CATALOGO DEI PRODOTTI DELLA RICERCA

MOTTES, Monica
 Distribuzione geografica
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Continente #
NA - Nord America 5.818
EU - Europa 4.678
AS - Asia 4.427
SA - Sud America 410
AF - Africa 31
OC - Oceania 25
Continente sconosciuto - Info sul continente non disponibili 3
Totale 15.392
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Nazione #
US - Stati Uniti d'America 5.754
CN - Cina 2.413
GB - Regno Unito 1.578
SG - Singapore 1.202
IT - Italia 740
SE - Svezia 404
DE - Germania 353
BR - Brasile 350
IE - Irlanda 349
FR - Francia 337
HK - Hong Kong 335
RU - Federazione Russa 324
FI - Finlandia 299
VN - Vietnam 147
UA - Ucraina 104
KR - Corea 97
NL - Olanda 53
ID - Indonesia 46
BE - Belgio 40
CA - Canada 40
JP - Giappone 40
TR - Turchia 33
IN - India 29
AU - Australia 23
AR - Argentina 19
AT - Austria 19
BD - Bangladesh 17
PL - Polonia 15
MX - Messico 14
IQ - Iraq 13
EC - Ecuador 10
PK - Pakistan 10
ZA - Sudafrica 10
ES - Italia 8
LT - Lituania 8
VE - Venezuela 8
CL - Cile 7
DK - Danimarca 7
SA - Arabia Saudita 7
BO - Bolivia 6
CZ - Repubblica Ceca 6
NO - Norvegia 5
RO - Romania 5
SK - Slovacchia (Repubblica Slovacca) 5
UZ - Uzbekistan 5
MA - Marocco 4
NP - Nepal 4
TG - Togo 4
TN - Tunisia 4
AE - Emirati Arabi Uniti 3
AZ - Azerbaigian 3
CO - Colombia 3
JM - Giamaica 3
LB - Libano 3
LV - Lettonia 3
PE - Perù 3
PS - Palestinian Territory 3
TH - Thailandia 3
UY - Uruguay 3
A2 - ???statistics.table.value.countryCode.A2??? 2
BG - Bulgaria 2
EG - Egitto 2
GR - Grecia 2
HN - Honduras 2
HR - Croazia 2
IL - Israele 2
IR - Iran 2
JO - Giordania 2
KE - Kenya 2
MD - Moldavia 2
PA - Panama 2
TW - Taiwan 2
AL - Albania 1
AM - Armenia 1
AO - Angola 1
BY - Bielorussia 1
CH - Svizzera 1
CR - Costa Rica 1
CW - ???statistics.table.value.countryCode.CW??? 1
CY - Cipro 1
DZ - Algeria 1
EE - Estonia 1
HU - Ungheria 1
IM - Isola di Man 1
KG - Kirghizistan 1
KI - Kiribati 1
LU - Lussemburgo 1
MN - Mongolia 1
MY - Malesia 1
NG - Nigeria 1
NI - Nicaragua 1
NZ - Nuova Zelanda 1
PY - Paraguay 1
RS - Serbia 1
SN - Senegal 1
SZ - Regno dello Swaziland 1
TJ - Tagikistan 1
VC - Saint Vincent e Grenadine 1
Totale 15.392
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Città #
Southend 1.370
Jacksonville 839
Chandler 804
Dallas 650
Singapore 621
Woodbridge 390
Ashburn 366
Dublin 348
Verona 334
Hong Kong 331
Ann Arbor 301
Houston 238
Beijing 180
New York 157
Wilmington 135
Princeton 127
Lawrence 126
Nanjing 126
Jinan 118
Shenyang 97
Helsinki 76
Sindelfingen 74
Hebei 73
Dong Ket 68
The Dalles 64
Boardman 63
Munich 63
Los Angeles 59
Tianjin 53
Hangzhou 47
Changsha 44
Jakarta 43
Ningbo 42
Milan 41
Haikou 40
Nanchang 40
Buffalo 38
Brussels 37
Redmond 37
Columbus 36
Redondo Beach 35
Taiyuan 35
Jiaxing 34
Turku 34
Council Bluffs 32
Guangzhou 32
San Francisco 32
Tokyo 32
São Paulo 31
Taizhou 31
Santa Clara 30
Zhengzhou 29
Seattle 27
Seoul 27
Falls Church 24
Fuzhou 23
Norwalk 22
Ho Chi Minh City 21
London 20
Moscow 19
Toronto 19
Kent 18
Lancaster 17
Rio de Janeiro 17
Lanzhou 16
Redwood City 16
Sant'Ambrogio di Valpolicella 16
Frankfurt am Main 15
Auburn Hills 14
Philadelphia 14
Amsterdam 13
Brisbane 13
Chicago 13
Lappeenranta 13
Phoenix 13
Vienna 12
Belo Horizonte 11
Bologna 11
Düsseldorf 11
Florence 11
Naples 11
Brooklyn 10
Dearborn 10
Rome 10
St Petersburg 10
Washington 10
Nuremberg 9
Warsaw 9
Atlanta 8
Cagliari 8
Fairfield 8
Mantova 8
Montreal 8
Boston 7
Brasília 7
Campinas 6
Curitiba 6
Des Moines 6
Detroit 6
Dhaka 6
Totale 9.712
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Nome #
CRISPR/Cas9 genome editing in melanoma cells: new insight of RUNT domain 1.225
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 219
An integrated approach identifies new oncotargets in melanoma 205
A common beta hexosaminidase gene mutation in adult Sandhoff disease patients. 201
Characterization and functional analysis of cis-acting elements of the human farnesyl diphosphate synthetase (FDPS) gene 5' flanking region. 197
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 178
Association of CTR and COLIA1 alleles with BMD values in peri and postmenopausal women 177
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 176
The genetic background of osteoporosis in cystic fibrosis: association analysis with polymorphic markers in four candidate genes 162
TREATMENT OF SKELETAL DISEASES WITH A NATURALLY DERIVED ANTIOXIDANT AND BISPHOSPHONATE EMBEDDED NANOPARTICLES 161
Can half-marathon affect overall health? The yin-yang of sport 161
Indagine sul coinvolgimento di gene LRP5 nella densità minerale ossea 159
