フォロー
Martin Pollak
Martin Pollak
BIDMC
確認したメール アドレス: bidmc.harvard.edu
タイトル
引用先
引用先
Association of trypanolytic ApoL1 variants with kidney disease in African Americans
G Genovese, DJ Friedman, MD Ross, L Lecordier, P Uzureau, ...
Science 329 (5993), 841-845, 2010
20232010
Mutations in ACTN4, encoding α-actinin-4, cause familial focal segmental glomerulosclerosis
JM Kaplan, S H Kim, KN North, H Rennke, L A Correia, HQ Tong, ...
Nature genetics 24 (3), 251-256, 2000
15992000
Mutations in the human Ca2+-sensing receptor gene cause familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism
MR Pollak, EM Brown, YHW Chou, SC Hebert, SJ Marx, B Stelnmann, ...
Cell 75 (7), 1297-1303, 1993
10651993
TRPC6 is a glomerular slit diaphragm-associated channel required for normal renal function
J Reiser, KR Polu, CC Möller, P Kenlan, MM Altintas, C Wei, C Faul, ...
Nature genetics 37 (7), 739-744, 2005
10232005
Stem cell engraftment at the endosteal niche is specified by the calcium-sensing receptor
GB Adams, KT Chabner, IR Alley, DP Olson, ZM Szczepiorkowski, ...
Nature 439 (7076), 599-603, 2006
9212006
APOL1 genetic variants in focal segmental glomerulosclerosis and HIV-associated nephropathy
JB Kopp, GW Nelson, K Sampath, RC Johnson, G Genovese, P An, ...
Journal of the American Society of Nephrology 22 (11), 2129-2137, 2011
8552011
Autosomal dominant hypocalcaemia caused by a Ca2+-sensing receptor gene mutation
MR Pollak, EM Brown, HL Estep, PN McLaine, O Kifor, J Park, SC Hebert, ...
Nature genetics 8 (3), 303-307, 1994
6331994
A mouse model of human familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism
C Ho, DA Conner, MR Pollak, DJ Ladd, O Kifor, HB Warren, EM Brown, ...
Nature genetics 11 (4), 389-394, 1995
6231995
Mutations in the formin gene INF2 cause focal segmental glomerulosclerosis
EJ Brown, JS Schlöndorff, DJ Becker, H Tsukaguchi, SJ Tonna, ...
Nature genetics 42 (1), 72-76, 2010
4932010
Expression and characterization of inactivating and activating mutations in the human Ca2+ o-sensing receptor
M Bai, S Quinn, S Trivedi, O Kifor, SHS Pearce, MR Pollak, K Krapcho, ...
Journal of Biological Chemistry 271 (32), 19537-19545, 1996
4851996
ADCK4 mutations promote steroid-resistant nephrotic syndrome through CoQ10 biosynthesis disruption
S Ashraf, HY Gee, S Woerner, LX Xie, V Vega-Warner, S Lovric, H Fang, ...
The Journal of clinical investigation 123 (12), 5179-5189, 2013
3682013
Calcium-ion–sensing cell-surface receptors
EM Brown, M Pollak, CE Seidman, JG Seidman, YHW Chou, D Riccardi, ...
New England Journal of Medicine 333 (4), 234-240, 1995
3571995
Mice deficient in α-actinin-4 have severe glomerular disease
CH Kos, TC Le, S Sinha, JM Henderson, SH Kim, H Sugimoto, R Kalluri, ...
The Journal of clinical investigation 111 (11), 1683-1690, 2003
3322003
Innate immunity pathways regulate the nephropathy gene Apolipoprotein L1
B Nichols, P Jog, JH Lee, D Blackler, M Wilmot, V D'agati, G Markowitz, ...
Kidney international 87 (2), 332-342, 2015
3312015
NPHS2 mutations in late-onset focal segmental glomerulosclerosis: R229Q is a common disease-associated allele
H Tsukaguchi, A Sudhakar, TC Le, T Nguyen, J Yao, JA Schwimmer, ...
The Journal of clinical investigation 110 (11), 1659-1666, 2002
3292002
Mutations causing medullary cystic kidney disease type 1 lie in a large VNTR in MUC1 missed by massively parallel sequencing
A Kirby, A Gnirke, DB Jaffe, V Barešová, N Pochet, B Blumenstiel, C Ye, ...
Nature genetics 45 (3), 299-303, 2013
3052013
Familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism. Effects of mutant gene dosage on phenotype.
MR Pollak, YH Chou, SJ Marx, B Steinmann, DE Cole, ML Brandi, ...
The Journal of clinical investigation 93 (3), 1108-1112, 1994
2991994
Arhgap24 inactivates Rac1 in mouse podocytes, and a mutant form is associated with familial focal segmental glomerulosclerosis
S Akilesh, H Suleiman, H Yu, MC Stander, P Lavin, R Gbadegesin, ...
The Journal of clinical investigation 121 (10), 4127-4137, 2011
2942011
Direct dynamin–actin interactions regulate the actin cytoskeleton
C Gu, S Yaddanapudi, A Weins, T Osborn, J Reiser, M Pollak, J Hartwig, ...
The EMBO journal 29 (21), 3593-3606, 2010
2762010
The apolipoprotein L1 (APOL1) gene and nondiabetic nephropathy in African Americans
BI Freedman, JB Kopp, CD Langefeld, G Genovese, DJ Friedman, ...
Journal of the American Society of Nephrology 21 (9), 1422-1426, 2010
2732010
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