Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Per, Wahlberg"'
Autor:
Aurélie Allais-Bonnet, Cécile Grohs, Ivica Medugorac, Stefan Krebs, Anis Djari, Alexander Graf, Sébastien Fritz, Doris Seichter, Aurélia Baur, Ingolf Russ, Stéphan Bouet, Sophie Rothammer, Per Wahlberg, Diane Esquerré, Chris Hoze, Mekki Boussaha, Bernard Weiss, Dominique Thépot, Marie-Noëlle Fouilloux, Marie-Noëlle Rossignol, Este van Marle-Köster, Gunnfríður Elín Hreiðarsdóttir, Sarah Barbey, Dominique Dozias, Emilie Cobo, Patrick Reversé, Olivier Catros, Jean-Luc Marchand, Pascal Soulas, Pierre Roy, Brigitte Marquant-Leguienne, Daniel Le Bourhis, Laetitia Clément, Laura Salas-Cortes, Eric Venot, Maëlle Pannetier, Florence Phocas, Christophe Klopp, Dominique Rocha, Michel Fouchet, Laurent Journaux, Carine Bernard-Capel, Claire Ponsart, André Eggen, Helmut Blum, Yves Gallard, Didier Boichard, Eric Pailhoux, Aurélien Capitan
Publikováno v:
PLoS ONE, Vol 8, Iss 5, p e63512 (2013)
Despite massive research efforts, the molecular etiology of bovine polledness and the developmental pathways involved in horn ontogenesis are still poorly understood. In a recent article, we provided evidence for the existence of at least two differe
Externí odkaz:
https://doaj.org/article/f085e21b9eb648f68096624ff77990e5
Autor:
Emmanuelle Bourneuf, Per Wahlberg, Jordi Estellé, Jérôme Lecardonnel, A. Blin, Sylvain Marthey, Francoise Créchet, F. Tessiot, Claire Rogel-Gaillard
Publikováno v:
Molecular Genetics and Genomics
Molecular Genetics and Genomics, Springer Verlag, 2020, 295 (5), pp.1239-1252. ⟨10.1007/s00438-020-01694-6⟩
Molecular Genetics and Genomics, 2020, 295 (5), pp.1239-1252. ⟨10.1007/s00438-020-01694-6⟩
Molecular Genetics and Genomics, Springer Verlag, 2020, 295 (5), pp.1239-1252. ⟨10.1007/s00438-020-01694-6⟩
Molecular Genetics and Genomics, 2020, 295 (5), pp.1239-1252. ⟨10.1007/s00438-020-01694-6⟩
International audience; The genetic mechanisms underlying cutaneous melanoma onset and progression need to be further understood to improve patients' care. Several studies have focused on the genetic determinism of melanoma development in the MeLiM p
Autor:
Marco Moroldo, Sylvain Marthey, Núria Mach, Amanda Y. Chong, Claire Rogel-Gaillard, Simon Y. W. Ho, Carol Lee, Jérôme Lecardonnel, Per Wahlberg, Jaime Gongora, Alvaro Perdomo-Sabogal, Jordi Estellé
Publikováno v:
Immunogenetics
Immunogenetics, Springer Verlag, 2018, 70 (6), pp.401-417. ⟨10.1007/s00251-017-1048-9⟩
Immunogenetics, Springer Verlag, 2018, 70 (6), pp.401-417. ⟨10.1007/s00251-017-1048-9⟩
International audience; The major histocompatibility complex (MHC) is a key genomic model region for understanding the evolution of gene families and the co-evolution between host and pathogen. To date, MHC studies have mostly focused on species from
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ea5dc99b752cee61bc7a4ee820972be1
https://doi.org/10.1007/s00251-017-1048-9
https://doi.org/10.1007/s00251-017-1048-9
Autor:
Linda Olsson, Mikael Behrendtz, Marianne Rissler, Anders Isaksson, Anders Castor, Henrik Lilljebjörn, Per Wahlberg, Anders Lundmark, Kajsa Paulsson, Kristina B. Lundin-Ström, Andrea Biloglav, Sebastian DiLorenzo, Rebeqa Gunnarsson, Thoas Fioretos, Bertil Johansson
Publikováno v:
Leukemia
