FIND

researchers

DISCOVER

relevant articles

PROMOTE

your research

now for free

Maurizia Valli

Research Profile

Disorders

Chemicals & Drugs

Concepts & Ideas

Anatomy

Physiology

Procedures

Co-author Network

Publications

TOP 3
Maurizia Valli; Simona Viglio; M A Weis; F Antoniazzi; A M Barnes; W A Cabral; David R Eyre; Angelo Gallanti; Sergey Leikin; Elena Makareeva; J C Marini; Monica Mottes
Deficiency of CRTAP in non-lethal recessive osteogenesis imperfecta reduces collagen deposition into matrix.
Giacomo Venturi; Monica Vincenzi; Attilio Boner; Massimiliano Corradi; Luca Dalle Carbonare; Alberto Gandini; Elena Monti; Monica Mottes; Enrico Pelilli; Maria Teresa Valenti; Maurizia Valli; Franco Antoniazzi
Lack of expression of SERPINF1, the gene coding for pigment epithelium-derived factor, causes progressively deforming osteogenesis imperfecta with normal type I collagen.
Salvatore Savasta; Marri Chiara Leoni; Luisa Strocchio; Daniela Pizzo; Maria Valentina Spartà; Mario Lima; Maurizia Valli; Antonietta Marchi
A rare cause of recurrent spontaneous pneumothorax.

Register for free to view:

Visualized networks:

See your personal network in
sophisticated graphical views

GeoTargeted Searches:

Locate experts around the world
and connect with global collaborators

Research Profiles:

See the research activity
of experts around the globe

Geonetwork of Maurizia Valli (preview)

Cities where this author has publications
Cities where co-authors of this author have publications

