Gache Y - Search Results

1

Basal Cell Carcinoma in Gorlin's Patients: a Matter of Fibroblasts-Led Protumoral Microenvironment?

Gache Y, Brellier F, Rouanet S, Al-Qaraghuli S, Goncalves-Maia M, Burty-Valin E, Barnay S, Scarzello S, Ruat M, Sevenet N, Avril MF, Magnaldo T. Gache Y, et al. PLoS One. 2015 Dec 22;10(12):e0145369. doi: 10.1371/journal.pone.0145369. eCollection 2015. PLoS One. 2015. PMID: 26694869 Free PMC article.

2

NK Cell and Fibroblast-Mediated Regulation of Skin Squamous Cell Carcinoma Invasion by CLEC2A Is Compromised in Xeroderma Pigmentosum.

Gonçalves-Maia M, Gache Y, Basante M, Cosson E, Salavagione E, Muller M, Bernerd F, Avril MF, Schaub S, Sarasin A, Braud VM, Magnaldo T. Gonçalves-Maia M, et al. Among authors: gache y. J Invest Dermatol. 2020 Sep;140(9):1723-1732. doi: 10.1016/j.jid.2020.01.021. Epub 2020 Feb 13. J Invest Dermatol. 2020. PMID: 32061658 Free article.

3

Genetic correction of stem cells in the treatment of inherited diseases and focus on xeroderma pigmentosum.

Rouanet S, Warrick E, Gache Y, Scarzello S, Avril MF, Bernerd F, Magnaldo T. Rouanet S, et al. Among authors: gache y. Int J Mol Sci. 2013 Oct 9;14(10):20019-36. doi: 10.3390/ijms141020019. Int J Mol Sci. 2013. PMID: 24113582 Free PMC article. Review.

4

Deficient expression of aldehyde dehydrogenase 1A1 is consistent with increased sensitivity of Gorlin syndrome patients to radiation carcinogenesis.

Wright AT, Magnaldo T, Sontag RL, Anderson LN, Sadler NC, Piehowski PD, Gache Y, Weber TJ. Wright AT, et al. Among authors: gache y. Mol Carcinog. 2015 Jun;54(6):473-84. doi: 10.1002/mc.22115. Epub 2013 Nov 27. Mol Carcinog. 2015. PMID: 24285572 Free PMC article.

5

Absence of the Integrin α3 Subunit Induces an Activated Phenotype in Human Keratinocytes.

Pazzagli C, He Y, Busch H, Esser P, Kiritsi D, Gache Y, Bruckner-Tuderman L, Boerries M, Has C. Pazzagli C, et al. Among authors: gache y. J Invest Dermatol. 2017 Jun;137(6):1387-1391. doi: 10.1016/j.jid.2017.01.018. Epub 2017 Feb 3. J Invest Dermatol. 2017. PMID: 28163067 Free article. No abstract available.

6

Correction of dog dystrophic epidermolysis bullosa by transplantation of genetically modified epidermal autografts.

Gache Y, Pin D, Gagnoux-Palacios L, Carozzo C, Meneguzzi G. Gache Y, et al. J Invest Dermatol. 2011 Oct;131(10):2069-78. doi: 10.1038/jid.2011.172. Epub 2011 Jun 23. J Invest Dermatol. 2011. PMID: 21697889 Free article.

7

Genetic bases of severe junctional epidermolysis bullosa presenting spontaneous amelioration with aging.

Gache Y, Allegra M, Bodemer C, Pisani-Spadafora A, de Prost Y, Ortonne JP, Meneguzzi G. Gache Y, et al. Hum Mol Genet. 2001 Oct 1;10(21):2453-61. doi: 10.1093/hmg/10.21.2453. Hum Mol Genet. 2001. PMID: 11689492

8

Splicing modulation of integrin beta4 pre-mRNA carrying a branch point mutation underlies epidermolysis bullosa with pyloric atresia undergoing spontaneous amelioration with ageing.

Chavanas S, Gache Y, Vailly J, Kanitakis J, Pulkkinen L, Uitto J, Ortonne J, Meneguzzi G. Chavanas S, et al. Among authors: gache y. Hum Mol Genet. 1999 Oct;8(11):2097-105. doi: 10.1093/hmg/8.11.2097. Hum Mol Genet. 1999. PMID: 10484780

9

Rapid decay of alpha6 integrin caused by a mis-sense mutation in the propeller domain results in severe junctional epidermolysis bullosa with pyloric atresia.

Allegra M, Gagnoux-Palacios L, Gache Y, Roques S, Lestringant G, Ortonne JP, Meneguzzi G. Allegra M, et al. Among authors: gache y. J Invest Dermatol. 2003 Dec;121(6):1336-43. doi: 10.1111/j.1523-1747.2003.12625.x. J Invest Dermatol. 2003. PMID: 14675179 Free article.

10

Construction of skin equivalents for gene therapy of recessive dystrophic epidermolysis bullosa.

Gache Y, Baldeschi C, Del Rio M, Gagnoux-Palacios L, Larcher F, Lacour JP, Meneguzzi G. Gache Y, et al. Hum Gene Ther. 2004 Oct;15(10):921-33. doi: 10.1089/hum.2004.15.921. Hum Gene Ther. 2004. PMID: 15585108

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