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There are 70666 results for: content related to: Computational Approaches and Tools for Establishing Structural Models for Short Amyloid-forming Peptides

  1. Non-syndromic, autosomal-recessive deafness

    Clinical Genetics

    Volume 69, Issue 5, May 2006, Pages: 371–392, MB Petersen and PJ Willems

    Version of Record online : 27 APR 2006, DOI: 10.1111/j.1399-0004.2006.00613.x

  2. Crystal Structure of the DFNKF Segment of Human Calcitonin Unveils Aromatic Interactions between Phenylalanines

    Chemistry - A European Journal

    Volume 23, Issue 9, February 10, 2017, Pages: 2051–2058, Dr. Arianna Bertolani, Andrea Pizzi, Dr. Lisa Pirrie, Dr. Lara Gazzera, Dr. Giulia Morra, Dr. Massimiliano Meli, Dr. Giorgio Colombo, Prof. Alessandro Genoni, Dr. Gabriella Cavallo, Prof. Giancarlo Terraneo and Prof. Pierangelo Metrangolo

    Version of Record online : 15 DEC 2016, DOI: 10.1002/chem.201604639

  3. You have free access to this content
    DFNA5 (ICERE-1) contributes to acquired etoposide resistance in melanoma cells

    FEBS Letters

    Volume 494, Issue 1-2, April 06, 2001, Pages: 54–59, Hermann Lage, Heike Helmbach, Claudia Grottke, Manfred Dietel and Dirk Schadendorf

    Version of Record online : 4 APR 2001, DOI: 10.1016/S0014-5793(01)02304-3

  4. You have free access to this content
    A DFNA5 Mutation Identified in Japanese Families with Autosomal Dominant Hereditary Hearing Loss

    Annals of Human Genetics

    Volume 78, Issue 2, March 2014, Pages: 83–91, Ayako Nishio, Yoshihiro Noguchi, Tatsuya Sato, Taeko K. Naruse, Akinori Kimura, Akira Takagi and Ken Kitamura

    Version of Record online : 10 FEB 2014, DOI: 10.1111/ahg.12053

  5. Structural stability and aggregation behavior of the VEALYL peptide derived from human insulin: A molecular dynamics simulation study

    Peptide Science

    Volume 94, Issue 3, 2010, Pages: 269–278, Yeh-Fon Lin, Jian-Hua Zhao, Hsuan-Liang Liu, Kung-Tien Liu, Jenn-Tzong Chen, Wei-Bor Tsai and Yih Ho

    Version of Record online : 6 OCT 2009, DOI: 10.1002/bip.21322

  6. Shear-aggregated fibronectin with anti-adhesive properties

    Journal of Tissue Engineering and Regenerative Medicine

    Volume 5, Issue 1, January 2011, Pages: 20–31, O. A. Branford, R. A. Brown, D. A. McGrouther, A. O. Grobbelaar and V. Mudera

    Version of Record online : 22 JUL 2010, DOI: 10.1002/term.284

  7. Structural diversity of amyloid fibril formed in human calcitonin as revealed by site-directed 13C solid-state NMR spectroscopy

    Magnetic Resonance in Chemistry

    Volume 42, Issue 2, February 2004, Pages: 247–257, Akira Naito, Miya Kamihira, Ryozo Inoue and Hazime Saitô

    Version of Record online : 14 JAN 2004, DOI: 10.1002/mrc.1323

  8. Genotype phenotype correlations for hearing impairment: Approaches to management

    Clinical Genetics

    Volume 85, Issue 6, June 2014, Pages: 514–523, L. H. Hoefsloot, I. Feenstra, H. P. M. Kunst and H. Kremer

    Version of Record online : 18 FEB 2014, DOI: 10.1111/cge.12339

  9. A comprehensive study to determine heterogeneity of autosomal recessive nonsyndromic hearing loss in Iran

    American Journal of Medical Genetics Part A

    Volume 158A, Issue 10, October 2012, Pages: 2485–2492, Mojgan Babanejad, Zohreh Fattahi, Niloofar Bazazzadegan, Carla Nishimura, Nicole Meyer, Nooshin Nikzat, Elahe Sohrabi, Amin Najmabadi, Peyman Jamali, Farkhonde Habibi, Richard J.H. Smith, Kimia Kahrizi and Hossein Najmabadi

    Version of Record online : 17 AUG 2012, DOI: 10.1002/ajmg.a.35572

  10. Fine mapping of autosomal dominant nonsyndromic hearing impairment DFNA21 to chromosome 6p24.1-22.3

    American Journal of Medical Genetics Part A

    Volume 137A, Issue 1, 15 August 2005, Pages: 41–46, Arjan P.M. de Brouwer, Hendrikus P.M. Kunst, Alice Krebsova, Karin van Asseldonk, André Reis, Rik L. Snoeckx, Guy Van Camp, Cor W.R.J. Cremers, Frans P.M. Cremers and Hannie Kremer

