CATALOGO DEI PRODOTTI DELLA RICERCA

MOTTES, Monica
 Distribuzione geografica
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Continente #
EU - Europa 6.744
NA - Nord America 6.472
AS - Asia 5.188
SA - Sud America 528
AF - Africa 60
OC - Oceania 25
Continente sconosciuto - Info sul continente non disponibili 3
Totale 19.020
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Nazione #
US - Stati Uniti d'America 6.366
CN - Cina 2.584
RU - Federazione Russa 2.253
GB - Regno Unito 1.620
SG - Singapore 1.557
IT - Italia 754
BR - Brasile 413
SE - Svezia 412
DE - Germania 360
IE - Irlanda 350
FR - Francia 339
HK - Hong Kong 337
FI - Finlandia 305
VN - Vietnam 288
KR - Corea 132
UA - Ucraina 107
NL - Olanda 62
ID - Indonesia 54
CA - Canada 52
JP - Giappone 47
AR - Argentina 42
BE - Belgio 40
TR - Turchia 40
IN - India 39
PL - Polonia 35
MX - Messico 33
BD - Bangladesh 28
AU - Australia 23
ES - Italia 22
ZA - Sudafrica 21
AT - Austria 19
EC - Ecuador 19
IQ - Iraq 16
LT - Lituania 14
CL - Cile 13
PK - Pakistan 11
SA - Arabia Saudita 9
VE - Venezuela 9
DK - Danimarca 8
CO - Colombia 7
MA - Marocco 7
UY - Uruguay 7
BJ - Benin 6
BO - Bolivia 6
CZ - Repubblica Ceca 6
PE - Perù 6
TN - Tunisia 6
AE - Emirati Arabi Uniti 5
NO - Norvegia 5
PA - Panama 5
PY - Paraguay 5
RO - Romania 5
SK - Slovacchia (Repubblica Slovacca) 5
UZ - Uzbekistan 5
AZ - Azerbaigian 4
DZ - Algeria 4
EG - Egitto 4
IL - Israele 4
LB - Libano 4
MD - Moldavia 4
NP - Nepal 4
TG - Togo 4
HN - Honduras 3
JM - Giamaica 3
JO - Giordania 3
LV - Lettonia 3
NI - Nicaragua 3
PS - Palestinian Territory 3
TH - Thailandia 3
A2 - ???statistics.table.value.countryCode.A2??? 2
AL - Albania 2
BG - Bulgaria 2
CH - Svizzera 2
CR - Costa Rica 2
DM - Dominica 2
GR - Grecia 2
HR - Croazia 2
IR - Iran 2
KE - Kenya 2
NG - Nigeria 2
TW - Taiwan 2
AM - Armenia 1
AO - Angola 1
BY - Bielorussia 1
CW - ???statistics.table.value.countryCode.CW??? 1
CY - Cipro 1
DO - Repubblica Dominicana 1
EE - Estonia 1
ET - Etiopia 1
GT - Guatemala 1
GY - Guiana 1
HU - Ungheria 1
IM - Isola di Man 1
KG - Kirghizistan 1
KI - Kiribati 1
LK - Sri Lanka 1
LU - Lussemburgo 1
MN - Mongolia 1
MY - Malesia 1
NZ - Nuova Zelanda 1
Totale 19.015
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Città #
Southend 1.370
Jacksonville 839
Chandler 804
Singapore 803
Moscow 747
Dallas 655
Ashburn 574
Woodbridge 390
Dublin 349
Verona 337
Hong Kong 333
Ann Arbor 301
Houston 249
Beijing 231
New York 193
Wilmington 135
Princeton 127
Lawrence 126
Nanjing 126
The Dalles 126
Jinan 118
Los Angeles 103
Shenyang 97
Helsinki 76
Sindelfingen 74
Hebei 73
Ho Chi Minh City 73
Dong Ket 68
Boardman 63
Munich 63
Tianjin 60
São Paulo 55
Buffalo 48
Hangzhou 47
Changsha 45
Jakarta 45
Redondo Beach 45
Milan 42
Ningbo 42
Haikou 40
Nanchang 40
Tokyo 39
Brussels 37
Redmond 37
Columbus 36
Santa Clara 36
Guangzhou 35
Taiyuan 35
Turku 35
Jiaxing 34
London 33
San Francisco 33
Council Bluffs 32
Taizhou 31
Warsaw 29
Zhengzhou 29
Seattle 27
Seoul 27
Hanoi 26
Falls Church 24
Fuzhou 23
Norwalk 22
Toronto 22
Denver 21
Orem 20
Rio de Janeiro 20
Amsterdam 19
Brooklyn 18
Kent 18
Chicago 17
Lancaster 17
Phoenix 17
Atlanta 16
Lanzhou 16
Lappeenranta 16
Redwood City 16
Sant'Ambrogio di Valpolicella 16
Frankfurt am Main 15
Johannesburg 15
Auburn Hills 14
Mexico City 14
Montreal 14
Philadelphia 14
Poplar 14
Brisbane 13
Stockholm 13
Belo Horizonte 12
Biên Hòa 12
Boston 12
Naples 12
Rome 12
Vienna 12
Bologna 11
Düsseldorf 11
Florence 11
Ankara 10
Buenos Aires 10
Dearborn 10
Nuremberg 10
San Jose 10
Totale 11.342
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Nome #
CRISPR/Cas9 genome editing in melanoma cells: new insight of RUNT domain 1.269
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 268
An integrated approach identifies new oncotargets in melanoma 259
A common beta hexosaminidase gene mutation in adult Sandhoff disease patients. 251
Characterization and functional analysis of cis-acting elements of the human farnesyl diphosphate synthetase (FDPS) gene 5' flanking region. 240
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 239
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 225
Association of CTR and COLIA1 alleles with BMD values in peri and postmenopausal women 214
Can half-marathon affect overall health? The yin-yang of sport 212
A 931 +2T-C transition in one COL1A2 allele causes exon 16 skipping in pro alpha 2(I) mRNA and produces moderately severe OI 201
Type VI Osteogenesis imperfecta: effect of plasma transfusion on bone metabolism 192
Indagine sul coinvolgimento di gene LRP5 nella densità minerale ossea 192
