CATALOGO DEI PRODOTTI DELLA RICERCA

MOTTES, Monica
 Distribuzione geografica
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Continente #
NA - Nord America 9.034
EU - Europa 7.170
AS - Asia 6.031
SA - Sud America 615
Continente sconosciuto - Info sul continente non disponibili 174
AF - Africa 127
OC - Oceania 29
Totale 23.180
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Nazione #
US - Stati Uniti d'America 8.840
CN - Cina 2.661
RU - Federazione Russa 2.258
SG - Singapore 1.903
GB - Regno Unito 1.668
IT - Italia 997
BR - Brasile 464
VN - Vietnam 443
SE - Svezia 416
DE - Germania 381
HK - Hong Kong 371
FR - Francia 370
IE - Irlanda 351
FI - Finlandia 315
KR - Corea 161
UA - Ucraina 109
CA - Canada 101
BD - Bangladesh 91
NL - Olanda 76
IN - India 69
JP - Giappone 64
ID - Indonesia 63
MX - Messico 48
AR - Argentina 47
TR - Turchia 45
BE - Belgio 43
NG - Nigeria 39
PL - Polonia 38
IQ - Iraq 33
ZA - Sudafrica 28
AU - Australia 27
ES - Italia 27
EC - Ecuador 26
AT - Austria 21
CL - Cile 19
PK - Pakistan 19
SA - Arabia Saudita 16
CO - Colombia 15
LT - Lituania 15
VE - Venezuela 14
PH - Filippine 12
DK - Danimarca 11
UZ - Uzbekistan 11
CH - Svizzera 10
MA - Marocco 10
EG - Egitto 9
PE - Perù 9
JM - Giamaica 8
LB - Libano 8
NI - Nicaragua 8
TN - Tunisia 8
AE - Emirati Arabi Uniti 7
PY - Paraguay 7
RO - Romania 7
UY - Uruguay 7
AZ - Azerbaigian 6
BJ - Benin 6
BO - Bolivia 6
CR - Costa Rica 6
CZ - Repubblica Ceca 6
DZ - Algeria 6
HN - Honduras 6
JO - Giordania 6
MY - Malesia 6
AL - Albania 5
GR - Grecia 5
IL - Israele 5
NO - Norvegia 5
NP - Nepal 5
PA - Panama 5
PS - Palestinian Territory 5
SK - Slovacchia (Repubblica Slovacca) 5
KE - Kenya 4
MD - Moldavia 4
SI - Slovenia 4
TG - Togo 4
TH - Thailandia 4
EE - Estonia 3
KZ - Kazakistan 3
LV - Lettonia 3
RS - Serbia 3
TW - Taiwan 3
A2 - ???statistics.table.value.countryCode.A2??? 2
BG - Bulgaria 2
CG - Congo 2
CW - ???statistics.table.value.countryCode.CW??? 2
CY - Cipro 2
DM - Dominica 2
ET - Etiopia 2
GT - Guatemala 2
HR - Croazia 2
HU - Ungheria 2
IR - Iran 2
MT - Malta 2
PT - Portogallo 2
SC - Seychelles 2
SN - Senegal 2
AM - Armenia 1
AO - Angola 1
BA - Bosnia-Erzegovina 1
Totale 22.986
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Città #
Southend 1.370
Ashburn 1.172
Singapore 1.096
Jacksonville 840
Chandler 804
San Jose 757
Moscow 748
Dallas 684
Verona 476
Woodbridge 390
Hong Kong 364
Dublin 349
Ann Arbor 301
Houston 254
The Dalles 251
Beijing 238
Council Bluffs 231
New York 221
Los Angeles 136
Wilmington 135
Princeton 127
Lawrence 126
Nanjing 126
Ho Chi Minh City 124
Jinan 118
Shenyang 97
Helsinki 84
Santa Clara 84
São Paulo 78
Sindelfingen 74
Hebei 73
Buffalo 68
Dong Ket 68
Hanoi 65
Boardman 63
Munich 63
Tianjin 61
Milan 51
Tokyo 50
Hangzhou 47
Jakarta 47
Changsha 45
Redondo Beach 45
Ningbo 42
Orem 42
London 41
Nanchang 41
Haikou 40
Toronto 40
Brussels 39
San Francisco 38
Columbus 37
Guangzhou 37
Redmond 37
Abuja 35
Taiyuan 35
Turku 35
Jiaxing 34
Warsaw 32
Taizhou 31
Frankfurt am Main 30
Phoenix 30
Zhengzhou 30
Montreal 29
Seattle 29
Denver 28
Chicago 27
Seoul 27
Amsterdam 26
Atlanta 25
Annandale 24
Falls Church 24
Fuzhou 23
Norwalk 22
Philadelphia 22
Brooklyn 21
Johannesburg 21
Naples 21
Rio de Janeiro 21
Mexico City 20
Lancaster 19
Kent 18
Lappeenranta 18
Belo Horizonte 16
Lanzhou 16
Redwood City 16
Sant'Ambrogio di Valpolicella 16
Stockholm 16
Biên Hòa 15
Boston 15
Da Nang 15
Poplar 15
Rome 15
Auburn Hills 14
Brisbane 14
Florence 14
Vienna 14
Washington 14
Chennai 13
Manchester 13
Totale 14.043
