תוצאות חיפוש - Kenneth Morgan

  • Showing 1 - 20 results of 20
Refine Results
  1. 1
    THE EFFECT OF INTRAGENIC RECOMBINATION ON THE NUMBER OF ALLELES IN A FINITE POPULATION

    THE EFFECT OF INTRAGENIC RECOMBINATION ON THE NUMBER OF ALLELES IN A FINITE POPULATION מאת Curtis Strobeck, Kenneth Morgan

    יצא לאור 1978
    קבל טקסט מלא קבל טקסט מלא
    Artigo
    הוספה למועדפים
    שמור ב:
  2. 2
    Impairment of Protective Immunity to Blood-Stage Malaria by Concurrent Nematode Infection

    Impairment of Protective Immunity to Blood-Stage Malaria by Concurrent Nematode Infection מאת Zhong Su, Mariela Segura, Kenneth Morgan, J. Concepción Loredo‐Osti, Mary M. Stevenson

    יצא לאור 2005
    קבל טקסט מלא
    Artigo
    הוספה למועדפים
    שמור ב:
  3. 3
    Limb-Girdle Muscular Dystrophy Type 2H Associated with Mutation in TRIM32, a Putative E3-Ubiquitin–Ligase Gene

    Limb-Girdle Muscular Dystrophy Type 2H Associated with Mutation in TRIM32, a Putative E3-Ubiquitin–Ligase Gene מאת Patrick Frosk, Tracey Weiler, Edward Nylen, Thangirala Sudha, Cheryl R. Greenberg, Kenneth Morgan, Takuya Fujiwara, Klaus Wrogemann

    יצא לאור 2002
    קבל טקסט מלא קבל טקסט מלא
    Artigo
    הוספה למועדפים
    שמור ב:
  4. 4
    A Gene for Autosomal Recessive Limb-Girdle Muscular Dystrophy in Manitoba Hutterites Maps to Chromosome Region 9q31-q33: Evidence for Another Limb-Girdle Muscular Dystrophy Locus

    A Gene for Autosomal Recessive Limb-Girdle Muscular Dystrophy in Manitoba Hutterites Maps to Chromosome Region 9q31-q33: Evidence for Another Limb-Girdle Muscular Dystrophy Locus מאת Tracey Weiler, Cheryl R. Greenberg, Teresa Zelinski, Edward Nylen, Gail Coghlan, M. JOYCE CRUMLEY, Takuya Fujiwara, Kenneth Morgan, Klaus Wrogemann

    יצא לאור 1998
    קבל טקסט מלא קבל טקסט מלא
    Artigo
    הוספה למועדפים
    שמור ב:
  5. 5
    Linkage of Tuberculosis to Chromosome 2q35 Loci, Including NRAMP1, in a Large Aboriginal Canadian Family

    Linkage of Tuberculosis to Chromosome 2q35 Loci, Including NRAMP1, in a Large Aboriginal Canadian Family מאת Celia M.T. Greenwood, Takuya Fujiwara, Lucy J. Boothroyd, Mark A. Miller, Danielle Frappier, E A Fanning, Erwin Schurr, Kenneth Morgan

    יצא לאור 2000
    קבל טקסט מלא
    Artigo
    הוספה למועדפים
    שמור ב:
  6. 6
    Dietary patterns and risk for Crohnʼs disease in children

    Dietary patterns and risk for Crohnʼs disease in children מאת Savio D’Souza, Émile Lévy, David R. Mack, David M. Israel, Philippe Lambrette, Parviz Ghadirian, Colette Deslandres, Kenneth Morgan, Ernest G. Seidman, Devendra Amre

    יצא לאור 2007
    קבל טקסט מלא קבל טקסט מלא
    Artigo
    הוספה למועדפים
    שמור ב:
  7. 7
    The Human Mammary-Derived Growth Inhibitor (MDGI) Gene: Genomic Structure and Mutation Analysis in Human Breast Tumors

    The Human Mammary-Derived Growth Inhibitor (MDGI) Gene: Genomic Structure and Mutation Analysis in Human Breast Tumors מאת Catherine M. Phelan, Catharina Larsson, Stephen Baird, P. Andrew Futreal, Martin Ruttledge, Kenneth Morgan, Patricia N. Tonin, Hung Huynh, Robert G. Korneluk, Michaël Pollak, Steven A. Narod

    יצא לאור 1996
    קבל טקסט מלא
    Artigo
    הוספה למועדפים
    שמור ב:
  8. 8
    Molecular scanning of the human PPARα gene: association of the L162V mutation with hyperapobetalipoproteinemia

    Molecular scanning of the human PPARα gene: association of the L162V mutation with hyperapobetalipoproteinemia מאת Marie‐Claude Vohl, Patricia Lepage, Daniel Gaudet, Carl G. Brewer, Christine Bétard, Patrice Perron, Ghislaine Houde, Christine Cellier, Janet Faith, Jean‐Pierre Després, Kenneth Morgan, Thomas J. Hudson

