Literature DB >> 10631162

A gene for an autosomal dominant scleroatrophic syndrome predisposing to skin cancer (Huriez syndrome) maps to chromosome 4q23.

Y A Lee, H P Stevens, E Delaporte, U Wahn, A Reis.   

Abstract

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Mesh：

Year:  2000        PMID： 10631162      PMCID： PMC1288338          DOI： 10.1086/302718

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN： 0002-9297            Impact factor:   11.025


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  30 in total

1.  [Sclero-atrophic and keratodermic genodermatosis of the extremities].

Authors:  D Lambert; H Planche; J L Chapuis
Journal:  Ann Dermatol Venereol       Date:  1977-10       Impact factor: 0.777

2.  [Scleroatrophying and degenerative keratodermic genodermatosis of the extremities].

Authors:  M Shaw; E Formentini; A R de Kaminsky; C A Kaminsky; J Abulafia
Journal:  Med Cutan Ibero Lat Am       Date:  1978

Review 3.  Epidermal growth factor.

Authors:  G Carpenter; S Cohen
Journal:  Annu Rev Biochem       Date:  1979       Impact factor: 23.643

Review 4.  Marjolin's ulcer: a review and reevaluation of a difficult problem.

Authors:  M D Fleming; J L Hunt; G F Purdue; J Sandstad
Journal:  J Burn Care Rehabil       Date:  1990 Sep-Oct

5.  Immunohistologic detection of the epidermal growth factor receptor in human esophageal squamous cell carcinoma.

Authors:  H Yano; H Shiozaki; K Kobayashi; T Yano; H Tahara; S Tamura; T Mori
Journal:  Cancer       Date:  1991-01-01       Impact factor: 6.860

6.  Human chromosomal mapping of genes for insulin-like growth factors I and II and epidermal growth factor.

Authors:  J E Brissenden; A Ullrich; U Francke
Journal:  Nature       Date:  1984 Aug 30-Sep 5       Impact factor: 49.962

7.  Squamous cell carcinoma in localized scleroderma following immunosuppressive therapy with azathioprine.

Authors:  F Nachbar; W Stolz; M Volkenandt; M Meurer
Journal:  Acta Derm Venereol       Date:  1993-06       Impact factor: 4.437

8.  Strategies for multilocus linkage analysis in humans.

Authors:  G M Lathrop; J M Lalouel; C Julier; J Ott
Journal:  Proc Natl Acad Sci U S A       Date:  1984-06       Impact factor: 11.205

9.  Allelotype analysis of cervical carcinoma.

Authors:  A B Mitra; V V Murty; R G Li; M Pratap; U K Luthra; R S Chaganti
Journal:  Cancer Res       Date:  1994-08-15       Impact factor: 12.701

10.  Patterns of epidermal growth factor receptors in basal and squamous cell carcinoma.

Authors:  E A Springer; J K Robinson
Journal:  J Dermatol Surg Oncol       Date:  1991-01
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  8 in total

Review 1.  Cutaneous Manifestations of Scleroderma and Scleroderma-Like Disorders: a Comprehensive Review.

Authors:  Caterina Ferreli; Giulia Gasparini; Aurora Parodi; Emanuele Cozzani; Franco Rongioletti; Laura Atzori
Journal:  Clin Rev Allergy Immunol       Date:  2017-12       Impact factor: 8.667

2.  A mortality gene(s) for the human adenocarcinoma line HeLa maps to a 130-kb region of human chromosome 4q22-q23.

Authors:  Steven D Bryce; Vivienne Morrison; Nicola J Craig; Nicholas R Forsyth; Sara A Fitzsimmons; Hazel Ireland; Andrew P Cuthbert; Robert F Newbold; E Kenneth Parkinson
Journal:  Neoplasia       Date:  2002 Nov-Dec       Impact factor: 5.715

3.  Association between Mutation in SMARCAD1 and Basan Syndrome with Cutaneous Squamous Cell Carcinoma.

Authors:  Ying Xiong; Ting Chen; Jia Yu; He Zhou; Baozhen Lu; Lijie Chen; Liwei Sun; Can Wang; Sujun Li; Bo Wu
Journal:  Dis Markers       Date:  2022-05-10       Impact factor: 3.464

4.  A Rare Syndrome Resembling Scleroderma: Huriez Syndrome.

Authors:  Nil Su Çelik; Şirin Yaşar; Sema Aytekin; Pembegül Güneş
Journal:  Skin Appendage Disord       Date:  2017-08-12

5.  [Genodermatoses with malignant skin tumors].

Authors:  L Hübinger; J Frank
Journal:  Hautarzt       Date:  2014-06       Impact factor: 0.751

Review 6.  [Palmoplantar dermatoses: when should genes be considered?].

Authors:  C Seebode; S Schiller; S Emmert; K Giehl
Journal:  Hautarzt       Date:  2014-06       Impact factor: 0.751

7.  Poikiloderma a varied presentation - Huriez syndrome.

Authors:  Priyadarshini Kharge; Carol Fernendes; Vijayeeta Jairath; Madan Mohan; Suresh Chandra
Journal:  Indian Dermatol Online J       Date:  2015 Jan-Feb

8.  Two SMARCAD1 Variants Causing Basan Syndrome in a Canadian and a Dutch Family.

Authors:  Youssef Elhaji; Tessa M A van Henten; Claudia A L Ruivenkamp; Mathew Nightingale; Gijs We Santen; Lydia E Vos; Peter R Hull
Journal:  JID Innov       Date:  2021-05-06
  8 in total

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