Glutathione S-transferase omega-1 modifies age-at-onset of Alzheimer disease and Parkinson disease (English)
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- New search for: Scherzer, Clemens R.
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In:
Human molecular genetics
;
12
, 24
;
3259-
;
2003
- Article (Journal) / Electronic Resource
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Title:Glutathione S-transferase omega-1 modifies age-at-onset of Alzheimer disease and Parkinson disease
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Contributors:Li, Yi-Ju ( author ) / Oliveira, Sofia A. ( author ) / Xu, Puting ( author ) / Martin, Eden R. ( author ) / Stenger, Judith E. ( author ) / Scherzer, Clemens R. ( author ) / Hauser, Michael A. ( author ) / Scott, William K. ( author ) / Small, Gary W. ( author ) / Nance, Martha A. ( author )
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Published in:Human molecular genetics ; 12, 24 ; 3259-
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Publisher:
- New search for: Oxford University Press
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Publication date:2003-12-15
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ISSN:
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DOI:
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Type of media:Article (Journal)
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Type of material:Electronic Resource
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Language:English
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Source:
Table of contents – Volume 12, Issue 24
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.
- 3207
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Functional haplotypes of the RET proto-oncogene promoter are associated with Hirschsprung disease (HSCR)Fitze, Guido / Appelt, Hella / König, Inke R. / Görgens, Heike / Stein, Ulrike / Walther, Wolfgang / Gossen, Manfred / Schreiber, Matthias / Ziegler, Andreas / Roesner, Dietmar et al. | 2003
- 3215
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PCDH15 is expressed in the neurosensory epithelium of the eye and ear and mutant alleles are responsible for both USH1F and DFNB23Ahmed, Zubair M. / Riazuddin, Saima / Ahmad, Jamil / Bernstein, Steve L. / Guo, Yan / Sabar, Muhammad F. / Sieving, Paul / Riazuddin, Sheikh / Griffith, Andrew J. / Friedman, Thomas B. et al. | 2003
- 3225
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Parent-of-origin effects on handedness and schizophrenia susceptibility on chromosome 2p12-q11Francks, Clyde / DeLisi, Lynn E. / Shaw, Sarah H. / Fisher, Simon E. / Richardson, Alex J. / Stein, John F. / Monaco, Anthony P. et al. | 2003
- 3231
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Autophagy regulates the processing of amino terminal huntingtin fragmentsQin, Zheng-Hong / Wang, Yumei / Kegel, Kimberly B. / Kazantsev, Aleksey / Apostol, Barbara L. / Thompson, Leslie Michels / Yoder, Jennifer / Aronin, Neil / DiFiglia, Marian et al. | 2003
- 3245
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Classifying the estrogen receptor status of breast cancers by expression profiles reveals a poor prognosis subpopulation exhibiting high expression of the ERBB2 receptorKun, Yu / How, Lee Chee / Hoon, Tan Puay / Bajic, Vladimir B. / Lam, Tan Sin / Aggarwal, Amit / Sze, Hong Ga / Bok, Wee Siew / Yin, Wong Chow / Tan, Patrick et al. | 2003
- 3259
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Glutathione S-transferase omega-1 modifies age-at-onset of Alzheimer disease and Parkinson diseaseLi, Yi-Ju / Oliveira, Sofia A. / Xu, Puting / Martin, Eden R. / Stenger, Judith E. / Scherzer, Clemens R. / Hauser, Michael A. / Scott, William K. / Small, Gary W. / Nance, Martha A. et al. | 2003
- 3269
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Abnormalities of the vitreoretinal interface caused by dysregulated Hedgehog signaling during retinal developmentBlack, Graeme C.M. / Mazerolle, Chantal J. / Wang, Yaping / Campsall, Katrina D. / Petrin, Dino / Leonard, Brian C. / Damji, Karim F. / Evans, D. Gareth / McLeod, David / Wallace, Valerie A. et al. | 2003
- 3277
