Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Ingrid K, Svenson"'
Autor:
Redford B, Williams, Douglas A, Marchuk, Ilene C, Siegler, John C, Barefoot, Michael J, Helms, Beverly H, Brummett, Richard S, Surwit, James D, Lane, Cynthia M, Kuhn, Kishore M, Gadde, Allison, Ashley-Koch, Ingrid K, Svenson, Edward C, Suarez, Saul M, Schanberg
Publikováno v:
Psychosomatic Medicine. 70:32-39
To test the hypothesis that low socioeconomic status (SES) and the 5HTTLPR L allele are associated with increased cardiovascular reactivity (CVR) to stress in a larger sample and that SES and 5HTTLPR genotypes interact to enhance CVR to stress. CVR t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e711ebd3d179e763e447fd789937c8fe
https://doi.org/10.1097/psy.0b013e31815f66c3
https://doi.org/10.1097/psy.0b013e31815f66c3
Autor:
Carol J. Gallione, Michael D. Ehlers, Amy Jacon, Margaret A. Pericak-Vance, Douglas A. Marchuk, April C. Horton, Ingrid K. Svenson, Mark T. Kloos
Publikováno v:
Neurogenetics. 6:135-141
Hereditary spastic paraplegia (HSP) is a group of clinically and genetically heterogeneous diseases characterized by neuronal degeneration that is maximal at the distal ends of the longest axons of the central nervous system. The most common cause of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::66f739a3ce1f9c08cfca7582c806df3b
https://doi.org/10.1007/s10048-005-0219-2
https://doi.org/10.1007/s10048-005-0219-2
Autor:
Greg L. Clary, Kishore M. Gadde, Ingrid K. Svenson, Ilene C. Siegler, Katherine P. Grichnik, Douglas A. Marchuk, Mark Stafford-Smith, Michael J. Helms, Redford B. Williams, John C. Barefoot, Saul M. Schanberg, Cynthia M. Kuhn, Edward C. Suarez, James G. Lewis
Publikováno v:
Neuropsychopharmacology. 28:533-541
Central nervous system (CNS) serotonergic function affects a wide range of biological and behavioral functions affecting health and disease. Our objective in this study was to determine whether functional polymorphisms of the genes that encode for th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::645e719b4cf1dc38d7b692a74df177ee
https://doi.org/10.1038/sj.npp.1300054
https://doi.org/10.1038/sj.npp.1300054
Autor:
Ilene C. Siegler, Ingrid K. Svenson, Douglas A. Marchuk, Judith C. Hays, David C. Steffens, Robert M. Levy, Elizabeth P. Flint, K. Ranga Rama Krishnan
Publikováno v:
The American Journal of Geriatric Psychiatry. 10:185-191
Previous studies have examined the role of genetic variations in the serotonin transporter-linked polymorphic region (5HTTLPR) in affective disorders. The authors studied 182 older depressed subjects and 107 elderly control subjects and obtained DNA
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::90256034a6e91a451639cb69474e3d15
https://doi.org/10.1097/00019442-200203000-00009
https://doi.org/10.1097/00019442-200203000-00009
Autor:
P. Craig Gaskell, W. J.Ken Cumming, Ingrid K. Svenson, Margaret A. Pericak-Vance, Travis J. Riney, Martha Nance, Edward L. Hogan, Rose-Mary Boustany, Douglas A. Marchuk, Helen Kingston, Allison E. Ashley-Koch, Jeffery M. Vance
Publikováno v:
The American Journal of Human Genetics. 68:1077-1085
Pure hereditary spastic paraplegia (SPG) type 4 is the most common form of autosomal dominant hereditary SPG, a neurodegenerative disease characterized primarily by hyperreflexia and progressive spasticity of the lower limbs. It is caused by mutation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b1422b392cf1c94e67cec72e256d910e
https://doi.org/10.1086/320111
https://doi.org/10.1086/320111
Autor:
Douglas A. Marchuk, Katherine P. Grichnik, Greg L. Clary, Redford B. Williams, John C. Barefoot, Cynthia M. Kuhn, Mark Stafford-Smith, Ilene C. Siegler, Ingrid K. Svenson, Saul M. Schanberg, Edward C. Suarez, James G. Lewis, Kishore M. Gadde, Michael J. Helms
Publikováno v:
Psychosomatic Medicine. 63:300-305
Objective The objective of this study was to evaluate the impact of indices of central nervous system (CNS) serotonin function on cardiovascular reactivity to mental stress. Methods Lumbar puncture was performed on 54 healthy volunteers to obtain cer
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::367cd3350de0b1d5e86a39bcf690ab64
https://doi.org/10.1097/00006842-200103000-00016
https://doi.org/10.1097/00006842-200103000-00016
Autor:
Ingrid K. Svenson, Perry C. Gaskell, Margaret A. Pericak-Vance, Martha Nance, Douglas A. Marchuk, Stephan Züchner, Allison E. Ashley-Koch, Melanie E. Kail
Publikováno v:
Neurogenetics. 7:127-129
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9da80d345c6e99b850b15102a36b3335
https://doi.org/10.1007/s10048-006-0029-1
https://doi.org/10.1007/s10048-006-0029-1
Autor:
James Y. Garbern, Douglas A. Marchuk, Margaret A. Pericak-Vance, Ingrid K. Svenson, P. Craig Gaskell, Martha Nance, Shin-ichi Hisanaga, Allison E. Ashley-Koch, Mark T. Kloos
Publikováno v:
Neurogenetics. 5(3)
Hereditary spastic paraplegia (HSP) is a genetically heterogeneous neurodegenerative disease characterized by wide variability in phenotypic expression, both within and among families. The most-common cause of autosomal dominant HSP is mutation of th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4551dd62f179ae37d5d0d499d67a1699
https://pubmed.ncbi.nlm.nih.gov/15248095
https://pubmed.ncbi.nlm.nih.gov/15248095
Autor:
Ilene C. Siegler, David C. Steffens, Beverly H. Brummett, Ingrid K. Svenson, Douglas R. McQuoid, Douglas A. Marchuk
Publikováno v:
Psychiatric genetics. 13(1)
OBJECTIVE: The short variant of the serotonin transporter gene-linked functional polymorphic region (5-HTTLPR) has been associated with personality traits related to anxiety, hostility, and depression. We attempted to replicate findings suggesting a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ea28df66c33d97bd0590f2df37648293
https://pubmed.ncbi.nlm.nih.gov/12605095
https://pubmed.ncbi.nlm.nih.gov/12605095
Autor:
Jeffery M. Vance, William K. Scott, Allison E. Ashley-Koch, Margaret A. Pericak-Vance, Ingrid K. Svenson, Sandra G. West, Chantelle M. Wolpert, Douglas A. Marchuk, Martha Nance, Erin Bonner, Richard W. Tim, Rodney Jones, Rose-Mary Boustany, Carolyn Farrell, P. Craig Gaskell
Publikováno v:
Neurogenetics. 3(2)
We evaluated seven families segregating pure, autosomal dominant familial spastic paraplegia (SPG) for linkage to four recently identified SPG loci on chromosomes 2q (1), 8q (2), 12q (3), and 19q (4). These families were previously shown to be unlink
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e883d4f2ed23cb1d6baf62ed1ef73e93
https://pubmed.ncbi.nlm.nih.gov/11354831
https://pubmed.ncbi.nlm.nih.gov/11354831