Zobrazeno 1 - 8
of 8
pro vyhledávání: '"alele"'
Autor:
Diaconu Rodica, Dumitrașcu Andreea-Ramona, Liehn Elisa, Pîrvu Andrei, Ioana Mihai, Alexandru Dragoș, Țieranu Eugen, Bălșeanu Tudor-Adrian, Donoiu Ionuț
Publikováno v:
Romanian Journal of Cardiology, Vol 33, Iss 1, Pp 19-24 (2023)
Background: Apolipoprotein E (ApoE) is a ubiquitous protein involved in maintaining cholesterol homeostasis and lipoprotein clearance from circulation. It is coded by three alleles (ε2, ε3, ε4) with six genotypes (ε3/ε3, ε3/ε4, ε2/ε3, ε4/ε
Externí odkaz:
https://doaj.org/article/62a4242869b843bf87f21c233ab1c2c9
Publikováno v:
Arta Medica, Vol 83, Iss 2 (2022)
Obiective. Studierea markerilor genetici proinflamatori ai artritei psoriazice și importanța diagnosticului precoce a acesteia. Materiale și metode. Studiul actual a inclus 104 pacienți cu artrită psoriazică. Diagnosticul de artrită psoriazi
Externí odkaz:
https://doaj.org/article/cffeb8b642d24ea3917d02e89fa39614
Molekularno određivanje alela RHD u populaciji RhD negativni davatelja krvi sjeverozapadne Hrvatske
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=57a035e5b1ae::c613fb9d98a083c1c0eb75639af2176c
https://www.bib.irb.hr/1167917
https://www.bib.irb.hr/1167917
Autor:
Fojtíková, Markéta
Fojtikova 2011 INTRODUCTION: Several factors like genetic susceptibility is required for systemic rheumatic diseases development. Immunomodulatory PRL effect supports autoimmunity. AIMS: 1. To detect the immunogenetic background (alleles HLA class I,
Externí odkaz:
http://www.nusl.cz/ntk/nusl-441655
Autor:
Volskienė, Rasa
Darbo tikslas – atlikti Baltijos šalių vietinių avių veislių: Estijos baltagalvių, Estijos juodgalvių, Estijos Ruhnu, Latvijos tamsiagalvių, Lietuvos vietinių šiurkščiavilnių, Lietuvos juodgalvių prioninio baltymo genetinės įvairov
Externí odkaz:
http://vddb.library.lt/fedora/get/LT-eLABa-0001:E.02~2008~D_20081215_130610-35367/DS.005.0.02.ETD
Autor:
Volskienė, Rasa
Darbo tikslas – atlikti Baltijos šalių vietinių avių veislių: Estijos baltagalvių, Estijos juodgalvių, Estijos Ruhnu, Latvijos tamsiagalvių, Lietuvos vietinių šiurkščiavilnių, Lietuvos juodgalvių prioninio baltymo genetinės įvairov
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______1338::66c03f09b918547c2744fd89d9850ab9
http://vddb.library.lt/fedora/get/LT-eLABa-0001:E.02~2008~D_20081215_130610-35367/DS.005.0.02.ETD
http://vddb.library.lt/fedora/get/LT-eLABa-0001:E.02~2008~D_20081215_130610-35367/DS.005.0.02.ETD
Autor:
Paolo Vezzoni, David Mellis, Julie C. Crockett, Fraser P. Coxon, Alessandra Pangrazio, Daniele Moratto, Evelina Mazzolari, Anna Villa, Mario Abinun, Paul J. Orchard, Jill Clayton-Smith, Luigi D. Notarangelo, Ilhan Tezcan, Michael J. Rogers, Barbara Cassani, Sara Sebnem Kilic, Miep H. Helfrich, Annalisa Frattini, Ashok Vellodi, Cristina Sobacchi, Matteo M Guerrini
Publikováno v:
American journal of human genetics 83 (2008): 64–76. doi:10.1016/j.ajhg.2008.06.015
info:cnr-pdr/source/autori:Guerrini MM; Sobacchi C; Cassani B; Abinun M; Kilic SS; Pangrazio A; Moratto D; Mazzolari E; Clayton-Smith J; Orchard P; Coxon FP; Helfrich MH; Crockett JC; Mellis D; Vellodi A; Tezcan I; Notarangelo LD; Rogers MJ; Vezzoni P; Villa A; Frattini A./titolo:Human osteoclast-poor osteopetrosis with hypogammaglobulinemia due to TNFRSF11A (RANK) mutations./doi:10.1016%2Fj.ajhg.2008.06.015/rivista:American journal of human genetics/anno:2008/pagina_da:64/pagina_a:76/intervallo_pagine:64–76/volume:83
info:cnr-pdr/source/autori:Guerrini MM; Sobacchi C; Cassani B; Abinun M; Kilic SS; Pangrazio A; Moratto D; Mazzolari E; Clayton-Smith J; Orchard P; Coxon FP; Helfrich MH; Crockett JC; Mellis D; Vellodi A; Tezcan I; Notarangelo LD; Rogers MJ; Vezzoni P; Villa A; Frattini A./titolo:Human osteoclast-poor osteopetrosis with hypogammaglobulinemia due to TNFRSF11A (RANK) mutations./doi:10.1016%2Fj.ajhg.2008.06.015/rivista:American journal of human genetics/anno:2008/pagina_da:64/pagina_a:76/intervallo_pagine:64–76/volume:83
Autosomal-Recessive Osteopetrosis (ARO) comprises a heterogeneous group of bone diseases for which mutations in five genes are known as causative. Most ARO are classified as osteoclast-rich, but recently a subset of osteoclast-poor ARO has been recog
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::868813390919efb5303f6e2b4af5955d
http://www.cnr.it/prodotto/i/56024
http://www.cnr.it/prodotto/i/56024