Human Genome Epidemiology Literature Finder
Records 1 - 8 (of 8 Records) |
Query Trace: KLF7[original query] |
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Single nucleotide polymorphisms in the gene encoding Krüppel-like factor 7 are associated with type 2 diabetes. Diabetologia 2005 Jul 48 (7): 1315-22. Kanazawa A, Kawamura Y, Sekine A, Iida A, Tsunoda T, Kashiwagi A, Tanaka Y, Babazono T, Matsuda M, Kawai K, Iiizumi T, Fujioka T, Imanishi M, Kaku K, Iwamoto Y, Kawamori R, Kikkawa R, Nakamura Y, Maeda |
Variation in the gene encoding Krüppel-like factor 7 influences body fat: studies of 14 818 Danes. European journal of endocrinology / European Federation of Endocrine Societies 2009 Apr 160 (4): 603-9. Zobel Dorit P, Andreasen Camilla H, Burgdorf Kristoffer S, Andersson Ehm A, Sandbaek Annelli, Lauritzen Torsten, Borch-Johnsen Knut, Jørgensen Torben, Maeda Shiro, Nakamura Yusuke, Eiberg Hans, Pedersen Oluf, Pederse Oluf, Hansen Torb |
Investigation of susceptibility genes triggering lachrymal/salivary gland lesion complications in Japanese patients with type 1 autoimmune pancreatitis.
PloS one 2015 10 (5): e0127078. Oguchi Takaya, Ota Masao, Ito Tetsuya, Hamano Hideaki, Arakura Norikazu, Katsuyama Yoshihiko, Meguro Akira, Kawa Shigeyu |
Genomic Study of Cardiovascular Continuum Comorbidity. Acta naturae 0 7 (3): 89-99. Makeeva O A, Sleptsov A A, Kulish E V, Barbarash O L, Mazur A M, Prokhorchuk E B, Chekanov N N, Stepanov V A, Puzyrev V |
Molecular genetic contributions to self-rated health.
International journal of epidemiology 2016 Nov . Harris Sarah E, Hagenaars Saskia P, Davies Gail, David Hill W, Liewald David C M, Ritchie Stuart J, Marioni Riccardo E, , Sudlow Cathie L M, Wardlaw Joanna M, McIntosh Andrew M, Gale Catharine R, Deary Ian |
Combining CDKN1A gene expression and genome-wide SNPs in a twin cohort to gain insight into the heritability of individual radiosensitivity. Functional & integrative genomics 2019 2 19 (4): 575-585. Zyla Joanna, Kabacik Sylwia, O'Brien Grainne, Wakil Salma, Al-Harbi Najla, Kaprio Jaakko, Badie Christophe, Polanska Joanna, Alsbeih Gha |
A Missense Mutation in the KLF7 Gene Is a Potential Candidate Variant for Congenital Deafness in Australian Stumpy Tail Cattle Dogs. Genes 2021 4 12 (4): . Xu Fangzheng, Shan Shuwen, Sommerlad Susan, Seddon Jennifer M, Brenig Bertr |
Analysis of KLF7 and KLF5 transcription factors genes variants in coronary artery disease. Revista portuguesa de cardiologia : orgao oficial da Sociedade Portuguesa de Cardiologia = Portuguese journal of cardiology : an official journal of the Portuguese Society of Cardiology 2023 6 . Vahid Akbari Kordkheyli, Arash Poursheikhani, Seyed Hasan Sharobandi, Sayed Mostafa Hossei |
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