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au.\*:("ST GEORGE-HYSLOP, Peter")

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Intracellular traffic and neurodegenerative disordersSt. George-Hyslop, Peter; Mobley, William C; Christen, Yves et al.Research and perspectives in Alzheimer's disease. 2009, isbn 978-3-540-87940-4 3-540-87940-4, 1Vol, XIV-183 p, isbn 978-3-540-87940-4 3-540-87940-4Conference Proceedings

Molecular biology and genetics of Alzheimer's diseaseST GEORGE-HYSLOP, Peter H; PETIT, Agnès.Comptes rendus. Biologies. 2005, Vol 328, Num 2, pp 119-130, issn 1631-0691, 12 p.Article

Recurrent fetal loss associated with bilineal inheritance of type 1 Autosomal dominant polycystic kidney diseasePATERSON, Andrew D; KAI RONG WANG; LUPEA, Doina et al.American journal of kidney diseases. 2002, Vol 40, Num 1, pp 16-20, issn 0272-6386Article

Differential display analysis of presenilin 1-deficient mouse brainsLIAUW, Jennifer; NGUYEN, Van; HUANG, Jean et al.Molecular brain research. 2002, Vol 109, Num 1-2, pp 56-62, issn 0169-328X, 7 p.Article

Presenilin-directed inhibitors of γ-secretase trigger caspase 3 activation in presenilin-expressing and presenilin-deficient cellsDA COSTA, Cristine Alves; AYRAL, Erwan; HERNANDEZ, Jean-Francois et al.Journal of neurochemistry. 2004, Vol 90, Num 4, pp 800-806, issn 0022-3042, 7 p.Article

Loss of nicastrin elicits an apoptotic phenotype in mouse embryosNGUYEN, Van; HAWKINS, Cynthia; BERGERON, Catherine et al.Brain research. 2006, Vol 1086, pp 76-84, issn 0006-8993, 9 p.Article

Lack of association between Alzheimer's disease and the promoter region polymorphisms of the nicastrin geneORLACCHIO, Antonio; KAWARAI, Toshitaka; POLIDORO, Mario et al.Neuroscience letters. 2004, Vol 363, Num 1, pp 49-53, issn 0304-3940, 5 p.Article

New locus for hereditary spastic paraplegia maps to chromosome 1p31.1-1p21.1ORLACCHIO, Antonio; KAWARAI, Toshitaka; GAUDIELLO, Fabrizio et al.Annals of neurology. 2005, Vol 58, Num 3, pp 423-429, issn 0364-5134, 7 p.Article

TMP21 is a presenilin complex component that modulates γ-secretase but not ε-secretase activityFUSHENG CHEN; HASEGAWA, Hiroshi; WAKUTANI, Yosuke et al.Nature (London). 2006, Vol 440, Num 7088, pp 1208-1212, issn 0028-0836, 5 p.Article

Novel SPG6 mutation p.A100T in a japanese family with autosomal dominant form of hereditary spastic paraplegiaKANEKO, Satoshi; KAWARAI, Toshitaka; ST GEORGE-HYSLOP, Peter et al.Movement disorders. 2006, Vol 21, Num 9, pp 1531-1533, issn 0885-3185, 3 p.Article

Investigation of C9orf72 in 4 Neurodegenerative DisordersZHENGRUI XI; ZINMAN, Lome; MORON, Francisco J et al.Archives of neurology (Chicago). 2012, Vol 69, Num 12, pp 1583-1590, issn 0003-9942, 8 p.Article

T313M PINK1 mutation in an extended highly consanguineous saudi family with early-onset parkinson diseaseCHISHTI, Muhammad A; BOHLEGA, Saeed; AHMED, Maqbool et al.Archives of neurology (Chicago). 2006, Vol 63, Num 10, pp 1483-1485, issn 0003-9942, 3 p.Article

Analysis of the glucocerebrosidase gene in Parkinson's diseaseSATO, Christine; MORGAN, Angharad; LANG, Anthony E et al.Movement disorders. 2004, Vol 20, Num 3, pp 367-370, issn 0885-3185, 4 p.Article

Brain levels of CDK5 activator p25 are not increased in Alzheimer's or other neurodegenerative diseases with neurofibrillary tanglesTANDON, Anurag; HAUNG YU; FRASER, Paul E et al.Journal of neurochemistry. 2003, Vol 86, Num 3, pp 572-581, issn 0022-3042, 10 p.Article

Frontotemporal dementia with novel tau pathology and a Glu342Val tau mutationLIPPA, Carol F; ZHUKAREVA, Victoria; LEE, Virginia M.-Y et al.Annals of neurology. 2000, Vol 48, Num 6, pp 850-858, issn 0364-5134Article

SPATACSIN mutations cause autosomal recessive juvenile amyotrophic lateral sclerosisORLACCHIO, Antonio; BABALINI, Carla; KAWARAI, Toshitaka et al.Brain. 2010, Vol 133, pp 591-598, issn 0006-8950, 8 p., 2Article

Functional variants of OCTN cation transporter genes are associated with Crohn diseasePELTEKOVA, Vanya D; WINTLE, Richard F; GRIFFITHS, Anne M et al.Nature genetics. 2004, Vol 36, Num 5, pp 471-475, issn 1061-4036, 5 p.Article

No evidence for tau duplications in frontal temporal dementia families showing genetic linkage to the tau locus in which tau mutations have not been foundJOHNSON, Janel; OSTOJIC, Jovanka; PASTOR, Pau et al.Neuroscience letters. 2004, Vol 363, Num 2, pp 99-101, issn 0304-3940, 3 p.Article

Distinguishable effects of Presenilin-1 and APP717 mutations on amyloid plaque depositionISHII, Kazuhiro; LIPPA, Carol; POLLEN, Dan A et al.Neurobiology of aging. 2001, Vol 22, Num 3, pp 367-376, issn 0197-4580Article

Meta-analysis of the Association Between Variants in SORL1 and Alzheimer DiseaseREITZ, Christiane; RONG CHENG; SHIBATA, Nobuto et al.Archives of neurology (Chicago). 2011, Vol 68, Num 1, pp 99-106, issn 0003-9942, 8 p.Article

Candidate Single-Nucleotide Polymorphisms From a Genomewide Association Study of Alzheimer DiseaseHAO LI; WETTEN, Sally; COLETTA, Natalie et al.Archives of neurology (Chicago). 2008, Vol 65, Num 1, pp 45-53, issn 0003-9942, 9 p.Article

The neuronal sortilin-related receptor SORL1 is genetically associated with Alzheimer diseaseROGAEVA, Ekaterina; YAN MENG; FUSHENG CHEN et al.Nature genetics. 2007, Vol 39, Num 2, pp 168-177, issn 1061-4036, 10 p.Article

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