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Functional interaction between BMPR-II and Tctex-1, a light chain of Dynein, is isoform-specific and disrupted by mutations underlying primary pulmonary hypertensionMachado, Rajiv D. / Rudarakanchana, Nung / Atkinson, Carl / Flanagan, Julia A. / Harrison, Rachel / Morrell, Nicholas W. / Trembath, Richard C. et al. | 2003
- 3287
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Molecular interaction of connexin 30.3 and connexin 31 suggests a dominant-negative mechanism associated with erythrokeratodermia variabilisPlantard, Laure / Huber, Marcel / Macari, Francoise / Meda, Paolo / Hohl, Daniel et al. | 2003
- 3295
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Phosphorylation influences the translation state of FMRP-associated polyribosomesCeman, Stephanie / O'Donnell, William T. / Reed, Matt / Patton, Stephana / Pohl, Jan / Warren, Stephen T. et al. | 2003
- 3307
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Hnf6 and Tcf2 (MODY5) are linked in a gene network operating in a precursor cell domain of the embryonic pancreasMaestro, Miguel A. / Boj, Sylvia F. / Luco, Reini F. / Pierreux, Christophe E. / Cabedo, Judit / Servitja, Joan M. / German, Michael S. / Rousseau, Guy G. / Lemaigre, Frédéric P. / Ferrer, Jorge et al. | 2003
- 3315
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Analysis of the ARMD1 locus: evidence that a mutation in HEMICENTIN-1 is associated with age-related macular degeneration in a large familySchultz, Dennis W. / Klein, Michael L. / Humpert, Andrea J. / Luzier, Christina W. / Persun, Vesna / Schain, Mitchell / Mahan, Alison / Runckel, Charles / Cassera, Maria / Vittal, Vasavi et al. | 2003
- 3325
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Impact of selection, mutation rate and genetic drift on human genetic variationSunyaev, Shamil / Kondrashov, Fyodor A. / Bork, Peer / Ramensky, Vasily et al. | 2003
- 3331
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Reduction in frataxin causes progressive accumulation of mitochondrial damageKarthikeyan, Gopalakrishnan / Santos, Janine H. / Graziewicz, Maria A. / Copeland, William C. / Isaya, Grazia / Houten, Bennett Van / Resnick, Michael A. et al. | 2003
- 3343
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Promoter-restricted H3 Lys 4 di-methylation is an epigenetic mark for monoallelic expressionRougeulle, Claire / Navarro, Pablo / Avner, Philip et al. | 2003
- 3349
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Mouse model of N-acetylgalactosamine-6-sulfate sulfatase deficiency (Galns-/-) produced by targeted disruption of the gene defective in Morquio A diseaseTomatsu, Shunji / Orii, Koji O. / Vogler, Carole / Nakayama, Jun / Levy, Beth / Grubb, Jeffrey H. / Gutierrez, Monica A. / Shim, Soomin / Yamaguchi, Seiji / Nishioka, Tatsuo et al. | 2003
- 3359
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Dramatic tissue-specific mutation length increases are an early molecular event in Huntington disease pathogenesisKennedy, Laura / Evans, Elizabeth / Chen, Chiung-Mei / Craven, Lyndsey / Detloff, Peter J. / Ennis, Margaret / Shelbourne, Peggy F. et al. | 2003
- 3369
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Allelism of MCKD, FJHN and GCKD caused by impairment of uromodulin export dynamicsRampoldi, Luca / Caridi, Gianluca / Santon, Daniela / Boaretto, Francesca / Bernascone, Ilenia / Lamorte, Giuseppe / Tardanico, Regina / Dagnino, Monica / Colussi, Giacomo / Scolari, Francesco et al. | 2003
- 3385
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Complement factor H mutations and gene polymorphisms in haemolytic uraemic syndrome: the C-257T, the A2089G and the G2881T polymorphisms are strongly associated with the diseaseCaprioli, Jessica / Castelletti, Federica / Bucchioni, Sara / Bettinaglio, Paola / Bresin, Elena / Pianetti, Gaia / Gamba, Sara / Brioschi, Simona / Daina, Erica / Remuzzi, Giuseppe et al. | 2003
- 3397
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Molecular basis of the functional podocin-nephrin complex: mutations in the NPHS2 gene disrupt nephrin targeting to lipid raft microdomainsHuber, Tobias B. / Simons, Matias / Hartleben, Björn / Sernetz, Leonie / Schmidts, Miriam / Gundlach, Enken / Saleem, Moin A. / Walz, Gerd / Benzing, Thomas et al. | 2003