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| First Name: | Stanislav | | Last Name: | Karsten | | Title: | Assistant Professor | | Advanced Degrees: | Ph.D. | | Affiliation: | UCLA | | Department: | Neurology | | Street Address 1: | Harbor-UCLA Medical Center | | Street Address 2: | 1000 W. Carson Street, Box 492 | | City: | Los Angeles | | State/Province: | CA | | Zip/Postal Code: | 90509 | Country/Territory: | U.S.A. | | Phone: | 310-8743275 | | Fax: | 310-5338905 | | Email Address: |  |
Disclosure:
(view policy)
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Member reports no financial or other potential conflicts of interest. [Last Modified: 26 August 2007]
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Neurodevelopmental Disorders (Down syndrome, etc.), Neuromuscular Disorders (ALS, etc.), Tauopathies, Alzheimer Disease, Aging Process
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DNA microarrays, Neurobiology, Genetics, Tau/Cytoskeleton, Animal Models, Stem cells
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Karsten SL, Sang T-K, Gehman LT, Liu J, Chatterjee S, Lawless G, Sengupta S, Berry RW, Wiedau-Pazos M, Pomakian J, Schulz C, Vinters HV, Binder LI, Geschwind DH, Jackson GR. (2006) A genomic screen for modifiers of tauopathy identifies puromycin-sensitive aminopeptidase as an inhibitor of tau-induced neurodegeneration. Neuron. 51(5): 549-560.
Lobo MK., Karsten SL, Gray M, Geschwind DH, Yang XW. (2006) FACS-array profiling of striatal projection neuron subtypes in juvenile and adult mouse brains. Nature Neuroscience 9(3): 443-452
Karsten S, Kudo L, Sabatti C, Jackson R, Kornblum H, Geschwind D (2003) Global analysis of gene expression in neural progenitors reveals specific cell-cycle, signaling and metabolic networks. Developmental Biology 261(1): 165-182.
Karsten S, Van Deerlin V, Sabatti C, Gill L, Geschwind D. (2002) An evaluation of tyramide signal amplification and archived and frozen tissue in microarray gene expression analysis. Nucleic Acids Research 30(2).
Sabatti C, Karsten S, Geschwind D. (2002) Thresholding rules to recover a sparse signal from microarray experiments. Mathematical Biosciences 176: 17-34.
Karsten S, Voskoboeva E, Krasnopolskaja X. and Bondeson ML. (1999) A Novel Type of Genetic Rearrangement in the Iduronate-2-Sulfatase (IDS) Gene Involving Deletion, Duplications and Inversions. Human Mutation 14 (6): 471-476.
Karsten S, Voskoboeva E, Tishkanina S, Pettersson U, Krasnopolskaja X and Bondeson ML. (1998) Mutation Spectrum of the Iduronate-2-Sulfatase (IDS) Gene in 36 Russian Unrelated MPS II Patients. Human Genetics 103: 732-735.
Karsten S, Voskoboeva E, Carlberg BM, Kleijer WJ, Tonnesen T, Pettersson U and Bondeson ML. (1998) Identification of 9 Novel IDS Gene Mutations in 19 Unrelated Hunter Syndrome (Mucopolysaccharidosis Type II) Patients. Human Mutation 12 (6): 433. Mutation in Brief #202
Lagerstedt K, Karsten S, Carlberg BM, Kleijer W, Tonnesen T, Pettersson U and Bondeson ML. (1997) Double-strand Breaks May Initiate the Inversion Mutation Causing the Hunter Syndrome. Human Molecular Genetics 6 (4): 627-633.
Karsten S, Lagerstedt K, Carlberg BM, Kleijer W, Pettersson U and Bondeson ML. (1997) Two Distinct Deletions in the IDS Gene and the IDS-2 Locus: a Novel Type of Mutation Causing the Hunter Syndrome. Genomics 43 (2): 123-129.
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