Ngā hua rapu - J. M. MacKenzie
- E whakaatu ana i te 1 - 3 hua o te 3
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1
Frontotemporal dementia with Pick‐type histology associated with Q336R mutation in the tau gene mā Stuart Pickering‐Brown, Matthew Baker, Takashi Nonaka, Keiichi Ikeda, Suvasini Sharma, J. M. MacKenzie, Sharon Simpson, Joan Moore, Julie S. Snowden, R. de Silva, Tamás Révész, Masato Hasegawa, M. Hutton, David Mann
I whakaputaina 2004Artigo -
2
Mutations in the pre-replication complex cause Meier-Gorlin syndrome mā Louise S. Bicknell, Ernie M.H.F. Bongers, Andrea Leitch, Stephen Brown, Jeroen Schoots, Margaret E Harley, Salim Aftimos, Jumana Y. Al‐Aama, Michael B. Bober, Paul A. Brown, Hans van Bokhoven, John Dean, Alaa Edrees, Murray Feingold, Alan Fryer, Lies H. Hoefsloot, Nikolaus Kau, Nine Knoers, J. M. MacKenzie, John M. Opitz, Pierre Sarda, Alison Ross, I. Karen Temple, Annick Toutain, Carol A. Wise, Michael Wright, Andrew P. Jackson
I whakaputaina 2011Artigo -
3
Mutations in the colony stimulating factor 1 receptor (CSF1R) gene cause hereditary diffuse leukoencephalopathy with spheroids mā Rosa Rademakers, Matt Baker, Alexandra M. Nicholson, Nicola J. Rutherford, NiCole A. Finch, Alexandra I. Soto‐Ortolaza, Jennifer Lash, Christian Wider, Aleksandra Wojtas, Mariely DeJesus‐Hernandez, Jennifer Adamson, Naomi Kouri, Christina Sundal, Elizabeth A. Shuster, Jan Aasly, J. M. MacKenzie, Sigrun Roeber, Hans A. Kretzschmar, Bradley F. Boeve, David S. Knopman, Ronald C. Petersen, Nigel J. Cairns, Bernardino Ghetti, Salvatore Spina, James Garbern, Alexandros Tselis, Ryan J. Uitti, Pritam Das, Jay A. van Gerpen, James F. Meschia, Shawn Levy, Daniel F. Broderick, Neill R. Graff‐Radford, Owen A. Ross, Bradley B. Miller, Russell H. Swerdlow, Dennis W. Dickson, Zbigniew K. Wszołek
I whakaputaina 2011Artigo
Ngā utauta rapu:
Ngā marau whai pānga
Biology
Gene
Genetics
Disease
Medicine
Mutation
Pathology
Alzheimer's disease
Central nervous system disease
Control of chromosome duplication
DNA replication
DNA replication factor CDT1
Degenerative disease
Dementia
Eukaryotic DNA replication
Exome sequencing
Frontotemporal dementia
Gene isoform
Genetic heterogeneity
Leukoencephalopathy
Locus (genetics)
Microcephaly
Missense mutation
Neurodegeneration
Neuroscience
Origin of replication
Origin recognition complex
Phenotype
Pick's disease
Pre-replication complex