A 931 +2T-C transition in one COL1A2 allele causes exon 16 skipping in pro alpha 2(I) mRNA and produces moderately severe OI 154
Lack of expression of SERPINF1, the gene coding for pigment epithelium derived factor, causes progressively deforming Osteogenesis Imperfecta with normal type I collagen 151
Molecole, cellule e organismi 150
A novel mutation which represents the fifth non-pathogenic polymorphism in the coding sequence of the arylsulfatase A gene 148
Type VI Osteogenesis imperfecta: effect of plasma transfusion on bone metabolism 145
Analisi di linkage di geni candidati per densità minerale 142
A potential role of RUNX2- RUNT domain in modulating the expression of genes involved in bone metastases: an in vitro study with melanoma cells 142
Linkage analysis for prenatal diagnosis in a familial case of Stickler syndrome 141
Defects of SERPINF1 cause progressively deforming recessive osteogenesis imperfecta with normal Collagen I 141
Hypophosphatasia and mesenchymal stem cells: a therapeutic promise 141
Haplotype analysis of collagen type I genes in the general population and in osteogenesis imperfecta families. 139
Two novel frameshift mutations in the adrenoleukodystrophy gene in Italian patients 138
Allelic frequencies of FBN1 gene polymorphisms and genetic analysis of Italian families with Marfan syndrome 137
The Runt domain of RUNX2 induces the migration of melanoma cells to bone 137
Splicing mutation causes infantile Sandhoff disease 136
Runx2 overexpression compromises bone quality in acromegalic patients 134
Clodronate as a Therapeutic Strategy against Osteoarthritis 133
Genetic testing for adult-type hypolactasia in Italian families 132
Detection of mutations in the ALD gene (ABCD1) in seven Italian families: description of four novel mutations 131
Densità dei siti variabili in sequenze codificanti del gene COL1A1 con diversa rilevanza funzionale 131
Bone histomorphometry in acromegaly patients with fragility vertebral fractures 130
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 129
Runx2 stimulates neoangiogenesis through the Runt domain in melanoma 129
Identificazione ed analisi della regione 5' del gene umano per l'enzima farnesil difosfato sintetasi (FDPS). 128
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 127
Four new cases of lethal Osteogenesis Imperfecta due to glycine substitutions in the COL1A1 and COL1A2 genes 127
The recurrent causal mutation for osteogenesis imperfecta type V occurs at a highly methylated CpG dinucleotide within the IFITM5 gene 125
A novel 4-bp deletion creates a premature stop codon and dramatically decreases HEXB mRNA levels in a severe case of Sandhoff disease 124
Effects of oral anticoagulant therapy on gene expression in crosstalk between osteogenic progenitor cells and endothelial cells 123
Autosomal dominant benign recurrent intrahepatic cholestasis (BRIC) unlinked to 18q21 and 2q24 121
BEL β‐Trefoil Reduces the Migration Ability of RUNX2 Expressing Melanoma Cells in Xenotransplanted Zebrafish 121
Association of BK virus with human brain tumors and tumors of pancreatic islets 120
Osteogenesi Imperfetta 120
Immunosenesscence and physical exercise: search for healthy ageing 120
Molecular screening in OI patients at Verona reference center: typical mutations 119
Osteogenesis Imperfecta: clinical, biochemical and molecular findings 119
Effects of intense physical exercise on osteogenic commitment of mesenchymal progenitors 119
A new type of EcoRI polymorphism of the human ribosomal DNA repeating unit revealed by analysis of cloned DNA fragments 118
Restoration by T4 ligase of DNA sequences sensitive to "flush" cleaving restriction enzyme 118
Intarfamilial variable expressivity of osteogenesis imperfecta due to mosaicism for a lethal G382R substitution in the COL1A1 gene 118
New Insights into the Runt Domain of RUNX2 in Melanoma Cell Proliferation and Migration 118
Clodronate as a Therapeutic Strategy against Osteoarthritis 118
Enhanced osteogenic differentiation in Zoledronate-treated osteoporotic patients 117
Segregation analysis of dominant osteogenesis imperfecta in Italy 116
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)) 116
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 115
Osteogenesis Imperfecta: Practical treatment guidelines 114
Two novel missense mutations causing adrenoleukodystrophy in Italian patients 114
Convergent transcription of the Escherichia coli hisG gene cloned in Bacillus subtilis stops in the vicinity of the attenuator 113
Studio di associazione del gene per il recettore alpha degli estrogeni con densità minerale ossea in donne italiane 111