High-throughput sequencing was applied to investigate the mutation/methylation patterns on 1q and gene expression profiles in pediatric B-cell precursor acute lymphoblastic leukemia (BCP ALL) with/without (w/wo) dup(1q). Sequencing of the breakpoint
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ec3387a968c68bfe20bdf6a59a0900f6
http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-367402
http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-367402
Autor:
Juleen R. Zierath, Paul B. Siegel, D. Michael Denbow, Leif Andersson, Finn Hallböök, Sojeong Ka, Svante Pääbo, Mohammad Harun-Or-Rashid, Frank W. Albert, Ellen Markljung, Henrik Ring, Pablo M. Garcia-Roves, Per Wahlberg
Publikováno v:
Physiological Genomics
Carnitine palmitoyl-CoA transferase-1B is a mitochondrial enzyme in the fatty acid oxidation pathway. In a previous study, CPT1B was identified as differentially expressed in the hypothalamus of two lines of chickens established by long-term selectio
Publikováno v:
Nucleic Acids Research
Sodium bisulphite treatment of DNA combined with next generation sequencing (NGS) is a powerful combination for the interrogation of genome-wide DNA methylation profiles. Library preparation for whole genome bisulphite sequencing (WGBS) is challengin
Autor:
Karolina Tandre, Per Wahlberg, Anders Lundmark, Daniel Sinnett, Tomi Pastinen, Stephan Busche, Lars Rönnblom, Erik Forestier, Ann-Christine Syvänen, Gudmar Lönnerholm, Jessica Nordlund, Amanda Raine
Aim: To identify regions of aberrant DNA methylation in acute lymphoblastic leukemia (ALL) cells of different subtypes on a genome-wide scale. Materials & methods: Whole-genome bisulfite sequencing (WGBS) was used to determine the DNA methylation lev
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::65b6151f7cff7ffe55a61ef9dd6ecfe4
http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-308929
http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-308929
Autor:
Michelle, Alexander, Simon Y W, Ho, Martyna, Molak, Ross, Barnett, Örjan, Carlborg, Ben, Dorshorst, Christa, Honaker, Francois, Besnier, Per, Wahlberg, Keith, Dobney, Paul, Siegel, Leif, Andersson, Greger, Larson
Publikováno v:
Biology Letters
Mitochondrial genomes represent a valuable source of data for evolutionary research, but studies of their short-term evolution have typically been limited to invertebrates, humans and laboratory organisms. Here we present a detailed study of 12 mitoc
Publikováno v:
Poultry Science. 83:1825-1831
A large mapping population, with 874 F2 individuals, was generated by reciprocally intercrossing 2 chicken lines. A genetic map of 2,426.6 cM comprising 25 linkage groups was established based on 145 microsatellite markers. Chromosome locations were
Autor:
Carl Mårten Lindqvist, Stefan Söderhäll, Jonas Abrahamsson, Gudmar Lönnerholm, Ann-Christine Syvänen, Per Wahlberg, Rolf Larsson, Elin Övernäs, Josefine Palle, Erik Forestier, Mats Heyman, Anna Johansson, Diana Ekman, Eva C. Berglund, Amanda Raine, Johan Dahlberg, Jessica Nordlund, Behrooz Torabi Moghadam, Dan Grandér, Britt-Marie Frost, Niklas Henriksson
Publikováno v:
Human Mutation
Genomic characterization of pediatric acute lymphoblastic leukemia (ALL) has identified distinct patterns of genes and pathways altered in patients with well-defined genetic aberrations. To extend the spectrum of known somatic variants in ALL, we per