No association with common Caucasian genotypes in exons 8, 13 and 14 of the human cytoplasmic dynein heavy chain gene (DNCHC1) and familial motor neuron disorders

Informa UK Limited - Tập 4 Số 3 - Trang 150-157 - 2003
Azlina Ahmad‐Annuar1, Paresh Shah2, Majid Hafezparast3, Holger Hummerich4, Abi Witherden5, Karen Morrison6, Pamela J. Shaw1, Janine Kirby2, Thomas T. Warner3, Andrew H. Crosby4, Christos Proukakis5, Philip A. Wilkinson6, Richard W. Orrell1, Lloyd Bradley2, Joanne E. Martin3, Elizabeth Fisher4
1Department of Neurodegenerative Disease, Institute of Neurology, National Hospital for Neurology and Neurosurgery, Queen Square, London WC1N 3BG, UK
2Department of Neurology, The Medical School, University of Birmingham, Edgbaston B15 2TT, UK
3Academic Neurology Unit, The Medical School, University of Sheffield, Sheffield S10 2RX, UK
4Department of Clinical Neurosciences, Royal Free and University College Medical School, Rowland Hill Street, London, NW3 2PF, UK
5Department of Medical Genetics, St George’s Hospital Medical School, Cranmer Terrace, London, SW17 0RE, UK
6Department of Histopathology, Queen Mary and Westfield College, The Royal London Hospital, Whitechapel, London E1 1BB, UK

Tóm tắt

Từ khóa


Tài liệu tham khảo

Cleveland DW, 2001, Nat Rev Neurosci, 2, 806, 10.1038/35097565

Julien JP., 2001, unfolding the toxicity of the misfolded. Cell, 104, 581

Hofmann Y, 2002, Hum Mol Genet, 11, 2037, 10.1093/hmg/11.17.2037

Crosby AH, 2002, Am J Hum Genet, 71, 1009, 10.1086/344206

10.1136/jnnp.69.2.150

Hafezparast M, 2003, Mutations in dynein link motor neuron degeneration to defects in retrograde transport. Science, 300, 808

Susalka SJ, 2000, Biochim Biophys Acta, 1496, 76, 10.1016/S0167-4889(00)00010-0

Puls I, 2003, Mutant dynactin in motor neuron disease. Nat Genet, 33, 455

Kozak M., 1999, Gene, 234, 187, 10.1016/S0378-1119(99)00210-3

Thông tin
Thông tin xuất bản

Informa UK Limited

Tập 4 Số 3

150-157

Thông tin tác giả