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Items: 1 to 50 of 190

1.

Eltrombopag for the treatment of inherited thrombocytopenias: a phase 2 clinical trial.

Zaninetti C, Gresele P, Bertomoro A, Klersy C, De Candia E, Veneri D, Barozzi S, Fierro T, Alberelli MA, Musella V, Noris P, Fabris F, Balduini CL, Pecci A.

Haematologica. 2019 Jul 4. pii: haematol.2019.223966. doi: 10.3324/haematol.2019.223966. [Epub ahead of print]

2.

Mapping the neurosteroid binding sites on glycine receptors.

Alvarez LD, Pecci A.

J Steroid Biochem Mol Biol. 2019 Jun 6;192:105388. doi: 10.1016/j.jsbmb.2019.105388. [Epub ahead of print]

PMID:
31176751
3.

Natural Heteroplasmy and Mitochondrial Inheritance in Bivalve Molluscs.

Ghiselli F, Maurizii MG, Reunov A, Ariño-Bassols H, Cifaldi C, Pecci A, Alexandrova Y, Bettini S, Passamonti M, Franceschini V, Milani L.

Integr Comp Biol. 2019 May 23. pii: icz061. doi: 10.1093/icb/icz061. [Epub ahead of print]

PMID:
31120503
4.

Eltrombopag in preparation for surgery in patients with severe MYH9-related thrombocytopenia.

Zaninetti C, Barozzi S, Bozzi V, Gresele P, Balduini CL, Pecci A.

Am J Hematol. 2019 Aug;94(8):E199-E201. doi: 10.1002/ajh.25500. Epub 2019 May 8. No abstract available.

PMID:
31034630
5.

The role of an accurate diagnosis of inherited thrombocytopenia as the basis for an effective treatment. A case of MYH9 syndrome treated with a TPO-RA.

Porrazzo M, Baldacci E, Ferretti A, Miulli E, Chistolini A, Pecci A, Mazzucconi MG, Foà R, Santoro C.

Haemophilia. 2019 Jul;25(4):e288-e290. doi: 10.1111/hae.13757. Epub 2019 Apr 17. No abstract available.

PMID:
30993846
6.

Liver X receptor-α activation enhances cholesterol secretion in lactating mammary epithelium.

Grinman DY, Careaga VP, Wellberg EA, Dansey MV, Kordon EC, Anderson SM, Maier MS, Burton G, MacLean PS, Rudolph MC, Pecci A.

Am J Physiol Endocrinol Metab. 2019 Jun 1;316(6):E1136-E1145. doi: 10.1152/ajpendo.00548.2018. Epub 2019 Apr 9.

PMID:
30964702
7.

MYH9-related disease mutations cause abnormal red blood cell morphology through increased myosin-actin binding at the membrane.

Smith AS, Pal K, Nowak RB, Demenko A, Zaninetti C, Da Costa L, Favier R, Pecci A, Fowler VM.

Am J Hematol. 2019 Jun;94(6):667-677. doi: 10.1002/ajh.25472. Epub 2019 Apr 17.

PMID:
30916803
8.

Heme Oxygenase 1 Impairs Glucocorticoid Receptor Activity in Prostate Cancer.

Leonardi DB, Anselmino N, Brandani JN, Jaworski FM, Páez AV, Mazaira G, Meiss RP, Nuñez M, Nemirovsky SI, Giudice J, Galigniana M, Pecci A, Gueron G, Vazquez E, Cotignola J.

Int J Mol Sci. 2019 Feb 26;20(5). pii: E1006. doi: 10.3390/ijms20051006.

9.

Loss-of-function mutations in PTPRJ cause a new form of inherited thrombocytopenia.

Marconi C, Di Buduo CA, LeVine K, Barozzi S, Faleschini M, Bozzi V, Palombo F, McKinstry S, Lassandro G, Giordano P, Noris P, Balduini CL, Savoia A, Balduini A, Pippucci T, Seri M, Katsanis N, Pecci A.

Blood. 2019 Mar 21;133(12):1346-1357. doi: 10.1182/blood-2018-07-859496. Epub 2018 Dec 27.

PMID:
30591527
10.

In Search of GABAA Receptor's Neurosteroid Binding Sites.

