar ataxia with the molar tooth - The  Lancet Neurology
Joubert syndrome: congenital cerebellar ataxia with the molar tooth - The Lancet Neurology

TMEM67 Polyclonal Antibody | EpigenTek
TMEM67 Polyclonal Antibody | EpigenTek

TMEM67 Fusion Protein Ag5174 | Proteintech
TMEM67 Fusion Protein Ag5174 | Proteintech

Meckelin (TMEM67) Antibody | Abbexa Ltd
Meckelin (TMEM67) Antibody | Abbexa Ltd

TMEM67 Gene - GeneCards | MKS3 Protein | MKS3 Antibody
TMEM67 Gene - GeneCards | MKS3 Protein | MKS3 Antibody

Hypomorphic mutations in meckelin (MKS3/TMEM67) cause nephronophthisis with  liver fibrosis (NPHP11) | Journal of Medical Genetics
Hypomorphic mutations in meckelin (MKS3/TMEM67) cause nephronophthisis with liver fibrosis (NPHP11) | Journal of Medical Genetics

The ciliary Frizzled-like receptor Tmem67 regulates canonical Wnt/β-catenin  signalling in the developing cerebellum via Hoxb5 | Scientific Reports
The ciliary Frizzled-like receptor Tmem67 regulates canonical Wnt/β-catenin signalling in the developing cerebellum via Hoxb5 | Scientific Reports

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

Characterizing the morbid genome of ciliopathies | Genome Biology | Full  Text
Characterizing the morbid genome of ciliopathies | Genome Biology | 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

JCI Insight - TRPV4 antagonists ameliorate ventriculomegaly in a rat model  of hydrocephalus
JCI Insight - TRPV4 antagonists ameliorate ventriculomegaly in a rat model of hydrocephalus

Anti-TMEM67 Antibody Products | Biocompare
Anti-TMEM67 Antibody Products | Biocompare

Meckel syndrome | Polycystic Kidney Disease: from Bench to Bedside
Meckel syndrome | Polycystic Kidney Disease: from Bench to Bedside

TMEM67 Polyclonal Antibody (PA5-141155)
TMEM67 Polyclonal Antibody (PA5-141155)

The ciliary Frizzled-like receptor Tmem67 regulates canonical Wnt/β-catenin  signalling in the developing cerebellum via Hoxb5 | Scientific Reports
The ciliary Frizzled-like receptor Tmem67 regulates canonical Wnt/β-catenin signalling in the developing cerebellum via Hoxb5 | Scientific Reports

What is TMEM67 Gene Joubert syndrome type 6 NGS Genetic DNA Test ?
What is TMEM67 Gene Joubert syndrome type 6 NGS Genetic DNA Test ?