Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Michael W. Booze"'
Autor:
Christopher J. Jones, Kath Roche, David C. Crossman, Elizabeth R. Hauser, Charles Dennis, Michael A. Hauser, Vincent Mooser, Scott S. Sundseth, Li Ling Huang, Brendan McAdam, Lefkos T. Middleton, Bernhard R. Winkelmann, Jeffery M. Vance, Allen D. Roses, Christopher B. Granger, Sanjay Sharma, Svati H. Shah, Karen Eggleston, Sandra G. West, Bonnie Pedersen, Elaine Dowdy, Alan H. Wiseman, Sheila E. Francis, William E. Kraus, Paula W. Clevenger, Carol Haynes, Michael W. Booze, Donny Asper, Silke Schmidt, Susan E. Estabrooks, Jonathan L. Haines, J. Brent Muhlestein, Alan G. Bartel, Margaret A. Pericak-Vance
Publikováno v:
The American Journal of Human Genetics. 75:436-447
A family history of coronary artery disease (CAD), especially when the disease occurs at a young age, is a potent risk factor for CAD. DNA collection in families in which two or more siblings are affected at an early age allows identification of gene
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::72aadb12fc732b503e7863e3166f7eb9
https://doi.org/10.1086/423900
https://doi.org/10.1086/423900
Autor:
Bradley C. Hiner, William C. Koller, Jeffery M. Vance, Christopher G. Goetz, William K. Scott, Jonathan L. Haines, Rajesh Pahwa, Francis Mastaglia, Xuejun Qin, M.B. Stern, Margaret A. Pericak-Vance, Yi-Ju Li, Eden R. Martin, Joseph Jankovic, Gary W. Small, Michael A. Hauser, Jean P. Hubble, Michael W. Booze, M. Nance, Jeffrey W. Walter
Publikováno v:
Neurology. 62:2005-2009
Background: Similarities between Alzheimer disease (AD) and Parkinson disease (PD) suggest a possible role for apolipoprotein E (APOE) in PD. Most previous studies seeking to establish such a link used case-control datasets and results have been inco
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4fd299a2b3c204309baeea3424730fd8
https://doi.org/10.1212/01.wnl.0000128089.53030.ac
https://doi.org/10.1212/01.wnl.0000128089.53030.ac
Autor:
Rajesh Pahwa, Fred H. Allen, William G. Ondo, Bradley C. Hiner, William C. Koller, Eden R. Martin, Ray L. Watts, Kelly E. Lyons, Margaret A. Pericak-Vance, Jeffery M. Vance, Joshua A. Reaves, William K. Scott, Jean P. Hubble, Fengyu Zhang, Jonathan L. Haines, Sofia A. Oliveira, Joseph Jankovic, Martha Nance, Frank L. Mastaglia, Michael W. Booze, Gary W. Small, Burton L. Scott, Christopher G. Goetz, Lefkos T. Middleton, Matthew B. Stern, Jeffrey M. Stajich
Publikováno v:
Archives of neurology. 60(7)
Background Previously, we detected linkage of idiopathic Parkinson disease (PD) to the region on chromosome 6 that contains the Parkin gene (D6S305; logarithm of odds score, 5.47) in families with at least one individual with age at onset younger tha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7b4d5fc44441ea0b8cc04ea3df4a295a
https://pubmed.ncbi.nlm.nih.gov/12873854
https://pubmed.ncbi.nlm.nih.gov/12873854
Autor:
Bradley C. Hiner, Jeffery M. Vance, Margaret A. Pericak-Vance, Rajesh Pahwa, Ray L. Watts, Lefkos T. Middleton, Fred H. Allen, Michelle P. Winn, Martha Nance, Fengyu Zhang, Jonathan L. Haines, Sofia A. Oliveira, Gary W. Small, Frank L. Mastaglia, William K. Scott, Jeffrey M. Stajich, Burton L. Scott, Christopher G. Goetz, William C. Koller, William G. Ondo, Jean P. Hubble, Michael W. Booze, Matthew B. Stern, Eden R. Martin
Publikováno v:
Annals of neurology. 53(5)
Parkin, an E2-dependent ubiquitin protein ligase, carries pathogenic mutations in patients with autosomal recessive juvenile parkinsonism, but its role in the late-onset form of Parkinson's disease (PD) is not firmly established. Previously, we detec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::28009b38be51ae85d05ec1bdb98fef60
