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There are 27723 results for: content related to: A meta-analysis of the relationship of the Parkin p.Val380Leu polymorphism to Parkinson's disease

  1. Construction and validation of a Parkinson's disease mutation genotyping array for the Parkin gene

    Movement Disorders

    Volume 22, Issue 7, 15 May 2007, Pages: 932–937, Lorraine N. Clark, Eneli Haamer, Helen Mejia-Santana, Juliette Harris, Suzanne Lesage, Alexandra Durr, Sabine Janin Bs, Katja Hedrich, Elan D. Louis, Lucien J. Cote, Howard Andrews, Stanley Fahn, Cheryl Waters, Blair Ford, Steven Frucht, William Scott, Christine Klein, Alexis Brice, Hanno Roomere, Ruth Ottman and Karen Marder

    Version of Record online : 5 APR 2007, DOI: 10.1002/mds.21419

  2. Complex relationship between Parkin mutations and Parkinson disease

    American Journal of Medical Genetics

    Volume 114, Issue 5, 8 July 2002, Pages: 584–591, Andrew West, Magali Periquet, Sarah Lincoln, Christoph B. Lücking, David Nicholl, Vincenzo Bonifati, Nina Rawal, Thomas Gasser, Ebba Lohmann, Jean-François Deleuze, Demetrius Maraganore, Allan Levey, Nick Wood, Alexandra Dürr, John Hardy, Alexis Brice and Matt Farrer

    Version of Record online : 10 MAY 2002, DOI: 10.1002/ajmg.10525

  3. You have free access to this content
    Inconsistency between hepatic expression and serum concentration of transthyretin in mice humanized at the transthyretin locus

    Genes to Cells

    Volume 13, Issue 12, December 2008, Pages: 1257–1268, Gang Zhao, Zhenghua Li, Kimi Araki, Kyoko Haruna, Kazuhito Yamaguchi, Masatake Araki, Motohiro Takeya, Yukio Ando and Ken-ichi Yamamura

    Version of Record online : 19 NOV 2008, DOI: 10.1111/j.1365-2443.2008.01242.x

  4. Parkin gene variations in late-onset Parkinson's disease: comparison between Norwegian and German cohorts

    Acta Neurologica Scandinavica

    Volume 113, Issue 1, January 2006, Pages: 9–13, A. M. Schlitter, M. Kurz, J. P. Larsen, D. Woitalla, T. Müller, J. T. Epplen and G. Dekomien

    Version of Record online : 18 NOV 2005, DOI: 10.1111/j.1600-0404.2005.00532.x

  5. You have full text access to this OnlineOpen article
    Familial adult onset hyperinsulinism due to an activating glucokinase mutation: implications for pharmacological glucokinase activation

    Clinical Endocrinology

    Volume 81, Issue 6, December 2014, Pages: 855–861, Benjamin G. Challis, Julie Harris, Alison Sleigh, Iona Isaac, Steve M. Orme, Nandini Seevaratnam, Ketan Dhatariya, Helen L. Simpson and Robert K. Semple

    Version of Record online : 2 JUL 2014, DOI: 10.1111/cen.12517

  6. Genetic and environmental findings in early-onset Parkinson's disease Brazilian patients

    Movement Disorders

    Volume 23, Issue 9, 15 July 2008, Pages: 1228–1233, Patricia de Carvalho Aguiar, Patricia Silva Lessa, Clecio Godeiro Junior, Orlando Barsottini, Andre Carvalho Felício, Vanderci Borges, Sonia Maria de Azevedo Silva, Roberta Arb Saba, Henrique Ballalai Ferraz, Carlos A. Moreira-Filho and Luiz Augusto F. Andrade

    Version of Record online : 7 MAY 2008, DOI: 10.1002/mds.22032

  7. Parkin mutations and susceptibility alleles in late-onset Parkinson's disease

    Annals of Neurology

    Volume 53, Issue 5, May 2003, Pages: 624–629, Sofia A. Oliveira, William K. Scott, Eden R. Martin, Martha A. Nance, Ray L. Watts, Jean P. Hubble, William C. Koller, Rajesh Pahwa, Matthew B. Stern, Bradley C. Hiner, William G. Ondo, Fred H. Allen Jr., Burton L. Scott, Christopher G. Goetz, Gary W. Small, Frank Mastaglia, Jeffrey M. Stajich, Fengyu Zhang, Michael W. Booze, Michelle P. Winn, Lefkos T. Middleton, Jonathan L. Haines, Margaret A. Pericak-Vance and Jeffery M. Vance

    Version of Record online : 1 APR 2003, DOI: 10.1002/ana.10524

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    Coagulation factor XIII polymorphisms and the risk of myocardial infarction and ischaemic stroke in young women

    British Journal of Haematology

    Volume 116, Issue 2, February 2002, Pages: 376–382, Alexander P. Reiner, Michele B. Frank, Stephen M. Schwartz, Michael L. Linenberger, W. T. Longstreth Jr, Gayle Teramura, Frits R. Rosendaal, Bruce M. Psaty and David S. Siscovick

    Version of Record online : 1 FEB 2002, DOI: 10.1046/j.1365-2141.2002.03265.x

  9. Novel mutations in the KCND3-encoded Kv4.3 K+ channel associated with autopsy-negative sudden unexplained death

    Human Mutation

    Volume 33, Issue 6, June 2012, Pages: 989–997, John R. Giudicessi, Dan Ye, Chad J. Kritzberger, Vladislav V. Nesterenko, David J. Tester, Charles Antzelevitch and Michael J. Ackerman

