引用次数
引用: 3,717
H-指数: 29
I10-指数 : 66
出版物: 143
Relationship among VDR (BsmI and FokI), COLIA1, and CTR polymorphisms with bone mass, bone turnover markers, and sex hormones in men.
V. Braga , A. Sangalli , G. Malerba , M. Mottes
Calcified Tissue International 70 ( 6) 457 -462
35
2002
Association of CTR and COLIA1 alleles with BMD values in peri- and postmenopausal women.
V. Braga , M. Mottes , S. Mirandola , V. Lisi
Calcified Tissue International 67 ( 5) 361 -366
43
2000
Expression of Hepatitis B Surface Antigen in Human Cells by a Recombinant BK Virus DNA Vector
A. Caputo , G. Barbanti-Brodano , P. Reschiglian , M. Gianni
Journal of General Virology 69 ( 2) 459 -466
5
1988
Restoration by T4 ligase of DNA sequences sensitive to “flush”-cleaving restriction enzyme
M. Mottes , C. Morandi , S. Cremaschi , V. Sgaramella
Nucleic Acids Research 4 ( 7) 2467 -2476
9
1977
Substitution of an aspartic acid for glycine 700 in the alpha 2(I) chain of type I collagen in a recurrent lethal type II osteogenesis imperfecta dramatically affects the mineralization of bone.
L Zylberberg , L Cohen-Solal , A Sangalli , M Mottes
Journal of Biological Chemistry 269 ( 20) 14751 -14758
27
1994
Determination of a new collagen type I alpha 2 gene point mutation which causes a Gly640 Cys substitution in osteogenesis imperfecta and prenatal diagnosis by DNA hybridisation.
M Gomez-Lira , A Sangalli , P F Pignatti , M C Digilio
Journal of Medical Genetics 31 ( 12) 965 -968
7
1994
Three novel polymorphic sequence variants in the type I collagen gene COL1A1, the main disease locus for Osteogenesis Imperfecta.
S Mirandola , PF Pignatti , M Mottes
Molecular and Cellular Probes 14 ( 6) 329 -332
2000
Segregation analysis of dominant osteogenesis imperfecta in Italy.
M Mottes , L Cugola , N Cappello , P F Pignatti
Journal of Medical Genetics 27 ( 6) 367 -370
5
1990
Osteogenesis imperfecta: clinical, biochemical and molecular findings.
G Venturi , E Tedeschi , M Mottes , M Valli
Clinical Genetics 70 ( 2) 131 -139
45
2006
Deficiency of CRTAP in non-lethal recessive osteogenesis imperfecta reduces collagen deposition into matrix
M Valli , AM Barnes , A Gallanti , WA Cabral
Clinical Genetics 82 ( 5) 453 -459
27
2012
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.
M Valli , M Mottes , R Tenni , A Sangalli
Journal of Biological Chemistry 266 ( 3) 1872 -1878
39
1991
Type VI Osteogenesis Imperfecta: effect of plasma transfusion on bone metabolism
F Antoniazzi , A Pietrobelli , A Gandini , P Cavarzere
Journal of Biological Regulators and Homeostatic Agents 35 ( 5) 41 -51
1
2021
Type VI Osteogenesis imperfecta: effect of plasma transfusion on bone metabolism
F Antoniazzi , A Pietrobelli , A Gandini , P Cavarzere
JOURNAL OF BIOLOGICAL REGULATORS & HOMEOSTATIC AGENTS 36 ( 2) 389 -395
2022
Autosomal dominant benign recurrent intrahepatic cholestasis (BRIC) unlinked to 18q21 locus: Is it a new entity?
A Floreani , M Molaro , M Mottes , A Sangalli
HEPATOLOGY 28 ( 4) 420A -420A
1998
Relazione tra i polimorfismi VDR COL1A, CTR e massa ossea.
V Braga , M Mottes , Leonardo Sartori , G Bianchi
20 -20
1999
Linkage and association analysis of estrogen receptor a, collagen type I, calcitonin receptor, and vitamin B receptor genes with bone mineral density in Italian families
A Sangalli , G Malerba , L Xumerle , E Petrelli
Kurskiy nauchno-prakticheskiy vestnik «Chelovek i ego zdorov'e»[Kursk scientific and practical bulletin «Human health»] ( 2) 22 -9
2
2011
Osteogenesis Imperfecta: A Heterogeneous Heritable Disease
M Deiana , G Malerba , L Dalle Carbonare , M Mottes
Deform Bone Muscles 1 06 -15
2018
DNA probes to evaluate possible association of papovaviruses with human tumors.
Giuseppe BARBANTI BRODANO , E Silini , M Mottes , G Milanesi
Gallo RC, Della Porta G. and Albertini A., Raven Press 147 -155
7
1987
CCM analysis of collagen type I mutations in very severe and lethal OI
M Gomez Lira , M Mottes , F Zolezzi , L Cohen-Solal
Fifth International Conference on Osteogenesis Imperfecta
2
1993
A cellular test for Ehlers-Danlos syndromes diagnosis.
Marina Colombi , Nicoletta Zoppi , PJ Coucke , M Mottes
EUROPEAN JOURNAL OF HUMAN GENETICS 14 124 -124
2006