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Nome #
CRISPR/Cas9 genome editing in melanoma cells: new insight of RUNT domain 1.306
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 314
Characterization and functional analysis of cis-acting elements of the human farnesyl diphosphate synthetase (FDPS) gene 5' flanking region. 298
An integrated approach identifies new oncotargets in melanoma 295
Can half-marathon affect overall health? The yin-yang of sport 285
A common beta hexosaminidase gene mutation in adult Sandhoff disease patients. 277
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 267
A base substitution at IVS-19 3' splice junction causes exon 20 skipping in pro alpha 2(I) collagen mRNA and produces mild osteogenesis imperfecta 256
Association of CTR and COLIA1 alleles with BMD values in peri and postmenopausal women 249
Type VI Osteogenesis imperfecta: effect of plasma transfusion on bone metabolism 246
A 931 +2T-C transition in one COL1A2 allele causes exon 16 skipping in pro alpha 2(I) mRNA and produces moderately severe OI 230
The genetic background of osteoporosis in cystic fibrosis: association analysis with polymorphic markers in four candidate genes 227
TREATMENT OF SKELETAL DISEASES WITH A NATURALLY DERIVED ANTIOXIDANT AND BISPHOSPHONATE EMBEDDED NANOPARTICLES 227
Lack of expression of SERPINF1, the gene coding for pigment epithelium derived factor, causes progressively deforming Osteogenesis Imperfecta with normal type I collagen 226
Defects of SERPINF1 cause progressively deforming recessive osteogenesis imperfecta with normal Collagen I 225
A potential role for astaxanthin in the treatment of bone diseases (Review) 224
Indagine sul coinvolgimento di gene LRP5 nella densità minerale ossea 223
A novel mutation which represents the fifth non-pathogenic polymorphism in the coding sequence of the arylsulfatase A gene 221
Analisi di linkage di geni candidati per densità minerale 220
Runx2 stimulates neoangiogenesis through the Runt domain in melanoma 220
A potential role of RUNX2- RUNT domain in modulating the expression of genes involved in bone metastases: an in vitro study with melanoma cells 220
Bone histomorphometry in acromegaly patients with fragility vertebral fractures 218
Identificazione ed analisi della regione 5' del gene umano per l'enzima farnesil difosfato sintetasi (FDPS). 217
Haplotype analysis of collagen type I genes in the general population and in osteogenesis imperfecta families. 208
Linkage analysis for prenatal diagnosis in a familial case of Stickler syndrome 207
BEL β‐Trefoil Reduces the Migration Ability of RUNX2 Expressing Melanoma Cells in Xenotransplanted Zebrafish 205
The Runt domain of RUNX2 induces the migration of melanoma cells to bone 204
Detection of mutations in the ALD gene (ABCD1) in seven Italian families: description of four novel mutations 202
Effects of oral anticoagulant therapy on gene expression in crosstalk between osteogenic progenitor cells and endothelial cells 202
Allelic frequencies of FBN1 gene polymorphisms and genetic analysis of Italian families with Marfan syndrome 200
Osteogenesis Imperfecta: clinical, biochemical and molecular findings 200
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 198
Densità dei siti variabili in sequenze codificanti del gene COL1A1 con diversa rilevanza funzionale 197
Hypophosphatasia and mesenchymal stem cells: a therapeutic promise 195
Runx2 overexpression compromises bone quality in acromegalic patients 195
