LAMB3 Gene

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Liu, D. LAMB3 Gene. Encyclopedia. Available online: https://encyclopedia.pub/entry/4365 (accessed on 29 September 2026).

Liu D. LAMB3 Gene. Encyclopedia. Available at: https://encyclopedia.pub/entry/4365. Accessed September 29, 2026.

Liu, Dean. "LAMB3 Gene" Encyclopedia, https://encyclopedia.pub/entry/4365 (accessed September 29, 2026).

Liu, D. (2020, December 23). LAMB3 Gene. In Encyclopedia. https://encyclopedia.pub/entry/4365

Liu, Dean. "LAMB3 Gene." Encyclopedia. Web. 23 December, 2020.

LAMB3 Gene

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This entry is adapted from the peer-reviewed paper https://medlineplus.gov/genetics/gene/lamb3

Laminin subunit beta 3

genes

References

Aumailley M, Bruckner-Tuderman L, Carter WG, Deutzmann R, Edgar D, Ekblom P,Engel J, Engvall E, Hohenester E, Jones JC, Kleinman HK, Marinkovich MP, MartinGR, Mayer U, Meneguzzi G, Miner JH, Miyazaki K, Patarroyo M, Paulsson M, QuarantaV, Sanes JR, Sasaki T, Sekiguchi K, Sorokin LM, Talts JF, Tryggvason K, Uitto J, Virtanen I, von der Mark K, Wewer UM, Yamada Y, Yurchenco PD. A simplifiedlaminin nomenclature. Matrix Biol. 2005 Aug;24(5):326-32. Review.
Hartwig B, Borm B, Schneider H, Arin MJ, Kirfel G, Herzog V.Laminin-5-deficient human keratinocytes: defective adhesion results in asaltatory and inefficient mode of migration. Exp Cell Res. 2007 May1;313(8):1575-87.
Mühle C, Jiang QJ, Charlesworth A, Bruckner-Tuderman L, Meneguzzi G, SchneiderH. Novel and recurrent mutations in the laminin-5 genes causing lethal junctionalepidermolysis bullosa: molecular basis and clinical course of Herlitz disease.Hum Genet. 2005 Jan;116(1-2):33-42.
Nakano A, Chao SC, Pulkkinen L, Murrell D, Bruckner-Tuderman L, Pfendner E,Uitto J. Laminin 5 mutations in junctional epidermolysis bullosa: molecular basisof Herlitz vs. non-Herlitz phenotypes. Hum Genet. 2002 Jan;110(1):41-51.
Nakano A, Pfendner E, Hashimoto I, Uitto J. Herlitz junctional epidermolysisbullosa: novel and recurrent mutations in the LAMB3 gene and the populationcarrier frequency. J Invest Dermatol. 2000 Sep;115(3):493-8.
Pulkkinen L, Gerecke DR, Christiano AM, Wagman DW, Burgeson RE, Uitto J.Cloning of the beta 3 chain gene (LAMB3) of human laminin 5, a candidate gene in junctional epidermolysis bullosa. Genomics. 1995 Jan 1;25(1):192-8.
Pulkkinen L, Uitto J. Mutation analysis and molecular genetics ofepidermolysis bullosa. Matrix Biol. 1999 Feb;18(1):29-42. Review.
Schneider H, Mühle C, Pacho F. Biological function of laminin-5 and pathogenicimpact of its deficiency. Eur J Cell Biol. 2007 Dec;86(11-12):701-17.
Varki R, Sadowski S, Pfendner E, Uitto J. Epidermolysis bullosa. I. Molecular genetics of the junctional and hemidesmosomal variants. J Med Genet. 2006Aug;43(8):641-52.

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Subjects: Genetics & Heredity

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Update Date: 23 Dec 2020

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