Browse Items (2 total)

Tags: 2020, Ahram DF, Alders M, American Journal of Human Genetics, Bartolomaeus T, Bauer SB, Baum MA, Blok LS, Bouchard M, Brilstra EH, Buerger F, Challman TD, Chen E, Chen J, congenital anomalies of the kidney and urinary tract, Connaughton DM, Costin CE, Coyaud E, Daga A, Dai R, Daouk GH, Deutsch K, Dipple KM, Duijkers FA, Dworschak GC, Eid LA, extra-renal features, Ferguson M, Ferguson MA, Fick R, FIM, Fisher SE, Fitzpatrick DR, genetic kidney disease, genomic analysis, Gharavi AG, Glass IA, Graham-Paquin AL, Hermle T, Hildebrandt F, Hospital List, Hulick PJ, Hwang D-Y, Ityel H, journalArticle, Kause F, Khokha MK, Kitzler TM, Klämbt V, Kline AD, Kohl S, Kolb A, Kolvenbach CM, Krey I, Kumar S, Laricchia KM, Laurent EMN, Lek M, Lifton RP, Lim TY, Lu W, MacArthur DG, Majmundar AJ, Mane SM, Mann N, Marco EJ, Marquez J, Mefford HC, Nakayama M, Onuchic-Whitford AC, Ottlewski I, Owen DJ, Platzer K, Povolotskaya IS, Rao Jia, Rasouly HM, Raught B, Rehm HL, Reutter HM, Rieke JM, Rodig NM, Salmanullah D, Sanna-Cherchi S, Savatt JM, Schneider R, Seltzsam S, Senguttuvan P, Sharrocks AD, Shcherbakova NV, Shril S, Somers MJG, Squire AE, St-Germain JR, Stein DR, syndromic CAKUT, Tasic V, Terhal PA, Thiffault I, transcription regulator, Traum AZ, van Binsbergen E, van der Ven AT, Vino A, Vivante A, Voinova VY, Wentzensen IM, whole-exome sequencing, Wu CW, Xu H, Youying M, ZMYM2, ZNF198, Zyskind J

Tags: 2010, Alloosh M, artery-disease, Bratz I N, Byrd J P, calcium, calcium channel, Cardiovascular research, Cardiovascular System & Cardiology, cardiovascular-disease, channels, Coronary smooth muscle, diabetic dyslipidemia, Edwards J M, endothelial-cells, Hyperplasia, Intravascular ultrasound, Kumar S, Long X, Neeb Z P, neointimal, Obukhov A G, Orai1, Ossabaw miniature swine, Peller C R, porcine model, smooth-muscle, STIM1, Store-operated, Sturek M, Transient receptor potential 1 channel