    Version of Record online : 27 MAR 2012, DOI: 10.1002/humu.22058

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    Mutation of colocalized residues of the pore helix and transmembrane segments S5 and S6 disrupt deactivation and modify inactivation of KCNQ1 K+ channels

    The Journal of Physiology

    Volume 563, Issue 2, March 2005, Pages: 359–368, Guiscard Seebohm, Peter Westenskow, Florian Lang and Michael C. Sanguinetti

    Version of Record online : 21 FEB 2005, DOI: 10.1113/jphysiol.2004.080887

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    Novel missense polymorphism in the regulator of G-protein signaling 10 gene: analysis of association with schizophrenia

    Psychiatry and Clinical Neurosciences


    Version of Record online : 11 OCT 2004, DOI: 10.1111/j.1440-1819.2004.01303.x

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    A novel factor XI missense mutation (Val371Ile) in the activation loop is responsible for a case of mild type II factor XI deficiency

    The FEBS Journal

    Volume 274, Issue 23, December 2007, Pages: 6128–6138, Cristina Bozzao, Valeria Rimoldi, Rosanna Asselta, Meytal Landau, Rossella Ghiotto, Maria L. Tenchini, Raimondo De Cristofaro, Giancarlo Castaman and Stefano Duga

    Version of Record online : 30 OCT 2007, DOI: 10.1111/j.1742-4658.2007.06134.x

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    Binding to human dipeptidyl peptidase IV by adenosine deaminase and antibodies that inhibit ligand binding involves overlapping, discontinuous sites on a predicted β propeller domain

    European Journal of Biochemistry

    Volume 266, Issue 3, December (II) 1999, Pages: 798–810, Catherine A. Abbott, Geoffrey W. McCaughan, Miriam T. Levy, W. Bret Church and Mark D. Gorrell

    Version of Record online : 25 DEC 2001, DOI: 10.1046/j.1432-1327.1999.00902.x

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    Structural and functional comparison of 15S- and 15R-specific cyclooxygenases from the coral Plexaura homomalla

    European Journal of Biochemistry

    Volume 271, Issue 17, September 2004, Pages: 3533–3538, Karin Valmsen, William E. Boeglin, Ivar Järving, Claus Schneider, Külliki Varvas, Alan R. Brash and Nigulas Samel

    Version of Record online : 11 AUG 2004, DOI: 10.1111/j.0014-2956.2004.04289.x

  15. Amyloidogenic transthyretin Val30Met homozygote showing unusually early-onset familial amyloid polyneuropathy

    Muscle & Nerve

    Volume 37, Issue 6, June 2008, Pages: 796–803, Kana Tojo, Yoshiki Sekijima, Kazuko Machida, Ayako Tsuchiya, Masahide Yazaki and Shu-Ichi Ikeda

    Version of Record online : 27 MAY 2008, DOI: 10.1002/mus.21028

  16. A naturally occurring Leu33Val mutation in β3-integrin impairs the HPA-1a epitope: the third allele of HPA-1


    Volume 46, Issue 5, May 2006, Pages: 790–799, Sentot Santoso, Hartmut Kroll, Cornelia L. Andrei-Selmer, Ines Socher, Angela Rankin, Evelyne Kretzschmar, Nicholas A. Watkins and Willem H. Ouwehand

    Version of Record online : 13 MAR 2006, DOI: 10.1111/j.1537-2995.2006.00797.x

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    Contribution of C-tail residues of potato carboxypeptidase inhibitor to the binding to carboxypeptidase A

    European Journal of Biochemistry

    Volume 267, Issue 5, March 2000, Pages: 1502–1509, Cristina Marino-Buslje, Gabriela Venhudová, Miguel A. Molina, Baldomero Oliva, Xavier Jorba, Francesc Canals, Francesc X. Avilés and Enrique Querol

    Version of Record online : 25 DEC 2001, DOI: 10.1046/j.1432-1327.2000.01150.x

  18. Characterization of differences in substrate specificity among CYP1A1, CYP1A2 and CYP1B1: an integrated approach employing molecular docking and molecular dynamics simulations

    Journal of Molecular Recognition

    Volume 29, Issue 8, August 2016, Pages: 370–390, Siddharth S. Kesharwani, Prajwal P. Nandekar, Preeti Pragyan, Vijay Rathod and Abhay T. Sangamwar

    Version of Record online : 25 FEB 2016, DOI: 10.1002/jmr.2537

  19. PRKN, DJ-1, and PINK1 screening identifies novel splice site mutation in PRKN and two novel DJ-1 mutations

    Movement Disorders

    Volume 26, Issue 1, January 2011, Pages: 80–89, Farzaneh Ghazavi, Zeinab Fazlali, Setareh Sadat Banihosseini, Sayed-Rzgar Hosseini, Mohammad Hossein Kazemi, Seyedmehdi Shojaee, Khosro Parsa, Homa Sadeghi, Farzad Sina, Mohammad Rohani, Gholam-Ali Shahidi, Nasser Ghaemi, Mostafa Ronaghi and Elahe Elahi

    Version of Record online : 8 NOV 2010, DOI: 10.1002/mds.23417

  20. Factor XIII Val34Leu mutation accelerates the development of fibrosis in patients with chronic hepatitis B and C

    Hepatology Research

    Volume 42, Issue 7, July 2012, Pages: 668–676, Kathelijne Dik, Joep de Bruijne, R. Bart Takkenberg, Joris J. Roelofs, Marjan J. Tempelmans, Marcel G. W. Dijkgraaf, Huub C. Gelderblom, Henk W. Reesink, Joost C. M. Meijers, Peter L. Jansen and Marcel Levi

    Version of Record online : 5 MAR 2012, DOI: 10.1111/j.1872-034X.2011.00963.x