https://pubmed.ncbi.nlm.nih.gov/12953277
https://pubmed.ncbi.nlm.nih.gov/12953277
Autor:
Martha Nance, Michael A. Hauser, Margaret A. Pericak-Vance, Jeffrey M. Stajich, Allen D. Roses, Gary W. Small, Kelly E. Lyons, William K. Scott, William G. Ondo, Eden R. Martin, Jean P. Hubble, Jeffery M. Vance, Bradley C. Hiner, Ray L. Watts, Donna Masterman, Robert C. Ribble, Matthew B. Stern, Nigel G. Laing, Michael W. Booze, Lefkos T. Middleton, Allison R. Rogala, Frank L. Mastaglia, Fengyu Zhang, Christopher G. Goetz, Amy Colcher, Rajesh Pahwa, Joseph Jankovic, Fred H. Allen, Jonathan L. Haines, Burton L. Scott, William C. Koller, Rachel A. Gibson
Publikováno v:
University of Western Australia
Scopus-Elsevier
Scopus-Elsevier
CONTEXT The human tau gene, which promotes assembly of neuronal microtubules, has been associated with several rare neurologic diseases that clinically include parkinsonian features. We recently observed linkage in idiopathic Parkinson disease (PD) t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5c4ce697ece4d4a7a2678ec1405304a3
https://pubmed.ncbi.nlm.nih.gov/11851532
https://pubmed.ncbi.nlm.nih.gov/11851532
Autor:
William G. Ondo, Frank L. Mastaglia, Fred H. Allen, Jean P. Hubble, Lefkos T. Middleton, Christopher G. Goetz, Kelly E. Lyons, William K. Scott, Jeffery M. Vance, Jonathan L. Haines, Brandon D. Slotterbeck, Bradley C. Hiner, Allen D. Roses, Sandra G. West, Evadnie Rampersaud, Gary W. Small, William C. Koller, Margaret A. Pericak-Vance, Donna Masterman, Rachel A. Gibson, Burton L. Scott, Robert C. Ribble, Martha Nance, Jeffrey M. Stajich, Joseph Jankovic, Matthew B. Stern, Rajesh Pahwa, Amy Colcher, Nigel G. Laing, Michael W. Booze, Ray L. Watts
Publikováno v:
Scopus-Elsevier
ContextThe relative contribution of genes vs environment in idiopathic Parkinson disease (PD) is controversial. Although genetic studies have identified 2 genes in which mutations cause rare single-gene variants of PD and observational studies have s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e71b51fe7c9ef910a2070f8a2d542192
https://doi.org/10.1001/jama.286.18.2239
https://doi.org/10.1001/jama.286.18.2239
Autor:
Sofia A. Oliveira, William K. Scott, Eden R. Martin, Martha A. Nance, Ray L. Watts, Jean P. Hubble, William C. Koller, Rajesh Pahwa, Matthew B. Stern, Bradley C. Hiner, William G. Ondo, Fred H. Allen, Burton L. Scott, Christopher G. Goetz, Gary W. Small, Frank Mastaglia, Jeffrey M. Stajich, Fengyu Zhang, Michael W. Booze, Michelle P. Winn
Publikováno v:
Annals of Neurology; May2003, Vol. 53 Issue 5, p624-629, 6p
Autor:
Jeffery M. Vance, William K. Scott, Jeffrey M. Stajich, Kenichiro Fujiwara, William C. Koller, Gary W. Small, Kelly E. Lyons, William G. Ondo, Lefkos T. Middleton, Rachel A. Gibson, Fred H. Allen, Eden R. Martin, Jean P. Hubble, Fengyu Zhang, J. M. Van Der Walt, Ray L. Watts, Burton L. Scott, Amy Colcher, Rajesh Pahwa, Joseph Jankovic, Francis Mastaglia, Jonathan L. Haines, M.B. Stern, Margaret A. Pericak-Vance, Christopher G. Goetz, A. D. Roses, M. Nance, Michael W. Booze, Bradley C. Hiner
Publikováno v:
Scopus-Elsevier
Recently, the authors demonstrated linkage in idiopathic PD to a region on chromosome 8p that contains the N-acetyltransferase genes, NAT1 and NAT2. The authors examined NAT1 and NAT2 for association with PD using family-based association methods and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4b84dac8a79b98955de0077fabd0dbba
http://www.scopus.com/inward/record.url?eid=2-s2.0-0037426413&partnerID=MN8TOARS
http://www.scopus.com/inward/record.url?eid=2-s2.0-0037426413&partnerID=MN8TOARS
