Human Genome Epidemiology Literature Finder
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Records 1 - 16 (of 16 Records) |
| Query Trace: Disease and KIF1B[original query] |
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| Mitochondrial GTPase mitofusin 2 mutation in Charcot-Marie-Tooth neuropathy type 2A. Human genetics 2005 Jan 116 (1-2): 23-7. Kijima Kazuki, Numakura Chikahiko, Izumino Hiroko, Umetsu Kazuo, Nezu Atsuo, Shiiki Toshihide, Ogawa Masafumi, Ishizaki Yoshito, Kitamura Takeshi, Shozawa Yasunobu, Hayasaka Kiyos |
| Lack of replication of KIF1B gene in an Italian primary progressive multiple sclerosis cohort. European journal of neurology 2010 May 17 (5): 740-5. Martinelli-Boneschi F, Esposito F, Scalabrini D, Fenoglio C, Rodegher M E, Brambilla P, Colombo B, Ghezzi A, Capra R, Collimedaglia L, Coniglio G, De Riz M, Serpente M, Cantoni C, Scarpini E, Martinelli V, Galimberti D, Comi |
| Polymorphic locus rs10492972 of the KIF1B gene association with multiple sclerosis in Russia: case control study. Molecular genetics and metabolism 2011 Nov 104 (3): 390-4. Kudryavtseva Ekaterina A, Rozhdestvenskii Aleksei S, Kakulya Anastasia V, Khanokh Elena V, Delov Roman A, Malkova Nadezhda A, Korobko Denis S, Platonov Fedor A, Aref Eva Elena G, Zagorskaya Natalia N, Aliferova Valentina M, Titova Marina A, Babenko Sergei A, Smagina Inna V, El Chaninova Svetlana A, Zolovkina Anna G, Lifshits G I, Puzyrev Valerii P, Filipenko Maxim |
| When is the absence of evidence, evidence of absence? Use of equivalence-based analyses in genetic epidemiology and a conclusion for the KIF1B rs10492972*C allelic association in multiple sclerosis. Genetic epidemiology 2011 Sep 35 (6): 568-71. Gourraud Pierre-Antoine, |
| Role of single nucleotide polymorphisms of KIF1B gene in HBV-associated viral hepatitis. PloS one 2012 7 (9): 9. Al-Qahtani A, Al-Anazi M, Viswan NA, Khalaf N, Abdo AA, Sanai FM, Al-Ashgar H, Al-Ahdal M |
| [Clinical and electrophysiological and molecular genetic characteristics of the course of relapsing-remitting multiple sclerosis]. Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova / Ministerstvo zdravookhraneniia i meditsinsko? promyshlennosti Rossi?sko? Federatsii, Vserossi?skoe obshchestvo nevrologov [i] Vserossi?skoe obshchestvo psikhiatrov 2013 113 (10): 55-9. Delov R A, Rozhdestvenski? A S, Marks E A, Smialovski? V E, Khanokh E V, Kakulia A V, Sokolova E A, Agapova O |
| Host genetic variants influencing the clinical course of hepatitis B virus infection. Journal of medical virology 2015 Aug . Matsuura Kentaro, Isogawa Masanori, Tanaka Yasuhi |
| [The relationship between the KIF1B (rs17401966) single nucleotide polymorphism and the genetic susceptibility to Hepatocellular carcinoma]. Zhonghua yu fang yi xue za zhi [Chinese journal of preventive medicine] 2015 May 49 (5): 419-23. Pan Huanhuan, Su Chenghao, Lin Yong, Niu Jianj |
| PNPLA3 and TM6SF2 variants as risk factors of hepatocellular carcinoma across various etiologies and severity of underlying liver diseases. International journal of cancer 2018 Oct . Yang Jie, Trépo Eric, Nahon Pierre, Cao Qian, Moreno Christophe, Letouzé Eric, Imbeaud Sandrine, Gustot Thierry, Deviere Jacques, Debette Stéphanie, Amouyel Philippe, Bioulac-Sage Paulette, Calderaro Julien, Ganne-Carrié Nathalie, Laurent Alexis, Blanc Jean Frédéric, Guyot Erwan, Sutton Angela, Ziol Marianne, Zucman-Rossi Jessica, Nault Jean-Charl |
| Molecular analysis and clinical diversity of distal hereditary motor neuropathy. European journal of neurology 2020 4 27 (7): 1319-1326. Liu X, Duan X, Zhang Y, Sun A, Fan |
| Activation of RAS Signalling is Associated with Altered Cell Adhesion in Phaeochromocytoma. International journal of molecular sciences 2020 11 21 (21): . Rossitti Hugo M, Dutta Ravi Kumar, Larsson Catharina, Ghayee Hans K, Söderkvist Peter, Gimm Oliv |
| [Associations of single nucleotide polymorphisms of KIF1B gene with the severity of clinical manifestations of multiple sclerosis]. Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova 2019 119 (10. Vyp. 2): 58-62. Arbusova E E, Selyanina N V, Karakulova Yu |
| The Importance of Multiple Gene Analysis for Diagnosis and Differential Diagnosis in Charcot Marie Tooth Disease. Turkish neurosurgery 2021 6 31 (6): 888-895. Yalcintepe Sinem, Gurkan Hakan, Dogan Ipek Gungor, Demir Selma, Sag Sebnem Ozemri, Kabayegit Zehra Manav, Atli Emine Ikbal, Atli Engin, Eker Damla, Temel Sehime Guls |
| [Risk of Multiple Sclerosis: Analysis of Interactions Between Variants of Nuclear and Mitochondrial Genomes]. Molekuliarnaia biologiia 0 55 (6): 956-964. Kozin M S, Kiselev I S, Baulina N M, Pavlova G V, Boyko A N, Kulakova O G, Favorova O |
| Novel Germline PHD2 Variant in a Metastatic Pheochromocytoma and Chronic Myeloid Leukemia, but in the Absence of Polycythemia. Medicina (Kaunas, Lithuania) 2022 Aug 58 (8): . Provenzano Aldesia, Chetta Massimiliano, De Filpo Giuseppina, Cantini Giulia, La Barbera Andrea, Nesi Gabriella, Santi Raffaella, Martinelli Serena, Rapizzi Elena, Luconi Michaela, Maggi Mario, Mannelli Massimo, Ercolino Tonino, Canu Letiz |
| Mutations of 1p genes do not consistently abrogate tumor suppressor functions in 1p-intact neuroblastoma. BMC cancer 2022 6 22 (1): 717. Kuick Chik Hong, Tan Jia Ying, Jasmine Deborah, Sumanty Tohari, Ng Alvin Y J, Venkatesh Byrrappa, Chen Huiyi, Loh Eva, Jain Sudhanshi, Seow Wan Yi, Ng Eileen H Q, Lian Derrick W Q, Soh Shui Yen, Chang Kenneth T E, Chen Zhi Xiong, Loh Amos H |
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