Die meistzitierten Artikel
|
Rang |
Autoren |
Paper |
Zitierungen |
1. | Davies SW, Turmaine M, Cozens BA, DiFiglia M, Sharp AH, Ross CA, Scherzinger E, Wanker EE, Mangiarini L, Bates GP | Formation of neuronal intranuclear inclusions underlies the neurological dysfunction in mice transgenic for the HD mutation. CELL 90: (3) 537-548 AUG 8 1997 | 412 |
2. | Krüger R, Kuhn W, Muller T, Woitalla D, Graeber M, Kosel S, Przuntek H, Epplen JT, Schols L, Rieß O | Ala30Pro mutation in the gene encoding alpha-synuclein in Parkinsons disease. NATURE GENETICS 18: (2) 106-108 FEB 1998 | 316 |
3. | Otto F, Thornell AP, Crompton T, Denzel A, Gilmour KC, Rosewell IR, Stamp GWH, Beddington RSP, Mundlos S, Olsen BR, Selby PB, Owen MJ | Cbfa1, a candidate gene for cleidocranial dysplasia syndrome, is essential for osteoblast differentiation and bone development. CELL 89: (5) 765-771 MAY 30 1997 | 290 |
4. | Scherzinger E, Lurz R, Turmaine M, Mangiarini L, Hollenbach B, Hasenbank R, Bates GP, Davies SW, Lehrach H, Wanker EE | Huntingtin-encoded polyglutamine expansions form amyloid-like protein aggregates in vitro and in vivo. CELL 90: (3) 549-558 AUG 8 1997 | 239 |
5. | Bodzioch M, Orso E, Klucken T, Langmann T, Bottcher L, Diederich W, Drobnik W, Barlage S, Buchler C, Porsch-Ozcurumez M, Kaminski WE, Hahmann HW, Oette K, Rothe G, Aslanidis C, Lackner KJ, Schmitz G | The gene encoding ATP-binding cassette transporter 1 is mutated in Tangier disease. NATURE GENETICS 22: (4) 347-351 AUG 1999 | 211 |
6. | Mundlos S, Otto F, Mundlos C, Mulliken JB, Aylsworth AS, Albright S, Lindhout D, Cole WG, Henn W, Knoll JHM, Owen MJ, Mertelsmann R, Zabel BU, Olsen BR | Mutations involving the transcription factor CBFA1 cause cleidocranial dysplasia. CELL 89: (5) 773-779 MAY 30 1997 | 211 |
7. | Rust S, Rosier M, Funke H, Real J, Amoura Z, Piette JC, Deleuze JF, Brewer HB, Duverger N, Denefle P, Assmann G | Tangier disease is caused by mutations in the gene encoding ATP-binding cassette transporter 1. NATURE GENETICS 22: (4) 352-355 AUG 1999 | 207 |
8. | Borrego F, Ulbrecht M, Weiss EH, Coligan JE, Brooks AG | Recognition of human histocompatibility leukocyte antigen (HLA)-E complexed with HLA class I signal sequence-derived peptides by CD94/NKG2 confers protection from natural killer cell-mediated lysis. JOURNAL OF EXPERIMENTAL MEDICINE 187: (5) 813-818 MAR 2 1998 | 181 |
9. | Biervert C, Schroeder BC, Kubisch C, Berkovic SF, Propping P, Jentsch TJ, Steinlein OK | A potassium channel mutation in neonatal human epilepsy. SCIENCE 279: (5349) 403-406 JAN 16 1998 | 179 |
9. | Krude H, Biebermann H, Luck W, Horn R, Brabant G, Gruters A | Severe early-onset obesity, adrenal insufficiency and red hair pigmentation caused by POMC mutations in humans. NATURE GENETICS 19: (2) 155-157 JUN 1998 | 179 |
|