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Items: 30

1.

Absence of Dipeptidyl Peptidase 3 Increases Oxidative Stress and Causes Bone Loss.

Menale C, Robinson LJ, Palagano E, Rigoni R, Erreni M, Almarza AJ, Strina D, Mantero S, Lizier M, Forlino A, Besio R, Monari M, Vezzoni P, Cassani B, Blair HC, Villa A, Sobacchi C.

J Bone Miner Res. 2019 Jul 11. doi: 10.1002/jbmr.3829. [Epub ahead of print]

PMID:
31295380
2.

Prolidase enzyme is required for extracellular matrix integrity and impacts on postnatal cerebellar cortex development.

Insolia V, Priori EC, Gasperini C, Coppa F, Cocchia M, Iervasi E, Ferrari B, Besio R, Maruelli S, Bernocchi G, Forlino A, Bottone MG.

J Comp Neurol. 2019 Jun 27. doi: 10.1002/cne.24735. [Epub ahead of print]

PMID:
31246278
3.

Bone biology: insights from osteogenesis imperfecta and related rare fragility syndromes.

Besio R, Chow CW, Tonelli F, Marini JC, Forlino A.

FEBS J. 2019 Aug;286(15):3033-3056. doi: 10.1111/febs.14963. Epub 2019 Jul 5. Review.

PMID:
31220415
4.

Cellular stress due to impairment of collagen prolyl hydroxylation complex is rescued by the chaperone 4-phenylbutyrate.

Besio R, Garibaldi N, Leoni L, Cipolla L, Sabbioneda S, Biggiogera M, Mottes M, Aglan M, Otaify GA, Temtamy SA, Rossi A, Forlino A.

Dis Model Mech. 2019 Jun 20;12(6). pii: dmm038521. doi: 10.1242/dmm.038521.

5.

Steady-State and Pulse-Chase Analyses of Fibrillar Collagen.

Forlino A, Tonelli F, Besio R.

Methods Mol Biol. 2019;1952:45-53. doi: 10.1007/978-1-4939-9133-4_4.

PMID:
30825164
6.

Calcium activated nucleotidase 1 (CANT1) is critical for glycosaminoglycan biosynthesis in cartilage and endochondral ossification.

Paganini C, Monti L, Costantini R, Besio R, Lecci S, Biggiogera M, Tian K, Schwartz JM, Huber C, Cormier-Daire V, Gibson BG, Pirog KA, Forlino A, Rossi A.

Matrix Biol. 2019 Aug;81:70-90. doi: 10.1016/j.matbio.2018.11.002. Epub 2018 Nov 12.

7.

Expression characterization and functional implication of the collagen-modifying Leprecan proteins in mouse gonadal tissue and mature sperm.

Zimmerman SM, Besio R, Heard-Lipsmeyer ME, Dimori M, Castagnola P, Swain FL, Gaddy D, Diekman AB, Morello R.

AIMS Genet. 2018;5(1):24-40. doi: 10.3934/genet.2018.1.24. Epub 2018 Feb 7.

8.

Early Fracture Healing is Delayed in the Col1a2+/G610C Osteogenesis Imperfecta Murine Model.

Besio R, Maruelli S, Battaglia S, Leoni L, Villani S, Layrolle P, Rossi A, Trichet V, Forlino A.

Calcif Tissue Int. 2018 Dec;103(6):653-662. doi: 10.1007/s00223-018-0461-x. Epub 2018 Aug 3.

PMID:
30076439
9.

Severely Impaired Bone Material Quality in Chihuahua Zebrafish Resembles Classical Dominant Human Osteogenesis Imperfecta.

Fiedler IAK, Schmidt FN, Wölfel EM, Plumeyer C, Milovanovic P, Gioia R, Tonelli F, Bale HA, Jähn K, Besio R, Forlino A, Busse B.

J Bone Miner Res. 2018 Aug;33(8):1489-1499. doi: 10.1002/jbmr.3445. Epub 2018 Jun 15.

10.

4-PBA ameliorates cellular homeostasis in fibroblasts from osteogenesis imperfecta patients by enhancing autophagy and stimulating protein secretion.

Besio R, Iula G, Garibaldi N, Cipolla L, Sabbioneda S, Biggiogera M, Marini JC, Rossi A, Forlino A.

