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Comandant Revizuire comandant de vas tmem67 conform Circulaţie Energize

Hydrocephalus in a rat model of Meckel Gruber syndrome with a TMEM67  mutation | Scientific Reports
Hydrocephalus in a rat model of Meckel Gruber syndrome with a TMEM67 mutation | Scientific Reports

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

MKS3 (NPHP11 or Meckelin or TMEM67) (Xenopus) antibody - BiCell Scientific®
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
Association of novel TMEM67 variants with mild phenotypes of high gamma-glutamyl transpeptidase cholestasis and congenital hepatic fibrosis,Journal of Cellular Physiology - X-MOL

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

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

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

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

TMEM67 Polyclonal Antibody (PA5-99981)
TMEM67 Polyclonal Antibody (PA5-99981)

TMEM67 Antikörper (ABIN6263272)
TMEM67 Antikörper (ABIN6263272)

MKS3 antibody (13975-1-AP) | Proteintech
MKS3 antibody (13975-1-AP) | Proteintech

Defects in Purkinje cell morphology, ciliogenesis and Shh signalling in...  | Download Scientific Diagram
Defects in Purkinje cell morphology, ciliogenesis and Shh signalling in... | Download Scientific Diagram

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

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

MKS3/TMEM67 mutations in patients with nephronophthisis (NPHP) and... |  Download Scientific Diagram
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, TMEM237, and Embigin in Complex With Monocarboxylate Transporter MCT1 Are Unique Components of the Photoreceptor Outer Segment Plasma Membrane - ScienceDirect

What is TMEM67 Gene Meckel syndrome type 3 NGS Genetic DNA Test ?
What is TMEM67 Gene Meckel syndrome type 3 NGS Genetic DNA Test ?

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

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

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

TMEM67 is required for the gating function of the transition zone that  controls entry of membrane-associated proteins ARL13B and INPP5E into  primary cilia - ScienceDirect
TMEM67 is required for the gating function of the transition zone that controls entry of membrane-associated proteins ARL13B and INPP5E into primary cilia - ScienceDirect

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

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

anti-TMEM67 antibody | anti-Human, Mouse Meckelin Polyclonal  Antibody-NP_001135773.1
anti-TMEM67 antibody | anti-Human, Mouse Meckelin Polyclonal Antibody-NP_001135773.1

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

CILIA: before and after | Cilia | Full Text
CILIA: before and after | Cilia | Full Text

Hydrocephalus in a rat model of Meckel Gruber syndrome with a TMEM67  mutation | Scientific Reports
Hydrocephalus in a rat model of Meckel Gruber syndrome with a TMEM67 mutation | Scientific Reports