Martin R. Pollak - Publications

Harvard University, Cambridge, MA, United States 
Genetics, Molecular Biology, Cell Biology

126 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2016 Subramanian B, Sun H, Yan P, Charoonratana VT, Higgs HN, Wang F, Lai KV, Valenzuela DM, Brown EJ, Schlöndorff JS, Pollak MR. Mice with mutant Inf2 show impaired podocyte and slit diaphragm integrity in response to protamine-induced kidney injury. Kidney International. PMID 27350175 DOI: 10.1016/J.Kint.2016.04.020  0.88
2015 Olabisi OA, Zhang JY, VerPlank L, Zahler N, DiBartolo S, Heneghan JF, Schlöndorff JS, Suh JH, Yan P, Alper SL, Friedman DJ, Pollak MR. APOL1 kidney disease risk variants cause cytotoxicity by depleting cellular potassium and inducing stress-activated protein kinases. Proceedings of the National Academy of Sciences of the United States of America. PMID 26699492 DOI: 10.1073/Pnas.1522913113  0.88
2015 Feng D, DuMontier C, Pollak MR. The role of alpha-actinin-4 in human kidney disease. Cell & Bioscience. 5: 44. PMID 26301083 DOI: 10.1186/S13578-015-0036-8  0.88
2015 Sampson MG, Pollak MR. Opportunities and Challenges of Genotyping Patients With Nephrotic Syndrome in the Genomic Era. Seminars in Nephrology. 35: 212-21. PMID 26215859 DOI: 10.1016/J.Semnephrol.2015.04.002  0.88
2015 Toka HR, Pollak MR, Houillier P. Calcium Sensing in the Renal Tubule. Physiology (Bethesda, Md.). 30: 317-26. PMID 26136545 DOI: 10.1152/Physiol.00042.2014  0.88
2015 Pollak MR. Modifiers of Cardiac Phenotypes. Circulation. Cardiovascular Genetics. 8: 425-6. PMID 26082553 DOI: 10.1161/Circgenetics.115.001122  0.88
2015 Ruchi R, Genovese G, Lee J, Charoonratana VT, Bernhardy AJ, Alper SL, Kopp JB, Thadhani R, Friedman DJ, Pollak MR. Copy Number Variation at the APOL1 Locus. Plos One. 10: e0125410. PMID 25933006 DOI: 10.1371/Journal.Pone.0125410  0.88
2015 Ehrlicher AJ, Krishnan R, Guo M, Bidan CM, Weitz DA, Pollak MR. Alpha-actinin binding kinetics modulate cellular dynamics and force generation. Proceedings of the National Academy of Sciences of the United States of America. 112: 6619-24. PMID 25918384 DOI: 10.1073/Pnas.1505652112  0.88
2015 Pollak MR. Idiopathic pediatric chronic kidney disease: can genomic technology crack the case? The Journal of Clinical Investigation. 125: 1799-800. PMID 25893596 DOI: 10.1172/Jci81509  0.88
2015 Kopp JB, Winkler CA, Zhao X, Radeva MK, Gassman JJ, D'Agati VD, Nast CC, Wei C, Reiser J, Guay-Woodford LM, Pollak MR, Hildebrandt F, Moxey-Mims M, Gipson DS, Trachtman H, et al. Clinical Features and Histology of Apolipoprotein L1-Associated Nephropathy in the FSGS Clinical Trial. Journal of the American Society of Nephrology : Jasn. 26: 1443-8. PMID 25573908 DOI: 10.1681/Asn.2013111242  0.88
2015 Nichols B, Jog P, Lee JH, Blackler D, Wilmot M, D'Agati V, Markowitz G, Kopp JB, Alper SL, Pollak MR, Friedman DJ. Innate immunity pathways regulate the nephropathy gene Apolipoprotein L1. Kidney International. 87: 332-42. PMID 25100047 DOI: 10.1038/Ki.2014.270  0.88
2015 Ma L, Shelness GS, Snipes JA, Murea M, Antinozzi PA, Cheng D, Saleem MA, Satchell SC, Banas B, Mathieson PW, Kretzler M, Hemal AK, Rudel LL, Petrovic S, Weckerle A, ... Pollak MR, et al. Localization of APOL1 protein and mRNA in the human kidney: nondiseased tissue, primary cells, and immortalized cell lines. Journal of the American Society of Nephrology : Jasn. 26: 339-48. PMID 25012173 DOI: 10.1681/Asn.2013091017  0.88
2014 Sun H, Al-Romaih KI, MacRae CA, Pollak MR. Human Kidney Disease-causing INF2 Mutations Perturb Rho/Dia Signaling in the Glomerulus. Ebiomedicine. 1: 107-15. PMID 26086034 DOI: 10.1016/J.Ebiom.2014.11.009  0.88
2014 Pollak MR. Familial FSGS. Advances in Chronic Kidney Disease. 21: 422-5. PMID 25168831 DOI: 10.1053/j.ackd.2014.06.001  0.88
2014 Toka HR, Pollak MR. The role of the calcium-sensing receptor in disorders of abnormal calcium handling and cardiovascular disease. Current Opinion in Nephrology and Hypertension. 23: 494-501. PMID 24992569 DOI: 10.1097/Mnh.0000000000000042  0.88
2014 Grgic I, Hofmeister AF, Genovese G, Bernhardy AJ, Sun H, Maarouf OH, Bijol V, Pollak MR, Humphreys BD. Discovery of new glomerular disease-relevant genes by translational profiling of podocytes in vivo. Kidney International. 86: 1116-29. PMID 24940801 DOI: 10.1038/Ki.2014.204  0.88
