PMC Links for Gene (Select 7148) - PMC

Links from Gene

Items: 1 to 20 of 55

<< First< Prev

Page of 3

Select item 80771171.

A TNXB splice donor site variant as a cause of hypermobility type Ehlers–Danlos syndrome in patients with congenital adrenal hyperplasia

Qizong Lao, Ashwini Mallappa, Fabio Rueda Faucz, Elizabeth Joyal, Padmasree Veeraraghavan, Wuyan Chen, Deborah P. Merke

Mol Genet Genomic Med. 2021 Feb; 9(2): e1556. Published online 2020 Dec 17. doi: 10.1002/mgg3.1556

PMCID:: PMC8077117

Article PDF–833K

Select item 64372622.

Tenascin-X in amniotic fluid and reproductive tissues of pregnancies complicated by infection and preterm prelabor rupture of membranes

Kara M Rood, Catalin S Buhimschi, Guomao Zhao, Emily A Oliver, Taryn Summerfield, Mert Ozan Bahtiyar, Irina A Buhimschi

Biol Reprod. 2019 Mar; 100(3): 773–782. Published online 2018 Oct 2. doi: 10.1093/biolre/ioy216

PMCID:: PMC6437262

Article PDF–8.0M

Select item 61175623.

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

Article PDF–1.4M

Select item 47471084.

RARE VARIANTS IN TENASCIN GENES IN A COHORT OF CHILDREN WITH PRIMARY VESICOURETERIC REFLUX

Shan Elahi, Alison Homstad, Himani Vaidya, Jennifer Stout, Gentzon Hall, Guanghong Wu, Peter Conlon, jr, Jonathan C. Routh, John S. Wiener, Sherry S. Ross, Shashi Nagaraj, Delbert Wigfall, John Foreman, Adebowale Adeyemo, Indra R. Gupta, Patrick D. Brophy, C. Egla Rabinovich, Rasheed A. Gbadegesin

Pediatr Nephrol. Author manuscript; available in PMC 2016 May 1.

Published in final edited form as: Pediatr Nephrol. 2016 Feb; 31(2): 247–253. Published online 2015 Sep 25. doi: 10.1007/s00467-015-3203-6

PMCID:: PMC4747108

Article PDF–655K

Select item 44502425.

Secretome Identifies Tenascin-X as a Potent Marker of Ovarian Cancer

Marianne Kramer, Sandra Pierredon, Pascale Ribaux, Jean-Christophe Tille, Patrick Petignat, Marie Cohen

Biomed Res Int. 2015; 2015: 208017. Published online 2015 May 18. doi: 10.1155/2015/208017

PMCID:: PMC4450242

Article PDF–3.2M

Select item 44228026.

Tenascin-X: beyond the architectural function

Ulrich Valcourt, Lindsay B Alcaraz, Jean-Yves Exposito, Claire Lethias, Laurent Bartholin

Cell Adh Migr. 2015 Jan-Apr; 9(1-2): 154–165. Published online 2015 Mar 20. doi: 10.4161/19336918.2014.994893

PMCID:: PMC4422802

Article PDF–1.1M

Select item 37367177.

TNXB Mutations Can Cause Vesicoureteral Reflux

Rasheed A. Gbadegesin, Patrick D. Brophy, Adebowale Adeyemo, Gentzon Hall, Indra R. Gupta, David Hains, Bartlomeij Bartkowiak, C. Egla Rabinovich, Settara Chandrasekharappa, Alison Homstad, Katherine Westreich, Guanghong Wu, Yutao Liu, Danniele Holanda, Jason Clarke, Peter Lavin, Angelica Selim, Sara Miller, John S. Wiener, Sherry S. Ross, John Foreman, Charles Rotimi, Michelle P. Winn

J Am Soc Nephrol. 2013 Jul 31; 24(8): 1313–1322. Published online 2013 Apr 25. doi: 10.1681/ASN.2012121148

PMCID:: PMC3736717

Article

Select item 30057938.

Phenotypic effects of Ehlers–Danlos syndrome-associated mutation on the FnIII domain of tenascin-X

Shulin Zhuang, Apichart Linhananta, Hongbin Li

Protein Sci. 2010 Nov; 19(11): 2231–2239. doi: 10.1002/pro.503

PMCID:: PMC3005793

Article PDF–381K

Select item 27839949.

Tenascin-X is a novel diagnostic marker of malignant mesothelioma

Yuan Yuan, Dag André Nymoen, Helene Tuft Stavnes, Anne Katrine Rossnes, Ola Bjørang, Chuanyue Wu, Jahn M. Nesland, Ben Davidson

Am J Surg Pathol. Author manuscript; available in PMC 2010 Nov 1.

