PMC Links for Protein (Select 188528648) - PMC

Select item 63326951.

Whole-genome methylation profiling of the retinal pigment epithelium of individuals with age-related macular degeneration reveals differential methylation of the SKI, GTF2H4, and TNXB genes

Louise F. Porter, Neil Saptarshi, Yongxiang Fang, Sonika Rathi, Anneke I. den Hollander, Eiko K. de Jong, Simon J. Clark, Paul N. Bishop, Timothy W. Olsen, Triantafillos Liloglou, Venkata R. M. Chavali, Luminita Paraoan

Clin Epigenetics. 2019; 11: 6. Published online 2019 Jan 14. doi: 10.1186/s13148-019-0608-2

PMCID:: PMC6332695

Abstract Article PDF–1.9M

Select item 61175622.

The extracellular matrix glycoprotein tenascin‐X regulates peripheral sensory and motor neurones

Rubina Aktar, Madusha Peiris, Asma Fikree, Vincent Cibert‐Goton, Maxim Walmsley, Iain R. Tough, Paulo Watanabe, Eduardo J. A. Araujo, Sahar D. Mohammed, Jean‐Marie Delalande, David C. Bulmer, S. Mark Scott, Helen M. Cox, Nicol C. Voermans, Qasim Aziz, L. Ashley Blackshaw

J Physiol. 2018 Sep 1; 596(17): 4237–4251. Published online 2018 Jul 18. doi: 10.1113/JP276300

PMCID:: PMC6117562

Abstract Article PDF–1.4M

Select item 21195963.

Tenascin-X: a novel extracellular matrix protein encoded by the human XB gene overlapping P450c21B

J Cell Biol. 1993 Jul 1; 122(1): 265–278. doi: 10.1083/jcb.122.1.265

PMCID:: PMC2119596

Summary PDF–2.7M

Select item 3643844.

Mechanism and consequences of the duplication of the human C4/P450c21/gene X locus.

S E Gitelman, J Bristow, W L Miller

Mol Cell Biol. 1992 May; 12(5): 2124–2134. doi: 10.1128/mcb.12.5.2124

Correction in:: Mol Cell Biol. 1992 Jul; 12(7): 3313–3314.

PMCID:: PMC364384

Summary Page Browse PDF–2.5M

Select item 2978885.

Transcript encoded on the opposite strand of the human steroid 21-hydroxylase/complement component C4 gene locus.

Y Morel, J Bristow, S E Gitelman, W L Miller

Proc Natl Acad Sci U S A. 1989 Sep; 86(17): 6582–6586. doi: 10.1073/pnas.86.17.6582

PMCID:: PMC297888

Summary Page Browse PDF–1.0M

Select item 68958886.

Clinical and Molecular Characterization of Classical-Like Ehlers-Danlos Syndrome Due to a Novel TNXB Variant

Daisy Rymen, Marco Ritelli, Nicoletta Zoppi, Valeria Cinquina, Cecilia Giunta, Marianne Rohrbach, Marina Colombi

Genes (Basel) 2019 Nov; 10(11): 843. Published online 2019 Oct 25. doi: 10.3390/genes10110843

PMCID:: PMC6895888

Abstract Article PDF–1.8M

Select item 49832067.

Ehlers-Danlos Syndrome Caused by Biallelic TNXB Variants in Patients with Congenital Adrenal Hyperplasia

Wuyan Chen, Ashley F. Perritt, Rachel Morissette, Jennifer L. Dreiling, Markus-Frederik Bohn, Ashwini Mallappa, Zhi Xu, Martha Quezado, Deborah P. Merke

Hum Mutat. Author manuscript; available in PMC 2017 Sep 1.

Published in final edited form as: Hum Mutat. 2016 Sep; 37(9): 893–897. Published online 2016 Jul 8. doi: 10.1002/humu.23028

PMCID:: PMC4983206

Abstract Article PDF–1.9M

PMC

Result Filters

Article attributes

Text availability

Publication date

Custom date range

Research Funder

Additional filters

Display Settings:

Send to:

Links from Protein

Items: 7

Display Settings:

Send to:

Supplemental Content

Find related data

Recent activity