2014 Pollak MR, Quaggin SE, Hoenig MP, Dworkin LD. The glomerulus: the sphere of influence. Clinical Journal of the American Society of Nephrology : Cjasn. 9: 1461-9. PMID 24875196 DOI: 10.2215/Cjn.09400913  0.88
2014 Thomson R, Genovese G, Canon C, Kovacsics D, Higgins MK, Carrington M, Winkler CA, Kopp J, Rotimi C, Adeyemo A, Doumatey A, Ayodo G, Alper SL, Pollak MR, Friedman DJ, et al. Evolution of the primate trypanolytic factor APOL1. Proceedings of the National Academy of Sciences of the United States of America. 111: E2130-9. PMID 24808134 DOI: 10.1073/Pnas.1400699111  0.88
2014 Gbadegesin RA, Hall G, Adeyemo A, Hanke N, Tossidou I, Burchette J, Wu G, Homstad A, Sparks MA, Gomez J, Jiang R, Alonso A, Lavin P, Conlon P, Korstanje R, ... ... Pollak MR, et al. Mutations in the gene that encodes the F-actin binding protein anillin cause FSGS. Journal of the American Society of Nephrology : Jasn. 25: 1991-2002. PMID 24676636 DOI: 10.1681/Asn.2013090976  0.88
2014 Barua M, Stellacci E, Stella L, Weins A, Genovese G, Muto V, Caputo V, Toka HR, Charoonratana VT, Tartaglia M, Pollak MR. Mutations in PAX2 associate with adult-onset FSGS. Journal of the American Society of Nephrology : Jasn. 25: 1942-53. PMID 24676634 DOI: 10.1681/Asn.2013070686  0.88
2014 Brown EJ, Pollak MR, Barua M. Genetic testing for nephrotic syndrome and FSGS in the era of next-generation sequencing. Kidney International. 85: 1030-8. PMID 24599252 DOI: 10.1038/Ki.2014.48  0.88
2014 Ito K, Bick AG, Flannick J, Friedman DJ, Genovese G, Parfenov MG, Depalma SR, Gupta N, Gabriel SB, Taylor HA, Fox ER, Newton-Cheh C, Kathiresan S, Hirschhorn JN, Altshuler DM, ... Pollak MR, et al. Increased burden of cardiovascular disease in carriers of APOL1 genetic variants. Circulation Research. 114: 845-50. PMID 24379297 DOI: 10.1161/Circresaha.114.302347  0.88
2014 Bruggeman LA, O'Toole JF, Ross MD, Madhavan SM, Smurzynski M, Wu K, Bosch RJ, Gupta S, Pollak MR, Sedor JR, Kalayjian RC. Plasma apolipoprotein L1 levels do not correlate with CKD. Journal of the American Society of Nephrology : Jasn. 25: 634-44. PMID 24231663 DOI: 10.1681/Asn.2013070700  0.88
2014 Barua M, Shieh E, Schlondorff J, Genovese G, Kaplan BS, Pollak MR. Exome sequencing and in vitro studies identified podocalyxin as a candidate gene for focal and segmental glomerulosclerosis. Kidney International. 85: 124-33. PMID 24048372 DOI: 10.1038/Ki.2013.354  0.88
2014 Barua M, Pollak MR. Focal and segmental glomerulosclerosis Core Concepts in Parenchymal Kidney Disease. 2147483647: 33-49. DOI: 10.1007/978-1-4614-8166-9_4  0.88
2013 Williams WW, Pollak MR. Health disparities in kidney disease - Emerging data from the human genome New England Journal of Medicine. 369: 2260-2261. PMID 24206461 DOI: 10.1056/Nejme1312797  0.88
2013 Toka HR, Genovese G, Mount DB, Pollak MR, Curhan GC. Frequency of rare allelic variation in candidate genes among individuals with low and high urinary calcium excretion. Plos One. 8: e71885. PMID 23991001 DOI: 10.1371/Journal.Pone.0071885  0.88
2013 Toka HR, Yang J, Zera CA, Duffield JS, Pollak MR, Mount DB. Pregnancy-associated polyuria in familial renal glycosuria. American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation. 62: 1160-4. PMID 23871407 DOI: 10.1053/J.Ajkd.2013.05.018  0.88
2013 Sun H, Schlondorff J, Higgs HN, Pollak MR. Inverted formin 2 regulates actin dynamics by antagonizing Rho/diaphanous-related formin signaling. Journal of the American Society of Nephrology : Jasn. 24: 917-29. PMID 23620398 DOI: 10.1681/Asn.2012080834  0.88
2013 Romero JR, Youte R, Brown EM, Pollak MR, Goltzman D, Karaplis A, Pong LC, Chien L, Chattopadhyay N, Rivera A. Parathyroid hormone ablation alters erythrocyte parameters that are rescued by calcium-sensing receptor gene deletion European Journal of Haematology. 91: 37-45. PMID 23528155 DOI: 10.1111/Ejh.12110  0.88
2013 Genovese G, Friedman DJ, Pollak MR. APOL1 variants and kidney disease in people of recent African ancestry. Nature Reviews. Nephrology. 9: 240-4. PMID 23438974 DOI: 10.1038/Nrneph.2013.34  0.88
