Human Genome Epidemiology Literature Finder
Records 1 - 9 (of 9 Records) |
Query Trace: MAP2[original query] |
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The NEI/NCBI dbGAP database: genotypes and haplotypes that may specifically predispose to risk of neovascular age-related macular degeneration. BMC medical genetics 2008 9 (1): 51. Zhang Hong, Morrison Margaux A, Dewan Andy, Adams Scott, Andreoli Michael, Huynh Nancy, Regan Maureen, Brown Alison, Miller Joan W, Kim Ivana K, Hoh Josephine, Deangelis Margaret |
CREB1 is a strong genetic predictor of the variation in exercise heart rate response to regular exercise: the HERITAGE Family Study. Circulation. Cardiovascular genetics 2010 Jun 3 (3): 294-9. Rankinen Tuomo, Argyropoulos George, Rice Treva, Rao D C, Bouchard Clau |
Longitudinal mutational analysis of a cerebellar pilocytic astrocytoma recurring as a ganglioglioma. Pediatric blood & cancer 2016 Oct . Fiset Pierre O, Fontebasso Adam M, De Jay Nicolas, Gayden Tenzin, Nikbakht Hamid, Majewski Jacek, Jabado Nada, Albrecht Steff |
Handedness, language areas and neuropsychiatric diseases: insights from brain imaging and genetics.
Brain : a journal of neurology 2019 Oct 142 (10): 2938-2947. Wiberg Akira, Ng Michael, Al Omran Yasser, Alfaro-Almagro Fidel, McCarthy Paul, Marchini Jonathan, Bennett David L, Smith Stephen, Douaud Gwenaëlle, Furniss Domin |
Genetic variants in the liver kinase B1-AMP-activated protein kinase pathway genes and pancreatic cancer risk. Molecular carcinogenesis 2019 Apr . Xu Xinyuan, Qian Danwen, Liu Hongliang, Cruz Diana, Luo Sheng, Walsh Kyle M, Abbruzzese James L, Zhang Xuefeng, Wei Qing |
The molecular genetics of hand preference revisited.
Scientific reports 2019 Apr 9 (1): 5986. de Kovel Carolien G F, Francks Cly |
Proteomics in cerebrospinal fluid and spinal cord suggests UCHL1, MAP2 and GPNMB as biomarkers and underpins importance of transcriptional pathways in amyotrophic lateral sclerosis. Acta neuropathologica 2019 11 139 (1): 119-134. Oeckl Patrick, Weydt Patrick, Thal Dietmar R, Weishaupt Jochen H, Ludolph Albert C, Otto Mark |
Next-generation sequencing identified somatic alterations that may underlie the etiology of Chinese papillary thyroid carcinoma. European journal of cancer prevention : the official journal of the European Cancer Prevention Organisation (ECP) 2019 Nov . Yang Chuanjia, Gong Jian, Xu Weixue, Liu Zhen, Cui Dong |
Cognitive genomics of learning delay and low level of social performance monitoring in macaque. Scientific reports 2022 10 12 (1): 16539. Ninomiya Taihei, Noritake Atsushi, Tatsumoto Shoji, Go Yasuhiro, Isoda Masa |
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- Page last updated:Apr 29, 2024
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