Flash Player Required

All Publications

2012: Maurizia Valli; Simona Viglio; M A Weis; F Antoniazzi; A M Barnes; W A Cabral; David R Eyre; Angelo Gallanti; Sergey Leikin; Elena Makareeva; J C Marini; Monica Mottes
Deficiency of CRTAP in non-lethal recessive osteogenesis imperfecta reduces collagen deposition into matrix.
Clinical genetics 2012;82(5):453-9.
2012: Giacomo Venturi; Monica Vincenzi; Attilio Boner; Massimiliano Corradi; Luca Dalle Carbonare; Alberto Gandini; Elena Monti; Monica Mottes; Enrico Pelilli; Maria Teresa Valenti; Maurizia Valli; Franco Antoniazzi
Lack of expression of SERPINF1, the gene coding for pigment epithelium-derived factor, causes progressively deforming osteogenesis imperfecta with normal type I collagen.
Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research 2012;27(3):723-8.
2011: Salvatore Savasta; Marri Chiara Leoni; Luisa Strocchio; Daniela Pizzo; Maria Valentina Spartà; Mario Lima; Maurizia Valli; Antonietta Marchi
A rare cause of recurrent spontaneous pneumothorax.
Clinical pediatrics 2011;50(5):456-8.
2009: Lorenzo Dolcini; Alberto Sala; Monica Campagnoli; Sara Labò; Maurizia Valli; Livia Visai; Lorenzo Minchiotti; Hugo L Monaco; Monica Galliano
Identification of the amniotic fluid insulin-like growth factor binding protein-1 phosphorylation sites and propensity to proteolysis of the isoforms.
The FEBS journal 2009;276(20):6033-46.
2008: Simona Viglio; Nicoletta Zoppi; Antonella Sangalli; Angelo Gallanti; Sergio Barlati; Monica Mottes; Marina Colombi; Maurizia Valli
Rescue of migratory defects of Ehlers-Danlos syndrome fibroblasts in vitro by type V collagen but not insulin-like binding protein-1.
The Journal of investigative dermatology 2008;128(8):1915-9.
2008: Simona Viglio; Nicoletta Zoppi; Antonella Sangalli; Angelo Gallanti; Sergio Barlati; Monica Mottes; Marina Colombi; Maurizia Valli
Wound repair capability in EDS fibroblasts can be retrieved by exogenous type V collagen.
TheScientificWorldJournal 2008;8():956-8.
2007: Salvatore Savasta; Mario Crispino; Maurizia Valli; Alberto Calligaro; Cesare Zambelloni; Carlo Poggiani
Subependymal periventricular heterotopias in a patient with ehlers-danlos syndrome: a new case.
Journal of child neurology 2007;22(3):317-20.
2006: Claudia Colonna; Ida Genta; Paola Perugini; Franca Pavanetto; Tiziana Modena; Maurizia Valli; Corrado Muzzarelli; Bice Conti
5-methyl-pyrrolidinone chitosan films as carriers for buccal administration of proteins.
AAPS PharmSciTech 2006;7(3):70.
2005: Alberto Sala; Stefano Capaldi; Monica Campagnoli; Beniamino Faggion; Sara Labò; Massimiliano Perduca; Assunta Romano; Maria E Carrizo; Maurizia Valli; Livia Visai; Lorenzo Minchiotti; Monica Galliano; Hugo L Monaco
Structure and properties of the C-terminal domain of insulin-like growth factor-binding protein-1 isolated from human amniotic fluid.
The Journal of biological chemistry 2005;280(33):29812-9.
2001: Roberta Salvini; Anna Maria Bardoni; Maurizia Valli; M Trinchera
beta 1,3-Galactosyltransferase beta 3Gal-T5 acts on the GlcNAcbeta 1-->3Galbeta 1-->4GlcNAcbeta 1-->R sugar chains of carcinoembryonic antigen and other N-linked glycoproteins and is down-regulated in colon adenocarcinomas.
The Journal of biological chemistry 2001;276(5):3564-73.
1999: Anna Maria Bardoni; Maurizia Valli; M Trinchera
Differential expression of beta1,3galactosyltransferases in human colon cells derived from adenocarcinomas or normal mucosa.
FEBS letters 1999;451(1):75-80.
1999: Maurizia Valli; Anna Maria Bardoni; M Trinchera
Mouse C127 cells transfected with fucosyltransferase fuc-TIII express masked Lewisx but not Lewisx antigen.
Glycobiology 1999;9(1):83-91.
1998: Maurizia Valli; Angelo Gallanti; S Bozzaro; M Trinchera
Beta-1,3-galactosyltransferase and alpha-1,2-fucosyltransferase involved in the biosynthesis of type-1-chain carbohydrate antigens in human colon adenocarcinoma cell lines.
European journal of biochemistry / FEBS 1998;256(2):494-501.
1996: Franco Antoniazzi; Francesco Bertoldo; Monica Mottes; Maurizia Valli; S Sirpresi; Giorgio Zamboni; R Valentini; L Tató
Growth hormone treatment in osteogenesis imperfecta with quantitative defect of type I collagen synthesis.
The Journal of pediatrics 1996;129(3):432-9.
1996: KM Dyne; Maurizia Valli; Antonella Forlino; Monica Mottes; H Kresse; Giuseppe Cetta
Deficient expression of the small proteoglycan decorin in a case of severe/lethal osteogenesis imperfecta.
American journal of medical genetics 1996;63(1):161-6.
1995: F Zolezzi; Antonella Forlino; Monica Mottes; Maurizia Valli; A Sensi; E Calzolari; Pier Franco Pignatti; Giuseppe Cetta
