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Items: 1 to 50 of 88

1.

CLCN5 5'UTR isoforms in human kidneys: differential expression analysis between controls and patients with glomerulonephritis.

Ceol M, Gianesello L, Tosetto E, Priante G, Del Prete D, Anglani F.

J Investig Med. 2020 Feb 3. pii: jim-2019-001205. doi: 10.1136/jim-2019-001205. [Epub ahead of print]

PMID:
32019767
2.

Genetic Analyses in Dent Disease and Characterization of CLCN5 Mutations in Kidney Biopsies.

Gianesello L, Ceol M, Bertoldi L, Terrin L, Priante G, Murer L, Peruzzi L, Giordano M, Paglialonga F, Cantaluppi V, Musetti C, Valle G, Prete DD, Anglani F, Network DDI.

Int J Mol Sci. 2020 Jan 14;21(2). pii: E516. doi: 10.3390/ijms21020516.

3.

Protein uptake at glomerular level: is it just the work of podocytes?

Gianesello L, Anglani F, Del Prete D.

Nephrol Dial Transplant. 2019 Jun 26. pii: gfz127. doi: 10.1093/ndt/gfz127. [Epub ahead of print] No abstract available.

PMID:
31608931
4.

Dent disease: A window into calcium and phosphate transport.

Anglani F, Gianesello L, Beara-Lasic L, Lieske J.

J Cell Mol Med. 2019 Nov;23(11):7132-7142. doi: 10.1111/jcmm.14590. Epub 2019 Aug 31. Review.

5.

Cell Death in the Kidney.

Priante G, Gianesello L, Ceol M, Del Prete D, Anglani F.

Int J Mol Sci. 2019 Jul 23;20(14). pii: E3598. doi: 10.3390/ijms20143598. Review.

6.

Cell death in ectopic calcification of the kidney.

Priante G, Mezzabotta F, Cristofaro R, Quaggio F, Ceol M, Gianesello L, Del Prete D, Anglani F.

Cell Death Dis. 2019 Jun 13;10(6):466. doi: 10.1038/s41419-019-1697-8. No abstract available.

7.

Human proximal tubular cells can form calcium phosphate deposits in osteogenic culture: role of cell death and osteoblast-like transdifferentiation.

Priante G, Ceol M, Gianesello L, Furlan C, Del Prete D, Anglani F.

Cell Death Discov. 2019 Jan 28;5:57. doi: 10.1038/s41420-019-0138-x. eCollection 2019.

8.

Hypercalciuria and nephrolithiasis: Expanding the renal phenotype of Donnai-Barrow syndrome.

Anglani F, Terrin L, Brugnara M, Battista M, Cantaluppi V, Ceol M, Bertoldi L, Valle G, Joy MP, Pober BR, Longoni M.

Clin Genet. 2018 Jul;94(1):187-188. doi: 10.1111/cge.13242. Epub 2018 Mar 13.

9.

Caspase-independent programmed cell death triggers Ca2PO4 deposition in an in vitro model of nephrocalcinosis.

Priante G, Quaggio F, Gianesello L, Ceol M, Cristofaro R, Terrin L, Furlan C, Del Prete D, Anglani F.

Biosci Rep. 2018 Jan 17;38(1). pii: BSR20171228. doi: 10.1042/BSR20171228. Print 2018 Feb 28.

10.

Albumin uptake in human podocytes: a possible role for the cubilin-amnionless (CUBAM) complex.

Gianesello L, Priante G, Ceol M, Radu CM, Saleem MA, Simioni P, Terrin L, Anglani F, Del Prete D.

Sci Rep. 2017 Oct 20;7(1):13705. doi: 10.1038/s41598-017-13789-z.

11.

QueryOR: a comprehensive web platform for genetic variant analysis and prioritization.

Bertoldi L, Forcato C, Vitulo N, Birolo G, De Pascale F, Feltrin E, Schiavon R, Anglani F, Negrisolo S, Zanetti A, D'Avanzo F, Tomanin R, Faulkner G, Vezzi A, Valle G.

BMC Bioinformatics. 2017 Apr 28;18(1):225. doi: 10.1186/s12859-017-1654-4.

12.

Long-term renal outcome in children with OCRL mutations: retrospective analysis of a large international cohort.

Zaniew M, Bökenkamp A, Kolbuc M, La Scola C, Baronio F, Niemirska A, Szczepanska M, Bürger J, La Manna A, Miklaszewska M, Rogowska-Kalisz A, Gellermann J, Zampetoglou A, Wasilewska A, Roszak M, Moczko J, Krzemien A, Runowski D, Siten G, Zaluska-Lesniewska I, Fonduli P, Zurrida F, Paglialonga F, Gucev Z, Paripovic D, Rus R, Said-Conti V, Sartz L, Chung WY, Park SJ, Lee JW, Park YH, Ahn YH, Sikora P, Stefanidis CJ, Tasic V, Konrad M, Anglani F, Addis M, Cheong HI, Ludwig M, Bockenhauer D.

Nephrol Dial Transplant. 2018 Jan 1;33(1):85-94. doi: 10.1093/ndt/gfw350.

PMID:
27708066
13.

Glomerular Pathology in Dent Disease and Its Association with Kidney Function.

Wang X, Anglani F, Beara-Lasic L, Mehta AJ, Vaughan LE, Herrera Hernandez L, Cogal A, Scheinman SJ, Ariceta G, Isom R, Copelovitch L, Enders FT, Del Prete D, Vezzoli G, Paglialonga F, Harris PC, Lieske JC; Investigators of the Rare Kidney Stone Consortium.

Clin J Am Soc Nephrol. 2016 Dec 7;11(12):2168-2176. Epub 2016 Oct 3.

14.

Nephrolithiasis, kidney failure and bone disorders in Dent disease patients with and without CLCN5 mutations.

Anglani F, D'Angelo A, Bertizzolo LM, Tosetto E, Ceol M, Cremasco D, Bonfante L, Addis MA, Del Prete D; Dent Disease Italian Network.

Springerplus. 2015 Sep 15;4:492. doi: 10.1186/s40064-015-1294-y. eCollection 2015.

15.

Urine proteome analysis in Dent's disease shows high selective changes potentially involved in chronic renal damage.

Santucci L, Candiano G, Anglani F, Bruschi M, Tosetto E, Cremasco D, Murer L, D'Ambrosio C, Scaloni A, Petretto A, Caridi G, Rossi R, Bonanni A, Ghiggeri GM.

J Proteomics. 2016 Jan 1;130:26-32. doi: 10.1016/j.jprot.2015.08.024. Epub 2015 Sep 11.

PMID:
26370164
16.

Spontaneous calcification process in primary renal cells from a medullary sponge kidney patient harbouring a GDNF mutation.

Mezzabotta F, Cristofaro R, Ceol M, Del Prete D, Priante G, Familiari A, Fabris A, D'Angelo A, Gambaro G, Anglani F.

J Cell Mol Med. 2015 Apr;19(4):889-902. doi: 10.1111/jcmm.12514. Epub 2015 Feb 18.

17.

Characterization of 28 novel patients expands the mutational and phenotypic spectrum of Lowe syndrome.

Recker F, Zaniew M, Böckenhauer D, Miglietti N, Bökenkamp A, Moczulska A, Rogowska-Kalisz A, Laube G, Said-Conti V, Kasap-Demir B, Niemirska A, Litwin M, Siteń G, Chrzanowska KH, Krajewska-Walasek M, Sethi SK, Tasic V, Anglani F, Addis M, Wasilewska A, Szczepańska M, Pawlaczyk K, Sikora P, Ludwig M.

Pediatr Nephrol. 2015 Jun;30(6):931-43. doi: 10.1007/s00467-014-3013-2. Epub 2014 Dec 6.

PMID:
25480730
18.

Complexity of the 5'UTR region of the CLCN5 gene: eleven 5'UTR ends are differentially expressed in the human kidney.

Tosetto E, Casarin A, Salviati L, Familiari A, Lieske JC, Anglani F.

BMC Med Genomics. 2014 Jul 7;7:41. doi: 10.1186/1755-8794-7-41.

19.

Pregnancy in Alport syndrome: a report of two differently-evolving cases.

Alessi M, Fabris A, Zambon A, Cremasco D, Muraro E, Dosa L, Anglani F, Del Prete D.

J Obstet Gynaecol. 2014 Jan;34(1):98-100. doi: 10.3109/01443615.2013.834299. No abstract available.

PMID:
24359068
20.

Decreased transcriptional activity of calcium-sensing receptor gene promoter 1 is associated with calcium nephrolithiasis.

Vezzoli G, Terranegra A, Aloia A, Arcidiacono T, Milanesi L, Mosca E, Mingione A, Spotti D, Cusi D, Hou J, Hendy GN, Soldati L; GENIAL network (Genetics and Environment in Nephrolithiasis Italian Alliance), Paloschi V, Dogliotti E, Brasacchio C, Dell'Antonio G, Montorsi F, Bertini R, Bellinzoni P, Guazzoni G, Borghi L, Guerra A, Allegri F, Ticinesi A, Meschi T, Nouvenne A, Lupo A, Fabris A, Gambaro G, Strazzullo P, Rendina D, De Filippo G, Brandi ML, Croppi E, Cianferotti L, Trinchieri A, Caudarella R, Cupisti A, Anglani F, Del Prete D.

J Clin Endocrinol Metab. 2013 Sep;98(9):3839-47. doi: 10.1210/jc.2013-1834. Epub 2013 Jul 17.

21.

Hereditary causes of kidney stones and chronic kidney disease.

Edvardsson VO, Goldfarb DS, Lieske JC, Beara-Lasic L, Anglani F, Milliner DS, Palsson R.

Pediatr Nephrol. 2013 Oct;28(10):1923-42. doi: 10.1007/s00467-012-2329-z. Epub 2013 Jan 20. Review.

22.

Medullary sponge kidney: state of the art.

Fabris A, Anglani F, Lupo A, Gambaro G.

Nephrol Dial Transplant. 2013 May;28(5):1111-9. doi: 10.1093/ndt/gfs505. Epub 2012 Dec 9. Review.

PMID:
23229933
23.

Familial clustering of medullary sponge kidney is autosomal dominant with reduced penetrance and variable expressivity.

Fabris A, Lupo A, Ferraro PM, Anglani F, Pei Y, Danza FM, Gambaro G.

Kidney Int. 2013 Feb;83(2):272-7. doi: 10.1038/ki.2012.378. Epub 2012 Dec 5.

24.

An atypical Dent's disease phenotype caused by co-inheritance of mutations at CLCN5 and OCRL genes.

Addis M, Meloni C, Tosetto E, Ceol M, Cristofaro R, Melis MA, Vercelloni P, Del Prete D, Marra G, Anglani F.

Eur J Hum Genet. 2013 Jun;21(6):687-90. doi: 10.1038/ejhg.2012.225. Epub 2012 Oct 10.

25.

Involvement of the tubular ClC-type exchanger ClC-5 in glomeruli of human proteinuric nephropathies.

Ceol M, Tiralongo E, Baelde HJ, Vianello D, Betto G, Marangelli A, Bonfante L, Valente M, Della Barbera M, D'Angelo A, Anglani F, Del Prete D.

PLoS One. 2012;7(9):e45605. doi: 10.1371/journal.pone.0045605. Epub 2012 Sep 24.

26.

[Rare genomic variants and susceptibility to multifactorial diseases. The example of medullary sponge kidney].

Anglani F, Fabris A, Torregrossa R, Cristofaro R, Gambaro G, D'Angelo A.

G Ital Nefrol. 2011 May-Jun;28(3):246-8. Italian. No abstract available.

PMID:
21626485
27.

[Participation in the International Dent's disease registry: clinical spin-offs and research prospects].

Anglani F, Del Prete D, Peruzzi L.

G Ital Nefrol. 2011 Jan-Feb;28(1):7-8. Italian. No abstract available.

PMID:
21341234
28.

The regenerative potential of the kidney: what can we learn from developmental biology?

Anglani F, Mezzabotta F, Ceol M, Cristofaro R, Del Prete D, D'Angelo A.

Stem Cell Rev Rep. 2010 Dec;6(4):650-7. doi: 10.1007/s12015-010-9186-6.

PMID:
20714827
29.

Identification of GDNF gene sequence variations in patients with medullary sponge kidney disease.

Torregrossa R, Anglani F, Fabris A, Gozzini A, Tanini A, Del Prete D, Cristofaro R, Artifoni L, Abaterusso C, Marchionna N, Lupo A, D'Angelo A, Gambaro G.

Clin J Am Soc Nephrol. 2010 Jul;5(7):1205-10. doi: 10.2215/CJN.07551009. Epub 2010 May 6.

30.

Primary IgA nephropathy is more severe in TGF-beta1 high secretor patients.

Brezzi B, Del Prete D, Lupo A, Magistroni R, Gomez-Lira M, Bernich P, Anglani F, Mezzabotta F, Turco A, Furci L, Ceol M, Antonucci F, Abaterusso C, Bonfante L, D'Angelo A, Albertazzi A, Gambaro G.

J Nephrol. 2009 Nov-Dec;22(6):747-59.

PMID:
19967654
31.

The origin of nephrocalcinosis, Randall's plaque and renal stones: a cell biology viewpoint.

Gambaro G, Abaterusso C, Fabris A, Ruggera L, Zattoni F, Del Prete D, D'Angelo A, Anglani F.

Arch Ital Urol Androl. 2009 Sep;81(3):166-70. Review.

PMID:
19911679
32.

Novel mutations of the CLCN5 gene including a complex allele and A 5' UTR mutation in Dent disease 1.

Tosetto E, Ceol M, Mezzabotta F, Ammenti A, Peruzzi L, Caruso MR, Barbano G, Vezzoli G, Colussi G, Vergine G, Giordano M, Glorioso N, Degortes S, Soldati L, Sayer J, D'Angelo A, Anglani F.

Clin Genet. 2009 Oct;76(4):413-6. doi: 10.1111/j.1399-0004.2009.01212.x. Epub 2009 Aug 10. No abstract available.

PMID:
19673950
33.

Early activation of fibrogenesis in transplanted kidneys: a study on serial renal biopsies.

Del Prete D, Ceol M, Anglani F, Vianello D, Tiralongo E, Valente M, Graziotto R, Bonfante L, Scaparrotta G, Furian L, Rigotti P, Gambaro G, D'Angelo A.

Exp Mol Pathol. 2009 Oct;87(2):141-5. doi: 10.1016/j.yexmp.2009.07.004. Epub 2009 Jul 16.

PMID:
19616542
34.

Locus heterogeneity of Dent's disease: OCRL1 and TMEM27 genes in patients with no CLCN5 mutations.

Tosetto E, Addis M, Caridi G, Meloni C, Emma F, Vergine G, Stringini G, Papalia T, Barbano G, Ghiggeri GM, Ruggeri L, Miglietti N, D Angelo A, Melis MA, Anglani F.

Pediatr Nephrol. 2009 Oct;24(10):1967-73. doi: 10.1007/s00467-009-1228-4. Epub 2009 Jul 7.

PMID:
19582483
35.

The renal stem cell system in kidney repair and regeneration.

Anglani F, Ceol M, Mezzabotta F, Torregrossa R, Tiralongo E, Tosetto E, Del Prete D, D'Angelo A.

Front Biosci. 2008 May 1;13:6395-405.

PMID:
18508667
36.

Encrusted cystitis by Corynebacterium urealyticum: a case report with novel insights into bladder lesions.

Del Prete D, Polverino B, Ceol M, Vianello D, Mezzabotta F, Tiralongo E, Iafrate M, De Canale E, Mengoli C, Valente M, Anglani F, D'Angelo A.

Nephrol Dial Transplant. 2008 Aug;23(8):2685-7. doi: 10.1093/ndt/gfn243. Epub 2008 May 8. No abstract available.

PMID:
18467375
37.

Pathogenesis of nephrolithiasis: recent insight from cell biology and renal pathology.

Gambaro G, Fabris A, Abaterusso C, Cosaro A, Ceol M, Mezzabotta F, Torregrossa R, Tiralongo E, Del Prete D, D'Angelo A, Anglani F.

Clin Cases Miner Bone Metab. 2008 May;5(2):107-9.

38.

Genes involved in TGF beta1-driven epithelial-mesenchymal transition of renal epithelial cells are topologically related in the human interactome map.

Campanaro S, Picelli S, Torregrossa R, Colluto L, Ceol M, Del Prete D, D'Angelo A, Valle G, Anglani F.

BMC Genomics. 2007 Oct 22;8:383.

39.

Interleukin-8 and CXCR1 receptor functional polymorphisms and susceptibility to acute pyelonephritis.

Artifoni L, Negrisolo S, Montini G, Zucchetta P, Molinari PP, Cassar W, Destro R, Anglani F, Rigamonti W, Zacchello G, Murer L.

J Urol. 2007 Mar;177(3):1102-6.

PMID:
17296422
40.

Phenotypic and genetic heterogeneity in Dent's disease--the results of an Italian collaborative study.

Tosetto E, Ghiggeri GM, Emma F, Barbano G, Carrea A, Vezzoli G, Torregrossa R, Cara M, Ripanti G, Ammenti A, Peruzzi L, Murer L, Ratsch IM, Citron L, Gambaro G, D'angelo A, Anglani F.

Nephrol Dial Transplant. 2006 Sep;21(9):2452-63. Epub 2006 Jul 5.

PMID:
16822791
41.

TGFbeta1 induces epithelial-mesenchymal transition, but not myofibroblast transdifferentiation of human kidney tubular epithelial cells in primary culture.

Forino M, Torregrossa R, Ceol M, Murer L, Della Vella M, Del Prete D, D'Angelo A, Anglani F.

Int J Exp Pathol. 2006 Jun;87(3):197-208.

42.

Perforin, Granzyme B, and fas ligand for molecular diagnosis of acute renal-allograft rejection: analyses on serial biopsies suggest methodological issues.

Graziotto R, Del Prete D, Rigotti P, Anglani F, Baldan N, Furian L, Valente M, Antonello A, Marchini F, D'Angelo A, Gambaro G.

Transplantation. 2006 Apr 27;81(8):1125-32.

PMID:
16641597
43.

Family history may be misleading in the diagnosis of Dent's disease.

Anglani F, Bernich P, Tosetto E, Cara M, Lupo A, Nalesso F, D'Angelo A, Gambaro G.

Urol Res. 2006 Feb;34(1):61-3. Epub 2006 Jan 14.

PMID:
16416111
44.

Dent's disease and prevalence of renal stones in dialysis patients in Northeastern Italy.

Tosetto E, Graziotto R, Artifoni L, Nachtigal J, Cascone C, Conz P, Piva M, Dell'Aquila R, De Paoli Vitali E, Citron L, Nalesso F, Antonello A, Vertolli U, Zagatti R, Lupo A, D'Angelo A, Anglani F, Gambaro G.

J Hum Genet. 2006;51(1):25-30. doi: 10.1007/s10038-005-0317-x. Epub 2005 Oct 25.

PMID:
16247550
45.

An unusual association of contralateral congenital small kidney, reduced renal function and hyperparathyroidism in sponge kidney patients: on the track of the molecular basis.

Gambaro G, Fabris A, Citron L, Tosetto E, Anglani F, Bellan F, Conte M, Bonfante L, Lupo A, D'Angelo A.

Nephrol Dial Transplant. 2005 Jun;20(6):1042-7. Epub 2005 Apr 6.

PMID:
15814540
46.

In search of adult renal stem cells.

Anglani F, Forino M, Del Prete D, Tosetto E, Torregrossa R, D'Angelo A.

J Cell Mol Med. 2004 Oct-Dec;8(4):474-87. Review.

47.

Crystals, Randall's plaques and renal stones: do bone and atherosclerosis teach us something?

Gambaro G, D'Angelo A, Fabris A, Tosetto E, Anglani F, Lupo A.

J Nephrol. 2004 Nov-Dec;17(6):774-7. Review.

PMID:
15593050
48.

Quantitave and qualitative changes in vascular endothelial growth factor gene expression in glomeruli of patients with type 2 diabetes.

Bortoloso E, Del Prete D, Dalla Vestra M, Gambaro G, Saller A, Antonucci F, Baggio B, Anglani F, Fioretto P.

Eur J Endocrinol. 2004 Jun;150(6):799-807.

PMID:
15191350
49.

Gene expression analysis in microdissected renal biopsy.

Del Prete D, Ceol M, Gambaro G, D'Angelo A, Anglani F.

Kidney Int. 2004 Jun;65(6):2445. No abstract available.

50.

GAPDH as housekeeping gene at renal level.

Ceol M, Del Prete D, Tosetto E, Graziotto R, Gambaro G, D'Angelo A, Anglani F.

Kidney Int. 2004 May;65(5):1972-3; author reply 1973-4. No abstract available.

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