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UnknownTNXB mutations can cause vesicoureteral reflux.
Not available
S-EPMC3736717 | biostudies-literature
UnknownNovel TNXB Variants in Two Italian Patients with Classical-Like Ehlers-Danlos Syndrome.
Not available
S-EPMC6947605 | biostudies-literature
UnknownEhlers-Danlos Syndrome Caused by Biallelic TNXB Variants in Patients with Congenital Adrenal Hyperplasia.
Not available
S-EPMC4983206 | biostudies-literature
UnknownAberrant methylation and expression of TNXB promote chondrocyte apoptosis and extracullar matrix degradation in hemophilic arthropathy via AKT signaling.
Not available
S-EPMC11142640 | biostudies-literature
GenomicsMus musculus
Transcriptomic Analysis of Tnxb-DDX4 Cre Mouse Testes
PRJNA1314753 | ENA
UnknownA TNXB splice donor site variant as a cause of hypermobility type Ehlers-Danlos syndrome in patients with congenital adrenal hyperplasia.
Not available
S-EPMC8077117 | biostudies-literature
UnknownCase report: A novel compound heterozygous variant in the TNXB gene causes single kidney agenesis and vesicoureteral reflux.
Not available
S-EPMC10869528 | biostudies-literature
UnknownHigh-Throughput Screening for CYP21A1P-TNXA/TNXB Chimeric Genes Responsible for Ehlers-Danlos Syndrome in Patients with Congenital Adrenal Hyperplasia.
Not available
S-EPMC6734858 | biostudies-literature
UnknownClinical and Molecular Characterization of Classical-Like Ehlers-Danlos Syndrome Due to a Novel TNXB Variant.
Not available
S-EPMC6895888 | biostudies-literature
UnknownGenome-wide association study of age-related macular degeneration identifies associated variants in the TNXB-FKBPL-NOTCH4 region of chromosome 6p21.3.
Not available
S-EPMC3428154 | biostudies-literature
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