Human Genome Epidemiology Literature Finder
Records 1 - 22 (of 22 Records) |
Query Trace: NCSTN[original query] |
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The gene encoding nicastrin, a major gamma-secretase component, modifies risk for familial early-onset Alzheimer disease in a Dutch population-based sample. American journal of human genetics 2002 Jun 70 (6): 1568-74. Dermaut Bart, Theuns Jessie, Sleegers Kristel, Hasegawa Hiroshi, Van den Broeck Marleen, Vennekens Krist'l, Corsmit Ellen, St George-Hyslop Peter, Cruts Marc, van Duijn Cornelia M, Van Broeckhoven Christi |
Association analysis between Alzheimer's disease and the Nicastrin gene polymorphisms. Neuroscience letters 2002 Nov 333 (2): 115-8. Orlacchio Antonio, Kawarai Toshitaka, Polidoro Mario, Stefani Alessandro, Orlacchio Aldo, St George-Hyslop Peter H, Bernardi Giorg |
No replication of the association between the Nicastrin gene and familial early-onset Alzheimer's disease. Neuroscience letters 2003 Dec 353 (2): 153-5. Cousin Emmanuelle, Hannequin Didier, Macé Sandrine, Dubois Bruno, Ricard Sylvain, Génin Emmanuelle, Brun Christophe, Chansac Céline, Pradier Laurent, Frebourg Thierry, Brice Alexis, Campion Dominique, Deleuze Jean-Franço |
Possible association of nicastrin polymorphisms and Alzheimer disease in the Finnish population. Neurology 2004 Jul 63 (1): 173-5. Helisalmi S, Dermaut B, Hiltunen M, Mannermaa A, Van den Broeck M, Lehtovirta M, Koivisto A M, Iivonen S, Cruts M, Soininen H, Van Broeckhoven |
Lack of association between Alzheimer's disease and the promoter region polymorphisms of the nicastrin gene. Neuroscience letters 2004 Jun 363 (1): 49-53. Orlacchio Antonio, Kawarai Toshitaka, Polidoro Mario, Paterson Andrew D, Rogaeva Ekaterina, Orlacchio Aldo, St George-Hyslop Peter H, Bernardi Giorg |
Nicastrin gene polymorphisms, cognitive ability level and cognitive ageing. Neuroscience letters 2005 Jan 373 (2): 110-4. Deary Ian J, Hamilton Gillian, Hayward Caroline, Whalley Lawrence J, Powell John, Starr John M, Lovestone Sim |
Systematic meta-analyses of Alzheimer disease genetic association studies: the AlzGene database. Nature genetics 2007 Jan 39 (1): 17-23. Bertram L, McQueen MB, Mullin K, Blacker D, Tanzi RE |
Genetic study of Sardinian patients with Alzheimer's disease. Neuroscience letters 2006 May 398 (1-2): 124-8. Piscopo Paola, Manfredi Antonella, Malvezzi-Campeggi Lorenzo, Crestini Alessio, Spadoni Ornella, Cherchi Rossella, Deiana Emiliano, Piras Maria Rita, Confaloni Annamar |
Replication study of candidate genes for cognitive abilities: the Lothian Birth Cohort 1936. Genes, brain, and behavior 2009 Mar 8 (2): 238-47. Houlihan L M, Harris S E, Luciano M, Gow A J, Starr J M, Visscher P M, Deary I |
Association between promoter polymorphisms of the nicastrin gene and sporadic Alzheimer's disease in North Chinese Han population. Neuroscience letters 2009 Jul 458 (3): 136-9. Ma Zhonghua, Han Di, Zuo Xiumei, Wang Fen, Jia Jianpi |
Analysis of the nicastrin promoter rs10752637 polymorphism and its association with Alzheimer's disease. The European journal of neuroscience 2009 Nov 30 (9): 1831-6. Zhong Li, Dong-hai Qiu, Hong-ying Liu, Qing-feng L |
