LAMA3 Gene

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Liu, D. LAMA3 Gene. Encyclopedia. Available online: https://encyclopedia.pub/entry/4362 (accessed on 29 September 2026).

Liu D. LAMA3 Gene. Encyclopedia. Available at: https://encyclopedia.pub/entry/4362. Accessed September 29, 2026.

Liu, Dean. "LAMA3 Gene" Encyclopedia, https://encyclopedia.pub/entry/4362 (accessed September 29, 2026).

Liu, D. (2020, December 23). LAMA3 Gene. In Encyclopedia. https://encyclopedia.pub/entry/4362

Liu, Dean. "LAMA3 Gene." Encyclopedia. Web. 23 December, 2020.

LAMA3 Gene

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This entry is adapted from the peer-reviewed paper https://medlineplus.gov/genetics/gene/lama3

Laminin subunit alpha 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.
Barzegar M, Mozafari N, Kariminejad A, Asadikani Z, Ozoemena L, McGrath JA. A new homozygous nonsense mutation in LAMA3A underlying laryngo-onycho-cutaneoussyndrome. Br J Dermatol. 2013 Dec;169(6):1353-6. doi: 10.1111/bjd.12522.
Hamill KJ, McLean WH. The alpha-3 polypeptide chain of laminin 5: insight intowound healing responses from the study of genodermatoses. Clin Exp Dermatol. 2005Jul;30(4):398-404. Review.
Hamill KJ, Paller AS, Jones JC. Adhesion and migration, the diverse functions of the laminin alpha3 subunit. Dermatol Clin. 2010 Jan;28(1):79-87. doi:10.1016/j.det.2009.10.009. 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.
Kim CC, Liang MG, Pfendner E, Kimonis VE. What syndrome is this?Laryngo-onycho-cutaneous syndrome. Pediatr Dermatol. 2007 May-Jun;24(3):306-8.
McLean WH, Irvine AD, Hamill KJ, Whittock NV, Coleman-Campbell CM, MellerioJE, Ashton GS, Dopping-Hepenstal PJ, Eady RA, Jamil T, Phillips R, Shabbir SG,Haroon TS, Khurshid K, Moore JE, Page B, Darling J, Atherton DJ, Van Steensel MA,Munro CS, Smith FJ, McGrath JA. An unusual N-terminal deletion of the lamininalpha3a isoform leads to the chronic granulation tissue disorderlaryngo-onycho-cutaneous syndrome. Hum Mol Genet. 2003 Sep 15;12(18):2395-409.Rodney J [corrected to Phillips Roderic J].
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.
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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