CATALOGO DEI PRODOTTI DELLA RICERCA

MOTTES, Monica
 Distribuzione geografica
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Continente #
NA - Nord America 7.801
EU - Europa 7.056
AS - Asia 5.939
SA - Sud America 580
AF - Africa 122
OC - Oceania 29
Continente sconosciuto - Info sul continente non disponibili 3
Totale 21.530
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Nazione #
US - Stati Uniti d'America 7.667
CN - Cina 2.653
RU - Federazione Russa 2.257
SG - Singapore 1.889
GB - Regno Unito 1.654
IT - Italia 914
BR - Brasile 444
VN - Vietnam 441
SE - Svezia 415
DE - Germania 379
FR - Francia 369
HK - Hong Kong 368
IE - Irlanda 350
FI - Finlandia 315
KR - Corea 161
UA - Ucraina 108
NL - Olanda 73
IN - India 69
CA - Canada 65
JP - Giappone 62
ID - Indonesia 59
AR - Argentina 46
TR - Turchia 45
MX - Messico 43
BE - Belgio 42
BD - Bangladesh 39
NG - Nigeria 39
PL - Polonia 38
IQ - Iraq 33
AU - Australia 27
ZA - Sudafrica 26
EC - Ecuador 25
ES - Italia 25
AT - Austria 21
PK - Pakistan 17
CL - Cile 15
LT - Lituania 15
SA - Arabia Saudita 15
VE - Venezuela 12
DK - Danimarca 11
PH - Filippine 11
UZ - Uzbekistan 11
CH - Svizzera 10
MA - Marocco 10
CO - Colombia 9
EG - Egitto 9
PE - Perù 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
CZ - Repubblica Ceca 6
DZ - Algeria 6
JO - Giordania 6
LB - Libano 6
AL - Albania 5
GR - Grecia 5
IL - Israele 5
JM - Giamaica 5
MY - Malesia 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
NI - Nicaragua 4
SI - Slovenia 4
TG - Togo 4
TH - Thailandia 4
CR - Costa Rica 3
HN - Honduras 3
KZ - Kazakistan 3
LV - Lettonia 3
RS - Serbia 3
TW - Taiwan 3
A2 - ???statistics.table.value.countryCode.A2??? 2
BG - Bulgaria 2
CY - Cipro 2
DM - Dominica 2
ET - Etiopia 2
HR - Croazia 2
HU - Ungheria 2
IR - Iran 2
MT - Malta 2
SN - Senegal 2
AM - Armenia 1
AO - Angola 1
BY - Bielorussia 1
CG - Congo 1
CW - ???statistics.table.value.countryCode.CW??? 1
DO - Repubblica Dominicana 1
EE - Estonia 1
GA - Gabon 1
GT - Guatemala 1
Totale 21.513
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Città #
Southend 1.370
Singapore 1.090
Ashburn 964
Jacksonville 839
Chandler 804
Moscow 748
Dallas 659
San Jose 601
Verona 474
Woodbridge 390
Hong Kong 361
Dublin 349
Ann Arbor 301
Houston 251
The Dalles 251
Beijing 234
New York 204
Wilmington 135
Princeton 127
Lawrence 126
Nanjing 126
Ho Chi Minh City 124
Los Angeles 120
Jinan 118
Shenyang 97
Helsinki 84
Sindelfingen 74
Hebei 73
Dong Ket 68
Hanoi 64
São Paulo 64
Boardman 63
Munich 63
Tianjin 61
Buffalo 60
Council Bluffs 56
Tokyo 49
Hangzhou 47
Jakarta 47
Changsha 45
Redondo Beach 45
Milan 43
Ningbo 42
London 41
Nanchang 41
Santa Clara 41
Haikou 40
Orem 40
Brussels 39
Guangzhou 37
Redmond 37
Columbus 36
Abuja 35
Taiyuan 35
Turku 35
Jiaxing 34
San Francisco 34
Warsaw 32
Taizhou 31
Zhengzhou 30
Frankfurt am Main 29
Seattle 28
Seoul 27
Amsterdam 26
Toronto 26
Denver 25
Falls Church 24
Fuzhou 23
Atlanta 22
Montreal 22
Norwalk 22
Phoenix 21
Rio de Janeiro 21
Chicago 19
Johannesburg 19
Brooklyn 18
Kent 18
Lappeenranta 18
Mexico City 18
Lancaster 17
Lanzhou 16
Redwood City 16
Sant'Ambrogio di Valpolicella 16
Stockholm 16
Belo Horizonte 15
Biên Hòa 15
Da Nang 15
Poplar 15
Auburn Hills 14
Boston 14
Brisbane 14
Philadelphia 14
Vienna 14
Chennai 13
Manchester 13
Naples 13
Paris 13
Florence 12
Rome 12
Bologna 11
Totale 13.253
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Nome #
CRISPR/Cas9 genome editing in melanoma cells: new insight of RUNT domain 1.298
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 291
An integrated approach identifies new oncotargets in melanoma 287
Characterization and functional analysis of cis-acting elements of the human farnesyl diphosphate synthetase (FDPS) gene 5' flanking region. 280
A common beta hexosaminidase gene mutation in adult Sandhoff disease patients. 268
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 261
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 247
Can half-marathon affect overall health? The yin-yang of sport 247
Association of CTR and COLIA1 alleles with BMD values in peri and postmenopausal women 237
A 931 +2T-C transition in one COL1A2 allele causes exon 16 skipping in pro alpha 2(I) mRNA and produces moderately severe OI 221
Type VI Osteogenesis imperfecta: effect of plasma transfusion on bone metabolism 219
Lack of expression of SERPINF1, the gene coding for pigment epithelium derived factor, causes progressively deforming Osteogenesis Imperfecta with normal type I collagen 216
