検索結果 - Jacques L Michaud

結果の絞り込み
  1. 1
    In vitro analyses of known and novel RUNX1/AML1 mutations in dominant familial platelet disorder with predisposition to acute myelogenous leukemia: implications for mechanisms of pathogenesis

    In vitro analyses of known and novel RUNX1/AML1 mutations in dominant familial platelet disorder with predisposition to acute myelogenous leukemia: implications for mechanisms of p... 著者: Jacques L. Michaud

    出版事項 2002
    全文の入手
    Artigo
    お気に入りに追加
    保存先:
  2. 2
    Expression of the mouse Gli and Ptc genes is adjacent to embryonic sources of hedgehog signals suggesting a conservation of pathways between flies and mice

    Expression of the mouse Gli and Ptc genes is adjacent to embryonic sources of hedgehog signals suggesting a conservation of pathways between flies and mice 著者: Kenneth A. Platt, Jacques L. Michaud, Alexandra L. Joyner

    出版事項 1997
    全文の入手
    Artigo
    お気に入りに追加
    保存先:
  3. 3
    Development of neuroendocrine lineages requires the bHLH–PAS transcription factor SIM1

    Development of neuroendocrine lineages requires the bHLH–PAS transcription factor SIM1 著者: Jacques L. Michaud, Thomas A. Rosenquist, Noah May, Chen‐Ming Fan

    出版事項 1998
    全文の入手 全文の入手
    Artigo
    お気に入りに追加
    保存先:
  4. 4
    ARNT2 acts as the dimerization partner of SIM1 for the development of the hypothalamus

    ARNT2 acts as the dimerization partner of SIM1 for the development of the hypothalamus 著者: Jacques L. Michaud, Charles DeRossi, Noah May, Bernadette C. Holdener, Chen‐Ming Fan

    出版事項 2000
    全文の入手
    Artigo
    お気に入りに追加
    保存先:
  5. 5
    Population history and its impact on medical genetics in Quebec

    Population history and its impact on medical genetics in Quebec 著者: A‐M Laberge, Jacques L. Michaud, Andréa Richter, Emmanuelle Lemyre, M Lambert, Bernard Brais, GA Mitchell

    出版事項 2005
    全文の入手 全文の入手
    Revisão
    お気に入りに追加
    保存先:
  6. 6
    Progressive impairment of developing neuroendocrine cell lineages in the hypothalamus of mice lacking the Orthopedia gene

    Progressive impairment of developing neuroendocrine cell lineages in the hypothalamus of mice lacking the Orthopedia gene 著者: Dario Acampora, Maria Pia Postiglione, Virginia Avantaggiato, M. Di Bonito, Flora M. Vaccarino, Jacques L. Michaud, Antonio Simeone

    出版事項 1999
    全文の入手 全文の入手
    Artigo
    お気に入りに追加
    保存先:
  7. 7
    Loss of Maged1 results in obesity, deficits of social interactions, impaired sexual behavior and severe alteration of mature oxytocin production in the hypothalamus

    Loss of Maged1 results in obesity, deficits of social interactions, impaired sexual behavior and severe alteration of mature oxytocin production in the hypothalamus 著者: Carlos Dombret, Tuan Huy Nguyen, Olivier Schakman, Jacques L. Michaud, Hélène Hardin‐Pouzet, Mathieu J.M. Bertrand, Olivier De Backer

    出版事項 2012
    全文の入手 全文の入手
    Artigo
    お気に入りに追加
    保存先:
  8. 8
    A Gain-of-Function Mutation in<i>NALCN</i>in a Child with Intellectual Disability, Ataxia, and Arthrogryposis

    A Gain-of-Function Mutation in<i>NALCN</i>in a Child with Intellectual Disability, Ataxia, and Arthrogryposis 著者: Kyota Aoyagi, Elsa Rossignol, Fadi F. Hamdan, Ben Mulcahy, Lin Xie, Shinya Nagamatsu, Guy A. Rouleau, Mei Zhen, Jacques L. Michaud

    出版事項 2015
    全文の入手
    Artigo
    お気に入りに追加
    保存先:
  9. 9
    A Missense Mutation (R565W) in Cirhin (FLJ14728) in North American Indian Childhood Cirrhosis

    A Missense Mutation (R565W) in Cirhin (FLJ14728) in North American Indian Childhood Cirrhosis 著者: Pierre Chagnon, Jacques L. Michaud, Grant A. Mitchell, Jocelyne Mercier, Jean-François Marion, Éric Drouin, Andrée Rasquin‐Weber, Thomas J. Hudson, Andréa Richter

    出版事項 2002
    全文の入手
    Artigo
    お気に入りに追加
    保存先:
  10. 10
    Ornithine delta-aminotransferase mutations in gyrate atrophy. Allelic heterogeneity and functional consequences.

    Ornithine delta-aminotransferase mutations in gyrate atrophy. Allelic heterogeneity and functional consequences. 著者: Larry Brody, Grant A. Mitchell, Cassandra Obie, Jacques L. Michaud, Gary Steel, G Fontaine, M.F. Robert, Ilkka Sipilä, Muriel I. Kaiser‐Kupfer, David Valle

    出版事項 1992
    全文の入手
    Artigo
    お気に入りに追加
    保存先:
  11. 11
    A homozygous mutation in <i><scp>SLC1A4</scp></i> in siblings with severe intellectual disability and microcephaly

    A homozygous mutation in <i><scp>SLC1A4</scp></i> in siblings with severe intellectual disability and microcephaly 著者: Myriam Srour, Fadi F. Hamdan, Ziv Gan‐Or, D. Labuda, Christina Nassif, Maryam Oskoui, Mali Gana‐Weisz, Avi Orr‐Urtreger, Guy A. Rouleau, Jacques L. Michaud

    出版事項 2015
    全文の入手 全文の入手
    Artigo
    お気に入りに追加
    保存先:
  12. 12
    Intellectual disability without epilepsy associated with STXBP1 disruption

    Intellectual disability without epilepsy associated with STXBP1 disruption 著者: Fadi F. Hamdan, Julie Gauthier, Sylvia Dobrzeniecka, Anne Lortie, Laurent Mottron, Michel Vanasse, Guy D’Anjou, Jean Claude Lacaille, Guy A. Rouleau, Jacques L. Michaud

    出版事項 2011
    全文の入手 全文の入手
    Artigo
    お気に入りに追加
    保存先:
  13. 13
    The genetic landscape of infantile spasms

    The genetic landscape of infantile spasms 著者: Jacques L. Michaud, Mathieu Lachance, Fadi F. Hamdan, Lionel Carmant, Anne Lortie, Paola Diadori, Philippe Major, Inge A. Meijer, Emmanuelle Lemyre, Patrick Cossette, Heather C. Mefford, Guy A. Rouleau, Elsa Rossignol

    出版事項 2014
    全文の入手 全文の入手
    Artigo
    お気に入りに追加
    保存先:
  14. 14
    Identification and Biochemical Characterization of a Novel Mutation in<i>DDX11</i>Causing Warsaw Breakage Syndrome

    Identification and Biochemical Characterization of a Novel Mutation in<i>DDX11</i>Causing Warsaw Breakage Syndrome 著者: José‐Mario Capo‐Chichi, Sanjay Kumar Bharti, Joshua A. Sommers, Tony Yammine, Éliane Chouery, Lysanne Patry, Guy A. Rouleau, Mark Samuels, Fadi F. Hamdan, Jacques L. Michaud, Robert Brosh, André Mégarbané, Zoha Kibar

    出版事項 2012
    全文の入手
    Artigo
    お気に入りに追加
    保存先:
  15. 15
    Identification of Novel Mutations Confirms<i>Pde4d</i>as a Major Gene Causing Acrodysostosis

    Identification of Novel Mutations Confirms<i>Pde4d</i>as a Major Gene Causing Acrodysostosis 著者: Danielle C. Lynch, David A. Dyment, Lijia Huang, Sarah M. Nikkel, Didier Lacombe, Philippe M. Campeau, Brendan Lee, Carlos A. Bacino, Jacques L. Michaud, François Bernier, FORGE Canada Consortium, Jillian S. Parboosingh, A. Micheil Innes

    出版事項 2012
    全文の入手
    Artigo
    お気に入りに追加
    保存先:
  16. 16
    Mutations in NOTCH2 in families with Hajdu-Cheney syndrome

    Mutations in NOTCH2 in families with Hajdu-Cheney syndrome 著者: Jacek Majewski, Jeremy Schwartzentruber, Aurore Caqueret, Lysanne Patry, Janet Marcadier, Jean‐Pierre Fryns, Kym M. Boycott, Louis‐Georges Ste‐Marie, Fergus E. McKiernan, Ivo Mařík, Hilde Van Esch, Jacques L. Michaud, Mark E. Samuels

    出版事項 2011
    全文の入手
    Artigo
    お気に入りに追加
    保存先:
  17. 17
    Loss-of-function de novo mutations play an important role in severe human neural tube defects

    Loss-of-function de novo mutations play an important role in severe human neural tube defects 著者: Philippe Lemay, Marie-Claude Guyot, Élizabeth Tremblay, Alexandre Dionne‐Laporte, Dan Spiegelman, Édouard Henrion, Ousmane Diallo, Patrizia De Marco, Elisa Merello, Christine Massicotte, Valérie Désilets, Jacques L. Michaud, Guy A. Rouleau, Valeria Capra, Zoha Kibar

    出版事項 2015
    全文の入手 全文の入手
    Artigo
    お気に入りに追加
    保存先:
  18. 18
    A homozygous loss-of-function variant in MYH11 in a case with megacystis-microcolon-intestinal hypoperistalsis syndrome

    A homozygous loss-of-function variant in MYH11 in a case with megacystis-microcolon-intestinal hypoperistalsis syndrome 著者: Julie Gauthier, Bouchra Ouled Amar Bencheikh, Fadi F. Hamdan, Steven M. Harrison, Linda A. Baker, Françoise Couture, Isabelle Thiffault, Réda Ouazzani, Mark E. Samuels, Grant A. Mitchell, Guy A. Rouleau, Jacques L. Michaud, J.‐F. Soucy

    出版事項 2014
    全文の入手 全文の入手
    Artigo
    お気に入りに追加
    保存先:
  19. 19
    Recessive and Dominant Mutations in Retinoic Acid Receptor Beta in Cases with Microphthalmia and Diaphragmatic Hernia

    Recessive and Dominant Mutations in Retinoic Acid Receptor Beta in Cases with Microphthalmia and Diaphragmatic Hernia 著者: Myriam Srour, David Chitayat, Véronique Caron, Nicolas Chassaing, Pierre Bitoun, Lysanne Patry, Marie‐Pierre Cordier, José‐Mario Capo‐Chichi, Christine Francannet, Patrick Calvas, Nicola Ragge, Sylvia Dobrzeniecka, Fadi F. Hamdan, Guy A. Rouleau, André Tremblay, Jacques L. Michaud

    出版事項 2013
    全文の入手
    Artigo
    お気に入りに追加
    保存先:
  20. 20
    Novel Jbts17 mutant mouse model of Joubert syndrome with cilia transition zone defects and cerebellar and other ciliopathy related anomalies

    Novel Jbts17 mutant mouse model of Joubert syndrome with cilia transition zone defects and cerebellar and other ciliopathy related anomalies 著者: Rama Rao Damerla, Cheng Cui, George C. Gabriel, Xiaoqin Liu, Branch Craige, Brian Gibbs, Richard Francis, You Li, Bishwanath Chatterjee, Jovenal T. San Agustin, Thibaut Eguether, Ramiah Subramanian, George B. Witman, Jacques L. Michaud, Gregory J. Pazour, Cecilia Lo

    出版事項 2015
    全文の入手
    Artigo
    お気に入りに追加
    保存先:

検索ツール: