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applebybs genetics [58 articles]

Neue Publikationen in applebybs Bibliothek eingetragen unter dem Bezeichner: genetics. You can also see everyone's genetics.
  • Atypical frontotemporal dementia as a new clinical phenotype of Gerstmann-Straussler-Scheinker disease with the PrP-P102L mutation. Description of a previously unreported Italian family
    Neurological Sciences
    by Anna Giovagnoli, Giuseppe Di Fede, Anna Aresi, Fabiola Reati, Giacomina Rossi, Fabrizio Tagliavini
    posted to prion phenotype gss genetics ftd by applebyb on 2008-11-27 14:59:46 as ****
  • Impact of Apolipoprotein E (ApoE) Polymorphism on Brain ApoE Levels
    J. Neurosci., Vol. 28, No. 45. (5 November 2008), pp. 11445-11453.
    by David R Riddell, Hua Zhou, Kevin Atchison, Helen K Warwick, Peter J Atkinson, Julius Jefferson, Lin Xu, Suzan Aschmies, Yolanda Kirksey, Yun Hu, Erik Wagner, Adrienne Parratt, Jane Xu, Zhuting Li, Margaret M Zaleska, Steve J Jacobsen, Menelas N Pangalos, Peter H Reinhart
    posted to polymorphism genetics apoe amyloid ad by applebyb on 2008-11-23 15:57:42 as *
  • Comparing test-specific distress of susceptibility versus deterministic genetic testing for Alzheimer's disease
    Alzheimer's and Dementia, Vol. 4, No. 6. (November 2008), pp. 406-413.
    by M Cassidy, J Roberts, T Bird, E Steinbart, L Cupples, C Chen, E Linnenbringer, R Green
    posted to ps-2 ps-1 genetics gad app apoe ad by applebyb on 2008-11-22 20:03:52 as ***
  • Familial Creutzfeldt-Jakob disease presenting as epilepsia partialis continua.
    Epileptic disorders : international epilepsy journal with videotape, Vol. 10, No. 4. (18 November 2008), pp. 271-275.
    by Max R R Lowden, Kevin Scott, Milind J J Kothari
    posted to prion_disease phenotype genetics gcjd diagnosis cjd by applebyb on 2008-11-21 14:45:47 as *****
  • A novel insertional mutation in the prion protein gene: clinical and bio-molecular findings.
    Journal of neurology, neurosurgery, and psychiatry, Vol. 79, No. 12. (December 2008), pp. 1395-1398.
    by C Mauro, G Giaccone, G Piscosquito, A Lavorgna, M Nigro, G Di Fede, A Leonardi, C Coppola, S Formisano, F Tagliavini, R Cotrufo, G Puoti
    posted to prnp prion_disease genetics by applebyb on 2008-11-21 14:38:55 as *****
  • Association between HFE 187 C>G (H63D) mutation and early-onset familial Alzheimer's disease PSEN-1 839A>C (E280A) mutation.
    Annals of hematology, Vol. 87, No. 8. (August 2008), pp. 671-673.
    by IC Avila-Gomez, M Jiménez-Del-Rio, F Lopera-Restrepo, C Velez-Pardo
    posted to yod ps-1 genetics ad by applebyb on 2008-11-21 14:19:33 as ***
  • Presenilin 1 Polymorphism Associated with Alzheimer’s Disease in Apolipoprotein E4Carriers
    posted to risk ps1 polymorphism genetics apoe ad by applebyb on 2008-10-29 00:03:44 as ***
  • A novel PRNP-P105S mutation associated with atypical prion disease and a rare PrPSc conformation
    Neurology, Vol. 71, No. 18. (28 October 2008), pp. 1431-1438.
    by E Tunnell, R Wollman, S Mallik, CJ Cortes, SJ Dearmond, JA Mastrianni
    posted to prpsc prion gss genetics by applebyb on 2008-10-28 00:37:31 as ****
  • Immune-Directed Gene Therapeutic Development for Alzheimer's, Prion, and Parkinson's Diseases.