2013 Genovese G, Handsaker RE, Li H, Altemose N, Lindgren AM, Chambert K, Pasaniuc B, Price AL, Reich D, Morton CC, Pollak MR, Wilson JG, McCarroll SA. Using population admixture to help complete maps of the human genome. Nature Genetics. 45: 406-14, 414e1-2. PMID 23435088 DOI: 10.1038/Ng.2565  0.88
2013 Kirby A, Gnirke A, Jaffe DB, Barešová V, Pochet N, Blumenstiel B, Ye C, Aird D, Stevens C, Robinson JT, Cabili MN, Gat-Viks I, Kelliher E, Daza R, DeFelice M, ... ... Pollak MR, et al. Mutations causing medullary cystic kidney disease type 1 lie in a large VNTR in MUC1 missed by massively parallel sequencing. Nature Genetics. 45: 299-303. PMID 23396133 DOI: 10.1038/Ng.2543  0.88
2013 Yao NY, Broedersz CP, Depken M, Becker DJ, Pollak MR, Mackintosh FC, Weitz DA. Stress-enhanced gelation: a dynamic nonlinearity of elasticity. Physical Review Letters. 110: 018103. PMID 23383843 DOI: 10.1103/Physrevlett.110.018103  0.88
2013 Quinn SJ, Thomsen ARB, Egbuna O, Pang J, Baxi K, Goltzman D, Pollak M, Brown EM. CaSR-mediated interactions between calcium and magnesium homeostasis in mice American Journal of Physiology - Endocrinology and Metabolism. 304: E724-E733. PMID 23360827 DOI: 10.1152/Ajpendo.00557.2012  0.88
2013 Quinn SJ, Thomsen ARB, Pang JL, Kantham L, Bräuner-Osborne H, Pollak M, Goltzman D, Brown EM. Interactions between calcium and phosphorus in the regulation of the production of fibroblast growth factor 23 in vivo American Journal of Physiology - Endocrinology and Metabolism. 304: E310-E320. PMID 23233539 DOI: 10.1152/Ajpendo.00460.2012  0.88
2013 Barua M, Brown EJ, Charoonratana VT, Genovese G, Sun H, Pollak MR. Mutations in the INF2 gene account for a significant proportion of familial but not sporadic focal and segmental glomerulosclerosis. Kidney International. 83: 316-22. PMID 23014460 DOI: 10.1038/Ki.2012.349  0.88
2012 Carrasquillo R, Tian D, Krishna S, Pollak MR, Greka A, Schlöndorff J. SNF8, a member of the ESCRT-II complex, interacts with TRPC6 and enhances its channel activity. Bmc Cell Biology. 13: 33. PMID 23171048 DOI: 10.1186/1471-2121-13-33  0.88
2012 Toka HR, Al-Romaih K, Koshy JM, DiBartolo S, Kos CH, Quinn SJ, Curhan GC, Mount DB, Brown EM, Pollak MR. Deficiency of the calcium-sensing receptor in the kidney causes parathyroid hormone-independent hypocalciuria. Journal of the American Society of Nephrology : Jasn. 23: 1879-90. PMID 22997254 DOI: 10.1681/Asn.2012030323  0.88
2012 Lee BT, Kumar V, Williams TA, Abdi R, Bernhardy A, Dyer C, Conte S, Genovese G, Ross MD, Friedman DJ, Gaston R, Milford E, Pollak MR, Chandraker A. The APOL1 genotype of African American kidney transplant recipients does not impact 5-year allograft survival American Journal of Transplantation. 12: 1924-1928. PMID 22487534 DOI: 10.1111/J.1600-6143.2012.04033.X  0.88
2012 Xue Y, Xiao Y, Liu J, Karaplis AC, Pollak MR, Brown EM, Miao D, Goltzman D. The calcium-sensing receptor complements parathyroid hormone-induced bone turnover in discrete skeletal compartments in mice. American Journal of Physiology. Endocrinology and Metabolism. 302: E841-51. PMID 22275754 DOI: 10.1152/Ajpendo.00599.2011  0.88
2012 Pollak MR, Genovese G, Friedman DJ. APOL1 and kidney disease. Current Opinion in Nephrology and Hypertension. 21: 179-82. PMID 22257798 DOI: 10.1097/Mnh.0B013E32835012Ab  0.88
2012 Boucher I, Yu W, Beaudry S, Negoro H, Tran M, Pollak MR, Henderson JM, Denker BM. Gα12 activation in podocytes leads to cumulative changes in glomerular collagen expression, proteinuria and glomerulosclerosis. Laboratory Investigation; a Journal of Technical Methods and Pathology. 92: 662-75. PMID 22249312 DOI: 10.1038/Labinvest.2011.198  0.88
2011 Kanji Z, Powe CE, Wenger JB, Huang C, Ankers E, Sullivan DA, Collerone G, Powe NR, Tonelli M, Bhan I, Bernhardy AJ, Dibartolo S, Friedman D, Genovese G, Pollak MR, et al. Genetic variation in APOL1 associates with younger age at hemodialysis initiation. Journal of the American Society of Nephrology : Jasn. 22: 2091-7. PMID 21997398 DOI: 10.1681/Asn.2010121234  0.88
2011 Friedman DJ, Kozlitina J, Genovese G, Jog P, Pollak MR. Population-based risk assessment of APOL1 on renal disease. Journal of the American Society of Nephrology : Jasn. 22: 2098-105. PMID 21997396 DOI: 10.1681/Asn.2011050519  0.88
2011 Kopp JB, Nelson GW, Sampath K, Johnson RC, Genovese G, An P, Friedman D, Briggs W, Dart R, Korbet S, Mokrzycki MH, Kimmel PL, Limou S, Ahuja TS, Berns JS, ... ... Pollak M, et al. APOL1 genetic variants in focal segmental glomerulosclerosis and HIV-associated nephropathy. Journal of the American Society of Nephrology : Jasn. 22: 2129-37. PMID 21997394 DOI: 10.1681/Asn.2011040388  0.88
2011 Akilesh S, Suleiman H, Yu H, Stander MC, Lavin P, Gbadegesin R, Antignac C, Pollak M, Kopp JB, Winn MP, Shaw AS. Arhgap24 inactivates Rac1 in mouse podocytes, and a mutant form is associated with familial focal segmental glomerulosclerosis. The Journal of Clinical Investigation. 121: 4127-37. PMID 21911940 DOI: 10.1172/Jci46458  0.88
2011 Friedman DJ, Pollak MR. Genetics of kidney failure and the evolving story of APOL1 Journal of Clinical Investigation. 121: 3367-3374. PMID 21881214 DOI: 10.1172/Jci46263  0.88
2011 Shankland SJ, Pollak MR. A suPAR circulating factor causes kidney disease. Nature Medicine. 17: 926-7. PMID 21818086 DOI: 10.1038/Nm.2443  0.88
2011 Yao NY, Becker DJ, Broedersz CP, Depken M, Mackintosh FC, Pollak MR, Weitz DA. Nonlinear viscoelasticity of actin transiently cross-linked with mutant α-actinin-4. Journal of Molecular Biology. 411: 1062-71. PMID 21762701 DOI: 10.1016/J.Jmb.2011.06.049  0.88
2011 Al-Romaih KI, Genovese G, Al-Mojalli H, Al-Othman S, Al-Manea H, Al-Suleiman M, Al-Jondubi M, Atallah N, Al-Rodayyan M, Weins A, Pollak MR, Adra CN. Genetic diagnosis in consanguineous families with kidney disease by homozygosity mapping coupled with whole-exome sequencing. American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation. 58: 186-95. PMID 21658830 DOI: 10.1053/J.Ajkd.2011.01.025  0.88
2011 Shu L, Ji J, Zhu Q, Cao G, Karaplis A, Pollak MR, Brown E, Goltzman D, Miao D. The calcium-sensing receptor mediates bone turnover induced by dietary calcium and parathyroid hormone in neonates. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. 26: 1057-71. PMID 21542007 DOI: 10.1002/Jbmr.300  0.88
2011 Liakopoulos V, Huerta A, Cohen S, Pollak MR, Sirota RA, Superdock K, Appel GB. Familial collapsing focal segmental glomerulosclerosis Clinical Nephrology. 75: 362-368. PMID 21426891 DOI: 10.5414/Cn106544  0.88
2011 Sun H, Schlondorff JS, Brown EJ, Higgs HN, Pollak MR. Rho activation of mDia formins is modulated by an interaction with inverted formin 2 (INF2). Proceedings of the National Academy of Sciences of the United States of America. 108: 2933-8. PMID 21278336 DOI: 10.1073/Pnas.1017010108  0.88
2011 Wyss HM, Henderson JM, Byfield FJ, Bruggeman LA, Ding Y, Huang C, Suh JH, Franke T, Mele E, Pollak MR, Miner JH, Janmey PA, Weitz DA, Miller RT. Biophysical properties of normal and diseased renal glomeruli. American Journal of Physiology. Cell Physiology. 300: C397-405. PMID 21123730 DOI: 10.1152/Ajpcell.00438.2010  0.88
2010 Broedersz CP, Depken M, Yao NY, Pollak MR, Weitz DA, MacKintosh FC. Cross-link-governed dynamics of biopolymer networks. Physical Review Letters. 105: 238101. PMID 21231506 DOI: 10.1103/Physrevlett.105.238101  0.88
2010 Shao H, Wang JH, Pollak MR, Wells A. α-actinin-4 is essential for maintaining the spreading, motility and contractility of fibroblasts. Plos One. 5: e13921. PMID 21085685 DOI: 10.1371/Journal.Pone.0013921  0.88
2010 Gu C, Yaddanapudi S, Weins A, Osborn T, Reiser J, Pollak M, Hartwig J, Sever S. Direct dynamin-actin interactions regulate the actin cytoskeleton. The Embo Journal. 29: 3593-606. PMID 20935625 DOI: 10.1038/Emboj.2010.249  0.88
2010 Feng J, Petersen CD, Coy DH, Jiang JK, Thomas CJ, Pollak MR, Wank SA. Calcium-sensing receptor is a physiologic multimodal chemosensor regulating gastric G-cell growth and gastrin secretion. Proceedings of the National Academy of Sciences of the United States of America. 107: 17791-6. PMID 20876097 DOI: 10.1073/Pnas.1009078107  0.88
2010 Parikh SM, Pollak MR. VEGF receptors and glomerular function. Journal of the American Society of Nephrology : Jasn. 21: 1599-600. PMID 20847145 DOI: 10.1681/Asn.2010080871  0.88
2010 Pollak MR. Genetics and genetic testing in kidney disease: introduction. Seminars in Nephrology. 30: 355. PMID 20807607 DOI: 10.1016/J.Semnephrol.2010.06.001  0.88