Amyloid precursor protein (APP) processing genes and cerebrospinal fluid APP cleavage product levels in Alzheimer's disease. Neurobiology of aging 2011 Mar 32 (3): 556.e13-23. Bekris L M, Galloway N M, Millard S, Lockhart D, Li G, Galasko D R, Farlow M R, Clark C M, Quinn J F, Kaye J A, Schellenberg G D, Leverenz J B, Seubert P, Tsuang D W, Peskind E R, Yu C |
Cerebrospinal fluid Aß42 levels and APP processing pathway genes in Parkinson's disease. Movement disorders : official journal of the Movement Disorder Society 2015 Jun 30 (7): 936-44. Bekris Lynn M, Tsuang Debby W, Peskind Elaine R, Yu Chang E, Montine Thomas J, Zhang Jing, Zabetian Cyrus P, Leverenz James |
NCSTN mutations in hidradenitis suppurativa/acne inversa do not influence cytokine production by peripheral blood mononuclear cells. The British journal of dermatology 2016 Sep . Xu H, He Y, Hui Y, Xiao X, Zhang X, Li C, Wang |
Somatic variants in autosomal dominant genes are a rare cause of sporadic Alzheimer's disease. Alzheimer's & dementia : the journal of the Alzheimer's Association 2018 8 14 (12): 1632-1639. Nicolas Gaël, Acuña-Hidalgo Rocío, Keogh Michael J, Quenez Olivier, Steehouwer Marloes, Lelieveld Stefan, Rousseau Stéphane, Richard Anne-Claire, Oud Manon S, Marguet Florent, Laquerrière Annie, Morris Chris M, Attems Johannes, Smith Colin, Ansorge Olaf, Al Sarraj Safa, Frebourg Thierry, Campion Dominique, Hannequin Didier, Wallon David, Gilissen Christian, Chinnery Patrick F, Veltman Joris A, Hoischen Alexand |
Evaluation of the prognostic significances of ?-secretase genes in pancreatic cancer. Oncology letters 2019 4 17 (5): 4614-4620. Jeon Yun Ho, Ha Mihyang, Kim Sung Won, Kim Mun Ju, Lee Chi-Seung, Oh Chang-Kyu, Han Myoung-Eun, Oh Sae-Ock, Kim Yun H |
Evaluation of PSEN1 subunit of the ?-secretase gene in patients with psoriasis vulgaris: a pilot study. Postepy dermatologii i alergologii 2020 Dec 37 (6): 915-920. Bergler-Czop Beata, Mizio?ek Bartosz, Sierant Katarzyna, Sazanów-Lubelski Jakub, Brzezi?ska-Wcis?o Lig |
Investigation of gamma secretase gene complex mutations in German population with Hidradenitis suppurativa designate a complex polygenic heritage. Journal of the European Academy of Dermatology and Venereology : JEADV 2021 Feb . Vural Seçil, Baumgartner Mark, Lichtner Peter, Eckstein Gertrud, Hariry Housien, Chen WenChieh, Ruzicka Thomas, Melnik Bodo, Plewig Gerd, Wagner Matthias, Giehl Kathrin |
Canine Somatic Mutations from Whole-Exome Sequencing of B-Cell Lymphomas in Six Canine Breeds-A Preliminary Study. Animals : an open access journal from MDPI 2023 9 13 (18): . Sungryong Kim, Namphil Kim, Hyo-Min Kang, Hye-Jin Jang, Amos Chungwon Lee, Ki-Jeong |
NCSTN In-Frame Deletion in Maltese Patients With Hidradenitis Suppurativa. JAMA dermatology 2023 7 . Dillon Mintoff, Nikolai Paul Pace, Isabella Bo |
An Updated Mutation Spectrum of the ?-Secretase Complex: Novel NCSTN Gene Mutation in an Indian Family with Hidradenitis Suppurativa and Acne Conglobata. Indian journal of dermatology 2023 6 68 (2): 141-147. Uppala Ratnamala, Nayan K Jain, Devendrasinh D Jhala, Pullabatla V S Prasad, Nazia Saiyed, Sreelatha Nair, Uppala Radhakrish |
Rare missense variants in the SH3 domain of PSTPIP1 are associated with hidradenitis suppurativa. HGG advances 2023 4 4 (2): 100187. Morales-Heil David J, Cao Li, Sweeney Cheryl, Malara Anna, Brown Frank, Milam Philip, Anadkat Milan, Kaffenberger Jessica, Kaffenberger Benjamin, Nagele Peter, Kirby Brian, Roberson Elisha D |
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