    Journal of neuroimmune pharmacology : the official journal of the Society on NeuroImmune Pharmacology (18 October 2008)
    by Kathleen A Maguire-Zeiss, Howard J Federoff
    posted to therapy prion pd genetics ad by applebyb on 2008-10-25 01:30:34 as ****
  • Review. The neuropathology of kuru and variant Creutzfeldt-Jakob disease.
    Philosophical transactions of the Royal Society of London. Series B, Biological sciences, Vol. 363, No. 1510. (27 November 2008), pp. 3685-3687.
    by CA McLean
    posted to vcjd prion phenotype kuru incubation genetics codon129 cjd by applebyb on 2008-10-20 00:07:40 as *****
  • A clinical study of kuru patients with long incubation periods at the end of the epidemic in Papua New Guinea.
    Philosophical transactions of the Royal Society of London. Series B, Biological sciences, Vol. 363, No. 1510. (27 November 2008), pp. 3725-3739.
    by J Collinge, J Whitfield, E McKintosh, A Frosh, S Mead, AF Hill, S Brandner, D Thomas, MP Alpers
    posted to risk prion phenotype kuru incubation genetics age by applebyb on 2008-10-20 00:01:37 as *****
  • Genetic susceptibility, evolution and the kuru epidemic.
    Philosophical transactions of the Royal Society of London. Series B, Biological sciences, Vol. 363, No. 1510. (27 November 2008), pp. 3741-3746.
    by S Mead, J Whitfield, M Poulter, P Shah, J Uphill, J Beck, T Campbell, H Al-Dujaily, H Hummerich, MP Alpers, J Collinge
    posted to risk prion kuru genetics codon129 anthropology by applebyb on 2008-10-19 23:59:39 as *****
  • Gene expression changes in the course of normal brain aging are sexually dimorphic
    Proceedings of the National Academy of Sciences, Vol. 105, No. 40. (7 October 2008), pp. 15605-15610.
    by Nicole C Berchtold, David H Cribbs, Paul D Coleman, Joseph Rogers, Elizabeth Head, Ronald Kim, Tom Beach, Carol Miller, Juan Troncoso, John Q Trojanowski, Ronald H Zielke, Carl W Cotman
    posted to neurodegeneration genetics age by applebyb on 2008-10-15 02:02:23 as *****
  • Arch Neurol -- Download Directly to Citation Manager
    posted to tau neurodegeneration gsk-3 genetics ftld dementia ad by applebyb on 2008-10-15 01:39:35 as *****
  • Apolipoprotein E Polymorphism and Brain Morphology in Mild Cognitive Impairment
    posted to genetics cognition apoe by applebyb on 2008-10-13 00:03:43 as *
  • Genetic variability in progranulin contributes to risk for clinically diagnosed Alzheimer disease.
    Neurology (18 June 2008)
    by N Brouwers, K Sleegers, S Engelborghs, S Maurer-Stroh, I Gijselinck, J van der Zee, B A A Pickut, M Van den Broeck, M Mattheijssens, K Peeters, J Schymkowitz, F Rousseau, J-J J Martin, M Cruts, P P P De Deyn, C Van Broeckhoven
    posted to risk prgn genetics ad by applebyb on 2008-10-03 14:39:28 as * along with 1 person giovanni
  • Update on recent molecular and genetic advances in frontotemporal lobar degeneration.
    Journal of neuropathology and experimental neurology, Vol. 67, No. 7. (July 2008), pp. 635-648.
    by EH Bigio
    posted to review genetics ftld by applebyb on 2008-09-26 01:13:11 as ***
  • The effect of apolipoprotein E genotype on expression of an autosomal dominant schizophreniform disorder with progressive dementia and neurofibrillary tangles.