Association study of Estrogen receptor-alpha gene with mineral bone density in a group of unrelated Italian females 111
Linkage analysis of LRP5 gene with bone mass density 110
A potential role for astaxanthin in the treatment of bone diseases (Review) 110
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 109
Osteogenesis imperfecta and type-I collagen mutations. A lethal variant caused by a Gly910-->Ala substitution in the alpha 1 (I) chain 109
Osteogenic differentiation in healthy and pathological conditions 109
Condrodisplasie e mucopolisaccaridosi. Fisipopatologia, Clinica e Terapia 108
Physical activity prevents cartilage degradation: a metabolomics study pinpoints the involvement of vitamin B6 107
Osteogenesis Imperfecta at the beginning of bone and joint decade 106
Expression of hepatitis B surface antigen in human cells by a recombinant BK virus DNA vector 105
Rapid and efficient genotype analysis of the COL1A1 Sp1 binding site dimorphism, a genetic marker for bone mineral density 103
No osteonecrosis of the jaw in children and adolescents treated with Neridronate for osteogenesis imperfecta. 102
Type I collagen molecular map lends insights into the domain structure of the fibril and the genotype-phenotype relationship for some collagen mutations 102
Circulating progenitor stem cells are important biomarkers of chondrogenesis and osteogenesis: employment in diagnosis and treatment follow up 101
Physical Exercise Modulates miR-21-5p, miR-129-5p, miR-378-5p, and miR-188-5p Expression in Progenitor Cells Promoting Osteogenesis 100
osteoporosis in (beta) - Thalassemia: Clinical and Genetic Aspect 99
Association study of Estrogen receptor-alpha gene with mineral bone density in a group of unrelated Italian females 98
Multiple forms of human dihydrofolate reductase messenger RNA. Cloning and expression in Escherichia coli of their DNA coding sequence 98
Current and emerging treatments for the management of osteogenesis imperfecta 98
Deficiency of CRTAP in non-lethal recessive osteogenesis imperfecta reduces collagen deposition into matrix 98
Different specific activities of the monomeric and oligomeric forms of plasmid DNA in transformation of B. subtilis and E. coli 96
Linkage analysis of three candidate gene polymorphisms with bone density in a sample of Italian families 96
Cellular stress due to impairment of collagen prolyl hydroxylation complex is rescued by the chaperone 4-phenylbutyrate 96
Relationship between vertebral fractures, bone mineral density, and osteometabolic profile in HIV and Hepatitis B and C-infected patients treated with ART 96
Paternal mosaicism for a COL1A1 dominant mutation (alpha 1 Ser-415) causes recurrent osteogenesis imperfecta 95
A novel intragenic polymorphism within the COL1A1 locus which can be detected by Taq I restriction of amplified genomic DNA 94
Increased Gene Expression of RUNX2 and SOX9 in Mesenchymal Circulating Progenitors Is Associated with Autophagy during Physical Activity 94
Possible hyperattenuation of transcription in the Escherichia coli hisG gene cloned in Bacillus subtilis 93
Two novel C-terminus RUNX2 mutations in two cleidocranial dysplasia (CCD) patients impairing p53 expression 93
Specific pattern of instability of Escherichia coli HisG gene cloned in Bacillus subtilis via the Staphylococcus aureus plasmid pCS194 92
Role of autophagy in bone and muscle biology 91
Role of microRNAs in progenitor cell commitment and osteogenic differentiation in health and disease (Review) 90
Molecular and lifestyle factors modulating obesity disease 90
Haplotype frequencies of the collagen type-I genes in the Italian population 89
Stickler syndrome and vitreoretinal degeneration: correlation between locus mitation and vitreous phenotype. Apropos of a case 89
Severe (type III) osteogenesis imperfecta due to glycine substitutions in the central domain of the collagen triple helix 88
Molecular defects and cellular dysfunctions in restricted growth conditions 87
Ectopic expression of the osteogenic master gene RUNX2 in melanoma 87
Totale 13.370
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Categoria #
all - tutte 52.967
article - articoli 40.651
book - libri 0
conference - conferenze 8.942
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 3.374
Totale 105.934
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021951 0 0 0 168 144 136 24 93 91 17 138 140
2021/20221.151 141 369 22 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
2025/20261.654 543 389 649 73 0 0 0 0 0 0 0 0
Totale 15.557