TREATMENT OF SKELETAL DISEASES WITH A NATURALLY DERIVED ANTIOXIDANT AND BISPHOSPHONATE EMBEDDED NANOPARTICLES 190
A novel mutation which represents the fifth non-pathogenic polymorphism in the coding sequence of the arylsulfatase A gene 187
Lack of expression of SERPINF1, the gene coding for pigment epithelium derived factor, causes progressively deforming Osteogenesis Imperfecta with normal type I collagen 186
Defects of SERPINF1 cause progressively deforming recessive osteogenesis imperfecta with normal Collagen I 184
Analisi di linkage di geni candidati per densità minerale 184
Bone histomorphometry in acromegaly patients with fragility vertebral fractures 183
A potential role of RUNX2- RUNT domain in modulating the expression of genes involved in bone metastases: an in vitro study with melanoma cells 182
A potential role for astaxanthin in the treatment of bone diseases (Review) 181
The genetic background of osteoporosis in cystic fibrosis: association analysis with polymorphic markers in four candidate genes 178
The Runt domain of RUNX2 induces the migration of melanoma cells to bone 175
Osteogenesis Imperfecta: clinical, biochemical and molecular findings 174
Detection of mutations in the ALD gene (ABCD1) in seven Italian families: description of four novel mutations 173
Haplotype analysis of collagen type I genes in the general population and in osteogenesis imperfecta families. 173
Allelic frequencies of FBN1 gene polymorphisms and genetic analysis of Italian families with Marfan syndrome 173
Runx2 stimulates neoangiogenesis through the Runt domain in melanoma 172
Linkage analysis for prenatal diagnosis in a familial case of Stickler syndrome 170
Densità dei siti variabili in sequenze codificanti del gene COL1A1 con diversa rilevanza funzionale 170
Identificazione ed analisi della regione 5' del gene umano per l'enzima farnesil difosfato sintetasi (FDPS). 166
Runx2 overexpression compromises bone quality in acromegalic patients 165
Effects of oral anticoagulant therapy on gene expression in crosstalk between osteogenic progenitor cells and endothelial cells 163
BEL β‐Trefoil Reduces the Migration Ability of RUNX2 Expressing Melanoma Cells in Xenotransplanted Zebrafish 163
Autosomal dominant benign recurrent intrahepatic cholestasis (BRIC) unlinked to 18q21 and 2q24 162
Molecole, cellule e organismi 162
New Insights into the Runt Domain of RUNX2 in Melanoma Cell Proliferation and Migration 162
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 161
Molecular screening in OI patients at Verona reference center: typical mutations 161
Hypophosphatasia and mesenchymal stem cells: a therapeutic promise 158
Clodronate as a Therapeutic Strategy against Osteoarthritis 158
Four new cases of lethal Osteogenesis Imperfecta due to glycine substitutions in the COL1A1 and COL1A2 genes 157
Clodronate as a Therapeutic Strategy against Osteoarthritis 157
A novel 4-bp deletion creates a premature stop codon and dramatically decreases HEXB mRNA levels in a severe case of Sandhoff disease 156
Association of BK virus with human brain tumors and tumors of pancreatic islets 154
Two novel frameshift mutations in the adrenoleukodystrophy gene in Italian patients 154
Association study of Estrogen receptor-alpha gene with mineral bone density in a group of unrelated Italian females 151
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 149
A new type of EcoRI polymorphism of the human ribosomal DNA repeating unit revealed by analysis of cloned DNA fragments 148
The recurrent causal mutation for osteogenesis imperfecta type V occurs at a highly methylated CpG dinucleotide within the IFITM5 gene 148
Splicing mutation causes infantile Sandhoff disease 147
Effects of intense physical exercise on osteogenic commitment of mesenchymal progenitors 147
Physical activity prevents cartilage degradation: a metabolomics study pinpoints the involvement of vitamin B6 147
Genetic testing for adult-type hypolactasia in Italian families 146
Enhanced osteogenic differentiation in Zoledronate-treated osteoporotic patients 146
Restoration by T4 ligase of DNA sequences sensitive to "flush" cleaving restriction enzyme 144
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 143
No osteonecrosis of the jaw in children and adolescents treated with Neridronate for osteogenesis imperfecta. 143
Current and emerging treatments for the management of osteogenesis imperfecta 142
Studio di associazione del gene per il recettore alpha degli estrogeni con densità minerale ossea in donne italiane 142