2010 Freedman BI, Kopp JB, Langefeld CD, Genovese G, Friedman DJ, Nelson GW, Winkler CA, Bowden DW, Pollak MR. The apolipoprotein L1 (APOL1) gene and nondiabetic nephropathy in African Americans. Journal of the American Society of Nephrology : Jasn. 21: 1422-6. PMID 20688934 DOI: 10.1681/Asn.2010070730  0.88
2010 Genovese G, Tonna SJ, Knob AU, Appel GB, Katz A, Bernhardy AJ, Needham AW, Lazarus R, Pollak MR. A risk allele for focal segmental glomerulosclerosis in African Americans is located within a region containing APOL1 and MYH9. Kidney International. 78: 698-704. PMID 20668430 DOI: 10.1038/Ki.2010.251  0.88
2010 Genovese G, Friedman DJ, Ross MD, Lecordier L, Uzureau P, Freedman BI, Bowden DW, Langefeld CD, Oleksyk TK, Uscinski Knob AL, Bernhardy AJ, Hicks PJ, Nelson GW, Vanhollebeke B, Winkler CA, ... ... Pollak MR, et al. Association of trypanolytic ApoL1 variants with kidney disease in African Americans. Science (New York, N.Y.). 329: 841-5. PMID 20647424 DOI: 10.1126/Science.1193032  0.88
2010 Genovese G, Leibon G, Pollak MR, Rockmore DN. Improved IBD detection using incomplete haplotype information. Bmc Genetics. 11: 58. PMID 20591167 DOI: 10.1186/1471-2156-11-58  0.88
2010 Rhee EP, Souza A, Farrell L, Pollak MR, Lewis GD, Steele DJ, Thadhani R, Clish CB, Greka A, Gerszten RE. Metabolite profiling identifies markers of uremia. Journal of the American Society of Nephrology : Jasn. 21: 1041-1051. PMID 20378825 DOI: 10.1681/Asn.2009111132  0.88
2010 Sun W, Sun W, Liu J, Zhou X, Xiao Y, Karaplis A, Pollak MR, Brown E, Goltzman D, Miao D. Alterations in phosphorus, calcium and PTHrP contribute to defects in dental and dental alveolar bone formation in calcium-sensing receptor-deficient mice. Development (Cambridge, England). 137: 985-92. PMID 20150282 DOI: 10.1242/Dev.045898  0.88
2010 Brown EJ, Schlöndorff JS, Becker DJ, Tsukaguchi H, Tonna SJ, Uscinski AL, Higgs HN, Henderson JM, Pollak MR. Mutations in the formin gene INF2 cause focal segmental glomerulosclerosis. Nature Genetics. 42: 72-6. PMID 20023659 DOI: 10.1038/Ng.505  0.88
2009 Pollak MR. Expanding the spectrum of NPHS1-associated disease. Kidney International. 76: 1221-3. PMID 19946311 DOI: 10.1038/Ki.2009.391  0.88
2009 Kantham L, Quinn SJ, Egbuna OI, Baxi K, Butters R, Pang JL, Pollak MR, Goltzman D, Brown EM. The calcium-sensing receptor (CaSR) defends against hypercalcemia independently of its regulation of parathyroid hormone secretion. American Journal of Physiology. Endocrinology and Metabolism. 297: E915-23. PMID 19797241 DOI: 10.1152/Ajpendo.00315.2009  0.88
2009 Pollak MR. Surprising results following conditional podocyte inactivation. Journal of the American Society of Nephrology : Jasn. 20: 2086-8. PMID 19762489 DOI: 10.1681/Asn.2009080854  0.88
2009 Henderson JM, Alexander MP, Pollak MR. Patients with ACTN4 mutations demonstrate distinctive features of glomerular injury. Journal of the American Society of Nephrology : Jasn. 20: 961-8. PMID 19357256 DOI: 10.1681/Asn.2008060613  0.88
2009 Schlöndorff J, Del Camino D, Carrasquillo R, Lacey V, Pollak MR. TRPC6 mutations associated with focal segmental glomerulosclerosis cause constitutive activation of NFAT-dependent transcription. American Journal of Physiology. Cell Physiology. 296: C558-69. PMID 19129465 DOI: 10.1152/Ajpcell.00077.2008  0.88
2008 Tonna SJ, Needham A, Polu K, Uscinski A, Appel GB, Falk RJ, Katz A, Al-Waheeb S, Kaplan BS, Jerums G, Savige J, Harmon J, Zhang K, Curhan GC, Pollak MR. NPHS2 variation in focal and segmental glomerulosclerosis. Bmc Nephrology. 9: 13. PMID 18823551 DOI: 10.1186/1471-2369-9-13  0.88
2008 Pollak MR. Kidney disease and African ancestry. Nature Genetics. 40: 1145-6. PMID 18818713 DOI: 10.1038/Ng1008-1145  0.88
2008 Ward SM, Weins A, Pollak MR, Weitz DA. Dynamic viscoelasticity of actin cross-linked with wild-type and disease-causing mutant alpha-actinin-4. Biophysical Journal. 95: 4915-23. PMID 18689451 DOI: 10.1529/Biophysj.108.131722  0.88
2008 Forman JP, Fisher ND, Pollak MR, Cox DG, Tonna S, Curhan GC. Renin-angiotensin system polymorphisms and risk of hypertension: influence of environmental factors. Journal of Clinical Hypertension (Greenwich, Conn.). 10: 459-66. PMID 18550936 DOI: 10.1111/J.1751-7176.2008.08007.X  0.88
2008 Leibon G, Rockmore DN, Pollak MR. A SNP streak model for the identification of genetic regions identical-by-descent. Statistical Applications in Genetics and Molecular Biology. 7: Article16. PMID 18518857 DOI: 10.2202/1544-6115.1340  0.88
2008 Tong Z, Yang Z, Patel S, Chen H, Gibbs D, Yang X, Hau VS, Kaminoh Y, Harmon J, Pearson E, Buehler J, Chen Y, Yu B, Tinkham NH, Zabriskie NA, ... ... Pollak MR, et al. Promoter polymorphism of the erythropoietin gene in severe diabetic eye and kidney complications. Proceedings of the National Academy of Sciences of the United States of America. 105: 6998-7003. PMID 18458324 DOI: 10.1073/Pnas.0800454105  0.88
2008 Pollak MR. Focal segmental glomerulosclerosis: recent advances. Current Opinion in Nephrology and Hypertension. 17: 138-42. PMID 18277145 DOI: 10.1097/Mnh.0B013E3282F5Dbe4  0.88
2008 Tonna S, Dandapani SV, Uscinski A, Appel GB, Schlöndorff JS, Zhang K, Denker BM, Pollak MR. Functional genetic variation in aminopeptidase A (ENPEP): lack of clear association with focal and segmental glomerulosclerosis (FSGS). Gene. 410: 44-52. PMID 18206321 DOI: 10.1016/J.Gene.2007.11.014  0.88
2008 Henderson JM, Al-Waheeb S, Weins A, Dandapani SV, Pollak MR. Mice with altered alpha-actinin-4 expression have distinct morphologic patterns of glomerular disease. Kidney International. 73: 741-50. PMID 18185509 DOI: 10.1038/Sj.Ki.5002751  0.88
2008 Lee SH, Weins A, Hayes DB, Pollak MR, Dominguez R. Crystal structure of the actin-binding domain of alpha-actinin-4 Lys255Glu mutant implicated in focal segmental glomerulosclerosis. Journal of Molecular Biology. 376: 317-24. PMID 18164029 DOI: 10.1016/J.Jmb.2007.11.084  0.88
2008 Weins A, Pollak MR. Inherited nephroses Molecular and Genetic Basis of Renal Disease. 141-150. DOI: 10.1016/B978-1-4160-0252-9.50013-6  0.88
2008 Pollak MR, Mount DB. The impact of molecular genetics on nephrology Molecular and Genetic Basis of Renal Disease. 1-2. DOI: 10.1016/B978-1-4160-0252-9.50005-7  0.88
2007 Mistry K, Ireland JH, Ng RC, Henderson JM, Pollak MR. Novel mutations in NPHP4 in a consanguineous family with histological findings of focal segmental glomerulosclerosis. American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation. 50: 855-64. PMID 17954299 DOI: 10.1053/J.Ajkd.2007.08.009  0.88
2007 Pollak MR, Alexander MP, Henderson JM. A case of familial kidney disease. Clinical Journal of the American Society of Nephrology : Cjasn. 2: 1367-74. PMID 17942774 DOI: 10.2215/Cjn.02040507  0.88
2007 Weins A, Schlondorff JS, Nakamura F, Denker BM, Hartwig JH, Stossel TP, Pollak MR. Disease-associated mutant alpha-actinin-4 reveals a mechanism for regulating its F-actin-binding affinity. Proceedings of the National Academy of Sciences of the United States of America. 104: 16080-5. PMID 17901210 DOI: 10.1073/Pnas.0702451104  0.88
2007 Copelovitch L, Guttenberg M, Pollak MR, Kaplan BS. Renin-angiotensin axis blockade reduces proteinuria in presymptomatic patients with familial FSGS. Pediatric Nephrology (Berlin, Germany). 22: 1779-84. PMID 17530296 DOI: 10.1007/S00467-007-0505-3  0.88
2007 Dandapani SV, Sugimoto H, Matthews BD, Kolb RJ, Sinha S, Gerszten RE, Zhou J, Ingber DE, Kalluri R, Pollak MR. Alpha-actinin-4 is required for normal podocyte adhesion. The Journal of Biological Chemistry. 282: 467-77. PMID 17082197 DOI: 10.1074/Jbc.M605024200  0.88
2007 Chattopadhyay N, Jeong KH, Yano S, Huang S, Pang JL, Ren X, Terwilliger E, Kaiser UB, Vassilev PM, Pollak MR, Brown EM. Calcium receptor stimulates chemotaxis and secretion of MCP-1 in GnRH neurons in vitro: potential impact on reduced GnRH neuron population in CaR-null mice. American Journal of Physiology. Endocrinology and Metabolism. 292: E523-32. PMID 17003237 DOI: 10.1152/Ajpendo.00372.2005  0.88
2006 Schlöndorff JS, Pollak MR. TRPC6 in glomerular health and disease: what we know and what we believe. Seminars in Cell & Developmental Biology. 17: 667-74. PMID 17116414 DOI: 10.1016/J.Semcdb.2006.11.003  0.88
2006 Dandapani SV, Pollak MR. The glomerular filter: Biologic and genetic complexity. Kidney International. 70: 980-2. PMID 16957744 DOI: 10.1038/Sj.Ki.5001801  0.88
2006 Möller CC, Pollak MR, Reiser J. The genetic basis of human glomerular disease. Advances in Chronic Kidney Disease. 13: 166-73. PMID 16580618 DOI: 10.1053/J.Ackd.2006.01.009  0.88
