Zobrazeno 1 - 10
of 64
pro vyhledávání: '"L. Giuffra"'
Autor:
Fabio Macciardi, Cecilia Marino, L. Ruocco, Enrico Smeraldi, V. Rinaldi, M. Ferrari, James L. Kennedy, L. Giuffra, Paola Carrera
Publikováno v:
Biological Psychiatry. 31:720-728
Some recent findings report that the area 5q11.2-13.3 of chromosome 5 segregates with schizophrenia in an uncle-nephew pair (Bassett et al 1988). However, linkage studies between chromosome 5 markers loci and schizophrenia lead to different results:
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a5726ab70ff8fa22a1735654af2ff83a
https://doi.org/10.1016/0006-3223(92)90282-5
https://doi.org/10.1016/0006-3223(92)90282-5
Autor:
Daniel E. Weeks, Mark H. Skolnick, Stuart Sherman, S.W. Guo, R.F. Kefford, Rudolph E. Tanzi, Erik W. Thompson, S. Williams-Blangero, Jack T. Rogers, Nancy R. Mendell, R.R. Frants, P.M. Stewart, B. McKnight, G.M. Cox, Darlene R. Goldstein, J. Ott, G.E. Bonney, Sarah R. Wilson, C.E. Aston, D.L. Duffy, Terence P. Speed, N. Risch, B.S. Weir, R.A. Lewis, G.P. Vogler, M. Frigge, M.A. Province, Gary A. Chase, A. Kong, D.E. Goldgar, A.C. Warren, C.M. Lewis, C. Tierney, Susan E. Hodge, N.G. Martin, Aravinda Chakravarti, A.P. Round, K.K. Amfoh, Deborah A. Meyers, D.R. Cox, H.M. Shaw, J.D. Elashoff, C.I. Amos, Katheleen Gardiner, Lisa A. Cannon-Albright, H. Yuan, C. Murigande, G.M. Petersen, D.F. Easton, M.B. Risman, Lynn R. Goldin, S.J. Bale, A.M. Macdonald, P. Van Eerdewegh, E.L. Harris, Sherri J. Bale, David Patterson, P. Watkms, Nan Rochberg, M.A. Tucker, E.B. Claus, Ellen M. Wijsman, J.D. Terwilliger, S. Lawrence, P. Szolovits, N. Risen, C.M. Kammerer, Stylianos E. Antonarakis, J.E. Reefer, Veronica J. Vieland, Timothy Bishop, G.P. Crockford, F.M. Demenais, Rudy Guerra, M.H. Skolnick, M.W. Piepkorn, S. Moldin, James A. Trofatter, N. Cox, L.A. Cupples, H. Blossey, J. Blangero, L.A. Farrer, V.L. Prenger, I.B. Borecki, J.A. Donald, N.A. Gruis, P. M. Conneally, L.R. Weitkamp, Terri H. Beaty, L.J. Meyer, B.G. Mellen, T.M. King, B. Towne, A.E. Laing, Richard H. Myers, J.J. Zone, P. Green, L.W. Konigsberg, D.T. Bishop, Rita M. Cantor, Chad Haynes, Joan E. Bailey-Wilson, Margaret A. Pericak-Vance, M. Boehnke, T.E. Dobbins, C.T. Falk, N. Morton, J.A. Salmon, S.L. Sherman, Jonathan Haines, W. Bergman, Mary Sara McPeek, L. Giuffra, R. Neuman, N.E. Maestri, David A. Greenberg, James F. Gusella, Maria Martinez, T. Rice, W.H. Wong, B.A.J. Ponder, W.H. McCarthy, Nancy S. Wexler, T. Lehner, M.C. Speer, A. Chakravarti, C.R. Colyer, J.K. Rivers, B.J.B. Keats, A.M. Goldstein, David R. Cox, Jean W. MacCluer, D.C. Thomas
Publikováno v:
Cytogenetic and Genome Research. 59:234-240
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::45f2fd4a6cb6488607748c9e46d2d8ba
https://doi.org/10.1159/000133257
https://doi.org/10.1159/000133257
Autor:
Barbro Sjögren, Tommy Martinsson, Joel Gelernter, Cathy L. Barr, James L. Kennedy, L. Bierut, Lennart Wetterberg, Kenneth K. Kidd, J. Kurth, L. Giuffra, Joachim Hallmayer, Jan Wahlström, A.J. Pakstis, Hans W. Moises, Claes Wadelius, Luigi Luca Cavalli-Sforza
Publikováno v:
American journal of medical genetics. 54(1)
Genetic linkage studies of a kindred from Sweden segregating for schizophrenia have been performed using a genetic model (autosomal dominant, f = 0.72, q = 0.02, phenocopies = 0.001) as described in Kennedy et al., 1988. Analyses of the restriction f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5f86fe5e442187e7fff4740022fc9661
https://pubmed.ncbi.nlm.nih.gov/7909991
https://pubmed.ncbi.nlm.nih.gov/7909991
Autor:
Lennart Wetterberg, Vincent P. Zarcone, Michael Litt, John Mauer, Olivier Civelli, James L. Kennedy, Barbro Sjögren, L. Giuffra, Hans W. Moises, Joel Gelernter, Luigi Luca Cavalli-Sforza, Kenneth K. Kidd, David K. Grandy, Sophia Vinogradov
Publikováno v:
Scopus-Elsevier
The dopamine hypothesis is one of the major etiological hypotheses of schizophrenia. The well-established role of genetic factors in schizophrenia together with reports of increased D2 dopamine receptor densities in untreated schizophrenic patients s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1a9a8b086143aefbed546d11c2df7b93
https://pubmed.ncbi.nlm.nih.gov/2069495
https://pubmed.ncbi.nlm.nih.gov/2069495
Autor:
Phillippa Newton, R. Mant, N.G. Irving, Alison Goate, Karen Rooke, Andrew Haynes, L. Giuffra, Louise James, Alien D. Roses, P Roques, Jeremy P Brown, Marie-Christine Chartier-Harlin, Christopher Talbot, Margaret A. Pericak-Vance, Michael Mullan, Fiona Crawford, Michael John Owen, John Hardy, Liana Fidani, Robert Williamson, Martin N. Rossor
Publikováno v:
Scopus-Elsevier
A locus segregating with familial Alzheimer's disease (AD) has been mapped to chromosome 21, close to the amyloid precursor protein (APP) gene. Recombinants between the APP gene and the AD locus have been reported which seemed to exclude it as the si
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::71a03ec9b60d5523bafdddf6bf2ff9d5
https://pubmed.ncbi.nlm.nih.gov/1901961
https://pubmed.ncbi.nlm.nih.gov/1901961
Autor:
L. Giuffra
Publikováno v:
Alcoholism ISBN: 9781468459487
Many human disorders are either partially or wholly determined by genetic factors. The identification of these genetic defects at the DNA level is a major goal with important implications. Such identification could greatly increase our understanding
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7938d92ca3ed2455b69df6cbceef69c3
https://doi.org/10.1007/978-1-4684-5946-3_17
https://doi.org/10.1007/978-1-4684-5946-3_17
Autor:
M. J. Owen, P. J. Newton, A. Haynes, Robert Williamson, I. Ovenstone, P. Luthert, L. Giuffra, John Hardy, Martin N. Rossor, P. Lantos, Alison Goate, P Roques, Michael Mullan, L James
Publikováno v:
Scopus-Elsevier
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5b6223b817411b1a930672f789702aa2
https://pubmed.ncbi.nlm.nih.gov/1776736
https://pubmed.ncbi.nlm.nih.gov/1776736
Publikováno v:
Human Genetics. 86
The Na+/H+ antiporter is a ubiquitous membrane-associated protein that plays an important role in the regulation of intracellular pH. APNH, a gene encoding the antiporter, has been cloned and mapped to the short arm of chromosome 1 by in situ hybridi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9b3c8acbfab16d98e56081f64e1413ae
https://doi.org/10.1007/bf00205179
https://doi.org/10.1007/bf00205179
Autor:
H G Harley, L. Giuffra, Jingshi Wu, Andrew J. Pakstis, Jeffrey Rogers, David C. Ward, Kenneth K. Kidd, James L. Kennedy, Peter Lichter, Trefor Jenkins, Judith R. Kidd
Publikováno v:
Genomics. 8(2)
A cDNA clone of the β subunit of human fibronectin receptor (FNRB) detects two different polymorphic loci: (a) a codominant system previously mapped to the pericentromeric region of chromosome 10, the site of the functional FNRB gene; and (b) a domi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8c69c8bc52d815990788a4aa152846dc
https://pubmed.ncbi.nlm.nih.gov/1979054
https://pubmed.ncbi.nlm.nih.gov/1979054
Publikováno v:
Nucleic Acids Research. 18:5326-5326
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5718929bb279546a4bd35f16349582e7
https://doi.org/10.1093/nar/18.17.5326
https://doi.org/10.1093/nar/18.17.5326