    יצא לאור 2000
    קבל טקסט מלא קבל טקסט מלא
    Artigo
    הוספה למועדפים
    שמור ב:
  9. 9
    Founder BRCA1 and BRCA2 Mutations in French Canadian Breast and Ovarian Cancer Families

    Founder BRCA1 and BRCA2 Mutations in French Canadian Breast and Ovarian Cancer Families מאת Patricia N. Tonin, Anne‐Marie Mes‐Masson, P. Andrew Futreal, Kenneth Morgan, Michelle G. Mahon, William D. Foulkes, David E.C. Cole, Diane Provencher, Parviz Ghadirian, Steven A. Narod

    יצא לאור 1998
    קבל טקסט מלא קבל טקסט מלא
    Artigo
    הוספה למועדפים
    שמור ב:
  10. 10
    Location Score and Haplotype Analyses of the Locus for Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay, in Chromosome Region 13q11

    Location Score and Haplotype Analyses of the Locus for Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay, in Chromosome Region 13q11 מאת Andréa Richter, John D. Rioux, Jean‐Pierre Bouchard, Jocelyne Mercier, Jean Mathieu, Bing Ge, Josée Poirier, Dominique Julien, Gàbor Gyapay, Jean Weissenbach, Thomas J. Hudson, Serge B. Melançon, Kenneth Morgan

    יצא לאור 1999
    קבל טקסט מלא קבל טקסט מלא
    Artigo
    הוספה למועדפים
    שמור ב:
  11. 11
    Epistasis between mouse Klra and major histocompatibility complex class I loci is associated with a new mechanism of natural killer cell–mediated innate resistance to cytomegalovirus infection

    Epistasis between mouse Klra and major histocompatibility complex class I loci is associated with a new mechanism of natural killer cell–mediated innate resistance to cytomegalovir... מאת Marie‐Pierre Desrosiers, Agnieszka Kielczewska, J. Concepción Loredo‐Osti, Sonia Girard Adam, Andrew P. Makrigiannis, Suzanne Lemieux, Trung H. M. Pham, Melissa B. Lodoen, Kenneth Morgan, Lewis L. Lanier, Silvia M. Vidal

    יצא לאור 2005
    קבל טקסט מלא
    Artigo
    הוספה למועדפים
    שמור ב:
  12. 12
    An aquaporin-2 water channel mutant which causes autosomal dominant nephrogenic diabetes insipidus is retained in the Golgi complex.

    An aquaporin-2 water channel mutant which causes autosomal dominant nephrogenic diabetes insipidus is retained in the Golgi complex. מאת S.M. Mulders, Daniel G. Bichet, J.P.L. Rijss, Erik‐Jan Kamsteeg, Marie‐Françoise Arthus, Michèle Lonergan, Masasuke Fujiwara, Kenneth Morgan, Richtje Leijendekker, Peter van der Sluijs, C.H. van Os, Peter M.T. Deen

    יצא לאור 1998
    קבל טקסט מלא קבל טקסט מלא
    Artigo
    הוספה למועדפים
    שמור ב:
  13. 13
    Report of 33 Novel AVPR2 Mutations and Analysis of 117 Families with X-Linked Nephrogenic Diabetes Insipidus

    Report of 33 Novel AVPR2 Mutations and Analysis of 117 Families with X-Linked Nephrogenic Diabetes Insipidus מאת Marie-FrancCOMBINING CEDILLAoise Arthus, MICHECombining Grave AccentLE LONERGAN, M. JOYCE CRUMLEY, Anna K. Naumova, Denis Morin, Luiz Armando De Marco, Bernard S. Kaplan, Gary L. Robertson, Sei Sasaki, Kenneth Morgan, Daniel G. Bichet, Takuya Fujiwara

    יצא לאור 2000
    קבל טקסט מלא
    Artigo
    הוספה למועדפים
    שמור ב:
  14. 14
    Filaggrin gene mutation associations with peanut allergy persist despite variations in peanut allergy diagnostic criteria or asthma status

    Filaggrin gene mutation associations with peanut allergy persist despite variations in peanut allergy diagnostic criteria or asthma status מאת Yuka Asai, Celia M.T. Greenwood, Peter Hull, Reza Alizadehfar, Moshe Ben‐Shoshan, Sara Brown, Linda Campbell, Déborah Michel, Johanne Bussières, François Rousseau, Takuya Fujiwara, Kenneth Morgan, Alan D. Irvine, W.H. Irwin McLean, Ann E. Clarke

    יצא לאור 2013
    קבל טקסט מלא קבל טקסט מלא
    Carta
    הוספה למועדפים
    שמור ב:
  15. 15
    Shwachman-Diamond Syndrome with Exocrine Pancreatic Dysfunction and Bone Marrow Failure Maps to the Centromeric Region of Chromosome 7

    Shwachman-Diamond Syndrome with Exocrine Pancreatic Dysfunction and Bone Marrow Failure Maps to the Centromeric Region of Chromosome 7 מאת Sharan Goobie, M. Popović, Jodi Morrison, Lynda Ellis, Hedy Ginzberg, Graeme R.B. Boocock, Nadia Ehtesham, Christine Bétard, Carl G. Brewer, Nicole M. Roslin, Thomas J. Hudson, Kenneth Morgan, Takuya Fujiwara, Peter R. Durie, Johanna M. Rommens

