Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Marisa, Acosta"'
Autor:
María del Carmen Castro-Mujica, Claudia Barletta-Carrillo, Julio A. Poterico, Marisa Acosta, Jesús Valer, Miguel De La Cruz
Publikováno v:
Revista Peruana de Medicina Experimental y Salud Pública, Vol 34, Iss 4, Pp 744-50 (2017)
El síndrome Gorlin (SG) es una condición genética, con patrón de herencia autosómico dominante, con penetrancia completa y expresividad variable, debida a mutaciones germinales en los genes PTCH1 o SUFU, los cuales son componentes de la vía mol
Externí odkaz:
https://doaj.org/article/8f5fce7abd6143eb97f473aacbd56de3
Autor:
George Mustoe, Marisa Acosta
Publikováno v:
Geosciences, Vol 6, Iss 2, p 25 (2016)
Fossil forests have world-wide distribution, commonly preserving mineralized wood that displays vivid hues and complex color patterns. However, the origin of petrified color has received little scientific attention. Color of silicified wood may be in
Externí odkaz:
https://doaj.org/article/76b11870583d493ba4ab5db008c382b0
Autor:
María Del Carmen, Castro-Mujica, Claudia, Barletta-Carrillo, Julio A, Poterico, Marisa, Acosta, Jesús, Valer, Miguel De La, Cruz
Publikováno v:
Revista peruana de medicina experimental y salud publica. 34(4)
Gorlin syndrome (GS) is a genetic disorder with an autosomal dominant inheritance pattern, with complete penetrance and variable expressivity. GS is caused by germline mutations in the genes PTCH1 or SUFU, which are components of the Sonic hedgehog m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1f73389d0e356c2e0fa0ede9d1cc6821
https://pubmed.ncbi.nlm.nih.gov/29364426
https://pubmed.ncbi.nlm.nih.gov/29364426
Autor:
María Del Carmen, Castro-Mujica, Claudia, Barletta-Carrillo, Marisa, Acosta-Aliaga, Ximena, Montenegro-Garreaud
Publikováno v:
Revista de gastroenterologia del Peru : organo oficial de la Sociedad de Gastroenterologia del Peru. 36(1)
Lynch syndrome (LS) is an autosomal-dominant inherited cancer predisposition syndrome caused by germline mutations in DNA mismatch repair genes (MLH1, MSH2, MSH6 or PMS2). Muir-Torre syndrome (MTS) is a phenotypic variant of LS that includes a predis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::388114395d8d3ab6694245b72a1c1b41
https://pubmed.ncbi.nlm.nih.gov/27131946
https://pubmed.ncbi.nlm.nih.gov/27131946
Autor:
Marisa Acosta, George E. Mustoe
Publikováno v:
Geosciences, Vol 6, Iss 2, p 25 (2016)
Geosciences; Volume 6; Issue 2; Pages: 25
Geosciences; Volume 6; Issue 2; Pages: 25
Fossil forests have world-wide distribution, commonly preserving mineralized wood that displays vivid hues and complex color patterns. However, the origin of petrified color has received little scientific attention. Color of silicified wood may be in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4e7acca2b88c1679e63ef6c0e06e8b3c
http://www.mdpi.com/2076-3263/6/2/25
http://www.mdpi.com/2076-3263/6/2/25
Publikováno v:
Revista Argentina de Cardioangiología Intervencionista. 5:0137-0139
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::58ab59273837479e515c20bc5d5fcb4d
https://doi.org/10.30567/raci/201402/0137-0139
https://doi.org/10.30567/raci/201402/0137-0139
Autor:
María del Carmen Castro-Mujica, Claudia Barletta-Carrillo, Julio A. Poterico, Marisa Acosta, Jesús Valer, Miguel De La Cruz
Publikováno v:
Revista Peruana de Medicina Experimental y Salud Pública, Vol 34, Iss 4, Pp 744-750
RESUMEN El síndrome Gorlin (SG) es una condición genética, con patrón de herencia autosómico dominante, con penetrancia completa y expresividad variable, debida a mutaciones germinales en los genes PTCH1 o SUFU, los cuales son componentes de la
Externí odkaz:
https://doaj.org/article/8c7d7239b00241d6803417d1c5748af6