González-Sarmiento R - Search Results

1

Cutaneous Squamous Cell Carcinoma: From Biology to Therapy.

Corchado-Cobos R, García-Sancha N, González-Sarmiento R, Pérez-Losada J, Cañueto J. Corchado-Cobos R, et al. Int J Mol Sci. 2020 Apr 22;21(8):2956. doi: 10.3390/ijms21082956. Int J Mol Sci. 2020. PMID: 32331425 Free PMC article. Review.

2

[The Philadelphia chromosome: from the gene to therapeutic methods].

Pérez-Losada J, González-Sarmiento R, Sánchez-García I. Pérez-Losada J, et al. Sangre (Barc). 1998 Apr;43(2):127-35. Sangre (Barc). 1998. PMID: 9656774 Review. Spanish. No abstract available.

3

Breast cancer, a stem cell disease.

González-Sarmiento R, Pérez-Losada J. González-Sarmiento R, et al. Curr Stem Cell Res Ther. 2008 Jan;3(1):55-65. doi: 10.2174/157488808783489453. Curr Stem Cell Res Ther. 2008. PMID: 18220924 Free article. Review.

4

The Emerging Picture of Human Breast Cancer as a Stem Cell-based Disease.

Cobaleda C, Cruz JJ, González-Sarmiento R, Sánchez-García I, Pérez-Losada J. Cobaleda C, et al. Stem Cell Rev. 2008 Summer;4(2):67-79. doi: 10.1007/s12015-008-9012-6. Stem Cell Rev. 2008. PMID: 18401767 Review.

5

Analysis of the STS gene in 40 patients with recessive X-linked ichthyosis: a high frequency of partial deletions in a Spanish population.

Cañueto J, Ciria S, Hernández-Martín A, Unamuno P, González-Sarmiento R. Cañueto J, et al. J Eur Acad Dermatol Venereol. 2010 Oct;24(10):1226-9. doi: 10.1111/j.1468-3083.2010.03612.x. J Eur Acad Dermatol Venereol. 2010. PMID: 20236202

6

Buschke-Ollendorff syndrome with striking phenotypic variation resulting from a novel c.2203C>T nonsense mutation in LEMD3.

Yuste-Chaves M, Cañueto J, Santos-Briz Á, Ciria S, González-Sarmiento R, Unamuno P. Yuste-Chaves M, et al. Pediatr Dermatol. 2011 Jul-Aug;28(4):447-50. doi: 10.1111/j.1525-1470.2010.01206.x. Epub 2010 Jul 29. Pediatr Dermatol. 2011. PMID: 20678097

7

A novel EDA gene mutation in a Spanish family with X-linked hypohidrotic ectodermal dysplasia.

Cañueto J, Zafra-Cobo MI, Ciria S, Unamuno P, González-Sarmiento R. Cañueto J, et al. Actas Dermosifiliogr. 2011 Nov;102(9):722-5. doi: 10.1016/j.ad.2011.04.004. Epub 2011 Jun 21. Actas Dermosifiliogr. 2011. PMID: 21696697 Free article.

8

Clinical, molecular and biochemical characterization of nine Spanish families with Conradi-Hünermann-Happle syndrome: new insights into X-linked dominant chondrodysplasia punctata with a comprehensive review of the literature.

Cañueto J, Girós M, Ciria S, Pi-Castán G, Artigas M, García-Dorado J, García-Patos V, Virós A, Vendrell T, Torrelo A, Hernández-Martín A, Martín-Hernández E, Garcia-Silva MT, Fernández-Burriel M, Rosell J, Tejedor M, Martínez F, Valero J, García JL, Sánchez-Tapia EM, Unamuno P, González-Sarmiento R. Cañueto J, et al. Br J Dermatol. 2012 Apr;166(4):830-8. doi: 10.1111/j.1365-2133.2011.10756.x. Epub 2012 Mar 2. Br J Dermatol. 2012. PMID: 22121851 Review.

9

The role of the abnormalities in the distal pathway of cholesterol biosynthesis in the Conradi-Hünermann-Happle syndrome.

Cañueto J, Girós M, González-Sarmiento R. Cañueto J, et al. Biochim Biophys Acta. 2014 Mar;1841(3):336-44. doi: 10.1016/j.bbalip.2013.09.002. Epub 2013 Sep 11. Biochim Biophys Acta. 2014. PMID: 24036494 Review.

10

Acral peeling skin syndrome resulting from mutations in TGM5.

Cañueto J, Bueno E, Rodríguez-Diaz E, Vicente-Díaz MA, Álvarez-Cuesta CC, Gonzalvo-Rodríguez P, González-Sarmiento R. Cañueto J, et al. J Eur Acad Dermatol Venereol. 2016 Mar;30(3):477-80. doi: 10.1111/jdv.12863. Epub 2014 Dec 16. J Eur Acad Dermatol Venereol. 2016. PMID: 25510201 No abstract available.

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