A 931 + 2T-->C transition in one COL1A2 allele causes exon 16 skipping in PRO alpha 2(I) mRNA and produces moderately severe OI.
Human mutation 1995;6(3):268-71.
1994: Antonella Forlino; F Zolezzi; Maurizia Valli; Pier Franco Pignatti; Giuseppe Cetta; P C Brunelli; Monica Mottes
Severe (type III) osteogenesis imperfecta due to glycine substitutions in the central domain of the collagen triple helix.
Human molecular genetics 1994;3(12):2201-6.
1994: Monica Mottes; A Sangalli; Maurizia Valli; Antonella Forlino; Macarena Gomez-Lira; Franco Antoniazzi; C D Constantinou-Deltas; Giuseppe Cetta; Pier Franco Pignatti
A base substitution at IVS-19 3'-end splice junction causes exon 20 skipping in pro alpha 2(I) collagen mRNA and produces mild osteogenesis imperfecta.
Human genetics 1994;93(6):681-7.
1993: Maurizia Valli; F Zolezzi; Monica Mottes; Franco Antoniazzi; F Stanzial; R Tenni; Pier Franco Pignatti; Giuseppe Cetta
Gly85 to Val substitution in pro alpha 1(I) chain causes mild osteogenesis imperfecta and introduces a susceptibility to protease digestion.
European journal of biochemistry / FEBS 1993;217(1):77-82.
1993: Maurizia Valli; Antonio Rossi; Antonella Forlino; R Tenni; Giuseppe Cetta
Extracellular matrix deposition in cultured dermal fibroblasts from four probands affected by osteogenesis imperfecta.
Matrix (Stuttgart, Germany) 1993;13(4):275-80.
1993: Maurizia Valli; A Sangalli; Antonio Rossi; Monica Mottes; Antonella Forlino; R Tenni; Pier Franco Pignatti; Giuseppe Cetta
Osteogenesis imperfecta and type-I collagen mutations. A lethal variant caused by a Gly910-->Ala substitution in the alpha 1 (I) chain.
European journal of biochemistry / FEBS 1993;211(3):415-9.
1993: R Tenni; Maurizia Valli; Antonio Rossi; Giuseppe Cetta
Possible role of overglycosylation in the type I collagen triple helical domain in the molecular pathogenesis of osteogenesis imperfecta.
American journal of medical genetics 1993;45(2):252-6.
1993: Monica Mottes; Macarena Gomez-Lira; Maurizia Valli; G Scarano; Fortunato Lonardo; Antonella Forlino; Giuseppe Cetta; Pier Franco Pignatti
Paternal mosaicism for a COL1A1 dominant mutation (alpha 1 Ser-415) causes recurrent osteogenesis imperfecta.
Human mutation 1993;2(3):196-204.
1993: Giuseppe Cetta; Antonio Rossi; R Tenni; Maurizia Valli; Antonella Forlino; G Zanaboni; KM Dyne; G R Burgio
Deposition of mutant type I collagen in the extracellular matrix of cultured dermal fibroblasts in osteogenesis imperfecta.
Connective tissue research 1993;29(1):41-9.
1992: Monica Mottes; A Sangalli; Maurizia Valli; Macarena Gomez-Lira; R Tenni; P Buttitta; Pier Franco Pignatti; Giuseppe Cetta
Mild dominant osteogenesis imperfecta with intrafamilial variability: the cause is a serine for glycine alpha 1(I) 901 substitution in a type-I collagen gene.
Human genetics 1992;89(5):480-4.
1991: Maurizia Valli; Monica Mottes; R Tenni; A Sangalli; Macarena Gomez-Lira; Antonio Rossi; Franco Antoniazzi; Giuseppe Cetta; Pier Franco Pignatti
A de novo G to T transversion in a pro-alpha 1 (I) collagen gene for a moderate case of osteogenesis imperfecta. Substitution of cysteine for glycine 178 in the triple helical domain.
The Journal of biological chemistry 1991;266(3):1872-8.
1990: Maurizia Valli; R Tenni; Giuseppe Cetta
Moderately severe osteogenesis imperfecta: biochemical studies showing variable defect localization in the triple-helical domain of type I collagen.
Matrix (Stuttgart, Germany) 1990;10(3):200-5.
1990: M Godfrey; Susan B Olson; R G Burgio; Alberto Martini; Maurizia Valli; Giuseppe Cetta; H Hori; D W Hollister
Unilateral microfibrillar abnormalities in a case of asymmetric Marfan syndrome.
American journal of human genetics 1990;46(4):661-71.
1990: R Tenni; Antonio Rossi; Maurizia Valli; Monica Mottes; Pier Franco Pignatti; Giuseppe Cetta
Anomalous cysteine in type I collagen. Localisation by chemical cleavage of the protein using 2-nitro-5-thiocyanobenzoic acid and by mismatch analysis of cDNA heteroduplexes.
Matrix (Stuttgart, Germany) 1990;10(1):20-6.
1989: G Zanaboni; M P De Agostini; Maurizia Valli; KM Dyne; Giuseppe Cetta; D W Hollister; A A Castellani
Marfan syndrome: a collagen disorder?
The Italian journal of biochemistry 1989;38(4):288A-289A.
1988: R Tenni; Giuseppe Cetta; KM Dyne; Maurizia Valli; G Zanaboni; A A Castellani
Severe nonlethal osteogenesis imperfecta: biochemical heterogeneity.
Annals of the New York Academy of Sciences 1988;543():73-82.
1980: Giuseppe Cetta; L Lenzi; Carlo L Balduini; Maurizia Valli; R Tenni; Giancarlo De Luca; A A Castellani
Glycosaminoglycan alterations in osteogenesis imperfecta.
The Italian journal of biochemistry 1980;29(5):337-50.