Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Michèle Jomphe"'
Autor:
Claudia Moreau, Jean-François Lefebvre, Michèle Jomphe, Claude Bhérer, Andres Ruiz-Linares, Hélène Vézina, Marie-Hélène Roy-Gagnon, Damian Labuda
Publikováno v:
PLoS ONE, Vol 8, Iss 6, p e65507 (2013)
For years, studies of founder populations and genetic isolates represented the mainstream of genetic mapping in the effort to target genetic defects causing Mendelian disorders. The genetic homogeneity of such populations as well as relatively homoge
Externí odkaz:
https://doaj.org/article/1c4887638ef94d09b7c4ba6c9852076b
Autor:
Julie St-Pierre, Michèle Jomphe
Ce livre résulte d'une pratique développée et éprouvée par une équipe d'enseignants en littérature du Cégep de Baie-Comeau depuis une dizaine d'années, à la recherche d'une méthode de travail permettant aux étudiant·e·s de développer l
Autor:
Lars Bosshard, Adrien Foucal, Kimberly J. Gilbert, Elias Gbeha, Vanessa Bruat, Alan Hodgkinson, Elodie Hip-Ki, Alexandre Gouy, Isabelle Dupanloup, Philip Awadalla, Laurent Excoffier, Hélène Vézina, Michèle Jomphe, Mawusse Agbessi, Jean-Christophe Grenier, Stephan Peischl
Publikováno v:
Genetics. 208(2)
Peischl et al. explore the way evolutionary forces shape genetic variability in expanding human populations. Over a few generations of separate evolution... Humans have colonized the planet through a series of range expansions, which deeply impacted
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::305855ae535e755437820897ebba1750
https://pubmed.ncbi.nlm.nih.gov/29187508
https://pubmed.ncbi.nlm.nih.gov/29187508
Autor:
Elodie Hip-Ki, Philip Awadalla, Jean-Christophe Grenier, Elias Gbeha, Vanessa Bruat, Laurent Excoffier, Lars Bosshard, Adrien Foucal, Stephan Peischl, Hélène Vézina, Michèle Jomphe, Isabelle Dupanloup, Mawusse Agbessi, Alan Hodgkinson, Alexandre Gouy
Humans have colonized the planet through a series of range expansions, which deeply impacted genetic diversity in newly settled areas and potentially increased the frequency of deleterious mutations on expanding wave fronts. To test this prediction,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ec882aeebda67cadc7562ea2bbbda4a9
Publikováno v:
Articles. 41:87-105
Dans le cadre d’un programme de recherche sur la diversité génétique des populations régionales du Québec, nous avons mesuré la contribution des ancêtres amérindiens au pool génique de 794 participants résidant dans les régions de Montr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::059cb8233bbe0ec03adaa4d2399ccd38
https://doi.org/10.7202/1012981ar
https://doi.org/10.7202/1012981ar
Publikováno v:
Journal of Historical Geography. 36:327-341
A series of mutations of tuberculosis, present in the 1990s among elderly persons in the Province of Quebec (Canada), is interpreted as the outcome of a suite of three episodes of high mobility. The most recent is the rapid urbanization of the 1950s.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d1a9f2bbec4591dd328cc7c7bef116b2
https://doi.org/10.1016/j.jhg.2009.10.003
https://doi.org/10.1016/j.jhg.2009.10.003
Autor:
Bertrand Desjardins, Marc St-Hilaire, Eric A. Shoubridge, Carol Macmillan, Louis Houde, Michèle Jomphe, Damian Labuda, Marc Tremblay, Bernard Brais, Anne-Marie Laberge, Hélène Vézina
Publikováno v:
The American Journal of Human Genetics. 77(2):313-317
The predominance of the T14484C mutation in French Canadians with Leber hereditary optic neuropathy is due to a founder effect. By use of genealogical reconstructions of maternal lineages, a woman married in Quebec City in 1669 is identified as the s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a58296ab6cd5f5d0a7f87bd4685d4290
Autor:
Daniel Gaudet, Pavel Hamet, Allen W. Cowley, Theodore A. Kotchen, Sergei N. Orlov, Hélène Vézina, Gérard Bouchard, Francis Gossard, Louis Houde, Johanne Tremblay, Zdenka Pausova, Michèle Jomphe
Publikováno v:
Obesity Research. 10:463-470
Objectives: To investigate genetic homogeneity in a set of hypertensive families and in subsets chosen for high and low prevalence of obesity; and to compare fasting insulin and lipids, ion transport, and water homeostasis in the obese and lean famil
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f148a3565394e9ea0a113c7461cd04e5
https://doi.org/10.1038/oby.2002.64
https://doi.org/10.1038/oby.2002.64
Autor:
Claudia Moreau, Claude Bhérer, Damian Labuda, Hélène Vézina, Laurent Excoffier, Michèle Jomphe
Publikováno v:
Science. 334:1148-1150
Since their origin, human populations have colonized the whole planet, but the demographic processes governing range expansions are mostly unknown. We analyzed the genealogy of more than one million individuals resulting from a range expansion in Que
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ef8bbba122d8ee518c093565ca67e084
https://doi.org/10.1126/science.1212880
https://doi.org/10.1126/science.1212880
Autor:
Severine Leclerc, Steven J.M. Jones, Harry C. Dietz, Silja Barbara Burkhard, Sandrine Faure, Philippe Chetaille, Gilles R.X. Hickson, Julie Castilloux, Gregor Andelfinger, Pascal de Santa Barbara, Jean-Marc Côté, Nour El Amine, Florian Wünnemann, Christoph Preuss, Natacha Gosset, Damian Labuda, Shing Hei Zhan, Maryse Thibeault, Jessica Piché, Jeroen Bakkers, D. Woodrow Benson, Michel Cameron, Claudia Moreau, Ines Boufaied, Christine Houde, Carmen Gagnon, Emmanuelle Lemyre, Elena Gallo-McFarlane, Anders Jonzon, Elizabeth Tuck, Antonella Galli, Yaoqing Shen, Michèle Jomphe
Publikováno v:
Nature Genetics
Nature Genetics, Nature Publishing Group, 2014, ⟨10.1038/ng.3113⟩
Nature Genetics, 46(11), 1245-9. Nature Publishing Group
Nature Genetics, Nature Publishing Group, 2014, ⟨10.1038/ng.3113⟩
Nature Genetics, 46(11), 1245-9. Nature Publishing Group
International audience; The pacemaking activity of specialized tissues in the heart and gut results in lifelong rhythmic contractions. Here we describe a new syndrome characterized by Chronic Atrial and Intestinal Dysrhythmia, termed CAID syndrome, i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eedd1e8c29dfb8157a608dfa10feb46b
https://hal.umontpellier.fr/hal-02543639
https://hal.umontpellier.fr/hal-02543639