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

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

Treatment of hydrocephalic Tmem67 -/-rats with TRPV4 agonist... | Download  Scientific Diagram
Treatment of hydrocephalic Tmem67 -/-rats with TRPV4 agonist... | Download Scientific Diagram

Current models of protein localization in the transition zone. a... |  Download Scientific Diagram
Current models of protein localization in the transition zone. a... | Download Scientific Diagram

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

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

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

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

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

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

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

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

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

TMEM67 Antibody (ABIN2856740)
TMEM67 Antibody (ABIN2856740)

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

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

Orientation defects in stereociliary hair bundles with uncoupling from... |  Download Scientific Diagram
Orientation defects in stereociliary hair bundles with uncoupling from... | 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

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

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

TMEM67 Polyclonal Antibody | EpigenTek
TMEM67 Polyclonal Antibody | EpigenTek

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

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

Novel compound heterozygous TMEM67 variants in a Vietnamese family with  Joubert syndrome: a case report | BMC Medical Genetics | Full Text
Novel compound heterozygous TMEM67 variants in a Vietnamese family with Joubert syndrome: a case report | BMC Medical Genetics | Full Text