Genome-wide SNP assay reveals structural genomic variation, extended homozygosity and cell-line induced alterations in normal individuals (English)
- New search for: Simon-Sanchez, J.
- New search for: Scholz, S.
- New search for: Fung, H. C.
- New search for: Matarin, M.
- New search for: Hernandez, D.
- New search for: Gibbs, J. R.
- New search for: Britton, A.
- New search for: de Vrieze, F. W.
- New search for: Peckham, E.
- New search for: Gwinn-Hardy, K.
- New search for: Simon-Sanchez, J.
- New search for: Scholz, S.
- New search for: Fung, H. C.
- New search for: Matarin, M.
- New search for: Hernandez, D.
- New search for: Gibbs, J. R.
- New search for: Britton, A.
- New search for: de Vrieze, F. W.
- New search for: Peckham, E.
- New search for: Gwinn-Hardy, K.
In:
HUMAN MOLECULAR GENETICS
;
16
, 1
;
1-14
;
2007
-
ISSN:
- Article (Journal) / Print
-
Title:Genome-wide SNP assay reveals structural genomic variation, extended homozygosity and cell-line induced alterations in normal individuals
-
Contributors:Simon-Sanchez, J. ( author ) / Scholz, S. ( author ) / Fung, H. C. ( author ) / Matarin, M. ( author ) / Hernandez, D. ( author ) / Gibbs, J. R. ( author ) / Britton, A. ( author ) / de Vrieze, F. W. ( author ) / Peckham, E. ( author ) / Gwinn-Hardy, K. ( author )
-
Published in:HUMAN MOLECULAR GENETICS ; 16, 1 ; 1-14
-
Publisher:
- New search for: Oxford University Press
-
Publication date:2007-01-01
-
Size:14 pages
-
ISSN:
-
Type of media:Article (Journal)
-
Type of material:Print
-
Language:English
- New search for: 572.8
- Further information on Dewey Decimal Classification
-
Classification:
DDC: 572.8 -
Source:
© Metadata Copyright the British Library Board and other contributors. All rights reserved.
Table of contents – Volume 16, Issue 1
The tables of contents are generated automatically and are based on the data records of the individual contributions available in the index of the TIB portal. The display of the Tables of Contents may therefore be incomplete.
- 1
-
Genome-wide SNP assay reveals structural genomic variation, extended homozygosity and cell-line induced alterations in normal individualsSimon-Sanchez, Javier / Scholz, Sonja / Fung, Hon-Chung / Matarin, Mar / Hernandez, Dena / Gibbs, J. Raphael / Britton, Angela / de Vrieze, Fabienne Wavrant / Peckham, Elizabeth / Gwinn-Hardy, Katrina et al. | 2007
- 15
-
The DYRK1A gene, encoded in chromosome 21 Down syndrome critical region, bridges between b-amyloid production and tau phosphorylation in Alzheimer diseaseKimura, R. / Kamino, K. / Yamamoto, M. / Nuripa, A. / Kida, T. / Kazui, H. / Hashimoto, R. / Tanaka, T. / Kudo, T. / Yamagata, H. et al. | 2007
- 15
-
The DYRK1A gene, encoded in chromosome 21 Down syndrome critical region, bridges between {beta}-amyloid production and tau phosphorylation in Alzheimer diseaseKimura, Ryo / Kamino, Kouzin / Yamamoto, Mitsuko / Nuripa, Aidaralieva / Kida, Tomoyuki / Kazui, Hiroaki / Hashimoto, Ryota / Tanaka, Toshihisa / Kudo, Takashi / Yamagata, Hidehisa et al. | 2007
- 24
-
Novel genes identified in a high-density genome wide association study for nicotine dependenceBierut, Laura Jean / Madden, Pamela A.F. / Breslau, Naomi / Johnson, Eric O. / Hatsukami, Dorothy / Pomerleau, Ovide F. / Swan, Gary E. / Rutter, Joni / Bertelsen, Sarah / Fox, Louis et al. | 2007
- 36
-
Cholinergic nicotinic receptor genes implicated in a nicotine dependence association study targeting 348 candidate genes with 3713 SNPsSaccone, Scott F. / Hinrichs, Anthony L. / Saccone, Nancy L. / Chase, Gary A. / Konvicka, Karel / Madden, Pamela A.F. / Breslau, Naomi / Johnson, Eric O. / Hatsukami, Dorothy / Pomerleau, Ovide et al. | 2007
- 50
-
Pael receptor induces death of dopaminergic neurons in the substantia nigra via endoplasmic reticulum stress and dopamine toxicity, which is enhanced under condition of parkin inactivationKitao, Yasuko / Imai, Yuzuru / Ozawa, Kentaro / Kataoka, Ayane / Ikeda, Toshio / Soda, Mariko / Nakimawa, Kazuhiko / Kiyama, Hiroshi / Stern, David M. / Hori, Osamu et al. | 2007
- 61
-
The first 17 amino acids of Huntingtin modulate its sub-cellular localization, aggregation and effects on calcium homeostasisRockabrand, Erica / Slepko, Natalia / Pantalone, Antonello / Nukala, Vidya N. / Kazantsev, Aleksey / Marsh, J. Lawrence / Sullivan, Patrick G. / Steffan, Joan S. / Sensi, Stefano L. / Thompson, Leslie Michels et al. | 2007
- 78
-
APC mutations in FAP-associated desmoid tumours are non-random but not 'just right'Latchford, Andrew / Volikos, Emmanouil / Johnson, Victoria / Rogers, Pauline / Suraweera, Nirosha / Tomlinson, Ian / Phillips, Robin / Silver, Andrew et al. | 2007
- 83
-
Involvement of hyperprolinemia in cognitive and psychiatric features of the 22q11 deletion syndromeRaux, Grégory / Bumsel, Emilie / Hecketsweiler, Bernadette / van Amelsvoort, Therese / Zinkstok, Janneke / Manouvrier-Hanu, Sylvie / Fantini, Carole / Brévière, Georges-Marie M. / Di Rosa, Gabriella / Pustorino, Giuseppina et al. | 2007
- 92
-
The mixed-lineage leukemia fusion partner AF4 stimulates RNA polymerase II transcriptional elongation and mediates coordinated chromatin remodelingBitoun, Emmanuelle / Oliver, Peter L. / Davies, Kay E. et al. | 2007
- 107
-
Identification of EFHC2 as a quantitative trait locus for fear recognition in Turner syndromeWeiss, Lauren A. / Purcell, Shaun / Waggoner, Skye / Lawrence, Kate / Spektor, David / Daly, Mark J. / Sklar, Pamela / Skuse, David et al. | 2007