Relationship between vertebral fractures, bone mineral density, and osteometabolic profile in HIV and Hepatitis B and C-infected patients treated with ART 194
Molecular screening in OI patients at Verona reference center: typical mutations 192
New Insights into the Runt Domain of RUNX2 in Melanoma Cell Proliferation and Migration 190
Autosomal dominant benign recurrent intrahepatic cholestasis (BRIC) unlinked to 18q21 and 2q24 189
Studio di associazione del gene per il recettore alpha degli estrogeni con densità minerale ossea in donne italiane 189
A novel 4-bp deletion creates a premature stop codon and dramatically decreases HEXB mRNA levels in a severe case of Sandhoff disease 186
Association of BK virus with human brain tumors and tumors of pancreatic islets 185
Molecole, cellule e organismi 185
Clodronate as a Therapeutic Strategy against Osteoarthritis 185
Physical activity prevents cartilage degradation: a metabolomics study pinpoints the involvement of vitamin B6 184
Methylsulfonylmethane enhances MSC chondrogenic commitment and promotes pre-osteoblasts formation 184
Association study of Estrogen receptor-alpha gene with mineral bone density in a group of unrelated Italian females 182
Four new cases of lethal Osteogenesis Imperfecta due to glycine substitutions in the COL1A1 and COL1A2 genes 180
The recurrent causal mutation for osteogenesis imperfecta type V occurs at a highly methylated CpG dinucleotide within the IFITM5 gene 180
Clodronate as a Therapeutic Strategy against Osteoarthritis 179
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 177
Association study of Estrogen receptor-alpha gene with mineral bone density in a group of unrelated Italian females 177
No osteonecrosis of the jaw in children and adolescents treated with Neridronate for osteogenesis imperfecta. 177
Two novel frameshift mutations in the adrenoleukodystrophy gene in Italian patients 176
Two novel C-terminus RUNX2 mutations in two cleidocranial dysplasia (CCD) patients impairing p53 expression 175
A new type of EcoRI polymorphism of the human ribosomal DNA repeating unit revealed by analysis of cloned DNA fragments 172
Restoration by T4 ligase of DNA sequences sensitive to "flush" cleaving restriction enzyme 172
Current and emerging treatments for the management of osteogenesis imperfecta 172
Genetic testing for adult-type hypolactasia in Italian families 171
Fisetin: an integrated approach to identify a strategy promoting osteogenesis 171
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 170
Effects of intense physical exercise on osteogenic commitment of mesenchymal progenitors 170
Osteogenesis Imperfecta: Practical treatment guidelines 169
Enhanced osteogenic differentiation in Zoledronate-treated osteoporotic patients 169
Splicing mutation causes infantile Sandhoff disease 168
Condrodisplasie e mucopolisaccaridosi. Fisipopatologia, Clinica e Terapia 165
Immunosenesscence and physical exercise: search for healthy ageing 165
osteoporosis in (beta) - Thalassemia: Clinical and Genetic Aspect 164
Linkage analysis of LRP5 gene with bone mass density 163
Type I collagen molecular map lends insights into the domain structure of the fibril and the genotype-phenotype relationship for some collagen mutations 162
Effects of a 4400 km ultra-cycling non-competitive race and related training on body composition and circulating progenitors differentiation 159
Osteogenesis imperfecta and type-I collagen mutations. A lethal variant caused by a Gly910-->Ala substitution in the alpha 1 (I) chain 159
Osteogenesi Imperfetta 159
