Zobrazeno 1 - 10
of 84
pro vyhledávání: '"Marja-Liisa Savontaus"'
Publikováno v:
European Journal of Entomology, Vol 101, Iss 4, Pp 495-502 (2004)
Analysis of the mitochondrial DNA (mtDNA) control region (CR) was used to examine the dispersal of females of a geometrid moth, Epirrita autumnata, in Fennoscandia. A 542-bp-portion of the CR of 200 individuals from four northern and four southern lo
Externí odkaz:
https://doaj.org/article/00972dfb8f074c07abc4be5afae5e577
Autor:
Elina Salmela, Tuuli Lappalainen, Jianjun Liu, Pertti Sistonen, Peter M Andersen, Stefan Schreiber, Marja-Liisa Savontaus, Kamila Czene, Päivi Lahermo, Per Hall, Juha Kere
Publikováno v:
PLoS ONE, Vol 6, Iss 2, p e16747 (2011)
The use of genome-wide single nucleotide polymorphism (SNP) data has recently proven useful in the study of human population structure. We have studied the internal genetic structure of the Swedish population using more than 350,000 SNPs from 1525 Sw
Externí odkaz:
https://doaj.org/article/328277c946fb46cd8d0c466810f30cd3
Autor:
Elina Salmela, Tuuli Lappalainen, Ingegerd Fransson, Peter M Andersen, Karin Dahlman-Wright, Andreas Fiebig, Pertti Sistonen, Marja-Liisa Savontaus, Stefan Schreiber, Juha Kere, Päivi Lahermo
Publikováno v:
PLoS ONE, Vol 3, Iss 10, p e3519 (2008)
Genome-wide data provide a powerful tool for inferring patterns of genetic variation and structure of human populations.In this study, we analysed almost 250,000 SNPs from a total of 945 samples from Eastern and Western Finland, Sweden, Northern Germ
Externí odkaz:
https://doaj.org/article/3d61a3dd41114a7c9ca00a3dfc33a4e3
Autor:
Karin Dahlman-Wright, Pertti Sistonen, Päivi Lahermo, Juha Kere, Marja-Liisa Savontaus, Elina Salmela, Tuuli Lappalainen, Stefan Schreiber, Peter M. Andersen
Publikováno v:
European Journal of Human Genetics. 18:471-478
Analyzing genetic variation of human populations for detecting loci that have been affected by positive natural selection is important for understanding adaptive history and phenotypic variation in humans. In this study, we analyzed recent positive s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::551d51024f91a93e7632033c75fba817
https://doi.org/10.1038/ejhg.2009.184
https://doi.org/10.1038/ejhg.2009.184
Autor:
Marja-Liisa Savontaus
Publikováno v:
Hereditas. 86:115-119
Nondisjunction of the second chromosome was induced by irradiating Drosophila melanogaster females with a dose of 3000 R. Forty-one percent of the offspring, derived from diplo-2 eggs, were nondisjunctionals (XX or nullo-X) for the X chromosomes, as
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dd9bb23372c570415fd5de052246380b
https://doi.org/10.1111/j.1601-5223.1977.tb01219.x
https://doi.org/10.1111/j.1601-5223.1977.tb01219.x
Autor:
Marja-Liisa Savontaus
Publikováno v:
Hereditas. 98:229-233
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::db44a1962a93fcdab620a23e177774dc
https://doi.org/10.1111/j.1601-5223.1983.tb00599.x
https://doi.org/10.1111/j.1601-5223.1983.tb00599.x
Autor:
Kai Ruohomäki, Jaan Viidalepp, Marja-Liisa Savontaus, Toomas Tammaru, Kirsi Huoponen, Niklas Wahlberg, Niina Snäll
Publikováno v:
Biological Journal of the Linnean Society. 92:241-252
Phylogenetic relationships of the tribe Operophterini (Lepidoptera, Geometridae): a case study of the evolution of female flightlessness
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9120c98376c3fe1744cc73f9752ecfe9
https://doi.org/10.1111/j.1095-8312.2007.00834.x
https://doi.org/10.1111/j.1095-8312.2007.00834.x
Autor:
Patrick Yu Wai Man, Joanna L. Elson, Valerio Carelli, Chiara La Morgia, Gavin Hudson, Maria Lucia Valentino, Patrick F. Chinnery, Liesbeth Spruijt, Kirsi Huoponen, Alessandro Achilli, Neil Howell, Catherine Mowbray, Massimo Zeviani, Angela Pyle, Philip G. Griffiths, Rita Horvath, Eeva Nikoskelainen, Mike Gerards, Marja-Liisa Savontaus, René de Coo, Antonio Torroni, Solange Rios Salomão, Hubert J T Smeets, Rubens Belfort, Alfredo A. Sadun
Publikováno v:
American Journal of Human Genetics, 81, 2, pp. 228-33
American Journal of Human Genetics, 81(2), 228-233. Cell Press
American Journal of Human Genetics, 81, 228-33
American Journal of Human Genetics, 81(2), 228-233. Cell Press
American Journal of Human Genetics, 81, 228-33
Contains fulltext : 52562.pdf (Publisher’s version ) (Closed access) Leber hereditary optic neuropathy (LHON) is due primarily to one of three common point mutations of mitochondrial DNA (mtDNA), but the incomplete penetrance implicates additional
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::67e91464f563b95f3561c2f7ca6a0ebd
https://doi.org/10.1086/519394
https://doi.org/10.1086/519394
Autor:
Petra Hämäläinen, Kirsi Huoponen, Eeva Nikoskelainen, Sanna Kivioja, Anu Puomila, Satu Koivumäki, Marja-Liisa Savontaus
Publikováno v:
European Journal of Human Genetics. 15:1079-1089
We have performed an entire-population-based survey of the epidemiology and penetrance of Leber hereditary optic neuropathy (LHON) in Finland - a country that is among the best-studied genetic isolates in the world. During our long-term clinical foll
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::62318f9b06c17c37768c8fb3650bd6fd
https://doi.org/10.1038/sj.ejhg.5201828
https://doi.org/10.1038/sj.ejhg.5201828
Autor:
Eeva Nikoskelainen, Petra Hämäläinen, Kirsi Huoponen, Maija Mäntyjärvi, Mirja Somer, Anu Puomila, Reetta Paananen, Marja-Liisa Savontaus, Eeva-Marja Sankila
Publikováno v:
Acta Ophthalmologica Scandinavica. 83:337-346
Purpose: To assess the clinical picture and molecular genetics of 14 Finnish families with dominant optic atrophy (DOA). Methods: The clinical status of family members was based on the assessment of visual acuity, colour vision, visual fields and opt
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::73a3c5b61bf447e23f84aba3b04a267a
https://doi.org/10.1111/j.1600-0420.2005.00448.x
https://doi.org/10.1111/j.1600-0420.2005.00448.x