Human Genome Epidemiology Literature Finder
Records 1 - 26 (of 26 Records) |
Query Trace: MME[original query] |
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Clinical, immunological, and genetic features of autoimmune primary adrenal insufficiency: observations from a Norwegian registry. The Journal of clinical endocrinology and metabolism 2009 Dec 94 (12): 4882-90. Erichsen Martina M, Løvås Kristian, Skinningsrud Beate, Wolff Anette B, Undlien Dag E, Svartberg Johan, Fougner Kristian J, Berg Tore J, Bollerslev Jens, Mella Bjarne, Carlson Joyce A, Erlich Henry, Husebye Eystein |
Identification of genetic factors associated with susceptibility to angiotensin-converting enzyme inhibitors-induced cough. Pharmacogenetics and genomics 2011 Jan 21 (1): 10-7. Grilo Antonio, Sáez-Rosas María P, Santos-Morano Juan, Sánchez Elena, Moreno-Rey Concha, Real Luis M, Ramírez-Lorca Reposo, Sáez María |
Multiple loci in the HLA complex are associated with Addison's disease. The Journal of clinical endocrinology and metabolism 2011 Oct 96 (10): E1703-8. Skinningsrud Beate, Lie Benedicte A, Lavant Ewa, Carlson Joyce A, Erlich Henry, Akselsen Hanne E, Gervin Kristina, Wolff Anette B, Erichsen Martina M, Løvås Kristian, Husebye Eystein S, Undlien Dag |
Genetic and functional effects of membrane metalloendopeptidase on diabetic nephropathy development. American journal of nephrology 2011 34 (5): 483-90. Zhang Dongying, Gu Tianwei, Forsberg Elisabete, Efendic Suad, Brismar Kerstin, Gu Harvest |
The role of ECE1 variants in cognitive ability in old age and Alzheimer's disease risk. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2012 Sep 159B (6): 696-709. Hamilton Gillian, Harris Sarah E, Davies Gail, Liewald David C, Tenesa Albert, Payton Antony, Horan Michael A, Ollier William E R, Pendleton Neil, , Starr John M, Porteous David, Deary Ian |
Genetic variation in MME in relation to neprilysin protein and enzyme activity, Aß levels, and Alzheimer's disease risk. International journal of molecular epidemiology and genetics 2012 3 (1): 30-8. Miners Scott, van Helmond Zoë, Barker Rachel, Passmore Peter A, Johnston Janet A, Todd Stephen, McGuinness Bernadette M, Panza Francesco, Seripa Davide, Solfrizzi Vincenzo, Love Seth, Prince Jonathan A, Kehoe Patrick |
Genetic variants associated with angiotensin-converting enzyme inhibitor-associated angioedema. Pharmacogenetics and genomics 2013 Sep 23 (9): 470-8. Pare Guillaume, Kubo Michiaki, Byrd James B, McCarty Catherine A, Woodard-Grice Alencia, Teo Koon K, Anand Sonia S, Zuvich Rebecca L, Bradford Yuki, Ross Stephanie, Nakamura Yusuke, Ritchie Marylyn, Brown Nancy |
Genetic gains and losses in oral squamous cell carcinoma: impact on clinical management. Cellular oncology (Dordrecht) 2014 Feb 37 (1): 29-39. Ribeiro Ilda Patrícia, Marques Francisco, Caramelo Francisco, Pereira João, Patrício Miguel, Prazeres Hugo, Ferrão José, Julião Maria José, Castelo-Branco Miguel, de Melo Joana Barbosa, Baptista Isabel Poiares, Carreira Isabel Marqu |
Genetic and nongenetic factors influencing pharmacokinetics of B-type natriuretic peptide. Journal of cardiac failure 2014 Sep 20 (9): 662-8. Lanfear David E, Chow Sheryl, Padhukasahasram Badri, Li Jia, Langholz David, Tang W H Wilson, Williams L Keoki, Sabbah Hani |