Published in final edited form as: Am J Surg Pathol. 2009 Nov; 33(11): 1673–1682. doi: 10.1097/PAS.0b013e3181b6bde3

PMCID:: PMC2783994

Article PDF–2.4M

Select item 641876410.

A novel role for the extracellular matrix glycoprotein‐Tenascin‐X in gastric function

Rubina Aktar, Madusha Peiris, Asma Fikree, Simon Eaton, Stamatiki Kritas, Stephen J. Kentish, Eduardo J. A. Araujo, Cristiano Bacarin, Amanda J. Page, Nicol C. Voermans, Qasim Aziz, L. Ashley Blackshaw

J Physiol. 2019 Mar 15; 597(6): 1503–1515. Published online 2019 Jan 23. doi: 10.1113/JP277195

PMCID:: PMC6418764

Article PDF–2.7M

Select item 498320611.

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

Article PDF–1.9M

Select item 238675112.

Analysis of obstetric complications and uterine connective tissue in tenascin-X-deficient humans and mice

David F. Egging, Ivonne van Vlijmen-Willems, Jiwon Choi, Anita C. T. M. Peeters, Desiree van Rens, Guido Veit, Manuel Koch, Elaine C. Davis, Joost Schalkwijk

Cell Tissue Res. 2008 Jun; 332(3): 523–532. Published online 2008 Mar 12. doi: 10.1007/s00441-008-0591-y

PMCID:: PMC2386751

Article PDF–844K

Select item 211959613.

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 36438414.

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 633269515.

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

Article PDF–1.9M

Select item 356511616.

Tenascin-X Haploinsufficiency Associated with Ehlers-Danlos Syndrome in Patients with Congenital Adrenal Hyperplasia

Deborah P. Merke, Wuyan Chen, Rachel Morissette, Zhi Xu, Carol Van Ryzin, Vandana Sachdev, Hwaida Hannoush, Sujata M. Shanbhag, Ana T. Acevedo, Miki Nishitani, Andrew E. Arai, Nazli B. McDonnell

J Clin Endocrinol Metab. 2013 Feb; 98(2): E379–E387. Published online 2013 Jan 2. doi: 10.1210/jc.2012-3148

PMCID:: PMC3565116

Article

Select item 29788817.

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 731663218.

Differential DNA methylation patterns in human Schlemm’s canal endothelial cells with glaucoma

Jingwen Cai, Michelle D. Drewry, Kristin Perkumas, W. Michael Dismuke, Michael A. Hauser, W. Daniel Stamer, Yutao Liu

Mol Vis. 2020; 26: 483–493. Published online 2020 Jun 26.

PMCID:: PMC7316632

Article PDF–1.1M

Select item 173546219.

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

P Koppens, H Smeets, I J de Wijs, H Degenhart

J Med Genet. 2003 May; 40(5): e53. doi: 10.1136/jmg.40.5.e53

PMCID:: PMC1735462

Summary PDF–235K

Select item 382013120.

A genome-wide association study of atopic dermatitis identifies loci with overlapping effects on asthma and psoriasis

Stephan Weidinger, Saffron A.G. Willis-Owen, Yoichiro Kamatani, Hansjörg Baurecht, Nilesh Morar, Liming Liang, Pauline Edser, Teresa Street, Elke Rodriguez, Grainne M. O'Regan, Paula Beattie, Regina Fölster-Holst, Andre Franke, Natalija Novak, Caoimhe M. Fahy, Mårten C.G. Winge, Michael Kabesch, Thomas Illig, Simon Heath, Cilla Söderhäll, Erik Melén, Göran Pershagen, Juha Kere, Maria Bradley, Agne Lieden, Magnus Nordenskjold, John I. Harper, W.H. Irwin Mclean, Sara J. Brown, William O.C. Cookson, G. Mark Lathrop, Alan D. Irvine, Miriam F. Moffatt

Hum Mol Genet. 2013 Dec 1; 22(23): 4841–4856. Published online 2013 Jul 25. doi: 10.1093/hmg/ddt317

PMCID:: PMC3820131

Article PDF–898K

PMC

Result Filters

Article attributes

Text availability

Publication date

Custom date range

Research Funder

Additional filters

Display Settings:

Send to:

Links from Gene

Items: 1 to 20 of 55

Display Settings:

Send to:

Supplemental Content

Find related data

Recent activity