Biochim Biophys Acta Mol Basis Dis. 2018 May;1864(5 Pt A):1642-1652. doi: 10.1016/j.bbadis.2018.02.002. Epub 2018 Feb 10.

11.

The scavenging chemokine receptor ACKR2 has a significant impact on acute mortality rate and early lesion development after traumatic brain injury.

Woodcock TM, Frugier T, Nguyen TT, Semple BD, Bye N, Massara M, Savino B, Besio R, Sobacchi C, Locati M, Morganti-Kossmann MC.

PLoS One. 2017 Nov 27;12(11):e0188305. doi: 10.1371/journal.pone.0188305. eCollection 2017.

12.

Cytoskeleton and nuclear lamina affection in recessive osteogenesis imperfecta: A functional proteomics perspective.

Gagliardi A, Besio R, Carnemolla C, Landi C, Armini A, Aglan M, Otaify G, Temtamy SA, Forlino A, Bini L, Bianchi L.

J Proteomics. 2017 Sep 7;167:46-59. doi: 10.1016/j.jprot.2017.08.007. Epub 2017 Aug 9.

13.

Sc65-Null Mice Provide Evidence for a Novel Endoplasmic Reticulum Complex Regulating Collagen Lysyl Hydroxylation.

Heard ME, Besio R, Weis M, Rai J, Hudson DM, Dimori M, Zimmerman SM, Kamykowski JA, Hogue WR, Swain FL, Burdine MS, Mackintosh SG, Tackett AJ, Suva LJ, Eyre DR, Morello R.

PLoS Genet. 2016 Apr 27;12(4):e1006002. doi: 10.1371/journal.pgen.1006002. eCollection 2016 Apr.

14.

A Rare Cause of Lower Extremity Ulcers: Prolidase Deficiency.

Adışen E, Erduran FB, Ezgü FS, Kasapkara ÇS, Besio R, Forlino A, Gürer MA.

Int J Low Extrem Wounds. 2016 Mar;15(1):86-91. doi: 10.1177/1534734615619550. Epub 2015 Dec 4.

PMID:
26637345
15.

Altered cytoskeletal organization characterized lethal but not surviving Brtl+/- mice: insight on phenotypic variability in osteogenesis imperfecta.

Bianchi L, Gagliardi A, Maruelli S, Besio R, Landi C, Gioia R, Kozloff KM, Khoury BM, Coucke PJ, Symoens S, Marini JC, Rossi A, Bini L, Forlino A.

Hum Mol Genet. 2015 Nov 1;24(21):6118-33. doi: 10.1093/hmg/ddv328. Epub 2015 Aug 11.

16.

Lack of prolidase causes a bone phenotype both in human and in mouse.

Besio R, Maruelli S, Gioia R, Villa I, Grabowski P, Gallagher O, Bishop NJ, Foster S, De Lorenzi E, Colombo R, Diaz JL, Moore-Barton H, Deshpande C, Aydin HI, Tokatli A, Kwiek B, Kasapkara CS, Adisen EO, Gurer MA, Di Rocco M, Phang JM, Gunn TM, Tenni R, Rossi A, Forlino A.

Bone. 2015 Mar;72:53-64. doi: 10.1016/j.bone.2014.11.009. Epub 2014 Nov 20.

PMID:
25460580
17.

Role of the advanced glycation end products receptor in Crohn's disease inflammation.

Ciccocioppo R, Vanoli A, Klersy C, Imbesi V, Boccaccio V, Manca R, Betti E, Cangemi GC, Strada E, Besio R, Rossi A, Falcone C, Ardizzone S, Fociani P, Danelli P, Corazza GR.

World J Gastroenterol. 2013 Dec 7;19(45):8269-81. doi: 10.3748/wjg.v19.i45.8269.

18.

Sc65 is a novel endoplasmic reticulum protein that regulates bone mass homeostasis.

Gruenwald K, Castagnola P, Besio R, Dimori M, Chen Y, Akel NS, Swain FL, Skinner RA, Eyre DR, Gaddy D, Suva LJ, Morello R.

J Bone Miner Res. 2014 Mar;29(3):666-75. doi: 10.1002/jbmr.2075.

19.

Kinetic and structural evidences on human prolidase pathological mutants suggest strategies for enzyme functional rescue.

Besio R, Gioia R, Cossu F, Monzani E, Nicolis S, Cucca L, Profumo A, Casella L, Tenni R, Bolognesi M, Rossi A, Forlino A.