    יצא לאור 2001
    קבל טקסט מלא
    Artigo
    הוספה למועדפים
    שמור ב:
  16. 16
    The most common mutation inFKRP causing limb girdle muscular dystrophy type 2I (LGMD2I) may have occurred only once and is present in Hutterites and other populations

    The most common mutation inFKRP causing limb girdle muscular dystrophy type 2I (LGMD2I) may have occurred only once and is present in Hutterites and other populations מאת Patrick Frosk, Cheryl R. Greenberg, Alysa A.P. Tennese, Ryan E. Lamont, Edward Nylen, Cheryl Hirst, Danielle Frappier, Nicole M. Roslin, M Zaik, Kate Bushby, Volker Straub, Mayana Zatz, Flavia Paula, Kenneth Morgan, Takuya Fujiwara, Klaus Wrogemann

    יצא לאור 2004
    קבל טקסט מלא
    Artigo
    הוספה למועדפים
    שמור ב:
  17. 17
    SLC34A3 Mutations in Patients with Hereditary Hypophosphatemic Rickets with Hypercalciuria Predict a Key Role for the Sodium-Phosphate Cotransporter NaPi-IIc in Maintaining Phosphate Homeostasis

    SLC34A3 Mutations in Patients with Hereditary Hypophosphatemic Rickets with Hypercalciuria Predict a Key Role for the Sodium-Phosphate Cotransporter NaPi-IIc in Maintaining Phospha... מאת Clemens Bergwitz, Nicole M. Roslin, Martin Tieder, Jorge Loredo‐Osti, Murat Bastepe, Hilal Abu-Zahra, Danielle Frappier, Kelly M. Burkett, Thomas O. Carpenter, Donald G. Anderson, Michèle Garabédian, Isabelle Sermet‐Gaudelus, Takuya Fujiwara, Kenneth Morgan, Harriet S. Tenenhouse, Harald Jüppner

    יצא לאור 2006
    קבל טקסט מלא
    Artigo
    הוספה למועדפים
    שמור ב:
  18. 18
    Study of Two Dose Regimens of Ticagrelor Compared With Clopidogrel in Patients Undergoing Percutaneous Coronary Intervention for Stable Coronary Artery Disease

    Study of Two Dose Regimens of Ticagrelor Compared With Clopidogrel in Patients Undergoing Percutaneous Coronary Intervention for Stable Coronary Artery Disease מאת Rachel C. Orme, William A. Parker, Mark R. Thomas, Heather M. Judge, Kathleen Baster, Wael Sumaya, Kenneth Morgan, Hannah McMellon, J. David Richardson, Ever Grech, Nigel Wheeldon, Ian Hall, Javaid Iqbal, David Barmby, Julian Gunn, Robert F. Storey, Robert A. Wilcox, John Walsh, William Smith, Allan M. Skene

    יצא לאור 2018
    קבל טקסט מלא
    Artigo
    הוספה למועדפים
    שמור ב:
  19. 19
    Loss-of-function variants in the filaggrin gene are a significant risk factor for peanut allergy

    Loss-of-function variants in the filaggrin gene are a significant risk factor for peanut allergy מאת Sara Brown, Yuka Asai, Heather J. Cordell, Linda Campbell, Yiwei Zhao, Haihui Liao, Kate Northstone, John Henderson, Reza Alizadehfar, Moshe Ben‐Shoshan, Kenneth Morgan, Graham Roberts, L. J. Masthoff, Suzanne G.M.A. Pasmans, Peter C. van den Akker, Cisca Wijmenga, Jonathan O’B Hourihane, Colin N. A. Palmer, Gideon Lack, Ann E. Clarke, Peter Hull, Alan D. Irvine, W.H. Irwin McLean

    יצא לאור 2011
    קבל טקסט מלא קבל טקסט מלא
    Artigo
    הוספה למועדפים
    שמור ב:
  20. 20
    Mutations in TMEM76 Cause Mucopolysaccharidosis IIIC (Sanfilippo C Syndrome)

    Mutations in TMEM76 Cause Mucopolysaccharidosis IIIC (Sanfilippo C Syndrome) מאת Martin Hřebı́ček, Lenka Mrázová, Volkan Seyrantepe, Stéphanie Durand, Nicole M. Roslin, Lenka Nosková, Hana Hartmannová, Robert Ivánek, Alena Čížková, Helena Poupětová, Jakub Sikora, Jana Uřinovská, Viktor Stránecký, J Zeman, Pierre Lepage, David Roquis, Andrei Verner, Jérôme Ausseil, Clare Beesley, Irène Maire, Ben J. H. M. Poorthuis, Jiddeke van de Kamp, Otto P. van Diggelen, Ron A. Wevers, Thomas J. Hudson, Takuya Fujiwara, Jacek Majewski, Kenneth Morgan, Stanislav Kmoch, Alexey V. Pshezhetsky

    יצא לאור 2006
    קבל טקסט מלא
    Artigo
    הוספה למועדפים
    שמור ב:

כלי חיפוש: