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Marcin Zaniew
Marcin Zaniew
未知所在单位机构
在 g.elearn.uz.zgora.pl 的电子邮件经过验证
标题
引用次数
引用次数
年份
Discovery of new risk loci for IgA nephropathy implicates genes involved in immunity against intestinal pathogens
K Kiryluk, Y Li, F Scolari, S Sanna-Cherchi, M Choi, M Verbitsky, D Fasel, ...
Nature genetics 46 (11), 1187-1196, 2014
6442014
Copy-number disorders are a common cause of congenital kidney malformations
S Sanna-Cherchi, K Kiryluk, KE Burgess, M Bodria, MG Sampson, ...
The American Journal of Human Genetics 91 (6), 987-997, 2012
2522012
The copy number variation landscape of congenital anomalies of the kidney and urinary tract
M Verbitsky, R Westland, A Perez, K Kiryluk, Q Liu, P Krithivasan, ...
Nature genetics 51 (1), 117-127, 2019
2032019
Whole-exome sequencing in adults with chronic kidney disease: a pilot study
S Lata, M Marasa, Y Li, DA Fasel, E Groopman, V Jobanputra, H Rasouly, ...
Annals of internal medicine 168 (2), 100-109, 2018
1962018
Genetic drivers of kidney defects in the DiGeorge syndrome
E Lopez-Rivera, YP Liu, M Verbitsky, BR Anderson, VP Capone, EA Otto, ...
New England Journal of Medicine 376 (8), 742-754, 2017
1472017
Treatment and long-term outcome in primary distal renal tubular acidosis
SC Lopez-Garcia, F Emma, SB Walsh, M Fila, N Hooman, M Zaniew, ...
Nephrology Dialysis Transplantation 34 (6), 981-991, 2019
1082019
Th1/Th2 balance and CD45-positive T cell subsets in primary nephrotic syndrome
J Stachowski, C Barth, J Michałkiewicz, T Krynicki, T Jarmoliński, ...
Pediatric Nephrology 14, 779-785, 2000
1042000
Exome-wide association study identifies GREB1L mutations in congenital kidney malformations
S Sanna-Cherchi, K Khan, R Westland, P Krithivasan, L Fievet, ...
The American Journal of Human Genetics 101 (5), 789-802, 2017
982017
Beneficial in vitro effect of N-acetyl-cysteine on oxidative stress and apoptosis
J Zachwieja, M Zaniew, W Bobkowski, E Stefaniak, A Warzywoda, ...
Pediatric Nephrology 20, 725-731, 2005
632005
Regulation of post-Golgi LH3 trafficking is essential for collagen homeostasis
B Banushi, F Forneris, A Straatman-Iwanowska, A Strange, AM Lyne, ...
Nature communications 7 (1), 12111, 2016
622016
HNF1B nephropathy has a slow-progressive phenotype in childhood—with the exception of very early onset cases: results of the German Multicenter HNF1B …
C Okorn, A Goertz, U Vester, BB Beck, C Bergmann, S Habbig, J König, ...
Pediatric Nephrology 34, 1065-1075, 2019
612019
Low levels of urinary epidermal growth factor predict chronic kidney disease progression in children
K Azukaitis, W Ju, M Kirchner, V Nair, M Smith, Z Fang, ...
Kidney international 96 (1), 214-221, 2019
552019
Characterization of 28 novel patients expands the mutational and phenotypic spectrum of Lowe syndrome
F Recker, M Zaniew, D Böckenhauer, N Miglietti, A Bökenkamp, ...
Pediatric nephrology 30, 931-943, 2015
532015
Risk factors for early dialysis dependency in autosomal recessive polycystic kidney disease
K Burgmaier, K Kunzmann, G Ariceta, C Bergmann, AK Buescher, ...
The Journal of pediatrics 199, 22-28. e6, 2018
522018
Long-term renal outcome in children with OCRL mutations: retrospective analysis of a large international cohort
M Zaniew, A Bökenkamp, M Kołbuc, C La Scola, F Baronio, A Niemirska, ...
Nephrology Dialysis Transplantation 33 (1), 85-94, 2018
522018
Resistance to therapy in primary nephrotic syndrome: effect of MDR1 gene activity
J Stachowski, CB Zanker, D Runowski, M Zaniew, A Peszko, A Medyńska, ...
Polski merkuriusz lekarski: organ Polskiego Towarzystwa Lekarskiego 8 (46 …, 2000
442000
Genome-wide association analyses define pathogenic signaling pathways and prioritize drug targets for IgA nephropathy
K Kiryluk, E Sanchez-Rodriguez, XJ Zhou, F Zanoni, L Liu, N Mladkova, ...
Nature genetics 55 (7), 1091-1105, 2023
432023
Intracellular cytokines of peripheral blood lymphocytes in nephrotic syndrome
J Zachwieja, W Bobkowski, A Dobrowolska-Zachwieja, ...
Pediatric Nephrology 17, 733-740, 2002
432002
Hypertensive nephropathy in children–do we diagnose early enough?
A Blumczynski, J Sołtysiak, K Lipkowska, M Silska, A Poprawska, ...
Blood pressure 21 (4), 233-239, 2012
392012
Retrospective cohort study of familial hypomagnesaemia with hypercalciuria and nephrocalcinosis due to CLDN16 mutations
P Sikora, M Zaniew, L Haisch, B Pulcer, M Szczepańska, A Moczulska, ...
Nephrology Dialysis Transplantation 30 (4), 636-644, 2015
372015
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