TNXB Gene - GeneCards | TENX Protein | TENX Antibody
Tenascin-X deficiency mimics Ehlers-Danlos syndrome in mice through alteration of collagen deposition | Nature Genetics
Compound heterozygous mutations of the TNXB gene cause primary myopathy - ScienceDirect
Differentially methylated region identified within tenascin X (TNXB).... | Download Scientific Diagram
PDF) A TNXB splice donor site variant as a cause of hypermobility type Ehlers–Danlos syndrome in patients with congenital adrenal hyperplasia
Genes | Free Full-Text | Novel TNXB Variants in Two Italian Patients with Classical-Like Ehlers-Danlos Syndrome
Tenascin-X (TenX) Ehlers-Danlos syndrome - EDS Wellness, Inc.
High-Throughput Screening for CYP21A1P-TNXA/TNXB Chimeric Genes Responsible for Ehlers-Danlos Syndrome in Patients with Congenital Adrenal Hyperplasia - ScienceDirect
The Prevalence of the Chimeric TNXA/TNXB Gene and Clinical Symptoms of Ehlers–Danlos Syndrome with 21-Hydroxylase Deficiency
What is tenascin x (TNXB)? This might be the gene I am asked about the most. Many people wonder if their EDS could be caused by TNXB, and… | Instagram
Identification of a significant association of a single nucleotide polymorphism in TNXB with systemic lupus erythematosus in a Japanese population | Journal of Human Genetics
TNXB Gene - GeneCards | TENX Protein | TENX Antibody
Missense mutations in TNXB as a cause of VUR. (A) Exons and protein... | Download Scientific Diagram
Tenascin-X Mediates Flow-Induced Suppression of EndMT and Atherosclerosis | Circulation Research
Tenascin XB Is a Novel Diagnostic Marker for Malignant Mesothelioma | Anticancer Research
Chimeric CYP21P/CYP21 and TNXA/TNXB genes in the RCCX module - ScienceDirect
Rare neurological manifestations in a Saudi Arabian patient with Ehlers–Danlos syndrome and a novel homozygous variant in the TNXB gene - Al‐Harbi - 2022 - American Journal of Medical Genetics Part A -
Biallelic CAH-X genetics and phenotypes. A: TNXB variants found on the... | Download Scientific Diagram
Schematic diagram of CYP21A1P/CYP21A2 and TNXA/TNXB chimera genes. (A)... | Download Scientific Diagram
Genes | Free Full-Text | Novel TNXB Variants in Two Italian Patients with Classical-Like Ehlers-Danlos Syndrome
Salt-wasting congenital adrenal hyperplasia phenotype as a result of the TNXA/TNXB chimera 1 (CAH-X CH-1) and the pathogenic IVS2-13A/C > G in CYP21A2 gene | Hormones
A TNXB splice donor site variant as a cause of hypermobility type Ehlers–Danlos syndrome in patients with congenital adrenal hyperplasia - Lao - 2021 - Molecular Genetics & Genomic Medicine - Wiley Online Library
Mutation analysis of the TNXB gene in CAH-X patients. A, Schematic of... | Download Scientific Diagram
Frontiers | Tenascin-X as a causal gene for classical-like Ehlers-Danlos syndrome