    Biological psychiatry, Vol. 41, No. 2. (15 January 1997), pp. 191-195.
    by D Tsuang, MA Raskind, J Leverenz, ER Peskind, G Schellenberg, TD Bird
    posted to tau sd-ftd genetics by applebyb on 2008-09-13 02:16:32 as read
  • Population distribution of the methionine allele at the PRNP codon 129 polymorphism in Europe and the Middle East.
    Human biology; an international record of research, Vol. 80, No. 2. (April 2008), pp. 181-190.
    by G Mercier, F Diéterlen, G Lucotte
    posted to risk prnp polymorphism genetics codon129 cjd by applebyb on 2008-09-01 23:12:26 as ****
  • Age of onset and death in inherited prion disease are heritable.
    American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics (26 August 2008)
    by T E F E Webb, J Whittaker, J Collinge, S Mead
    posted to survival prnp phenotype genetics gcjd epigenetics by applebyb on 2008-09-01 23:08:45 as *****
  • A novel presenilin 2 mutation (V393M) in early-onset dementia with profound language impairment.
    European journal of neurology : the official journal of the European Federation of Neurological Societies (21 August 2008)
    by S G G Lindquist, L Hasholt, J M C M Bahl, N H H H Heegaard, B B B Andersen, A Nørremølle, J Stokholm, M Schwartz, M Batbayli, H Laursen, R Pardossi-Piquard, F Chen, P St George-Hyslop, G Waldemar, J E E Nielsen
    posted to ps2 genetics ad by applebyb on 2008-09-01 22:07:10 as ***
  • Is the glass half empty or half full? Genetically determined disease in frontotemporal dementia.
    Neurology (13 August 2008)
    by Murray Grossman
    posted to ftd genetics by applebyb on 2008-08-19 01:44:44 as ***
  • Distinct genetic forms of frontotemporal dementia
    Neurology (13 August 2008), 01.wnl.0000319702.37497.72.
    by H Seelaar, W Kamphorst, SM Rosso, A Azmani, R Masdjedi, I de Koning, JA Maat-Kievit, B Anar, Donker L Kaat, GJ Breedveld, D Dooijes, JM Rozemuller, IF Bronner, P Rizzu, JC van Swieten
    posted to ftd genetics by applebyb on 2008-08-19 01:43:27 as *** along with 1 person giovanni
  • Housekeeping Genes Revisited - Different Expressions Depending On Gender, Brain Area And Stressor
    Neuroscience, Vol. In Press, Accepted Manuscript
    by N Derks, M Muller, B Gaszner, D Tilburg-Ouwens, EW Roubos, LT Kozicz
    posted to genetics by applebyb on 2008-08-05 01:53:19 as *
  • Gene Mutations and Cognitive Delay -- Leonard et al. 321 (5889): 640a -- Science
    posted to dementia genetics by applebyb on 2008-08-02 10:14:48 as ***
  • The Genetic Information Nondiscrimination Act -- A Half-Step toward Risk Sharing
    N Engl J Med, Vol. 359, No. 4. (24 July 2008), pp. 335-337.
    by Russell Korobkin, Rahul Rajkumar
    posted to genetics by applebyb on 2008-08-02 10:12:34 as **** along with 1 person mfm11
  • Effective gene therapy in a mouse model of prion diseases.
    PLoS ONE, Vol. 3, No. 7. (2008)
    by K Toupet, V Compan, C Crozet, C Mourton-Gilles, N Mestre-Francés, F Ibos, P Corbeau, JM Verdier, V Perrier
    posted to genetics prion_diseases by applebyb on 2008-08-02 01:47:58 as read
  • Mutation analysis of presenilin 1 gene in Alzheimer's disease
    The Lancet, Vol. 347, No. 8994. (13 January 1996), pp. 130-131.
    by K Boteva, M Vitek, H Mitsuda, Har de Silva, PT Xu, G Small, JR Gilbert
    posted to ad fad genetics ps-1 yod by applebyb on 2008-07-21 02:36:43 as read
  • Genomic structure and expression of STM2, the chromosome 1 familial Alzheimer disease gene.
