Literature DB >> 7525738

Genetic bases of epidermolysis bullosa simplex and epidermolytic hyperkeratosis.

E Fuchs1, P Coulombe, J Cheng, Y M Chan, E Hutton, A Syder, L Degenstein, Q C Yu, A Letai, R Vassar.   

Abstract

Keratins are the major structural proteins of the epidermis. Analyzing keratin gene sequences, appreciating the switch in keratin gene expression that takes place as epidermal cells commit to terminally differentiate, and elucidating how keratins assemble into 10-nm filaments have provided the foundation that has led to the discoveries of the genetic bases of two major classes of human skin diseases. In this report, we review the cell biology and human genetics of these diseases, epidermolysis bullosa simplex and epidermolytic hyperkeratosis. Both of these diseases are epidermal disorders of keratin, typified by cell fragility as a consequence of defects in the mechanical strength of basal epidermolysis bullosa simplex or suprabasal epidermolytic hyperkeratosis cells.

Entities:  

Mesh:

Substances:

Year:  1994        PMID: 7525738     DOI: 10.1111/1523-1747.ep12398924

Source DB:  PubMed          Journal:  J Invest Dermatol        ISSN: 0022-202X            Impact factor:   8.551


  12 in total

Review 1.  Lens intermediate filaments.

Authors:  Paul G FitzGerald
Journal:  Exp Eye Res       Date:  2008-11-24       Impact factor: 3.467

2.  Head and rod 1 interactions in vimentin: identification of contact sites, structure, and changes with phosphorylation using site-directed spin labeling and electron paramagnetic resonance.

Authors:  Atya Aziz; John F Hess; Madhu S Budamagunta; Paul G FitzGerald; John C Voss
Journal:  J Biol Chem       Date:  2008-12-31       Impact factor: 5.157

3.  Mutations Affecting Keratin 10 Surface-Exposed Residues Highlight the Structural Basis of Phenotypic Variation in Epidermolytic Ichthyosis.

Authors:  Haris Mirza; Anil Kumar; Brittany G Craiglow; Jing Zhou; Corey Saraceni; Richard Torbeck; Bruce Ragsdale; Paul Rehder; Annamari Ranki; Keith A Choate
Journal:  J Invest Dermatol       Date:  2015-06-15       Impact factor: 8.551

Review 4.  Lessons from skin blistering: molecular mechanisms and unusual patterns of inheritance?

Authors:  A S Paller
Journal:  Am J Pathol       Date:  1996-06       Impact factor: 4.307

5.  Autosomal-dominant congenital cataract associated with a deletion mutation in the human beaded filament protein gene BFSP2.

Authors:  P M Jakobs; J F Hess; P G FitzGerald; P Kramer; R G Weleber; M Litt
Journal:  Am J Hum Genet       Date:  2000-03-16       Impact factor: 11.025

6.  A transgenic mouse model with an inducible skin blistering disease phenotype.

Authors:  K Takahashi; P A Coulombe
Journal:  Proc Natl Acad Sci U S A       Date:  1996-12-10       Impact factor: 11.205

7.  KLF5 governs sphingolipid metabolism and barrier function of the skin.

Authors:  Ying Lyu; Yinglu Guan; Lisa Deliu; Ericka Humphrey; Joanna K Frontera; Youn Joo Yang; Daniel Zamler; Kun Hee Kim; Vakul Mohanty; Kevin Jin; Vakul Mohanty; Virginia Liu; Jinzhuang Dou; Lucas J Veillon; Shwetha V Kumar; Philip L Lorenzi; Yang Chen; Kathleen M McAndrews; Sergei Grivennikov; Xingzhi Song; Jianhua Zhang; Yuanxin Xi; Jing Wang; Ken Chen; Priyadharsini Nagarajan; Yejing Ge
Journal:  Genes Dev       Date:  2022-08-25       Impact factor: 12.890

8.  The function of intermediate filaments in cell shape and cytoskeletal integrity.

Authors:  R D Goldman; S Khuon; Y H Chou; P Opal; P M Steinert
Journal:  J Cell Biol       Date:  1996-08       Impact factor: 10.539

Review 9.  [Hereditary blistering disorders].

Authors:  C Has; J S Kern; L Bruckner-Tuderman
Journal:  Hautarzt       Date:  2004-10       Impact factor: 0.751

10.  Identifying the role of specific motifs in the lens fiber cell specific intermediate filament phakosin.

Authors:  Joshua T Pittenger; John F Hess; Paul G Fitzgerald
Journal:  Invest Ophthalmol Vis Sci       Date:  2007-11       Impact factor: 4.799

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.