A potential role of RUNX2- RUNT domain in modulating the expression of genes involved in bone metastases: an in vitro study with melanoma cells 213
A novel mutation which represents the fifth non-pathogenic polymorphism in the coding sequence of the arylsulfatase A gene 212
TREATMENT OF SKELETAL DISEASES WITH A NATURALLY DERIVED ANTIOXIDANT AND BISPHOSPHONATE EMBEDDED NANOPARTICLES 212
Defects of SERPINF1 cause progressively deforming recessive osteogenesis imperfecta with normal Collagen I 208
A potential role for astaxanthin in the treatment of bone diseases (Review) 208
Analisi di linkage di geni candidati per densità minerale 207
Indagine sul coinvolgimento di gene LRP5 nella densità minerale ossea 206
Bone histomorphometry in acromegaly patients with fragility vertebral fractures 206
The genetic background of osteoporosis in cystic fibrosis: association analysis with polymorphic markers in four candidate genes 201
Haplotype analysis of collagen type I genes in the general population and in osteogenesis imperfecta families. 199
Runx2 stimulates neoangiogenesis through the Runt domain in melanoma 197
Linkage analysis for prenatal diagnosis in a familial case of Stickler syndrome 195
BEL β‐Trefoil Reduces the Migration Ability of RUNX2 Expressing Melanoma Cells in Xenotransplanted Zebrafish 195
Detection of mutations in the ALD gene (ABCD1) in seven Italian families: description of four novel mutations 194
Allelic frequencies of FBN1 gene polymorphisms and genetic analysis of Italian families with Marfan syndrome 194
The Runt domain of RUNX2 induces the migration of melanoma cells to bone 193
Effects of oral anticoagulant therapy on gene expression in crosstalk between osteogenic progenitor cells and endothelial cells 192
Osteogenesis Imperfecta: clinical, biochemical and molecular findings 189
Identificazione ed analisi della regione 5' del gene umano per l'enzima farnesil difosfato sintetasi (FDPS). 188
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 187
Runx2 overexpression compromises bone quality in acromegalic patients 187
Densità dei siti variabili in sequenze codificanti del gene COL1A1 con diversa rilevanza funzionale 186
Molecular screening in OI patients at Verona reference center: typical mutations 182
New Insights into the Runt Domain of RUNX2 in Melanoma Cell Proliferation and Migration 182
Autosomal dominant benign recurrent intrahepatic cholestasis (BRIC) unlinked to 18q21 and 2q24 181
Hypophosphatasia and mesenchymal stem cells: a therapeutic promise 179
Clodronate as a Therapeutic Strategy against Osteoarthritis 178
Association of BK virus with human brain tumors and tumors of pancreatic islets 177
A novel 4-bp deletion creates a premature stop codon and dramatically decreases HEXB mRNA levels in a severe case of Sandhoff disease 176
Molecole, cellule e organismi 175
Studio di associazione del gene per il recettore alpha degli estrogeni con densità minerale ossea in donne italiane 173
Association study of Estrogen receptor-alpha gene with mineral bone density in a group of unrelated Italian females 173
Clodronate as a Therapeutic Strategy against Osteoarthritis 172
Physical activity prevents cartilage degradation: a metabolomics study pinpoints the involvement of vitamin B6 172
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 169
The recurrent causal mutation for osteogenesis imperfecta type V occurs at a highly methylated CpG dinucleotide within the IFITM5 gene 169
Restoration by T4 ligase of DNA sequences sensitive to "flush" cleaving restriction enzyme 167
Four new cases of lethal Osteogenesis Imperfecta due to glycine substitutions in the COL1A1 and COL1A2 genes 167
No osteonecrosis of the jaw in children and adolescents treated with Neridronate for osteogenesis imperfecta. 166
Effects of intense physical exercise on osteogenic commitment of mesenchymal progenitors 166
Two novel frameshift mutations in the adrenoleukodystrophy gene in Italian patients 165
Association study of Estrogen receptor-alpha gene with mineral bone density in a group of unrelated Italian females 165
Two novel C-terminus RUNX2 mutations in two cleidocranial dysplasia (CCD) patients impairing p53 expression 165
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 161
Genetic testing for adult-type hypolactasia in Italian families 161
Current and emerging treatments for the management of osteogenesis imperfecta 160
Immunosenesscence and physical exercise: search for healthy ageing 160