    Genomics, Vol. 34, No. 2. (1 June 1996), pp. 198-204.
    by E Levy-Lahad, P Poorkaj, K Wang, YH Fu, J Oshima, J Mulligan, GD Schellenberg
    posted to ad genetics young_onset_dementia by applebyb on 2008-07-19 22:39:11 as **
  • Segregation of a missense mutation in the amyloid precursor protein gene with familial Alzheimer's disease
    Nature, Vol. 349, No. 6311. (21 February 1991), pp. 704-706.
    by Alison Goate, Marie-Christine Chartier-Harlin, Mike Mullan, Jeremy Brown, Fiona Crawford, Liana Fidani, Luis Giuffra, Andrew Haynes, Nick Irving, Louise James, Rebecca Mant, Phillippa Newton, Karen Rooke, Penelope Roques, Chris Talbot, Margaret Pericak-Vance, Alien Roses, Robert Williamson, Martin Rossor, Mike Owen, John Hardy
    posted to ad genetics young_onset_dementia by applebyb on 2008-07-19 22:38:19 as *** along with 1 person jclau
  • Citation Results : Nature
    posted to genetics by applebyb on 2008-07-19 01:59:44 as ***
  • JAMA -- Download Directly to Citation Manager
    posted to genetics by applebyb on 2008-07-19 00:41:35 as ***
  • Citation Results : Nature
    posted to genetics by applebyb on 2008-07-14 10:48:58 as ****
  • Biochemical markers in persons with preclinical familial Alzheimer disease
    Neurology, Vol. 71, No. 2. (8 July 2008), pp. 85-92.
    by JM Ringman, SG Younkin, D Pratico, W Seltzer, GM Cole, DH Geschwind, Y Rodriguez-Agudelo, B Schaffer, J Fein, S Sokolow, ER Rosario, KH Gylys, A Varpetian, LD Medina, JL Cummings
    posted to ad genetics by applebyb on 2008-07-08 00:41:11 as ****
  • Clinicopathological and genetic correlates of frontotemporal lobar degeneration and corticobasal degeneration
    Journal of Neurology, Vol. 255, No. 4. (April 2008), pp. 488-494.
    by Llado, Albert, Sanchez-Valle, Raquel, Rey, Maria, Ezquerra, Mario, Tolosa, Eduardo, Ferrer, Isidro, Molinuevo, Jose
    posted to corticobasal_ganglionic_degeneration ftd genetics neuropathology by applebyb on 2008-07-05 01:19:03 as ****
  • Mutational Analysis in Early-Onset Familial Dementia in the Japanese Population
    posted to ad genetics young_onset_dementia by applebyb on 2008-06-28 02:33:52 as ****
  • From Darwin's Finches to Canaries in the Coal Mine -- Mining the Genome for New Biology
    N Engl J Med, Vol. 358, No. 26. (26 June 2008), pp. 2760-2763.
    by David J Hunter, David Altshuler, Daniel J Rader
    posted to genetics by applebyb on 2008-06-26 02:17:57 as *** along with 1 person guhjy
  • Journal of Clinical Investigation -- A HapMap harvest of insights into the genetics of common disease
    posted to genetics by applebyb on 2008-06-21 12:52:28 as *****
  • Citation Results : Nature
    posted to genetics by applebyb on 2008-06-21 12:47:55 as *****
  • A comprehensive review of genetic association studies.
    Genet Med, Vol. 4, No. 2. (r 2002), pp. 45-61.
    by JN Hirschhorn, K Lohmueller, E Byrne, K Hirschhorn
    posted to genetics by applebyb on 2008-06-21 12:46:41 as ***** along with 1 person mrkrause
  • Drinking from the fire hose--statistical issues in genomewide association studies.
