Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Laura Näätsaari"'
Autor:
Laura Näätsaari, Beate Mistlberger, Claudia Ruth, Tanja Hajek, Franz S Hartner, Anton Glieder
Publikováno v:
PLoS ONE, Vol 7, Iss 6, p e39720 (2012)
Targeted gene replacement to generate knock-outs and knock-ins is a commonly used method to study the function of unknown genes. In the methylotrophic yeast Pichia pastoris, the importance of specific gene targeting has increased since the genome seq
Externí odkaz:
https://doaj.org/article/5863615e58b84005b9071ab7a614da03
Publikováno v:
BMC Genomics
Background Horseradish peroxidases (HRPs) from Armoracia rusticana have long been utilized as reporters in various diagnostic assays and histochemical stainings. Regardless of their increasing importance in the field of life sciences and suggested us
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8cae37f10e06d90cb182268f93235c1d
http://openlib.tugraz.at/564f252f212d0
http://openlib.tugraz.at/564f252f212d0
Autor:
Leigha Senter, Pia Vahteristo, Stéphane Richard, Riitta Herva, Lauri A. Aaltonen, Erik Björck, Virpi Launonen, Marja Hietala, Rainer Lehtonen, Betty Gardie, Laura Näätsaari, Kristiina Aittomäki, Maija Ht Kiuru, Taru A. Koski, Ignacio Blanco, Satu-Leena Sallinen, Didier Bessis, Richard S. Houlston, Auli Karhu, Outi Vierimaa, Emmanuel Van Glabeke
Publikováno v:
Familial cancer. 9(2)
Hereditary leiomyomatosis and renal cell cancer (HLRCC) is a tumor predisposition syndrome caused by heterozygous germline mutations in the fumarate hydratase (FH) gene. Cutaneous and uterine leiomyomas are the most common clinical manifestations of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::07ea2f1bb23bbff38e85d5e61ab52cc4
https://pubmed.ncbi.nlm.nih.gov/20091131
https://pubmed.ncbi.nlm.nih.gov/20091131
Autor:
Tomi P. Mäkelä, Pia Alhopuro, F W M de Rooij, Lauri A. Aaltonen, Auli Karhu, Sanna K. Ylisaukko-oja, T Vogel, J.H.P. Wilson, P Katajisto, Virpi Launonen, Laura Näätsaari, I. P. M. Tomlinson, Gabriela Moeslein, Anne Marie Westerman, Rainer Lehtonen
Publikováno v:
University of Helsinki
British Journal of Cancer, 92(6), 1126-1129. Nature Publishing Group
British Journal of Cancer
British Journal of Cancer, 92(6), 1126-1129. Nature Publishing Group
British Journal of Cancer
Mutations in LKB1 lead to Peutz-Jeghers syndrome (PJS). However, only a subset of PJS patients harbours LKB1 mutations. We performed a mutation analysis of three genes encoding novel LKB1-interacting proteins, BRG1, STRADalpha, and MO25alpha, in 28 L
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d182aadd4b0b85af851562094225a595
http://ora.ox.ac.uk/objects/uuid:8ccffa64-b991-49b6-8890-8d9fc6ad5834
http://ora.ox.ac.uk/objects/uuid:8ccffa64-b991-49b6-8890-8d9fc6ad5834
Autor:
Maija Ht Kiuru, Stéphane Richard, Outi Vierimaa, Riitta Herva, Virpi Launonen, Lauri A. Aaltonen, Marja Hietala, Erik Björck, Laura Näätsaari, Satu-Leena Sallinen, Leigha Senter, Pia Vahteristo, Ignacio Blanco, Emmanuel Van Glabeke, Kristiina Aittomäki, Taru A. Koski, Auli Karhu, Betty Gardie, Rainer Lehtonen, Didier Bessis, Richard S. Houlston
Publikováno v:
Cancer Research. 70:1844-1844
Hereditary leiomyomatosis and renal cell cancer (HLRCC) is a hereditary tumor predisposition syndrome with fumarate hydratase (FH), which encodes a tricarboxylic acid cycle enzyme fumarase, as the predisposing gene. The HLRCC family members carry het
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c888ffa1f7db9909f59277ce629be6ab
https://doi.org/10.1158/1538-7445.am10-1844
https://doi.org/10.1158/1538-7445.am10-1844