2006 Adams GB, Chabner KT, Alley IR, Olson DP, Szczepiorkowski ZM, Poznansky MC, Kos CH, Pollak MR, Brown EM, Scadden DT. Stem cell engraftment at the endosteal niche is specified by the calcium-sensing receptor. Nature. 439: 599-603. PMID 16382241 DOI: 10.1038/Nature04247  0.88
2005 Weins A, Kenlan P, Herbert S, Le TC, Villegas I, Kaplan BS, Appel GB, Pollak MR. Mutational and Biological Analysis of alpha-actinin-4 in focal segmental glomerulosclerosis. Journal of the American Society of Nephrology : Jasn. 16: 3694-701. PMID 16251236 DOI: 10.1681/Asn.2005070706  0.88
2005 Reiser J, Polu KR, Möller CC, Kenlan P, Altintas MM, Wei C, Faul C, Herbert S, Villegas I, Avila-Casado C, McGee M, Sugimoto H, Brown D, Kalluri R, Mundel P, ... ... Pollak MR, et al. TRPC6 is a glomerular slit diaphragm-associated channel required for normal renal function. Nature Genetics. 37: 739-44. PMID 15924139 DOI: 10.1038/Ng1592  0.88
2005 Hunt JL, Pollak MR, Denker BM. Cultured podocytes establish a size-selective barrier regulated by specific signaling pathways and demonstrate synchronized barrier assembly in a calcium switch model of junction formation Journal of the American Society of Nephrology. 16: 1593-1602. PMID 15843471 DOI: 10.1681/Asn.2004080679  0.88
2005 Leykin I, Hao K, Cheng J, Meyer N, Pollak MR, Smith RJ, Wong WH, Rosenow C, Li C. Comparative linkage analysis and visualization of high-density oligonucleotide SNP array data. Bmc Genetics. 6: 7. PMID 15713228 DOI: 10.1186/1471-2156-6-7  0.88
2004 Ellinor PT, Moore RK, Patton KK, Ruskin JN, Pollak MR, Macrae CA. Mutations in the long QT gene, KCNQ1, are an uncommon cause of atrial fibrillation. Heart (British Cardiac Society). 90: 1487-8. PMID 15547041 DOI: 10.1136/Hrt.2003.027227  0.88
2004 Yao J, Le TC, Kos CH, Henderson JM, Allen PG, Denker BM, Pollak MR. Alpha-actinin-4-mediated FSGS: an inherited kidney disease caused by an aggregated and rapidly degraded cytoskeletal protein. Plos Biology. 2: e167. PMID 15208719 DOI: 10.1371/Journal.Pbio.0020167  0.88
2004 Pereira AC, Pereira AB, Mota GF, Cunha RS, Herkenhoff FL, Pollak MR, Mill JG, Krieger JE. NPHS2 R229Q functional variant is associated with microalbuminuria in the general population. Kidney International. 65: 1026-30. PMID 14871423 DOI: 10.1111/J.1523-1755.2004.00479.X  0.88
2003 Kos CH, Le TC, Sinha S, Henderson JM, Kim SH, Sugimoto H, Kalluri R, Gerszten RE, Pollak MR. Mice deficient in alpha-actinin-4 have severe glomerular disease. The Journal of Clinical Investigation. 111: 1683-90. PMID 12782671 DOI: 10.1172/Jci17988  0.88
2003 Pollak MR. The genetic basis of FSGS and steroid-resistant nephrosis. Seminars in Nephrology. 23: 141-6. PMID 12704574 DOI: 10.1053/Snep.2003.50014  0.88
2003 Kos CH, Karaplis AC, Peng JB, Hediger MA, Goltzman D, Mohammad KS, Guise TA, Pollak MR. The calcium-sensing receptor is required for normal calcium homeostasis independent of parathyroid hormone. The Journal of Clinical Investigation. 111: 1021-8. PMID 12671051 DOI: 10.1172/Jci17416  0.88
2002 Tsukaguchi H, Sudhakar A, Le TC, Nguyen T, Yao J, Schwimmer JA, Schachter AD, Poch E, Abreu PF, Appel GB, Pereira AB, Kalluri R, Pollak MR. NPHS2 mutations in late-onset focal segmental glomerulosclerosis: R229Q is a common disease-associated allele. The Journal of Clinical Investigation. 110: 1659-66. PMID 12464671 DOI: 10.1172/Jci16242  0.88
2002 Pollak MR. Inherited podocytopathies: FSGS and nephrotic syndrome from a genetic viewpoint. Journal of the American Society of Nephrology : Jasn. 13: 3016-23. PMID 12444222 DOI: 10.1097/01.Asn.0000039569.34360.5E  0.88
2001 Kaplan J, Pollak MR. Familial focal segmental glomerulosclerosis Current Opinion in Nephrology and Hypertension. 10: 183-187. PMID 11224692 DOI: 10.1097/00041552-200103000-00005  0.88
2000 Olszak IT, Poznansky MC, Evans RH, Olson D, Kos C, Pollak MR, Brown EM, Scadden DT. Extracellular calcium elicits a chemokinetic response from monocytes in vitro and in vivo Journal of Clinical Investigation. 105: 1299-1305. PMID 10792005 DOI: 10.1172/Jci9799  0.88