A new type of EcoRI polymorphism of the human ribosomal DNA repeating unit revealed by analysis of cloned DNA fragments 159
Enhanced osteogenic differentiation in Zoledronate-treated osteoporotic patients 159
Fisetin: an integrated approach to identify a strategy promoting osteogenesis 159
Methylsulfonylmethane enhances MSC chondrogenic commitment and promotes pre-osteoblasts formation 159
Splicing mutation causes infantile Sandhoff disease 158
Osteogenesis Imperfecta: Practical treatment guidelines 156
Increased Gene Expression of RUNX2 and SOX9 in Mesenchymal Circulating Progenitors Is Associated with Autophagy during Physical Activity 153
Condrodisplasie e mucopolisaccaridosi. Fisipopatologia, Clinica e Terapia 151
Osteogenesi Imperfetta 150
Relationship between vertebral fractures, bone mineral density, and osteometabolic profile in HIV and Hepatitis B and C-infected patients treated with ART 150
Osteogenesis imperfecta and type-I collagen mutations. A lethal variant caused by a Gly910-->Ala substitution in the alpha 1 (I) chain 148
Segregation analysis of dominant osteogenesis imperfecta in Italy 148
Convergent transcription of the Escherichia coli hisG gene cloned in Bacillus subtilis stops in the vicinity of the attenuator 148
Effects of a 4400 km ultra-cycling non-competitive race and related training on body composition and circulating progenitors differentiation 147
Linkage analysis of LRP5 gene with bone mass density 147
Expression of hepatitis B surface antigen in human cells by a recombinant BK virus DNA vector 145
Physical Exercise Modulates miR-21-5p, miR-129-5p, miR-378-5p, and miR-188-5p Expression in Progenitor Cells Promoting Osteogenesis 145
Modulation of miR-204 expression during chondrogenesis 144
A novel intragenic polymorphism within the COL1A1 locus which can be detected by Taq I restriction of amplified genomic DNA 143
Effects of physical exercise on the prevention of stem cells senescence 143
Physical activity modulates miRNAs levels and enhances MYOD expression in myoblasts 143
Cellular stress due to impairment of collagen prolyl hydroxylation complex is rescued by the chaperone 4-phenylbutyrate 139
Two novel missense mutations causing adrenoleukodystrophy in Italian patients 138
Intarfamilial variable expressivity of osteogenesis imperfecta due to mosaicism for a lethal G382R substitution in the COL1A1 gene 138
osteoporosis in (beta) - Thalassemia: Clinical and Genetic Aspect 137
Osteogenic differentiation in healthy and pathological conditions 136
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 135
Type I collagen molecular map lends insights into the domain structure of the fibril and the genotype-phenotype relationship for some collagen mutations 135
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)) 134
Expression of FBXW11 in normal and disease-associated osteogenic cells 133
Different specific activities of the monomeric and oligomeric forms of plasmid DNA in transformation of B. subtilis and E. coli 133
Severe (type III) osteogenesis imperfecta due to glycine substitutions in the central domain of the collagen triple helix 133
Linkage analysis of three candidate gene polymorphisms with bone density in a sample of Italian families 132
Deficiency of CRTAP in non-lethal recessive osteogenesis imperfecta reduces collagen deposition into matrix 132
Osteogenesis Imperfecta at the beginning of bone and joint decade 131
Specific pattern of instability of Escherichia coli HisG gene cloned in Bacillus subtilis via the Staphylococcus aureus plasmid pCS194 126
Rapid and efficient genotype analysis of the COL1A1 Sp1 binding site dimorphism, a genetic marker for bone mineral density 126
Circulating progenitor stem cells are important biomarkers of chondrogenesis and osteogenesis: employment in diagnosis and treatment follow up 126
Molecular and lifestyle factors modulating obesity disease 124
Haplotype frequencies of the collagen type-I genes in the Italian population 122
Multiple forms of human dihydrofolate reductase messenger RNA. Cloning and expression in Escherichia coli of their DNA coding sequence 122
Totale 18.489
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Categoria #
all - tutte 64.495
article - articoli 49.601
book - libri 0
conference - conferenze 10.806
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 4.088
Totale 128.990
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021295 0 0 0 0 0 0 0 0 0 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
2025/20267.797 543 389 649 1.293 2.012 576 787 455 632 461 0 0
Totale 21.700