    Version of Record online : 8 JUL 2005, DOI: 10.1002/ajmg.a.30844

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    Identification of a novel frameshift mutation in the DFNB31/WHRN gene in a Tunisian consanguineous family with hereditary non-syndromic recessive hearing loss

    Human Mutation

    Volume 25, Issue 5, May 2005, Page: 503, Abdelaziz Tlili, Ilhem Charfedine, Imed Lahmar, Zaineb Benzina, Ben Amor Mohamed, Dominique Weil, Nabil Idriss, Mohamed Drira, Saber Masmoudi and Hammadi Ayadi

    Version of Record online : 19 APR 2005, DOI: 10.1002/humu.9333

  12. Mutation spectrum of MYO7A and evaluation of a novel nonsyndromic deafness DFNB2 allele with residual function

    Human Mutation

    Volume 29, Issue 4, April 2008, Pages: 502–511, Saima Riazuddin, Sabiha Nazli, Zubair M. Ahmed, Yi Yang, Fareeha Zulfiqar, Rehan S. Shaikh, Ahmed U. Zafar, Shaheen N. Khan, Farooq Sabar, Fouzia T. Javid, Edward R. Wilcox, Ekaterini Tsilou, Erich T. Boger, James R. Sellers, Inna A. Belyantseva, Sheikh Riazuddin and Thomas B. Friedman

    Version of Record online : 7 JAN 2008, DOI: 10.1002/humu.20677

  13. A recessive Mendelian model to predict carrier probabilities of DFNB1 for nonsyndromic deafness

    Human Mutation

    Volume 27, Issue 11, November 2006, Pages: 1135–1142, Juan R. González, Wenyi Wang, Ester Ballana and Xavier Estivill

    Version of Record online : 29 AUG 2006, DOI: 10.1002/humu.20390

  14. Electrophysiologic response recorded in the first dorsal interosseous muscle with stimulation of the tibial and deep fibular nerves

    Clinical Anatomy

    Volume 17, Issue 4, 2004, Pages: 312–317, Kathleen M. Galloway, David G. Greathouse, Ronald Olson and Mary Tracy

    Version of Record online : 20 APR 2004, DOI: 10.1002/ca.10244

  15. Combined MODFLOW-FRACTRAN Application to Assess Chlorinated Solvent Transport and Remediation in Fractured Sedimentary Rock

    Remediation Journal

    Volume 23, Issue 3, Summer 2013, Pages: 7–35, Steven W. Chapman, Beth L. Parker, John A. Cherry, Shane D. McDonald, Kenneth J. Goldstein, Jeffrey J. Frederick, Daniel J. St. Germain, Diana M. Cutt and Charles E. Williams

    Version of Record online : 13 JUN 2013, DOI: 10.1002/rem.21355

  16. High frequency of autosomal-recessive DFNB59 hearing loss in an isolated Arab population in Israel

    Clinical Genetics

    Volume 82, Issue 3, September 2012, Pages: 271–276, G Borck, L Rainshtein, S Hellman-Aharony, AE Volk, K Friedrich, E Taub, N Magal, M Kanaan, C Kubisch, M Shohat and L Basel-Vanagaite

    Version of Record online : 18 JUL 2011, DOI: 10.1111/j.1399-0004.2011.01741.x

  17. Synthetic fracture network characterization with transdimensional inversion

    Water Resources Research

    Accepted manuscript online: 7 JUN 2017, Márk Somogyvári, Mohammadreza Jalali, Santos Jimenez Parras and Peter Bayer

    DOI: 10.1002/2016WR020293

  18. A novel nonsense mutation in MYO6 is associated with progressive nonsyndromic hearing loss in a Danish DFNA22 family

    American Journal of Medical Genetics Part A

    Volume 146A, Issue 8, 15 April 2008, Pages: 1017–1025, Kirsten M. Sanggaard, Klaus W. Kjaer, Hans Eiberg, Gudrun Nürnberg, Peter Nürnberg, Katrin Hoffman, Hanne Jensen, Charlotte Sørum, Nanna D. Rendtorff and Lisbeth Tranebjærg

    Version of Record online : 17 MAR 2008, DOI: 10.1002/ajmg.a.32174

  19. Aggregation of small peptides studied by molecular dynamics simulations

    Proteins: Structure, Function, and Bioinformatics

    Volume 65, Issue 4, 1 December 2006, Pages: 914–921, Dagmar Flöck, Giulia Rossetti, Isabella Daidone, Andrea Amadei and Alfredo Di Nola

    Version of Record online : 15 SEP 2006, DOI: 10.1002/prot.21168

  20. DFNB74, a novel autosomal recessive nonsyndromic hearing impairment locus on chromosome 12q14.2-q15

    Clinical Genetics

    Volume 76, Issue 3, September 2009, Pages: 270–275, AM Waryah, A Rehman, ZM Ahmed, Z-H Bashir, SY Khan, AU Zafar, S Riazuddin, TB Friedman and S Riazuddin

    Version of Record online : 24 JUL 2009, DOI: 10.1111/j.1399-0004.2009.01209.x