Literature DB >> 22058051

The COL7A1 mutation database.

Katarzyna Wertheim-Tysarowska1, Agnieszka Sobczyńska-Tomaszewska, Cezary Kowalewski, Michał Skroński, Grzegorz Swięćkowski, Anna Kutkowska-Kaźmierczak, Katarzyna Woźniak, Jerzy Bal.   

Abstract

Dystrophic Epidermolysis Bullosa (DEB) is a genetic disease caused by mutations in the COL7A1 gene that is inherited in the autosomal dominant or recessive mode. We have developed a curated, freely accessible COL7A1 specific database (http://www.col7.info), which contains more than 730 reported and unpublished sequence variants of the gene. Molecular defects are reported according to HGVS recommendation. The clinical description module is provided with an advanced search tool together with a CSV (comm. separated values) data format download option. This compilation of COL7A1 data and nomenclature is aimed at assisting molecular and clinical geneticists to enhance the collaboration between researchers worldwide.
© 2011 Wiley Periodicals, Inc.

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Year:  2011        PMID: 22058051     DOI: 10.1002/humu.21651

Source DB:  PubMed          Journal:  Hum Mutat        ISSN: 1059-7794            Impact factor:   4.878


  27 in total

1.  Aminoglycosides restore full-length type VII collagen by overcoming premature termination codons: therapeutic implications for dystrophic epidermolysis bullosa.

Authors:  Jon Cogan; Jacqueline Weinstein; Xinyi Wang; Yingping Hou; Sabrina Martin; Andrew P South; David T Woodley; Mei Chen
Journal:  Mol Ther       Date:  2014-07-23       Impact factor: 11.454

2.  Genome-wide DNA methylation in neonates exposed to maternal depression, anxiety, or SSRI medication during pregnancy.

Authors:  Amy L Non; Alexandra M Binder; Laura D Kubzansky; Karin B Michels
Journal:  Epigenetics       Date:  2014-04-21       Impact factor: 4.528

3.  High Local Concentrations of Intradermal MSCs Restore Skin Integrity and Facilitate Wound Healing in Dystrophic Epidermolysis Bullosa.

Authors:  Tobias Kühl; Markus Mezger; Ingrid Hausser; Rupert Handgretinger; Leena Bruckner-Tuderman; Alexander Nyström
Journal:  Mol Ther       Date:  2015-04-10       Impact factor: 11.454

4.  Gentamicin induces functional type VII collagen in recessive dystrophic epidermolysis bullosa patients.

Authors:  David T Woodley; Jon Cogan; Yingping Hou; Chao Lyu; M Peter Marinkovich; Douglas Keene; Mei Chen
Journal:  J Clin Invest       Date:  2017-07-10       Impact factor: 14.808

Review 5.  Amlexanox Enhances Premature Termination Codon Read-Through in COL7A1 and Expression of Full Length Type VII Collagen: Potential Therapy for Recessive Dystrophic Epidermolysis Bullosa.

Authors:  Velina S Atanasova; Qiujie Jiang; Marco Prisco; Christina Gruber; Josefina Piñón Hofbauer; Mei Chen; Cristina Has; Leena Bruckner-Tuderman; John A McGrath; Jouni Uitto; Andrew P South
Journal:  J Invest Dermatol       Date:  2017-05-24       Impact factor: 8.551

6.  Characterization of mutant type VII collagens underlying the inversa subtype of recessive dystrophic epidermolysis bullosa.

Authors:  David T Woodley; Jon Cogan; Daniel Mosallaei; Kaitlyn Yim; Mei Chen
Journal:  J Dermatol Sci       Date:  2021-09-23       Impact factor: 4.563

7.  [The many facets of inherited skin fragility].

Authors:  C Has; D Kiritsi
Journal:  Hautarzt       Date:  2014-06       Impact factor: 0.751

8.  From Clinical Phenotype to Genotypic Modelling: Incidence and Prevalence of Recessive Dystrophic Epidermolysis Bullosa (RDEB).

Authors:  Shaundra Eichstadt; Jean Y Tang; Daniel C Solis; Zurab Siprashvili; M Peter Marinkovich; Nedra Whitehead; Matthew Schu; Fang Fang; Stephen W Erickson; Mary E Ritchey; Max Colao; Kaye Spratt; Amir Shaygan; Mark J Ahn; Kavita Y Sarin
Journal:  Clin Cosmet Investig Dermatol       Date:  2019-12-24

Review 9.  Toward Combined Cell and Gene Therapy for Genodermatoses.

Authors:  Laura De Rosa; Maria Carmela Latella; Alessia Secone Seconetti; Cecilia Cattelani; Johann W Bauer; Sergio Bondanza; Michele De Luca
Journal:  Cold Spring Harb Perspect Biol       Date:  2020-05-01       Impact factor: 10.005

10.  Mouse models for dominant dystrophic epidermolysis bullosa carrying common human point mutations recapitulate the human disease.

Authors:  Blake R C Smith; Alexander Nyström; Cameron J Nowell; Ingrid Hausser; Christine Gretzmeier; Susan J Robertson; George A Varigos; Cristina Has; Johannes S Kern; Ken C Pang
Journal:  Dis Model Mech       Date:  2021-06-04       Impact factor: 5.758

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