Renal Mechanisms of Association between Fibroblast Growth Factor 1 and Blood Pressure. Journal of the American Society of Nephrology : JASN 2015 Apr . Tomaszewski Maciej, Eales James, Denniff Matthew, Myers Stephen, Chew Guat Siew, Nelson Christopher P, Christofidou Paraskevi, Desai Aishwarya, Büsst Cara, Wojnar Lukasz, Musialik Katarzyna, Jozwiak Jacek, Debiec Radoslaw, Dominiczak Anna F, Navis Gerjan, van Gilst Wiek H, van der Harst Pim, Samani Nilesh J, Harrap Stephen, Bogdanski Pawel, Zukowska-Szczechowska Ewa, Charchar Fadi |
Genetic Factors Influencing B-type Natriuretic Peptide-Mediated Production of Cyclic Guanosine Monophosphate and Blood Pressure Effects in Heart Failure Patients. Journal of cardiovascular translational research 2015 Nov . Lanfear David E, Li Jia, Abbas Raza, She Ricoung, Padhukasahasram Badri, Gupta Ramesh C, Langholz David, Tang W H Wilson, Williams L Keoki, Sabbah Hani N, Chow Sheryl |
Mutations in MME cause an autosomal-recessive Charcot-Marie-Tooth disease type 2. Annals of neurology 2016 Mar . Higuchi Yujiro, Hashiguchi Akihiro, Yuan Junhui, Yoshimura Akiko, Mitsui Jun, Ishiura Hiroyuki, Tanaka Masaki, Ishihara Satoshi, Tanabe Hajime, Nozuma Satoshi, Okamoto Yuji, Matsuura Eiji, Ohkubo Ryuichi, Inamizu Saeko, Shiraishi Wataru, Yamasaki Ryo, Ohyagi Yasumasa, Kira Jun-Ichi, Oya Yasushi, Yabe Hayato, Nishikawa Noriko, Tobisawa Shinsuke, Matsuda Nozomu, Masuda Masayuki, Kugimoto Chiharu, Fukushima Kazuhiro, Yano Satoshi, Yoshimura Jun, Doi Koichiro, Nakagawa Masanori, Morishita Shinichi, Tsuji Shoji, Takashima Hiros |
A genome-wide analysis in cluster headache points to neprilysin and PACAP receptor gene variants.
The journal of headache and pain 2016 Dec 17 (1): 114. Bacchelli Elena, Cainazzo Maria Michela, Cameli Cinzia, Guerzoni Simona, Martinelli Angela, Zoli Michele, Maestrini Elena, Pini Luigi Alber |
Screening of genetic variants in ADCYAP1R1, MME and 14q21 in a Swedish cluster headache cohort. The journal of headache and pain 2017 Aug 18 (1): 88. Ran Caroline, Fourier Carmen, Michalska Julia M, Steinberg Anna, Sjöstrand Christina, Waldenlind Elisabet, Belin Andrea Carmi |
The Association of MME microRNA Binding Site Polymorphism with the Risk of Late Onset Alzheimer's Disease in Northern Han Chinese. Current neurovascular research 2017 Mar . Liu Chun-Xia, Tan Lin, Sun Fu-Rong, Zhang Wei, Miao Dan, Tan Meng-Shan, Wan Yu, Tan Chen-Chen, Yu Jin-Tai, Tan L |
SNPs in A? clearance proteins: Lower CSF A? levels and earlier onset of dementia in PD. Neurology 2017 Nov . Brockmann Kathrin, Lerche Stefanie, Dilger Sarah Selina, Stirnkorb Johannes Georg, Apel Anja, Hauser Ann-Kathrin, Liepelt-Scarfone Inga, Berg Daniela, Gasser Thomas, Schulte Claudia, Maetzler Walt |
A prospective case-control study comparing optical coherence tomography characteristics in neuromyelitis optica spectrum disorder- optic neuritis and idiopathic optic neuritis. BMC ophthalmology 2018 9 18 (1): 247. Zhao Xiujuan, Qiu Wei, Zhang Yuxin, Luo Yan, Zhang Xiulan, Lu Lin, Yang H |
Genome sequencing for early-onset or atypical dementia: high diagnostic yield and frequent observation of multiple contributory alleles. Cold Spring Harbor molecular case studies 2019 12 5 (6): . Cochran J Nicholas, McKinley Emily C, Cochran Meagan, Amaral Michelle D, Moyers Bryan A, Lasseigne Brittany N, Gray David E, Lawlor James M J, Prokop Jeremy W, Geier Ethan G, Holt James M, Thompson Michelle L, Newberry J Scott, Yokoyama Jennifer S, Worthey Elizabeth A, Geldmacher David S, Love Marissa Natelson, Cooper Gregory M, Myers Richard M, Roberson Erik |
Genome-wide association study of angioedema induced by angiotensin-converting enzyme inhibitor and angiotensin receptor blocker treatment.
