Human Genome Epidemiology Literature Finder
|
Records 1 - 11 (of 11 Records) |
| Query Trace: Disease and SLC4A1[original query] |
|---|
| [Polymorphism analysis of G199A, Ncol in ANK1 and Memphis I in SLC4A1 genes in Mexican healthy individuals and subjects affected with hereditary spherocytosis]. Gaceta médica de México 0 142 (5): 435-7. Camacho-Torres Ana Luisa, Sánchez-López Josefina Yoaly, Mesa-Cornejo Viviana Matilde, Ibarra Bertha, Perea-Díaz Francisco Javi |
| Genetic polymorphisms associated with priapism in sickle cell disease. British journal of haematology 2007 May 137 (3): 262-7. Elliott Laine, Ashley-Koch Allison E, De Castro Laura, Jonassaint Jude, Price Jennifer, Ataga Kenneth I, Levesque Marc C, Brice Weinberg J, Eckman James R, Orringer Eugene P, Vance Jeffery M, Telen Marilyn |
| Distribution of Diego blood group alleles and identification of four novel mutations on exon 19 of SLC4A1 gene in the Chinese Han population by polymerase chain reaction sequence-based typing. Vox sanguinis 2011 Apr 100 (3): 317-21. Xu X G, He J, He Y M, Tao S D, Ying Y L, Zhu F M, Lv H J, Yan L |
| Genome-wide differential expression reveals candidate genes involved in the pathogenesis of lupus and lupus nephritis. International journal of rheumatic diseases 2015 Sep . AlFadhli Suad, Ghanem Aqeel A M, Nizam Rashee |
| Clinical and genetic analysis of distal renal tubular acidosis in three Chinese children. Renal failure 2018 9 40 (1): 520-526. Liu Jiaojiao, Shen Qian, Li Guomin, Zhai Yihui, Fang Xiaoyan, Xu Ho |
| Genotype-Phenotype Analysis in Pediatric Patients with Distal Renal Tubular Acidosis. Kidney & blood pressure research 2018 4 43 (2): 513-521. Park Eujin, Cho Myung Hyun, Hyun Hye Sun, Shin Jae Il, Lee Joo Hoon, Park Young Seo, Choi Hyun Jin, Kang Hee Gyung, Cheong Hae |
| Evaluation of phenotypic and genotypic features of children with distal kidney tubular acidosis. Pediatric nephrology (Berlin, Germany) 2020 7 35 (12): 2297-2306. Atmis Bahriye, Cevizli Derya, Melek Engin, Bisgin Atil, Unal Ilker, Anarat Ali, Bayazit Aysun |
Multiple-ancestry genome-wide association study identifies 27 loci associated with measures of hemolysis following blood storage.
The Journal of clinical investigation 2021 May . Page Grier P, Kanias Tamir, Guo Yuelong J, Lanteri Marion C, Zhang Xu, Mast Alan E, Cable Ritchard G, Spencer Bryan R, Kiss Joseph E, Fang Fang, Endres-Dighe Stacy M, Brambilla Donald, Nouraie Mehdi, Gordeuk Victor R, Kleinman Steve, Busch Michael P, Gladwin Mark T, |
| Systematic assessment of monogenic etiology in adult-onset kidney stone formers undergoing urological intervention-evidence for genetic pretest probability. American journal of medical genetics. Part C, Seminars in medical genetics 2022 8 190 (3): 279-288. Schönauer Ria, Scherer Lotte, Nemitz-Kliemchen Melanie, Hagemann Tobias, Hantmann Elena, Seidel Anna, Müller Luise, Kehr Stephanie, Voigt Cornelia, Stolzenburg Jens-Uwe, Halbritter J |
| Frequency of the DI*A, DI*B and Band 3 Memphis polymorphism among distinct groups in Brazil. Hematology, transfusion and cell therapy 2022 May . Kaliniczenko Alessandra, Martins Juliana Oliveira, Cruz Bruno Ribeiro, Chiba Akemi Kuroda, Filho João Paulo Botelho Vieira, Bordin José Orlan |
| Genetic testing enables a precision medicine approach for nephrolithiasis and nephrocalcinosis in pediatrics: a single-center cohort. Molecular genetics and genomics : MGG 2022 May . Huang Lin, Qi Chang, Zhu Gaohong, Ding Juanjuan, Yuan Li, Sun Jie, He Xuelian, Wang Xiaow |
- Page last reviewed:Feb 1, 2024
- Content source: