Human Genome Epidemiology Literature Finder
Records 1 - 12 (of 12 Records) |
Query Trace: Abnormalities and INS[original query] |
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The -141C Ins/Del polymorphism of the dopamine D2 receptor gene is not associated with either migraine or Parkinson's disease. Psychiatric genetics 2001 Mar 11 (1): 49-52. Maude S, Curtin J, Breen G, Collier D, Russell G, Shaw D, Clair D |
Molecular defects of the CYP21 gene in Spanish girls with isolated precocious pubarche. European journal of endocrinology / European Federation of Endocrine Societies 2002 Oct 147 (4): 485-8. Potau N, Riqué S, Eduardo I, Marcos V, Ibañez |
Human alpha2-macroglobulin: genotype-phenotype relation. Experimental neurology 2003 Nov 184 (1): 153-61. Birkenmeier G, Müller R, Huse K, Forberg J, Gläser C, Hedrich H, Nicklisch S, Reichenbach |
Lack of association between polymorphisms of dopamine receptors, type D2, and bipolar affective illness in a Polish population. Medical science monitor : international medical journal of experimental and clinical research 2005 Jun 11 (6): CR289-295. Leszczy?ska-Rodziewicz Anna, Hauser Joanna, Dmitrzak-Weglarz Monika, Skibi?ka Maria, Czerski Piotr, Zakrzewska Agnieszka, Kosmowska Magdalena, Rybakowski Janusz |
Endothelial nitric oxide synthase, angiotensin-converting enzyme and angiotensinogen gene polymorphisms in hypertensive disorders of pregnancy. Hypertension research : official journal of the Japanese Society of Hypertension 2010 May 33 (5): 473-7. Aggarwal Pardeep Kumar, Jain Vanita, Jha Vivekana |
Genetic polymorphisms of INS, INSR and IRS-1 genes are not associated with polycystic ovary syndrome in Croatian women. Collegium antropologicum 2013 Mar 37 (1): 141-6. Skrgati? Lana, Baldani Dinka Pavici?, Gersak Ksenija, Cerne Jasmina Ziva, Ferk Polonca, Cori? Mar |
CD36 haplotypes are associated with lipid profile in normal-weight subjects. Lipids in health and disease 2013 12 (1): 167. Ramos-Arellano Luz E, Salgado-Bernabé Aralia B, Guzmán-Guzmán Iris P, Salgado-Goytia Lorenzo, Muñoz-Valle José F, Parra-Rojas Ise |
Clinical characteristics and molecular genetic analysis of 22 patients with neonatal diabetes from the South-Eastern region of Turkey: predominance of non-KATP channel mutations. European journal of endocrinology / European Federation of Endocrine Societies 2015 Jun 172 (6): 697-705. Demirbilek Huseyin, Arya Ved Bhushan, Ozbek Mehmet Nuri, Houghton Jayne A L, Baran Riza Taner, Akar Melek, Tekes Selahattin, Tuzun Heybet, Mackay Deborah J, Flanagan Sarah E, Hattersley Andrew T, Ellard Sian, Hussain Khal |
Plasma soluble HLA-G levels in a cohort of heart failure patients exposed to chemicals. Human immunology 2019 Dec . Bortolotti Daria, Vitali Emanuela, Stendardo Mariarita, Fucili Alessandro, Rizzo Roberta, Boschetto Pie |
HLA-G14bp ins/del polymorphism and post-transplant weight gain in kidney transplantation: potential implications beyond tolerance. BMC nephrology 2020 4 21 (1): 109. Piancatelli Daniela, Maccarone Daniela, Colanardi Alessia, Sebastiani Pierluigi, Clemente Katia, Iesari Samuele, Lai Quirino, Pisani Frances |
3'UTR polymorphism of Thymidylate Synthase gene increased the risk of persistence of pre-neoplastic cervical lesions. BMC cancer 2020 4 20 (1): 323. Silva Nayara Nascimento Toledo, Santos Ana Carolina Silva, Nogueira Verlândia Mendes, Carneiro Cláudia Martins, Lima Angélica Alv |
Role of genetic variants of Vitamin D receptor, Toll-like receptor 2 and Toll-like receptor 4 in extrapulmonary tuberculosis. Microbial pathogenesis 2021 5 156 104911. Wani Bilal Ahmad, Shehjar Faheem, Shah Sonaullah, Koul Ajaz, Yusuf Adfar, Farooq Muzamil, Mir Mohmad Iqbal, Singh Rajni, Afroze D |
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- Page last updated:May 06, 2024
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