Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Maite Alvarez-Alvarez"'
Autor:
Marian M. de Pancorbo, Maite Alvarez-Alvarez, José Javier Marqueta-Gracia, Miriam Baeta, Juan R. Ordoñana, Leire Palencia-Madrid, Endika Prieto-Fernández
Publikováno v:
Forensic Science International: Genetics. 37:e1-e5
Discrimination between monozygotic (MZ) twins is a forensic limitation when using conventional DNA profiling techniques for human identification. Recent works based on epigenetics seem to open a new way to solve this issue due to methylation status o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0560bcba9149ec207d1f9a191f3f2d2b
https://doi.org/10.1016/j.fsigen.2018.08.013
https://doi.org/10.1016/j.fsigen.2018.08.013
Autor:
Cyril Goizet, Jordi Yagüe, Ana B. Rodríguez-Martínez, Agustín Ibáñez, Isabelle Coupry, N Cuevas, A. Castro, Antón Digón, Maite Alvarez-Alvarez, Raquel Sánchez-Valle, Ignacio Fernández-Manchola, Christian Barreau, Luis Galdós-Alcelay, Juan J. Zarranz, Marian M. de Pancorbo, Benoit Arveiler
Publikováno v:
Human Genetics. 117:61-69
Fatal familial insomnia (FFI) and familial Creutzfeldt-Jakob disease (fCJD) are familial prion diseases with autosomal dominant inheritance of the D178N mutation. FFI has been reported in at least 27 pedigrees around the world. Twelve apparently unre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0992681f46ed7595e2211b0c3e7c0a8c
https://doi.org/10.1007/s00439-005-1277-0
https://doi.org/10.1007/s00439-005-1277-0
Autor:
Sellama Nadifi, M. M. de Pancorbo, Maite Alvarez-Alvarez, Houssine Azeddoug, Faiza Chbel, C Martı́nez-Bouzas, M.-J. Rodriguez-Tojo
Publikováno v:
Russian Journal of Genetics. 39:1184-1190
Alu elements are the largest family of short tandem interspersed elements (SINEs) in human who have arisen to a copy number with an excess of 500 000 copies per haploid human genome and mobilize through an RNAse polymerase III derived transcript in a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d456868d0df15c0303793f599b16dc3b
https://doi.org/10.1023/a:1026135229528
https://doi.org/10.1023/a:1026135229528
Autor:
Victoria Garcı́a-Centeno, Maite Alvarez-Alvarez, Juan J. Zarranz, Ana B. Rodríguez-Martínez, Luis Galdos, Marian M. de Pancorbo, Caridad Arias-Arias, Manuel Fernández-Martínez, Fernando Gómez-Busto, Carmen Sánchez-Salazar
Publikováno v:
Neuroscience Letters. 339:85-87
Although there is considerable evidence implicating apolipoprotein E (ApoE) epsilon4 in the development of the Alzheimer's disease (AD), additional factors are also known to be involved. Thus, an association has been described between C267T polymorph
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b081f35d9aea75847ececb8904b612f7
https://doi.org/10.1016/s0304-3940(02)01425-8
https://doi.org/10.1016/s0304-3940(02)01425-8
Autor:
Elena Lezcano, Juan Carlos Gómez-Esteban, M.C. González-Fernández, Maite Alvarez-Alvarez, Owen A. Ross, Fernando Velasco, Marian M. de Pancorbo, Roberto Ciordia, Fernando Gómez-Busto, María B. Rodríguez-Martínez, Matthew J. Farrer, Juan J. Zarranz, Ignacio F. Mata
Publikováno v:
Parkinsonismrelated disorders. 13(8)
Herein we describe a comparative clinical and genetic study of Lrrk2-associated parkinsonism in Northern Spain. In our sample from the Basque region, Lrrk2 R1441G and G2019S account for 15 out of 50 kindreds (30%) with familial Parkinson’s disease.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::07731f5e5417b8897ecfbf5f2a91d6e0
https://pubmed.ncbi.nlm.nih.gov/17540608
https://pubmed.ncbi.nlm.nih.gov/17540608
Autor:
Xabier Elcoroaristizabal Martín, Sandra Inglés Borda, Iratxe Ugarriza Serrano, Begoña Indakoetxea Juanbeltz, Luis Galdos Alcelay, Juan María Uterga Valiente, Elisa Blanco Martín, Fernando Gómez Busto, Maite Alvarez-Alvarez, Myriam Barandiarán Amillano, Josefa Moraza López, Rocio Bereincua Gandarias, Manuel Fernández-Martínez, María Ángeles Gómez Beldarraín, Marian M. de Pancorbo, Ana Molano Salazar
Publikováno v:
BMJ Open
Objectives: Examine the role of single nucleotide polymorphisms (SNPs) in the oestrogen receptor (ER) genes: rs9340799, rs2234693, rs2228480 (in the ESR1 gene) and rs4986938 (in the ESR2 gene) as a risk factor for amnesic mild cognitive impairment (M
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ca4f4698d8212e02d192a5b3d080f4f4
https://doi.org/10.1136/bmjopen-2013-003200
https://doi.org/10.1136/bmjopen-2013-003200