PubMed (cited) for id: 190195

Year	Number of Results
1990	1
1991	2
1992	3
1995	2
1996	2
1997	2
1998	2
1999	3
2000	1
2001	4
2003	1
2005	1
2006	2
2007	1
2008	1
2009	4
2010	1
2011	1
2024	0

1

Analysis of TGM1, ALOX12B, ALOXE3, NIPAL4 and CYP4F22 in autosomal recessive congenital ichthyosis from Galicia (NW Spain): evidence of founder effects.

Rodríguez-Pazos L, Ginarte M, Fachal L, Toribio J, Carracedo A, Vega A. Rodríguez-Pazos L, et al. Br J Dermatol. 2011 Oct;165(4):906-11. doi: 10.1111/j.1365-2133.2011.10454.x. Epub 2011 Aug 4. Br J Dermatol. 2011. PMID: 21668430

2

Genotype-phenotype correlations with TGM1: clustering of mutations in the bathing suit ichthyosis and self-healing collodion baby variants of lamellar ichthyosis.

Hackett BC, Fitzgerald D, Watson RM, Hol FA, Irvine AD. Hackett BC, et al. Br J Dermatol. 2010 Feb 1;162(2):448-51. doi: 10.1111/j.1365-2133.2009.09537.x. Epub 2009 Oct 26. Br J Dermatol. 2010. PMID: 19863506 No abstract available.

3

Acral self-healing collodion baby: report of a new clinical phenotype caused by a novel TGM1 mutation.

Mazereeuw-Hautier J, Aufenvenne K, Deraison C, Ahvazi B, Oji V, Traupe H, Hovnanian A. Mazereeuw-Hautier J, et al. Br J Dermatol. 2009 Aug;161(2):456-63. doi: 10.1111/j.1365-2133.2009.09277.x. Epub 2009 Jun 4. Br J Dermatol. 2009. PMID: 19500103

4

Transglutaminase-1 and bathing suit ichthyosis: molecular analysis of gene/environment interactions.

Aufenvenne K, Oji V, Walker T, Becker-Pauly C, Hennies HC, Stöcker W, Traupe H. Aufenvenne K, et al. J Invest Dermatol. 2009 Aug;129(8):2068-71. doi: 10.1038/jid.2009.18. Epub 2009 Feb 12. J Invest Dermatol. 2009. PMID: 19212342 Free article. No abstract available.

5

Novel transglutaminase-1 mutations and genotype-phenotype investigations of 104 patients with autosomal recessive congenital ichthyosis in the USA.

Farasat S, Wei MH, Herman M, Liewehr DJ, Steinberg SM, Bale SJ, Fleckman P, Toro JR. Farasat S, et al. J Med Genet. 2009 Feb;46(2):103-11. doi: 10.1136/jmg.2008.060905. Epub 2008 Oct 23. J Med Genet. 2009. PMID: 18948357 Free PMC article.

6

The South African "bathing suit ichthyosis" is a form of lamellar ichthyosis caused by a homozygous missense mutation, p.R315L, in transglutaminase 1.

Arita K, Jacyk WK, Wessagowit V, van Rensburg EJ, Chaplin T, Mein CA, Akiyama M, Shimizu H, Happle R, McGrath JA. Arita K, et al. J Invest Dermatol. 2007 Feb;127(2):490-3. doi: 10.1038/sj.jid.5700550. Epub 2006 Sep 14. J Invest Dermatol. 2007. PMID: 16977323 Free article. No abstract available.

7

Bathing suit ichthyosis is caused by transglutaminase-1 deficiency: evidence for a temperature-sensitive phenotype.

Oji V, Hautier JM, Ahvazi B, Hausser I, Aufenvenne K, Walker T, Seller N, Steijlen PM, Küster W, Hovnanian A, Hennies HC, Traupe H. Oji V, et al. Hum Mol Genet. 2006 Nov 1;15(21):3083-97. doi: 10.1093/hmg/ddl249. Epub 2006 Sep 12. Hum Mol Genet. 2006. PMID: 16968736

8

Bathing-suit ichthyosis. A peculiar phenotype of lamellar ichthyosis in South African blacks.

Jacyk WK. Jacyk WK. Eur J Dermatol. 2005 Nov-Dec;15(6):433-6. Eur J Dermatol. 2005. PMID: 16280294

9

Self-healing collodion baby: a dynamic phenotype explained by a particular transglutaminase-1 mutation.

Raghunath M, Hennies HC, Ahvazi B, Vogel M, Reis A, Steinert PM, Traupe H. Raghunath M, et al. J Invest Dermatol. 2003 Feb;120(2):224-8. doi: 10.1046/j.1523-1747.2003.12032.x. J Invest Dermatol. 2003. PMID: 12542526 Free article.

10

Novel mutations of the transglutaminase 1 gene in lamellar ichthyosis.

Yang JM, Ahn KS, Cho MO, Yoneda K, Lee CH, Lee JH, Lee ES, Candi E, Melino G, Ahvazi B, Steinert PM. Yang JM, et al. J Invest Dermatol. 2001 Aug;117(2):214-8. doi: 10.1046/j.0022-202x.2001.01429.x. J Invest Dermatol. 2001. PMID: 11511296 Free article.

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