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Cortney Gensemer, PhD on Instagram: “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,
Cortney Gensemer, PhD on Instagram: “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,

Frontiers | Tenascin-X—Discovery and Early Research
Frontiers | Tenascin-X—Discovery and Early Research

Classical-like Ehlers-Danlos Linked to Newly ID'd Mutation in TNXB Gene
Classical-like Ehlers-Danlos Linked to Newly ID'd Mutation in TNXB Gene

New TNXB Mutation in EDS Patient May Be Cause of Rare Lung Collapse
New TNXB Mutation in EDS Patient May Be Cause of Rare Lung Collapse

Frontiers | Tenascin-X as a causal gene for classical-like Ehlers-Danlos  syndrome
Frontiers | Tenascin-X as a causal gene for classical-like Ehlers-Danlos syndrome

Tenascin-X (TenX) Ehlers-Danlos syndrome - EDS Wellness, Inc.
Tenascin-X (TenX) Ehlers-Danlos syndrome - EDS Wellness, Inc.

Tenascin X - Wikipedia
Tenascin X - Wikipedia

TNXB Gene - GeneCards | TENX Protein | TENX Antibody
TNXB Gene - GeneCards | TENX Protein | TENX Antibody

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 -
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 -

TNXB Gene - GeneCards | TENX Protein | TENX Antibody
TNXB Gene - GeneCards | TENX Protein | TENX Antibody

Tenascin XB Is a Novel Diagnostic Marker for Malignant Mesothelioma |  Anticancer Research
Tenascin XB Is a Novel Diagnostic Marker for Malignant Mesothelioma | Anticancer Research

Frontiers | Genes and Pseudogenes: Complexity of the RCCX Locus and Disease
Frontiers | Genes and Pseudogenes: Complexity of the RCCX Locus and Disease

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
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

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 | SpringerLink
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 | SpringerLink

Mapping of a de novo unequal crossover causing a deletion of the steroid  21-hydroxylase (CYP21A2) gene and a non-functional hybrid tenascin-X (TNXB)  gene | Journal of Medical Genetics
Mapping of a de novo unequal crossover causing a deletion of the steroid 21-hydroxylase (CYP21A2) gene and a non-functional hybrid tenascin-X (TNXB) gene | Journal of Medical Genetics

Genes | Free Full-Text | Novel TNXB Variants in Two Italian Patients with  Classical-Like Ehlers-Danlos Syndrome
Genes | Free Full-Text | Novel TNXB Variants in Two Italian Patients with Classical-Like Ehlers-Danlos Syndrome

Tenascin-X, Congenital Adrenal Hyperplasia, and the CAH-X Syndrome |  Semantic Scholar
Tenascin-X, Congenital Adrenal Hyperplasia, and the CAH-X Syndrome | Semantic Scholar

PDF] Broadening the Spectrum of Ehlers Danlos Syndrome in Patients With  Congenital Adrenal Hyperplasia. | Semantic Scholar
PDF] Broadening the Spectrum of Ehlers Danlos Syndrome in Patients With Congenital Adrenal Hyperplasia. | Semantic Scholar

TNXB Gene - GeneCards | TENX Protein | TENX Antibody
TNXB Gene - GeneCards | TENX Protein | TENX Antibody

Missense mutations in TNXB as a cause of VUR. (A) Exons and protein... |  Download Scientific Diagram
Missense mutations in TNXB as a cause of VUR. (A) Exons and protein... | Download Scientific Diagram

TNXB Gene - GeneCards | TENX Protein | TENX Antibody
TNXB Gene - GeneCards | TENX Protein | TENX Antibody

TNXB Gene - GeneCards | TENX Protein | TENX Antibody
TNXB Gene - GeneCards | TENX Protein | TENX Antibody

Recognizing the tenascin‐X deficient type of Ehlers–Danlos syndrome: a  cross‐sectional study in 17 patients - Demirdas - 2017 - Clinical Genetics  - Wiley Online Library
Recognizing the tenascin‐X deficient type of Ehlers–Danlos syndrome: a cross‐sectional study in 17 patients - Demirdas - 2017 - Clinical Genetics - Wiley Online Library

Mutation analysis of the TNXB gene in CAH-X patients. A, Schematic of... |  Download Scientific Diagram
Mutation analysis of the TNXB gene in CAH-X patients. A, Schematic of... | Download Scientific Diagram

Mutation in TNXB gene causes moderate to severe Ehlers-Danlos syndrome
Mutation in TNXB gene causes moderate to severe Ehlers-Danlos syndrome

TNXB Gene - GeneCards | TENX Protein | TENX Antibody
TNXB Gene - GeneCards | TENX Protein | TENX Antibody

Chimeric CYP21P/CYP21 and TNXA/TNXB genes in the RCCX module - ScienceDirect
Chimeric CYP21P/CYP21 and TNXA/TNXB genes in the RCCX module - ScienceDirect