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(A) The structure of meckelin protein encoded by TMEM67 gene and the ...
Domain structure of TMEM67 and clinical images of the patient with ...
TMEM67 Gene - GeneCards | MKS3 Protein | MKS3 Antibody
Increased canonical Wnt signalling following loss of TMEM67 is ...
Validation of C. elegans predictions of TMEM67 VUS pathogenicity in ...
| Missense variants of the TMEM67 gene in MKS and JBS. There were about ...
The ciliary Frizzled-like receptor Tmem67 regulates canonical Wnt/β ...
(PDF) The Meckel-Gruber syndrome protein TMEM67 controls basal body ...
TMEM67 Gene - Somatic Mutations in Cancer
Homeobox transcription factor Hoxb5 is up-regulated in the Tmem67 −/− ...
DNA sequence analysis of TMEM67 gene and amino acid alignment of ...
Characterization of the TMEM67 genotype in the Wpk rat. (a) Design of ...
TMEM67 - Wikipedia
Loss of Wnt5a-induced branching morphogenesis during Tmem67 − / − ...
Differential expression analysis of the Tmem67 −/− post-natal ...
(PDF) Interpreting TMEM67 missense variants of uncertain significance ...
Sequencing analysis for AQP2 and TMEM67 genes. (A) Sequencing analysis ...
Characteristic of TMEM67 variants identified in examined patients ...
A missense mutation in TMEM67 causes Meckel-Gruber syndrome type 3 ...
Over-proliferation and increased apoptosis at in the Tmem67 −/− ...
TMEM67 Polyclonal Antibody (PA5-22095)
Treatment of hydrocephalic Tmem67 -/-rats with TRPV4 agonist ...
TMEM67 sequence variations associated with a wide phenotype spectrum ...
Novel TMEM67 mutations and genotype-phenotype correlates in meckelin ...
Upgrading an intronic TMEM67 variant of unknown significance to likely ...
Hydrocephalus in a rat model of Meckel Gruber syndrome with a TMEM67 ...
Cleavage of the Meckel-Gruber syndrome protein TMEM67 by ADAMTS9 ...
(PDF) Novel compound heterozygous TMEM67 variants in a Vietnamese ...
Novel TMEM67 Mutations and Genotype-phenotype Correlates in Meckelin ...
Amelioration of cranial doming by P15 in hydrocephalic Tmem67 -/-rats ...
(PDF) Novel TMEM67 mutations and genotype-phenotype correlates in ...
TMEM67 mutations found in a case of Joubert syndrome with renal ...
TMEM67 Fusion Protein Ag5009 | Proteintech
TMEM67 Polyclonal Antibody | Invitrogen (PA5-141155)
MKS3/TMEM67 mutations are a major cause of COACH Syndrome, a Joubert ...
Frontiers | The transmembrane proteins (TMEM) and their role in cell ...
(a) Structural mapping of the two novel pathogenic mutations onto the ...
TMEM67, TMEM237, and Embigin in Complex With Monocarboxylate ...
(PDF) TMEM67, TMEM237, and Embigin in Complex With Monocarboxylate ...
MKS3 (NPHP11 or Meckelin or TMEM67) (Xenopus) antibody - BiCell Scientific®
Midline malformation and ciliary phenotype at birth in the TMEM67+/− ...
Defects in Purkinje cell morphology, ciliogenesis and Shh signalling in ...
Tmem67−/− cerebellar hypoplasia and foliation defects at perinatal and ...
Primary cilia prevent activation of the cGAS-STING pathway during mouse ...
Hypomorphic mutations in meckelin (MKS3/TMEM67) cause nephronophthisis ...
The Meckel syndrome protein meckelin (TMEM67) is a key regulator of ...
Custom Antibody Production with Guaranteed Success - BiCell Scientific®
TM6/TM7 dimerization interface in 10 structures of MT7-hM1 dimer ...
Figure 3 from A case of Joubert syndrome caused by novel compound ...
The transition zone. (A) Freeze-etch electron micrograph of tracheal ...
Functional validation of novel MKS3/TMEM67 mutations in COACH syndrome ...
(PDF) Hydrocephalus in a rat model of Meckel Gruber syndrome with a ...
mtor Haploinsufficiency Ameliorates Renal Cysts and Cilia Abnormality ...
Anti-TMEM67 antibody | Science Company | Labroots
兔抗TMEM67多克隆抗体,Anti-TMEM67 rabbit polyclonal antibody 生命科学产品与技术服务-生工生物工程 ...
MKS3 (NPHP11 or Meckelin or TMEM67) antibody - BiCell Scientific®
MKS3/TMEM67 mutations in patients with nephronophthisis (NPHP) and ...
Seven different MKS3/TMEM67 mutations in four families with ...
An ovine hepatorenal fibrocystic model of a Meckel-like syndrome ...
CCEP-290 belongs to a third transition zone module required for ...
Transmembrane proteins with unknown function (TMEMs) as ion channels ...
Magnetic Resonance Imaging (MRI) of the WT and heterozygous (TMEM67 +/− ...
Prenatal Versus Postnatal Diagnosis of Meckel–Gruber and Joubert ...
Regulation of the length of neuronal primary cilia and its potential ...
(PDF) The Meckel syndrome protein meckelin (TMEM67) is a key regulator ...
Primary cilia and their effects on immune cell functions and metabolism ...
All diagnostic variants were illustrated at the gene exon and protein ...
Primary Cilium Is Involved in Stem Cell Differentiation and Renewal ...
Identification of two missense mutations in TMEM67. (a) Sequence ...
Normal PCP and apical planar asymmetry in the organ of Corti of ...
Figure 2 from A case of Joubert syndrome caused by novel compound ...
The receptor tyrosine kinase-like orphan receptor ROR2 colocalises and ...
(PDF) Superresolution Pattern Recognition Reveals the Architectural Map ...