2000 Kaplan JM, Kim SH, North KN, Rennke H, Correia LA, Tong HQ, Mathis BJ, Rodríguez-Pérez JC, Allen PG, Beggs AH, Pollak MR. Mutations in ACTN4, encoding alpha-actinin-4, cause familial focal segmental glomerulosclerosis. Nature Genetics. 24: 251-6. PMID 10700177 DOI: 10.1038/73456  0.88
1998 Brown EM, Pollak M, Hebert SC. The extracellular calcium-sensing receptor: Its role in health and disease Annual Review of Medicine. 49: 15-29. PMID 9509247 DOI: 10.1146/Annurev.Med.49.1.15  0.88
1998 Mathis BJ, Kim SH, Calabrese K, Haas M, Seidman JG, Seidman CE, Pollak MR. A locus for inherited focal segmental glomerulosclerosis maps to chromosome 19q13: Rapid communication Kidney International. 53: 282-286. PMID 9461087 DOI: 10.1046/J.1523-1755.1998.00828.X  0.88
1997 Pollak MR, Brown EM. Chapter 8 Molecular aspects of familial hypocalciuric hypercalcemia Advances in Molecular and Cellular Endocrinology. 1: 229-239. DOI: 10.1016/S1569-2566(97)80039-7  0.88
1996 Pollak MR, Seidman CE, Brown EM. Three inherited disorders of calcium sensing Medicine. 75: 115-123. PMID 8965680 DOI: 10.1097/00005792-199605000-00001  0.88
1996 Bai M, Quinn S, Trivedi S, Kifor O, Pearce SHS, Pollak MR, Krapcho K, Hebert SC, Brown EM. Expression and characterization of inactivating and activating mutations in the human Ca2+(o)-sensing receptor Journal of Biological Chemistry. 271: 19537-19545. PMID 8702647 DOI: 10.1074/Jbc.271.32.19537  0.88
1995 Brown EM, Pollak M, Chou YH, Seidman CE, Seidman JG, Hebert SC. Cloning and functional characterization of extracellular Ca2+-sensing receptors from parathyroid and kidney Bone. 17. PMID 8579901 DOI: 10.1016/8756-3282(95)00199-N  0.88
1995 Brown EM, Pollak M, Hebert SC. Sensing of extracellular Ca2+ by parathyroid and kidney cells: Cloning and characterization of an extracellular Ca2+-sensing receptor American Journal of Kidney Diseases. 25: 506-513. PMID 7872334 DOI: 10.1016/0272-6386(95)90118-3  0.88
1995 Brown EM, Pollak M, Seidman CE, Seidman JG, Chou YHW, Riccardi D, Hebert SC. Calcium-ion-sensing cell-surface receptors New England Journal of Medicine. 333: 234-240. PMID 7791841 DOI: 10.1056/Nejm199507273330407  0.88
1995 Brown EM, Pollak M, Hebert SC. Molecular mechanisms underlying the sensing of extracellular Ca2+ by parathyroid and kidney cells European Journal of Endocrinology. 132: 523-531. PMID 7749489 DOI: 10.1530/Eje.0.1320523  0.88
1995 Brown EM, Pollak M, Chou YHW, Seidman CE, Seidman JG, Hebert SC. The cloning of extracellular Ca2+-sensing receptors from parathyroid and kidney: Molecular mechanisms of extracellular Ca2+-sensing Journal of Nutrition. 125. PMID 7602378 DOI: 10.1093/Jn/125.Suppl_7.1965S  0.88
1995 Hosokawa Y, Pollak MR, Brown EM, Arnold A. Mutational analysis of the extracellular Ca2+-sensing receptor gene in human parathyroid tumors Journal of Clinical Endocrinology and Metabolism. 80: 3107-3110. PMID 7593409 DOI: 10.1210/Jcem.80.11.7593409  0.88
1995 Ho C, Conner DA, Pollak MR, Ladd DJ, Kifor O, Warren HB, Brown EM, Seidman JG, Seidman CE. A mouse model of human familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism Nature Genetics. 11: 389-394. PMID 7493018 DOI: 10.1038/Ng1295-389  0.88
1994 Pollak MR, Chou YHW, Marx SJ, Steinmann B, Cole DEC, Brandi ML, Papapoulos SE, Menko FH, Hendy GN, Brown EM, Seidman CE, Seidman JG. Familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism: Effects of mutant gene dosage on phenotype Journal of Clinical Investigation. 93: 1108-1112. PMID 8132750 DOI: 10.1007/Bf02254188  0.88
1994 Pollak MR, Brown EM, Estep HL, McLaine PN, Kifor O, Park J, Hebert SC, Seidman CE, Seidman JG. Autosomal dominant hypocalcaemia caused by a Ca2+-sensing receptor gene mutation Nature Genetics. 8: 303-307. PMID 7874174 DOI: 10.1038/Ng1194-303  0.88
1993 Pollak MR, Chou YHW, Cerda JJ, Steinmann B, La Du BN, Seidman JG, Seidman CE. Homozygosity mapping of the gene for alkaptonuria to chromosome 3q2 Nature Genetics. 5: 201-204. PMID 8252048 DOI: 10.1038/Ng1093-201  0.88
1993 Pollak MR, Brown EM, Chou YHW, Hebert SC, Marx SJ, Stelnmann B, Levi T, Seidman CE, Seidman JG. Mutations in the human Ca2+-sensing receptor gene cause familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism Cell. 75: 1297-1303. PMID 7916660 DOI: 10.1016/0092-8674(93)90617-Y  0.88
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