Torthaí cuardaigh - Takuya Fujiwara

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  1. 1
    Molecular Biology of Hereditary Diabetes Insipidus

    Molecular Biology of Hereditary Diabetes Insipidus de réir Takuya Fujiwara, Daniel G. Bichet

    Foilsithe / Cruthaithe 2005
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    Revisão
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  2. 2
    Efficacy of brain-computer interface-driven neuromuscular electrical stimulation for chronic paresis after stroke

    Efficacy of brain-computer interface-driven neuromuscular electrical stimulation for chronic paresis after stroke de réir Masahiko Mukaino, Takashi Ono, Katsuro Shindo, Takuya Fujiwara, T. Ōta, Akio Kimura, Min Liu, Junichi Ushiba

    Foilsithe / Cruthaithe 2014
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    Artigo
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  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 de réir Patrick Frosk, Tracey Weiler, Edward Nylen, Thangirala Sudha, Cheryl R. Greenberg, Kenneth Morgan, Takuya Fujiwara, Klaus Wrogemann

    Foilsithe / Cruthaithe 2002
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  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 de réir Tracey Weiler, Cheryl R. Greenberg, Teresa Zelinski, Edward Nylen, Gail Coghlan, M. JOYCE CRUMLEY, Takuya Fujiwara, Kenneth Morgan, Klaus Wrogemann

    Foilsithe / Cruthaithe 1998
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    Artigo
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  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 de réir Celia M.T. Greenwood, Takuya Fujiwara, Lucy J. Boothroyd, Mark A. Miller, Danielle Frappier, E A Fanning, Erwin Schurr, Kenneth Morgan

    Foilsithe / Cruthaithe 2000
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    Artigo
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  6. 6
    Troglitazone increases the number of small adipocytes without the change of white adipose tissue mass in obese Zucker rats.

    Troglitazone increases the number of small adipocytes without the change of white adipose tissue mass in obese Zucker rats. de réir Akira Okuno, Hiroyuki Tamemoto, Kazuuki TOBE, Kohjiro Ueki, Yusaku Mori, K Iwamoto, Kazuhiko Umesono, Y. Akanuma, Takuya Fujiwara, Hiroyoshi Horikoshi, Y Yazaki, Takashi Kadowaki

    Foilsithe / Cruthaithe 1998
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  7. 7
    X-linked nephrogenic diabetes insipidus mutations in North America and the Hopewell hypothesis.

    X-linked nephrogenic diabetes insipidus mutations in North America and the Hopewell hypothesis. de réir Daniel G. Bichet, Marie‐Françoise Arthus, Michèle Lonergan, Geoffrey N. Hendy, A J Paradis, Takuya Fujiwara, K. Morgan, Martin C. Gregory, Walter Rosenthal, A Didwania

    Foilsithe / Cruthaithe 1993
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    Artigo
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  8. 8
    Homozygous Deletion of the Very Low Density Lipoprotein Receptor Gene Causes Autosomal Recessive Cerebellar Hypoplasia with Cerebral Gyral Simplification

    Homozygous Deletion of the Very Low Density Lipoprotein Receptor Gene Causes Autosomal Recessive Cerebellar Hypoplasia with Cerebral Gyral Simplification de réir Kym M. Boycott, Shauna Flavelle, Alexandre Bureau, Hannah C. Glass, Takuya Fujiwara, Elaine Wirrell, Krista Davey, Albert E. Chudley, James N. Scott, D. Ross McLeod, Jillian S. Parboosingh

    Foilsithe / Cruthaithe 2005
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  9. 9
    Three Families with Autosomal Dominant Nephrogenic Diabetes Insipidus Caused by Aquaporin-2 Mutations in the C-Terminus

    Three Families with Autosomal Dominant Nephrogenic Diabetes Insipidus Caused by Aquaporin-2 Mutations in the C-Terminus de réir Michio Kuwahara, Kazuyuki Iwai, Toru Ooeda, Takashi Igarashi, Eishin Ogawa, Yuriko Katsushima, Itsuki Shinbo, Shinichi Uchida, Yoshio Terada, Marie‐Françoise Arthus, Michèle Lonergan, Takuya Fujiwara, Daniel G. Bichet, Fumiaki Marumo, Sei Sasaki

    Foilsithe / Cruthaithe 2001
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  10. 10
    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 de réir 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

    Foilsithe / Cruthaithe 2000
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  11. 11
    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 de réir 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

    Foilsithe / Cruthaithe 2013
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  12. 12
    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 de réir 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

    Foilsithe / Cruthaithe 2001
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  13. 13
    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 de réir 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

    Foilsithe / Cruthaithe 2004
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  14. 14
    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... de réir 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

    Foilsithe / Cruthaithe 2006
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  15. 15
    Cell-Biologic and Functional Analyses of Five New Aquaporin-2 Missense Mutations that Cause Recessive Nephrogenic Diabetes Insipidus

    Cell-Biologic and Functional Analyses of Five New Aquaporin-2 Missense Mutations that Cause Recessive Nephrogenic Diabetes Insipidus de réir Nannette Marr, Daniel G. Bichet, Susan Hoefs, Paul J.M. Savelkoul, Irene B. M. Konings, Fabrizio De Mattia, Michael P. J. Graat, Marie-FrancCOMBINING CEDILLAoise Arthus, Michèle Lonergan, Takuya Fujiwara, Nine V.A.M. Knoers, Daniel Landau, William J. Balfe, A. Oksche, Walter Rosenthal, Dominik N. Müller, C.H. van Os, Peter M.T. Deen

    Foilsithe / Cruthaithe 2002
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  16. 16
    Mutations in TMEM76 Cause Mucopolysaccharidosis IIIC (Sanfilippo C Syndrome)

    Mutations in TMEM76 Cause Mucopolysaccharidosis IIIC (Sanfilippo C Syndrome) de réir 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

    Foilsithe / Cruthaithe 2006
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