Connexin 26 (GJB2) mutations in keratitis-ichthyosis-deafness syndrome presenting with squamous cell carcinoma-Reference-Cited by-同舟云学术

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Connexin 26 (GJB2) mutations in keratitis-ichthyosis-deafness syndrome presenting with squamous cell carcinoma

Published:2011-11-21 Issue:9 Volume:39 Page:814-815
ISSN:0385-2407
Container-title:The Journal of Dermatology
language:en
Short-container-title:

Author:

SAKABE Jun-Ichi,YOSHIKI Ryutaro,SUGITA Kazunari,HARUYAMA Sanehito,SAWADA Yu,KABASHIMA Rieko,BITO Toshinori,NAKAMURA Motonobu,TOKURA Yoshiki

Publisher

Wiley

Subject

Dermatology,General Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1346-8138.2011.01414.x/fullpdf

Reference12 articles.

1. Keratitis-ichthyosis- deafness syndrome: disease expression and spectrum of connexin 26 (GJB2) mutations in 14 patients;Mazereeuw-Hautier;Br J Dermatol,2007

2. Keratitis, ichthyosis, and deafness (KID) syndrome. Vertical transmission and death from multiple squamous cell carcinomas;Grob;Arch Dermatol,1987

3. Connexin26 mutations associated with nonsyndromic hearing loss;Park;Laryngoscope,2000

4. A novel connexin 26 mutation in a patient diagnosed with keratitis-ichthyosis-deafness syndrome;van Steensel;J Invest Dermatol,2002

5. Malignant proliferating pilar tumors arising in KID syndrome: a report of two patients;Nyquist;Am J Med Genet A,2007

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1. The Multifaceted Role of Connexins in Tumor Microenvironment Initiation and Maintenance;Biology;2023-01-28

2. Keratitis‐ichthyosis‐deafness syndrome: A comprehensive review of cutaneous and systemic manifestations;Pediatric Dermatology;2022-11-29

3. Ceramide/protein phosphatase 2A axis is engaged in gap junction impairment elicited by PCB153 in liver stem-like progenitor cells;Molecular and Cellular Biochemistry;2021-04-10

4. Gap junctions and cancer: communicating for 50 years;Nature Reviews Cancer;2016-10-21

5. Hereditary Disorders of Cornification;Hurwitz Clinical Pediatric Dermatology;2016

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