Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Carina Hirvelä"'
Autor:
Magdalena Benetkiewicz, Kiran Kumar Mantripragada, Donna G. Albertson, Britt-Inger Johnsson, Jan P. Dumanski, Charlotte Thyr, Teresita Díaz de Ståhl, Koichi Ichimura, Ian Dunham, David Beare, Nils Mandahl, Anna Wedell, Daniel Pinkel, John E. Collins, Uwe Menzel, Haider Ali, Elisabeth Blennow, Martin Hergersberg, Isabel Tapia-Páez, V. Peter Collins, Carina Hirvelä, Ingegerd Fransson, Patrick G. Buckley, Cecilia de Bustos, Magnus Rosenquist, Roger S. Lasken, Caroline Jarbo, A. Fawad Faruqi, Birgitta Sinder Wilén, Boris C. Bastian, Carl E.G. Bruder
Publikováno v:
Karolinska Institutet
Scopus-Elsevier
Scopus-Elsevier
We have constructed the first comprehensive microarray representing a human chromosome for analysis of DNA copy number variation. This chromosome 22 array covers 34.7 Mb, representing 1.1% of the genome, with an average resolution of 75 kb. To demons
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2195525684a6e005c9b483c51f751af6
https://doi.org/10.1093/hmg/11.25.3221
https://doi.org/10.1093/hmg/11.25.3221
Autor:
Kiran K, Mantripragada, Patrick G, Buckley, Magdalena, Benetkiewicz, Cecilia, De Bustos, Carina, Hirvelä, Caroline, Jarbo, Carl E G, Bruder, Helena, Wensman, Tiit, Mathiesen, Gunnar, Nyberg, Laura, Papi, V Peter, Collins, Koichi, Ichimura, Gareth, Evans, Jan P, Dumanski
Publikováno v:
International journal of oncology. 22(3)
Previous low-resolution schwannoma studies have reported diverse frequencies (30-80%) of 22q deletions, involving the neurofibromatosis-2 tumor suppressor (NF2) gene. We constructed an array spanning 11 million base pairs of 22q encompassing the NF2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::da2e10ed7f0e3cce13531c47921461ad
https://pubmed.ncbi.nlm.nih.gov/12579316
https://pubmed.ncbi.nlm.nih.gov/12579316
Autor:
George Poptodorov, Ingegerd Fransson, Lan Kluwe, Gene Hung, Greg Hamilton, Richard Segraves, Xiao Xiao Zhang, Daniel Pinkel, Sigrid Sahlén, Isabel Tapia-Páez, Eugene Boltshauser, Guy A. Rouleau, Martin Hergersberg, Albena Jordanova, Michael E. Baser, Mariko Honda, Elisabeth Blennow, Carl E.G. Bruder, Markku Sainio, Stefan M. Pulst, Henrik Harder, Carina Hirvelä, Helge Rask-Andersen, Jessica Zucman-Rossi, Victor F. Mautner, D. Gareth Evans, Arvid Heiberg, Jan P. Dumanski, Donna G. Albertson, Claes Möller, Laura Papi, Tiit Mathiesen, Andrew J Wallace, Michihito Niimura
Publikováno v:
Karolinska Institutet
Scopus-Elsevier
Human molecular genetics
Scopus-Elsevier
Human molecular genetics
Neurofibromatosis type 2 (NF2) is an autosomal dominant disorder whose hallmark is bilateral vestibular schwannoma. It displays a pronounced clinical heterogeneity with mild to severe forms. The NF2 tumor suppressor (merlin/schwannomin) has been clon
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8e83d95f8c46cfebb33d887b9d2da9ff
http://www.ncbi.nlm.nih.gov/pubmed/11159946
http://www.ncbi.nlm.nih.gov/pubmed/11159946
Autor:
Carina Hirvelä, Mats Fredrikson, Tomas Furmark, Gerhard Andersson, Leif Lyttkens, Maria Tillfors
Publikováno v:
Karolinska Institutet
CIÊNCIAVITAE
CIÊNCIAVITAE
Brain imaging of tinnitus has suggested central correlates of tinnitus perception. This study presents positron emission tomographic (PET) measurements of regional cerebral blood flow (rCBF) in a female tinnitus patient with bilateral left dominant t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c2dca58a7051b32116ab62f49f9b7355
http://www.ncbi.nlm.nih.gov/pubmed/11200593
http://www.ncbi.nlm.nih.gov/pubmed/11200593