PLoS One. 2013;8(3):e58792. doi: 10.1371/journal.pone.0058792. Epub 2013 Mar 13.

20.

Partial Rescue of Biochemical Parameters After Hematopoietic Stem Cell Transplantation in a Patient with Prolidase Deficiency Due to Two Novel PEPD Mutations.

Caselli D, Cimaz R, Besio R, Rossi A, De Lorenzi E, Colombo R, Cantarini L, Riva S, Spada M, Forlino A, Aricò M.

JIMD Rep. 2012;3:71-7. doi: 10.1007/8904_2011_62. Epub 2011 Sep 27.

21.

A Mn(II)-Mn(II) center in human prolidase.

Besio R, Baratto MC, Gioia R, Monzani E, Nicolis S, Cucca L, Profumo A, Casella L, Basosi R, Tenni R, Rossi A, Forlino A.

Biochim Biophys Acta. 2013 Jan;1834(1):197-204. doi: 10.1016/j.bbapap.2012.09.008. Epub 2012 Sep 19.

PMID:
22999980
22.

Differential response to intracellular stress in the skin from osteogenesis imperfecta Brtl mice with lethal and non lethal phenotype: a proteomic approach.

Bianchi L, Gagliardi A, Gioia R, Besio R, Tani C, Landi C, Cipriano M, Gimigliano A, Rossi A, Marini JC, Forlino A, Bini L.

J Proteomics. 2012 Aug 3;75(15):4717-33. doi: 10.1016/j.jprot.2012.01.038. Epub 2012 Feb 18.

PMID:
22846432
23.

Impaired osteoblastogenesis in a murine model of dominant osteogenesis imperfecta: a new target for osteogenesis imperfecta pharmacological therapy.

Gioia R, Panaroni C, Besio R, Palladini G, Merlini G, Giansanti V, Scovassi IA, Villani S, Villa I, Villa A, Vezzoni P, Tenni R, Rossi A, Marini JC, Forlino A.

Stem Cells. 2012 Jul;30(7):1465-76. doi: 10.1002/stem.1107.

24.

Improved prolidase activity assay allowed enzyme kinetic characterization and faster prolidase deficiency diagnosis.

Besio R, Monzani E, Gioia R, Nicolis S, Rossi A, Casella L, Forlino A.

Clin Chim Acta. 2011 Sep 18;412(19-20):1814-20. doi: 10.1016/j.cca.2011.06.011. Epub 2011 Jun 15.

PMID:
21699887
25.

Identifying the structure of the active sites of human recombinant prolidase.

Besio R, Alleva S, Forlino A, Lupi A, Meneghini C, Minicozzi V, Profumo A, Stellato F, Tenni R, Morante S.

Eur Biophys J. 2010 May;39(6):935-45. doi: 10.1007/s00249-009-0459-4. Epub 2009 May 5.

PMID:
19415262
26.

In utero transplantation of adult bone marrow decreases perinatal lethality and rescues the bone phenotype in the knockin murine model for classical, dominant osteogenesis imperfecta.

Panaroni C, Gioia R, Lupi A, Besio R, Goldstein SA, Kreider J, Leikin S, Vera JC, Mertz EL, Perilli E, Baruffaldi F, Villa I, Farina A, Casasco M, Cetta G, Rossi A, Frattini A, Marini JC, Vezzoni P, Forlino A.

Blood. 2009 Jul 9;114(2):459-68. doi: 10.1182/blood-2008-12-195859. Epub 2009 May 4.

27.

[Ontological and ethical status of anencephalic fetus].

Besio R M, Besio H F.

Rev Med Chil. 2008 Jun;136(6):783-8. doi: /S0034-98872008000600015. Epub 2008 Aug 26. Spanish.

28.

Oxalosis.

Besio R, Meerhoff E, Laza J, Venturini A.

Am J Ophthalmol. 1983 Mar;95(3):397-8. No abstract available.

PMID:
6829687
29.

Neonatal retinal hemorrhages and influence of perinatal factors.

Besio R, Caballero C, Meerhoff E, Schwarcz R.

Am J Ophthalmol. 1979 Jan;87(1):74-6.

PMID:
434055
30.

Familial bilateral optic nerve hypoplasia.

Hackenbruch Y, Meerhoff E, Besio R, Cardoso H.

Am J Ophthalmol. 1975 Feb;79(2):314-20.

PMID:
1115199

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