Alvarez LD, Pecci A, Estrin DA.

J Med Chem. 2019 Jun 13;62(11):5250-5260. doi: 10.1021/acs.jmedchem.8b01400. Epub 2018 Dec 31.

PMID:
30566352
11.

ACTN1 mutations lead to a benign form of platelet macrocytosis not always associated with thrombocytopenia.

Faleschini M, Melazzini F, Marconi C, Giangregorio T, Pippucci T, Cigalini E, Pecci A, Bottega R, Ramenghi U, Siitonen T, Seri M, Pastore A, Savoia A, Noris P.

Br J Haematol. 2018 Oct;183(2):276-288. doi: 10.1111/bjh.15531. Epub 2018 Oct 23.

PMID:
30351444
12.

Lemierre Syndrome: Clinical Update and Protocol for a Systematic Review and Individual Patient Data Meta-analysis.

Sacco C, Zane F, Granziera S, Holm K, Creemers-Schild D, Hotz MA, Turpini E, Valentini A, Righini C, Karkos PD, Verhamme P, Di Nisio M, Konstantinides S, Pecci A, Barco S; Lemierre Study Group .

Hamostaseologie. 2019 Feb;39(1):76-86. doi: 10.1055/s-0038-1654720. Epub 2018 Aug 2.

PMID:
30071559
13.

MYH9-Related Thrombocytopenia: Four Novel Variants Affecting the Tail Domain of the Non-Muscle Myosin Heavy Chain IIA Associated with a Mild Clinical Evolution of the Disorder.

Zaninetti C, De Rocco D, Giangregorio T, Bozzi V, Demeter J, Leoni P, Noris P, Ryhänen S, Barozzi S, Pecci A, Savoia A.

Hamostaseologie. 2019 Feb;39(1):87-94. doi: 10.1055/s-0038-1645840. Epub 2018 Jul 11.

PMID:
29996171
14.

Thrombopoietin receptor agonists in hereditary thrombocytopenias.

Rodeghiero F, Pecci A, Balduini CL.

J Thromb Haemost. 2018 Sep;16(9):1700-1710. doi: 10.1111/jth.14217. Epub 2018 Jul 27. Review.

PMID:
29956472
15.

Structure and dynamics of neurosteroid binding to the α1β2γ2 GABAA receptor.

Alvarez LD, Pecci A.

J Steroid Biochem Mol Biol. 2018 Sep;182:72-80. doi: 10.1016/j.jsbmb.2018.04.012. Epub 2018 Apr 26.

PMID:
29705269
16.

MYH9: Structure, functions and role of non-muscle myosin IIA in human disease.

Pecci A, Ma X, Savoia A, Adelstein RS.

Gene. 2018 Jul 20;664:152-167. doi: 10.1016/j.gene.2018.04.048. Epub 2018 Apr 19. Review.

17.

Synthesis and activity evaluation of a series of cholanamides as modulators of the liver X receptors.

Martínez MD, Ghini AA, Dansey MV, Veleiro AS, Pecci A, Alvarez LD, Burton G.

Bioorg Med Chem. 2018 Mar 1;26(5):1092-1101. doi: 10.1016/j.bmc.2018.01.025. Epub 2018 Jan 31.

PMID:
29428525
18.

Mapping the dynamical organization of the cell nucleus through fluorescence correlation spectroscopy.

Stortz M, Angiolini J, Mocskos E, Wolosiuk A, Pecci A, Levi V.

Methods. 2018 May 1;140-141:10-22. doi: 10.1016/j.ymeth.2017.12.008. Epub 2017 Dec 15.

PMID:
29253641
19.

Molecular dynamics simulations of the glucocorticoid receptor DNA-binding domain suggest a role of the lever-arm mobility in transcriptional output.

Álvarez LD, Presman DM, Pecci A.

PLoS One. 2017 Dec 15;12(12):e0189588. doi: 10.1371/journal.pone.0189588. eCollection 2017.

20.

Hereditary thrombocytopenias: a growing list of disorders.

Noris P, Pecci A.

Hematology Am Soc Hematol Educ Program. 2017 Dec 8;2017(1):385-399. doi: 10.1182/asheducation-2017.1.385. Review.

21.

Thrombopoietin mutation in congenital amegakaryocytic thrombocytopenia treatable with romiplostim.

Pecci A, Ragab I, Bozzi V, De Rocco D, Barozzi S, Giangregorio T, Ali H, Melazzini F, Sallam M, Alfano C, Pastore A, Balduini CL, Savoia A.

EMBO Mol Med. 2018 Jan;10(1):63-75. doi: 10.15252/emmm.201708168.

22.

Inherited thrombocytopenia caused by ANKRD26 mutations misdiagnosed and treated as myelodysplastic syndrome: report on two cases.

Zaninetti C, Santini V, Tiniakou M, Barozzi S, Savoia A, Pecci A.

J Thromb Haemost. 2017 Dec;15(12):2388-2392. doi: 10.1111/jth.13855. Epub 2017 Oct 28.

PMID:
28976612
23.

Germ cell line during the seasonal sexual rest of clams: finding niches of cells for gonad renewal.

Milani L, Pecci A, Ghiselli F, Passamonti M, Lazzari M, Franceschini V, Maurizii MG.

Histochem Cell Biol. 2018 Jan;149(1):105-110. doi: 10.1007/s00418-017-1607-z. Epub 2017 Sep 5.

PMID:
28875375
24.

Mapping the Dynamics of the Glucocorticoid Receptor within the Nuclear Landscape.

Stortz M, Presman DM, Bruno L, Annibale P, Dansey MV, Burton G, Gratton E, Pecci A, Levi V.

Sci Rep. 2017 Jul 24;7(1):6219. doi: 10.1038/s41598-017-06676-0.

25.

PL10 DEAD-Box Protein is Expressed during Germ Cell Differentiation in the Reptile Podarcis sicula (Family Lacertidae).

Milani L, Pecci A, Cifaldi C, Maurizii MG.

J Exp Zool B Mol Dev Evol. 2017 Jul;328(5):433-448. doi: 10.1002/jez.b.22744.

PMID:
28656658
26.

A new form of inherited thrombocytopenia due to monoallelic loss of function mutation in the thrombopoietin gene.

Noris P, Marconi C, De Rocco D, Melazzini F, Pippucci T, Loffredo G, Giangregorio T, Pecci A, Seri M, Savoia A.

Br J Haematol. 2018 Jun;181(5):698-701. doi: 10.1111/bjh.14694. Epub 2017 May 3. No abstract available.

PMID:
28466964
27.

Diagnosis of inherited platelet disorders on a blood smear: a tool to facilitate worldwide diagnosis of platelet disorders.

Greinacher A, Pecci A, Kunishima S, Althaus K, Nurden P, Balduini CL, Bakchoul T.

J Thromb Haemost. 2017 Jul;15(7):1511-1521. doi: 10.1111/jth.13729. Epub 2017 Jun 4.

28.

VASA expression suggests shared germ line dynamics in bivalve molluscs.

Milani L, Pecci A, Ghiselli F, Passamonti M, Bettini S, Franceschini V, Maurizii MG.

Histochem Cell Biol. 2017 Aug;148(2):157-171. doi: 10.1007/s00418-017-1560-x. Epub 2017 Apr 6.

29.

Bleeding risk of surgery and its prevention in patients with inherited platelet disorders.

Orsini S, Noris P, Bury L, Heller PG, Santoro C, Kadir RA, Butta NC, Falcinelli E, Cid AR, Fabris F, Fouassier M, Miyazaki K, Lozano ML, Zúñiga P, Flaujac C, Podda GM, Bermejo N, Favier R, Henskens Y, De Maistre E, De Candia E, Mumford AD, Ozdemir GN, Eker I, Nurden P, Bayart S, Lambert MP, Bussel J, Zieger B, Tosetto A, Melazzini F, Glembotsky AC, Pecci A, Cattaneo M, Schlegel N, Gresele P; European Hematology Association - Scientific Working Group (EHA-SWG) on thrombocytopenias and platelet function disorders.

Haematologica. 2017 Jul;102(7):1192-1203. doi: 10.3324/haematol.2016.160754. Epub 2017 Apr 6.

30.

MYH9 gene mutations associated with bleeding.

Savoia A, De Rocco D, Pecci A.

Platelets. 2017 May;28(3):312-315. doi: 10.1080/09537104.2017.1294250. Epub 2017 Apr 3. No abstract available.

PMID:
28368695
31.

Mutations of RUNX1 in families with inherited thrombocytopenia.

De Rocco D, Melazzini F, Marconi C, Pecci A, Bottega R, Gnan C, Palombo F, Giordano P, Coccioli MS, Glembotsky AC, Heller PG, Seri M, Savoia A, Noris P.

Am J Hematol. 2017 Jun;92(6):E86-E88. doi: 10.1002/ajh.24703. Epub 2017 Mar 24. No abstract available.

32.

5'UTR point substitutions and N-terminal truncating mutations of ANKRD26 in acute myeloid leukemia.

Marconi C, Canobbio I, Bozzi V, Pippucci T, Simonetti G, Melazzini F, Angori S, Martinelli G, Saglio G, Torti M, Pastan I, Seri M, Pecci A.

J Hematol Oncol. 2017 Jan 18;10(1):18. doi: 10.1186/s13045-016-0382-y.

33.

Severe to profound deafness may be associated with MYH9-related disease: report of 4 patients.

Canzi P, Pecci A, Manfrin M, Rebecchi E, Zaninetti C, Bozzi V, Benazzo M.

Acta Otorhinolaryngol Ital. 2016 Oct;36(5):415-420. doi: 10.14639/0392-100X-702.

34.

Platelets from glioblastoma patients promote angiogenesis of tumor endothelial cells and exhibit increased VEGF content and release.

Di Vito C, Navone SE, Marfia G, Abdel Hadi L, Mancuso ME, Pecci A, Crisà FM, Berno V, Rampini P, Campanella R, Riboni L.

Platelets. 2017 Sep;28(6):585-594. doi: 10.1080/09537104.2016.1247208. Epub 2016 Nov 29.

PMID:
27897101
35.

Clinical and pathogenic features of ETV6-related thrombocytopenia with predisposition to acute lymphoblastic leukemia.

Melazzini F, Palombo F, Balduini A, De Rocco D, Marconi C, Noris P, Gnan C, Pippucci T, Bozzi V, Faleschini M, Barozzi S, Doubek M, Di Buduo CA, Kozubik KS, Radova L, Loffredo G, Pospisilova S, Alfano C, Seri M, Balduini CL, Pecci A, Savoia A.

Haematologica. 2016 Nov;101(11):1333-1342. Epub 2016 Jun 30.

36.

Revealing eltrombopag's promotion of human megakaryopoiesis through AKT/ERK-dependent pathway activation.

Di Buduo CA, Currao M, Pecci A, Kaplan DL, Balduini CL, Balduini A.

Haematologica. 2016 Dec;101(12):1479-1488. Epub 2016 Aug 11.

37.

Fluorinated oxysterol analogues: Synthesis, molecular modelling and LXRβ activity.

Rodriguez CR, Alvarez LD, Dansey MV, Paolo LS, Veleiro AS, Pecci A, Burton G.

J Steroid Biochem Mol Biol. 2017 Jan;165(Pt B):268-276. doi: 10.1016/j.jsbmb.2016.07.001. Epub 2016 Jul 22.

PMID:
27452335
38.

Role of CREB on heme oxygenase-1 induction in adrenal cells: involvement of the PI3K pathway.

Astort F, Repetto EM, Rocha-Viegas L, Mercau ME, Puch SS, Finkielstein CV, Pecci A, Cymeryng CB.

J Mol Endocrinol. 2016 Aug;57(2):113-24. doi: 10.1530/JME-16-0005.

PMID:
27412767
39.

C(16)-C(22) oxygen-bridged analogues of ceDAF-12 and LXR ligands.

Del Fueyo MC, Dansey MV, Paolo LS, Pecci A, Veleiro AS, Burton G.

Steroids. 2016 Aug;112:109-14. doi: 10.1016/j.steroids.2016.05.009. Epub 2016 May 26.

PMID:
27235856
40.

Inherited thrombocytopenias-recent advances in clinical and molecular aspects.

Balduini CL, Melazzini F, Pecci A.

Platelets. 2017 Jan;28(1):3-13. doi: 10.3109/09537104.2016.1171835. Epub 2016 May 9. Review.

PMID:
27161842
41.

21-Hydroxy-6,19-epoxyprogesterone: A Promising Therapeutic Agent and a Molecular Tool for Deciphering Glucocorticoid Action.

Pecci A, Alvarez LD, Presman DM, Burton G.

Mini Rev Med Chem. 2018 Feb 14;18(5):428-438. doi: 10.2174/1389557516666160118112313. Review.

PMID:
26776223
42.

SLFN14-related thrombocytopenia: identification within a large series of patients with inherited thrombocytopenia.

Marconi C, Di Buduo CA, Barozzi S, Palombo F, Pardini S, Zaninetti C, Pippucci T, Noris P, Balduini A, Seri M, Pecci A.

Thromb Haemost. 2016 May 2;115(5):1076-9. doi: 10.1160/TH15-11-0884. Epub 2016 Jan 14. No abstract available.

PMID:
26769223
43.

Automated detection of Antarctic blue whale calls.

Socheleau FX, Leroy E, Pecci AC, Samaran F, Bonnel J, Royer JY.

J Acoust Soc Am. 2015 Nov;138(5):3105-17. doi: 10.1121/1.4934271.

PMID:
26627784
44.

Role of 3'-5'-cyclic adenosine monophosphate on the epidermal growth factor dependent survival in mammary epithelial cells.

Grinman DY, Romorini L, Presman DM, Rocha-Viegas L, Coso OA, Davio C, Pecci A.

Mol Cell Endocrinol. 2016 Jan 5;419:259-67. doi: 10.1016/j.mce.2015.10.026. Epub 2015 Oct 30.

PMID:
26522133
45.

Destabilization of the torsioned conformation of a ligand side chain inverts the LXRβ activity.

Álvarez LD, Dansey MV, Grinman DY, Navalesi D, Samaja GA, Del Fueyo MC, Bastiaensen N, Houtman R, Estrin DA, Veleiro AS, Pecci A, Burton G.

Biochim Biophys Acta. 2015 Dec;1851(12):1577-86. doi: 10.1016/j.bbalip.2015.09.007. Epub 2015 Oct 3.

PMID:
26434697
46.

The Expression of a Novel Mitochondrially-Encoded Gene in Gonadic Precursors May Drive Paternal Inheritance of Mitochondria.

Milani L, Ghiselli F, Pecci A, Maurizii MG, Passamonti M.

PLoS One. 2015 Sep 4;10(9):e0137468. doi: 10.1371/journal.pone.0137468. eCollection 2015.

47.

Nonmuscle Myosin Heavy Chain IIA Mutation Predicts Severity and Progression of Sensorineural Hearing Loss in Patients With MYH9-Related Disease.

Verver EJ, Topsakal V, Kunst HP, Huygen PL, Heller PG, Pujol-Moix N, Savoia A, Benazzo M, Fierro T, Grolman W, Gresele P, Pecci A.

Ear Hear. 2016 Jan-Feb;37(1):112-20. doi: 10.1097/AUD.0000000000000198.

PMID:
26226608
48.

Ex vivo immunosuppressive effects of mesenchymal stem cells on Crohn's disease mucosal T cells are largely dependent on indoleamine 2,3-dioxygenase activity and cell-cell contact.

Ciccocioppo R, Cangemi GC, Kruzliak P, Gallia A, Betti E, Badulli C, Martinetti M, Cervio M, Pecci A, Bozzi V, Dionigi P, Visai L, Gurrado A, Alvisi C, Picone C, Monti M, Bernardo ME, Gobbi P, Corazza GR.

Stem Cell Res Ther. 2015 Jul 24;6:137. doi: 10.1186/s13287-015-0122-1.

49.

MYH9-Related Disorders.

Savoia A, Pecci A.

In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Stephens K, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2019.
2008 Nov 20 [updated 2015 Jul 16].

50.

Particulate cytoplasmic structures with high concentration of ubiquitin-proteasome accumulate in myeloid neoplasms.

Pecci A, Necchi V, Barozzi S, Vitali A, Boveri E, Elena C, Bernasconi P, Noris P, Solcia E.

J Hematol Oncol. 2015 Jun 18;8:71. doi: 10.1186/s13045-015-0169-6.

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