The pharmacogenomics journal 2020 Feb . Rasmussen Eva Rye, Hallberg Pär, Baranova Ekaterina V, Eriksson Niclas, Karawajczyk Malgorzata, Johansson Caroline, Cavalli Marco, Maroteau Cyrielle, Veluchamy Abirami, Islander Gunilla, Hugosson Svante, Terreehorst Ingrid, Asselbergs Folkert W, Norling Pia, Johansson Hans-Erik, Kohnke Hugo, Syvänen Ann-Christine, Siddiqui Moneeza K, Lang Chim C, Magnusson Patrik K E, Yue Qun-Ying, Wadelius Claes, von Buchwald Christian, Bygum Anette, Alfirevic Ana, Maitland-van der Zee Anke H, Palmer Colin N A, Wadelius M |
Germline Genetic Variants of the Renin-Angiotensin System, Hypoxia and Angiogenesis in Non-Small Cell Lung Cancer Progression: Discovery and Validation Studies. Cancers 2020 Dec 12 (12): . Catarata Maria Joana, Medeiros Rui, Oliveira Maria José, Pêgo Alice, Frade João Gonçalo, Martins Maria Fátima, Robalo Cordeiro Carlos, Herth Felix J F, Thomas Michael, Kriegsmann Mark, Meister Michael, Schneider Marc A, Muley Thomas, Ribeiro Ricar |
The genetic landscape of axonal neuropathies in the middle-aged and elderly: Focus on MME. Neurology 2020 11 95 (24): e3163-e3179. Senderek Jan, Lassuthova Petra, Kabzi?ska Dagmara, Abreu Lisa, Baets Jonathan, Beetz Christian, Braathen Geir J, Brenner David, Dalton Joline, Dankwa Lois, Deconinck Tine, De Jonghe Peter, Dräger Bianca, Eggermann Katja, Ellis Melina, Fischer Carina, Stojkovic Tanya, Herrmann David N, Horvath Rita, Høyer Helle, Iglseder Stephan, Kennerson Marina, Kinslechner Katharina, Kohler Jennefer N, Kurth Ingo, Laing Nigel G, Lamont Phillipa J, Wolfgang N Löscher, Ludolph Albert, Marques Wilson, Nicholson Garth, Ong Royston, Petri Susanne, Ravenscroft Gianina, Rebelo Adriana, Ricci Giulia, Rudnik-Schöneborn Sabine, Schirmacher Anja, Schlotter-Weigel Beate, Schoels Ludger, Schüle Rebecca, Synofzik Matthis, Francou Bruno, Strom Tim M, Wagner Johannes, Walk David, Wanschitz Julia, Weinmann Daniela, Weishaupt Jochen, Wiessner Manuela, Windhager Reinhard, Young Peter, Züchner Stephan, Toegel Stefan, Seeman Pavel, Kocha?ski Andrzej, Auer-Grumbach Michae |
High Genetic Addiction Risk Score (GARS) in Chronically Prescribed Severe Chronic Opioid Probands Attending Multi-pain Clinics: an Open Clinical Pilot Trial. Molecular neurobiology 2021 Mar . Moran Mark, Blum Kenneth, Ponce Jessica Valdez, Lott Lisa, Gondré-Lewis Marjorie C, Badgaiyan Sampada, Brewer Raymond, Downs B William, Fynman Philip, Weingarten Alexander, Cadet Jean Lud, Smith David E, Baron David, Thanos Panayotis K, Modestino Edward J, Badgaiyan Rajendra D, Elman Igor, Gold Mark |
Interaction between glycolysis?cholesterol synthesis axis and tumor microenvironment reveal that gamma-glutamyl hydrolase suppresses glycolysis in colon cancer. Frontiers in immunology 2022 12 13 979521. Chen Yan-Jie, Guo Xi, Liu Meng-Ling, Yu Yi-Yi, Cui Yue-Hong, Shen Xi-Zhong, Liu Tian-Shu, Liang |
A patient with demyelinating CMT carrying the p.Y347C heterozygous variant of the MME gene and the p.L131F heterozygous variant of the HARS1 gene. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2022 12 . Parisi Mattia, Canosa Antonio, Tessa Alessandra, Ferrero Bruno, Gallone Salvato |
Multiple gene variants linked to Alzheimer's-type clinical dementia via GWAS are also associated with non-Alzheimer's neuropathologic entities. Neurobiology of disease 2022 10 174 105880. Katsumata Yuriko, Shade Lincoln M, Hohman Timothy J, Schneider Julie A, Bennett David A, Farfel Jose M, , Kukull Walter A, Fardo David W, Nelson Peter |
Functional mutation, splice, distribution, and divergence analysis of impactful genes associated with heart failure and other cardiovascular diseases. Scientific reports 2023 10 13 (1): 16769. Ishani Mhatre, Habiba Abdelhalim, William Degroat, Shreya Ashok, Bruce T Liang, Zeeshan Ahm |
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- Page last updated:Apr 22, 2024
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