Immunosenesscence and physical exercise: search for healthy ageing 140
Osteogenesi Imperfetta 139
Two novel C-terminus RUNX2 mutations in two cleidocranial dysplasia (CCD) patients impairing p53 expression 139
Osteogenesis Imperfecta: Practical treatment guidelines 137
Association study of Estrogen receptor-alpha gene with mineral bone density in a group of unrelated Italian females 137
Linkage analysis of LRP5 gene with bone mass density 133
Segregation analysis of dominant osteogenesis imperfecta in Italy 130
Physical Exercise Modulates miR-21-5p, miR-129-5p, miR-378-5p, and miR-188-5p Expression in Progenitor Cells Promoting Osteogenesis 130
Increased Gene Expression of RUNX2 and SOX9 in Mesenchymal Circulating Progenitors Is Associated with Autophagy during Physical Activity 130
Osteogenesis imperfecta and type-I collagen mutations. A lethal variant caused by a Gly910-->Ala substitution in the alpha 1 (I) chain 129
Convergent transcription of the Escherichia coli hisG gene cloned in Bacillus subtilis stops in the vicinity of the attenuator 129
Fisetin: an integrated approach to identify a strategy promoting osteogenesis 129
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)) 128
Intarfamilial variable expressivity of osteogenesis imperfecta due to mosaicism for a lethal G382R substitution in the COL1A1 gene 128
A novel intragenic polymorphism within the COL1A1 locus which can be detected by Taq I restriction of amplified genomic DNA 128
Two novel missense mutations causing adrenoleukodystrophy in Italian patients 127
Methylsulfonylmethane enhances MSC chondrogenic commitment and promotes pre-osteoblasts formation 126
Physical activity modulates miRNAs levels and enhances MYOD expression in myoblasts 126
Expression of hepatitis B surface antigen in human cells by a recombinant BK virus DNA vector 124
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 124
Modulation of miR-204 expression during chondrogenesis 124
Condrodisplasie e mucopolisaccaridosi. Fisipopatologia, Clinica e Terapia 123
Type I collagen molecular map lends insights into the domain structure of the fibril and the genotype-phenotype relationship for some collagen mutations 121
Relationship between vertebral fractures, bone mineral density, and osteometabolic profile in HIV and Hepatitis B and C-infected patients treated with ART 121
Effects of physical exercise on the prevention of stem cells senescence 119
Effects of a 4400 km ultra-cycling non-competitive race and related training on body composition and circulating progenitors differentiation 118
Osteogenic differentiation in healthy and pathological conditions 118
osteoporosis in (beta) - Thalassemia: Clinical and Genetic Aspect 117
Linkage analysis of three candidate gene polymorphisms with bone density in a sample of Italian families 117
Osteogenesis Imperfecta at the beginning of bone and joint decade 117
Deficiency of CRTAP in non-lethal recessive osteogenesis imperfecta reduces collagen deposition into matrix 117
Cellular stress due to impairment of collagen prolyl hydroxylation complex is rescued by the chaperone 4-phenylbutyrate 117
Rapid and efficient genotype analysis of the COL1A1 Sp1 binding site dimorphism, a genetic marker for bone mineral density 115
Circulating progenitor stem cells are important biomarkers of chondrogenesis and osteogenesis: employment in diagnosis and treatment follow up 115
Molecular and lifestyle factors modulating obesity disease 115
Expression of FBXW11 in normal and disease-associated osteogenic cells 113
Different specific activities of the monomeric and oligomeric forms of plasmid DNA in transformation of B. subtilis and E. coli 111
Multiple forms of human dihydrofolate reductase messenger RNA. Cloning and expression in Escherichia coli of their DNA coding sequence 109
Haplotype frequencies of the collagen type-I genes in the Italian population 107
Specific pattern of instability of Escherichia coli HisG gene cloned in Bacillus subtilis via the Staphylococcus aureus plasmid pCS194 107
Possible hyperattenuation of transcription in the Escherichia coli hisG gene cloned in Bacillus subtilis 106
Totale 16.439
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Categoria #
all - tutte 59.680
article - articoli 45.860
book - libri 0
conference - conferenze 10.030
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 3.790
Totale 119.360
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021639 0 0 0 0 0 136 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
2025/20265.286 543 389 649 1.293 2.012 400 0 0 0 0 0 0
Totale 19.189