Increased Gene Expression of RUNX2 and SOX9 in Mesenchymal Circulating Progenitors Is Associated with Autophagy during Physical Activity 158
Segregation analysis of dominant osteogenesis imperfecta in Italy 157
Convergent transcription of the Escherichia coli hisG gene cloned in Bacillus subtilis stops in the vicinity of the attenuator 156
Effects of physical exercise on the prevention of stem cells senescence 156
Expression of hepatitis B surface antigen in human cells by a recombinant BK virus DNA vector 155
Physical Exercise Modulates miR-21-5p, miR-129-5p, miR-378-5p, and miR-188-5p Expression in Progenitor Cells Promoting Osteogenesis 154
Physical activity modulates miRNAs levels and enhances MYOD expression in myoblasts 154
Modulation of miR-204 expression during chondrogenesis 151
Cellular stress due to impairment of collagen prolyl hydroxylation complex is rescued by the chaperone 4-phenylbutyrate 148
Osteogenic differentiation in healthy and pathological conditions 148
A novel intragenic polymorphism within the COL1A1 locus which can be detected by Taq I restriction of amplified genomic DNA 147
Molecular genetic characterization of two metachromatic leukodystrophy patients who carry the T799G mutation acid show different phenotypes; description of a novel null-type mutation (Human Genetics (1998) 102 (459-463)) 145
Two novel missense mutations causing adrenoleukodystrophy in Italian patients 145
Intarfamilial variable expressivity of osteogenesis imperfecta due to mosaicism for a lethal G382R substitution in the COL1A1 gene 145
Deficiency of CRTAP in non-lethal recessive osteogenesis imperfecta reduces collagen deposition into matrix 145
Different specific activities of the monomeric and oligomeric forms of plasmid DNA in transformation of B. subtilis and E. coli 142
Severe (type III) osteogenesis imperfecta due to glycine substitutions in the central domain of the collagen triple helix 142
Osteogenesis Imperfecta at the beginning of bone and joint decade 141
Expression of FBXW11 in normal and disease-associated osteogenic cells 140
Linkage analysis of three candidate gene polymorphisms with bone density in a sample of Italian families 140
Haplotype frequencies of the collagen type-I genes in the Italian population 139
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 139
Rapid and efficient genotype analysis of the COL1A1 Sp1 binding site dimorphism, a genetic marker for bone mineral density 137
Circulating progenitor stem cells are important biomarkers of chondrogenesis and osteogenesis: employment in diagnosis and treatment follow up 133
Molecular and lifestyle factors modulating obesity disease 133
Possible hyperattenuation of transcription in the Escherichia coli hisG gene cloned in Bacillus subtilis 131
Specific pattern of instability of Escherichia coli HisG gene cloned in Bacillus subtilis via the Staphylococcus aureus plasmid pCS194 131
Totale 19.682
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Categoria #
all - tutte 73.887
article - articoli 57.116
book - libri 0
conference - conferenze 12.134
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 4.637
Totale 147.774
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022619 0 0 0 62 28 37 10 59 35 25 89 274
2022/20232.370 160 236 221 402 202 562 24 151 303 12 52 45
2023/20242.350 42 92 136 139 179 1.246 107 104 2 56 167 80
2024/20252.689 167 203 134 468 169 75 104 146 350 148 192 533
2025/20268.157 543 389 649 1.293 2.012 576 787 455 632 491 182 148
2026/20271.120 114 165 402 439 0 0 0 0 0 0 0 0
Totale 23.180