Zobrazeno 1 - 9
of 9
pro vyhledávání: '"T J Moscarillo"'
Autor:
William DeJong, Deborah Blacker, Rodney C.P. Go, Joan M. Stoler, Marilyn S. Albert, B J Miles, T J Moscarillo, S Goldberg, L Cortellini, Marissa J. Perman, H Holt
Publikováno v:
Public Health Genomics. 10:97-102
Objectives: In preparation for the development of an educational intervention on Alzheimer disease (AD) genetics, we undertook a pilot survey of knowledge in this area and attitudes toward genetic testing for AD among individuals with a family histor
Autor:
Karunya Ramasamy, K. David Becker, Bradley T. Hyman, T J Moscarillo, Gonul Velicelebi, Christoph Lange, Martin Ingelsson, Steven L. Wagner, Kristina Mullin, Michele Parkinson, Lars Bertram, Monica Y. Hsiao, Rashmi Menon, Deborah Blacker, Andrew J. Sampson, Kathryn J. Elliott, Mikko Hiltunen, Rudolph E. Tanzi
Publikováno v:
New England Journal of Medicine. 352:884-894
background Recent analyses suggest that the known Alzheimer’s disease genes account for less than half the genetic variance in this disease. The gene encoding ubiquilin 1 ( UBQLN1 ) is one of several candidate genes for Alzheimer’s disease locate
Autor:
R Menon, Monica Hsiao, T J Moscarillo, Deborah Blacker, Rudolph E. Tanzi, Kristina Mullin, Michele Parkinson, Lars Bertram
Publikováno v:
Molecular Psychiatry. 10:522-524
Autor:
Andrew J. Sampson, Rudolph E. Tanzi, S S Basset, T J Moscarillo, Kristina Mullin, Rodney C.P. Go, Deborah Blacker, Aleister J. Saunders, Lars Bertram
Publikováno v:
Molecular Psychiatry. 8:571-573
Autor:
T J Moscarillo, Marie Ryder, Basavaraj Hooli, Lars Bertram, Kari Lynn Ohlsen, Iuliana Ionita, Brit Maren Michaud Schjeide, Diane Hu-Lince, Amy Murphy, K. David Becker, Kristina Mullin, Michele Parkinson, Steven L. Wagner, Rudolph E. Tanzi, Deborah Blacker, Kathryn J. Elliott, Xin Wang, Nan M. Laird, Monica Hsiao, Christoph Lange, Hongyu Jiang, Meghan F. Hogan, Jason DiVito
Alzheimer's disease (AD) is a genetically complex and heterogeneous disorder. To date four genes have been established to either cause early-onset autosomal-dominant AD (APP, PSEN1, and PSEN2(1-4)) or to increase susceptibility for late-onset AD (APO
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0d3cde32cfba8ecadb8b41dd2d031130
https://europepmc.org/articles/PMC2668052/
https://europepmc.org/articles/PMC2668052/
Autor:
R Menon, Deborah Blacker, T J Moscarillo, Matthew B. McQueen, Rudolph E. Tanzi, Monica Hsiao, Kristina Mullin, Michele Parkinson, Lars Bertram
Objectives: Several studies suggested chromosome 12 harbours an Alzheimer’s disease (AD) risk factor gene. Significant association of a single nucleotide polymorphism (SNP) in the 3′ UTR of transcription factor CP2 ( LBP-1c/CP2/LSF or TFCP2 ) at
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5a31ed9cf8706993989f6469638aeeaa
https://europepmc.org/articles/PMC1735943/
https://europepmc.org/articles/PMC1735943/
Autor:
Elizabeth W. Pugh, Howard W. Wiener, Marilyn S. Albert, Kimberly Doheny, Melvin G. McInnis, Susan Spear Bassett, Gary A. Chase, M. Danielle Fallin, Deborah Blacker, Amy Mahoney, Lindy E. Harrell, Aleister J. Saunders, Terri H. Beaty, Rudolph E. Tanzi, T J Moscarillo, Rodney T. Perry, Rodney C.P. Go, Lars Bertram, Dimitrios Avramopoulos, Marshal F. Folstein, Julianne S. Collins
Publikováno v:
Human molecular genetics. 12(1)
Alzheimer's disease (AD) is a devastating neurodegenerative disorder of late life with complex inheritance. Mutations in three known genes lead to the rare early-onset autosomal dominant form of AD, while a common polymorphism (epsilon 4) in the gene
Autor:
Gonul Velicelebi, K. D. Becker, Monica Hsiao, Kristina Mullin, Deborah Blacker, Rudolph E. Tanzi, Michele Parkinson, Steven L. Wagner, Lars Bertram, T J Moscarillo
Publikováno v:
Journal of Medical Genetics. 44:e63-e63
Background: Recently, conflicting reports have been published on the potential role of genetic variants in the α-T catenin gene ( VR22 ; CTNNA3 ) on the risk for Alzheimer’s disease. In these papers, evidence for association is mostly observed in
Autor:
Hilkka Soininen, T J Moscarillo, Kathryn J. Elliott, Kristina Mullin, Michele Parkinson, Rudolph E. Tanzi, Mikko Hiltunen, Deborah Blacker, K. D. Becker, Lars Bertram
Publikováno v:
Neurobiology of Aging. 25:S509