    N Engl J Med, Vol. 357, No. 5. (2 August 2007), pp. 436-439.
    by DJ Hunter, P Kraft
    posted to genetics by applebyb on 2008-06-21 12:45:07 as ***** along with 2 people guhjy jasonbobe
  • BREAKTHROUGH OF THE YEAR: Human Genetic Variation
    Science, Vol. 318, No. 5858. (21 December 2007), pp. 1842-1843.
    by Elizabeth Pennisi
    posted to genetics by applebyb on 2008-06-21 12:44:12 as ***** along with 3 people jasonbobe lorettawilliams frohike
  • Genes contributing to prion pathogenesis.
    The Journal of general virology, Vol. 89, No. Pt 7. (July 2008), pp. 1777-1788.
    by G Tamgüney, K Giles, DV Glidden, P Lessard, H Wille, P Tremblay, DF Groth, F Yehiely, C Korth, RC Moore, J Tatzelt, E Rubinstein, C Boucheix, X Yang, P Stanley, MP Lisanti, RA Dwek, PM Rudd, J Moskovitz, CJ Epstein, TD Cruz, WA Kuziel, N Maeda, J Sap, KH Ashe, GA Carlson, I Tesseur, T Wyss-Coray, L Mucke, KH Weisgraber, RW Mahley, FE Cohen, SB Prusiner
    posted to genetics prion_diseases by applebyb on 2008-06-20 02:28:20 as ***** along with 1 person cicada
  • Evaluation of Choline Acetyltransferase Gene Polymorphism (2384 G/A) in Alzheimer’s Disease and Mild Cognitive Impairment
    posted to ad genetics snps by applebyb on 2008-06-20 01:18:42 as *****
  • First demonstrated de novo insertion in the prion protein gene in a young patient with dementia
    J Neurol Neurosurg Psychiatry, Vol. 79, No. 7. (1 July 2008), pp. 845-846.
    by Raquel Sanchez-Valle, Juan I Arostegui, Jordi Yague, Lorena Rami, Albert Llado, Jose L Molinuevo
    posted to genetics prion_diseases by applebyb on 2008-06-17 01:55:53 as *****
  • Tau haplotype influences cerebral perfusion pattern in frontotemporal lobar degeneration and related disorders
    Acta Neurologica Scandinavica, Vol. 117, No. 5. (May 2008), pp. 359-366.
    by Borroni, , Perani, , Agosti, , Anchisi, , Paghera, , Archetti, , Alberici, , Di Luca, , Padovani,
    posted to frontotemporal_dementia genetics neuroimaging tau by applebyb on 2008-06-14 16:14:47 as ****
  • JAMA -- Download Directly to Citation Manager
    posted to genetics polymorphisms by applebyb on 2008-05-27 21:44:42 as *****
  • Novel PRNP mutation in a patient with a slow progressive dementia syndrome.
    Medical science monitor : international medical journal of experimental and clinical research, Vol. 14, No. 5. (May 2008)
    by U Heinemann, A Krasnianski, B Meissner, EM Grasbon-Frodl, HA Kretzschmar, I Zerr
    posted to dementia genetics prnp by applebyb on 2008-05-01 09:41:03 as *****
  • PRNP mutations in a series of apparently sporadic neurodegenerative dementias in China.
    American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics (18 April 2008)
    by Liu Zheng, Jia Longfei, Ye Jing, Zhang Xinqing, Song Haiqing, Lv Haiyan, Wang Fen, Dong Xiumin, Jia Jianping
    posted to genetics prnp by applebyb on 2008-04-24 11:31:40 as *****
  • Genetic aspects of Alzheimer disease.
    Genetics in medicine : official journal of the American College of Medical Genetics, Vol. 10, No. 4. (April 2008), pp. 231-239.
    by TD Bird
    posted to ad genetics by applebyb on 2008-04-18 00:57:06 as ****
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