Kcnrg-flox 基因敲除小鼠

1. Cho, Yong Gu, Kim, Chang Jae, Song, Jae Hwi, Lee, Jung Young, Park, Won Sang. . Genetic and expression analysis of the KCNRG gene in hepatocellular carcinomas. In Experimental & molecular medicine, 38, 247-55. doi:. https://pubmed.ncbi.nlm.nih.gov/16819283/

2. Ivanov, D V, Tyazhelova, T V, Lemonnier, L, Yankovsky, N K, Baranova, A V. . A new human gene KCNRG encoding potassium channel regulating protein is a cancer suppressor gene candidate located in 13q14.3. In FEBS letters, 539, 156-60. doi:. https://pubmed.ncbi.nlm.nih.gov/12650944/

3. Birerdinc, Aybike, Nohelty, Elizabeth, Marakhonov, Andrey, Chandhoke, Vikas, Baranova, Ancha. 2009. Pro-apoptotic and antiproliferative activity of human KCNRG, a putative tumor suppressor in 13q14 region. In Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine, 31, 33-45. doi:10.1007/s13277-009-0005-0. https://pubmed.ncbi.nlm.nih.gov/20237900/

4. Lu, Xiaotian, Suo, Langda, Yan, Xiaochun, Wu, Yujiang, Su, Rui. 2024. Genome-wide association analysis of fleece traits in Northwest Xizang white cashmere goat. In Frontiers in veterinary science, 11, 1409084. doi:10.3389/fvets.2024.1409084. https://pubmed.ncbi.nlm.nih.gov/38872797/

5. Alimohammadi, Mohammad, Dubois, Noémie, Sköldberg, Filip, Kämpe, Olle, Carel, Jean-Claude. 2009. Pulmonary autoimmunity as a feature of autoimmune polyendocrine syndrome type 1 and identification of KCNRG as a bronchial autoantigen. In Proceedings of the National Academy of Sciences of the United States of America, 106, 4396-401. doi:10.1073/pnas.0809986106. https://pubmed.ncbi.nlm.nih.gov/19251657/

6. Popler, Jonathan, Alimohammadi, Mohammad, Kämpe, Olle, Soep, Jennifer B, Deterding, Robin R. 2011. Autoimmune polyendocrine syndrome type 1: Utility of KCNRG autoantibodies as a marker of active pulmonary disease and successful treatment with rituximab. In Pediatric pulmonology, 47, 84-7. doi:10.1002/ppul.21520. https://pubmed.ncbi.nlm.nih.gov/21901851/

7. Lacey, Cameron J, Doudney, Kit, Bridgman, Paul G, Cameron, Vicky A, Kennedy, Martin A. 2018. Copy number variants implicate cardiac function and development pathways in earthquake-induced stress cardiomyopathy. In Scientific reports, 8, 7548. doi:10.1038/s41598-018-25827-5. https://pubmed.ncbi.nlm.nih.gov/29765130/

8. Zhou, Weixun, Zeng, Xuan, Liu, Tonghua. . Aberrations of chromosome 13q in gastrointestinal stromal tumors: analysis of 91 cases by fluorescence in situ hybridization (FISH). In Diagnostic molecular pathology : the American journal of surgical pathology, part B, 18, 72-80. doi:10.1097/PDM.0b013e318181fa1f. https://pubmed.ncbi.nlm.nih.gov/19430298/

9. Zúñiga-García, Violeta, Chávez-López, María de Guadalupe, Quintanar-Jurado, Valeria, Pérez-Carreón, Julio Isael, Camacho, Javier. 2015. Differential Expression of Ion Channels and Transporters During Hepatocellular Carcinoma Development. In Digestive diseases and sciences, 60, 2373-83. doi:10.1007/s10620-015-3633-9. https://pubmed.ncbi.nlm.nih.gov/25842354/

10. Wild, Philipp S, Felix, Janine F, Schillert, Arne, Vasan, Ramachandran S, Dörr, Marcus. 2017. Large-scale genome-wide analysis identifies genetic variants associated with cardiac structure and function. In The Journal of clinical investigation, 127, 1798-1812. doi:10.1172/JCI84840. https://pubmed.ncbi.nlm.nih.gov/28394258/