CATALOGO DEI PRODOTTI DELLA RICERCA

MOTTES, Monica
 Distribuzione geografica
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Continente #
NA - Nord America 4.654
EU - Europa 4.405
AS - Asia 3.131
SA - Sud America 23
OC - Oceania 22
AF - Africa 10
Continente sconosciuto - Info sul continente non disponibili 2
Totale 12.247
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Nazione #
US - Stati Uniti d'America 4.637
CN - Cina 2.291
GB - Regno Unito 1.566
IT - Italia 708
SG - Singapore 577
SE - Svezia 404
IE - Irlanda 349
FR - Francia 319
RU - Federazione Russa 319
DE - Germania 265
FI - Finlandia 249
VN - Vietnam 108
UA - Ucraina 100
ID - Indonesia 37
BE - Belgio 36
NL - Olanda 34
JP - Giappone 27
KR - Corea 27
AU - Australia 21
TR - Turchia 21
CA - Canada 14
IN - India 11
AT - Austria 8
BR - Brasile 7
CL - Cile 6
DK - Danimarca 6
PL - Polonia 6
CZ - Repubblica Ceca 5
HK - Hong Kong 5
PK - Pakistan 5
AR - Argentina 4
ES - Italia 4
TG - Togo 4
LV - Lettonia 3
NO - Norvegia 3
RO - Romania 3
SA - Arabia Saudita 3
SK - Slovacchia (Repubblica Slovacca) 3
A2 - ???statistics.table.value.countryCode.A2??? 2
AE - Emirati Arabi Uniti 2
AZ - Azerbaigian 2
BO - Bolivia 2
EG - Egitto 2
GR - Grecia 2
HR - Croazia 2
LT - Lituania 2
MD - Moldavia 2
PE - Perù 2
TH - Thailandia 2
TW - Taiwan 2
UZ - Uzbekistan 2
AM - Armenia 1
BD - Bangladesh 1
BG - Bulgaria 1
BY - Bielorussia 1
CO - Colombia 1
CR - Costa Rica 1
CY - Cipro 1
EC - Ecuador 1
EE - Estonia 1
HU - Ungheria 1
IL - Israele 1
IM - Isola di Man 1
IQ - Iraq 1
IR - Iran 1
JM - Giamaica 1
KE - Kenya 1
KG - Kirghizistan 1
LU - Lussemburgo 1
MA - Marocco 1
MN - Mongolia 1
NP - Nepal 1
NZ - Nuova Zelanda 1
PA - Panama 1
RS - Serbia 1
TN - Tunisia 1
ZA - Sudafrica 1
Totale 12.247
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Città #
Southend 1.391
Jacksonville 848
Chandler 804
Singapore 469
Woodbridge 400
Dublin 348
Verona 330
Ashburn 319
Ann Arbor 301
Houston 236
Beijing 165
New York 142
Wilmington 136
Princeton 128
Lawrence 127
Nanjing 126
Jinan 118
Shenyang 97
Sindelfingen 75
Hebei 73
Dong Ket 68
Helsinki 67
Boardman 63
Tianjin 50
Hangzhou 48
Changsha 42
Ningbo 42
Haikou 41
Nanchang 40
Jakarta 37
Milan 37
Redmond 37
Taiyuan 35
Brussels 33
Jiaxing 33
Taizhou 31
Guangzhou 29
Zhengzhou 29
San Francisco 26
Seattle 26
Falls Church 24
Fuzhou 24
Seoul 24
Norwalk 22
Tokyo 21
Dallas 19
Kent 19
Lanzhou 18
Moscow 18
Lancaster 17
Los Angeles 16
Redwood City 16
Sant'Ambrogio di Valpolicella 16
Santa Clara 15
Auburn Hills 14
Philadelphia 13
Brisbane 12
Düsseldorf 12
Toronto 12
Bologna 11
Florence 11
London 11
Dearborn 10
St Petersburg 10
Washington 10
Chicago 9
Cagliari 8
Fairfield 8
Mantova 8
Vienna 8
Rome 7
Des Moines 6
Detroit 6
Naples 6
Phoenix 6
Riva 6
Tombolo 6
Andover 5
Binetto 5
Melbourne 5
Amsterdam 4
Brno 4
Cambridge 4
Clearwater 4
Esslingen am Neckar 4
Lappeenranta 4
Leawood 4
Lomé 4
Munich 4
Pomezia 4
Sala Di Cesenatico 4
Schio 4
Tomsk 4
Turin 4
Bratislava 3
Brescia 3
Bruino 3
Buk-gu 3
Edinburgh 3
Ikast 3
Totale 8.015
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Nome #
CRISPR/Cas9 genome editing in melanoma cells: new insight of RUNT domain 1.194
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 155
Association of CTR and COLIA1 alleles with BMD values in peri and postmenopausal women 145
Indagine sul coinvolgimento di gene LRP5 nella densità minerale ossea 142
A common beta hexosaminidase gene mutation in adult Sandhoff disease patients. 140
TREATMENT OF SKELETAL DISEASES WITH A NATURALLY DERIVED ANTIOXIDANT AND BISPHOSPHONATE EMBEDDED NANOPARTICLES 140
Characterization and functional analysis of cis-acting elements of the human farnesyl diphosphate synthetase (FDPS) gene 5' flanking region. 137
Molecole, cellule e organismi 131
Lack of expression of SERPINF1, the gene coding for pigment epithelium derived factor, causes progressively deforming Osteogenesis Imperfecta with normal type I collagen 130
An integrated approach identifies new oncotargets in melanoma 129
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 128
The genetic background of osteoporosis in cystic fibrosis: association analysis with polymorphic markers in four candidate genes 123
Can half-marathon affect overall health? The yin-yang of sport 123
Genetic testing for adult-type hypolactasia in Italian families 122
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 119
Hypophosphatasia and mesenchymal stem cells: a therapeutic promise 118
A 931 +2T-C transition in one COL1A2 allele causes exon 16 skipping in pro alpha 2(I) mRNA and produces moderately severe OI 117
Splicing mutation causes infantile Sandhoff disease 114
Two novel frameshift mutations in the adrenoleukodystrophy gene in Italian patients 113
Allelic frequencies of FBN1 gene polymorphisms and genetic analysis of Italian families with Marfan syndrome 112
Defects of SERPINF1 cause progressively deforming recessive osteogenesis imperfecta with normal Collagen I 112
A novel mutation which represents the fifth non-pathogenic polymorphism in the coding sequence of the arylsulfatase A gene 111
Linkage analysis for prenatal diagnosis in a familial case of Stickler syndrome 111
Haplotype analysis of collagen type I genes in the general population and in osteogenesis imperfecta families. 111
Analisi di linkage di geni candidati per densità minerale 107
Clodronate as a Therapeutic Strategy against Osteoarthritis 107
Bone histomorphometry in acromegaly patients with fragility vertebral fractures 105
The Runt domain of RUNX2 induces the migration of melanoma cells to bone 105
Detection of mutations in the ALD gene (ABCD1) in seven Italian families: description of four novel mutations 104
Identificazione ed analisi della regione 5' del gene umano per l'enzima farnesil difosfato sintetasi (FDPS). 104
The recurrent causal mutation for osteogenesis imperfecta type V occurs at a highly methylated CpG dinucleotide within the IFITM5 gene 104
A new type of EcoRI polymorphism of the human ribosomal DNA repeating unit revealed by analysis of cloned DNA fragments 103
Densità dei siti variabili in sequenze codificanti del gene COL1A1 con diversa rilevanza funzionale 103
Four new cases of lethal Osteogenesis Imperfecta due to glycine substitutions in the COL1A1 and COL1A2 genes 103
A potential role of RUNX2- RUNT domain in modulating the expression of genes involved in bone metastases: an in vitro study with melanoma cells 103
Type VI Osteogenesis imperfecta: effect of plasma transfusion on bone metabolism 100
Restoration by T4 ligase of DNA sequences sensitive to "flush" cleaving restriction enzyme 100
Association of BK virus with human brain tumors and tumors of pancreatic islets 100
Runx2 stimulates neoangiogenesis through the Runt domain in melanoma 100
Autosomal dominant benign recurrent intrahepatic cholestasis (BRIC) unlinked to 18q21 and 2q24 99
Effects of intense physical exercise on osteogenic commitment of mesenchymal progenitors 99
Segregation analysis of dominant osteogenesis imperfecta in Italy 98
Intarfamilial variable expressivity of osteogenesis imperfecta due to mosaicism for a lethal G382R substitution in the COL1A1 gene 98
Convergent transcription of the Escherichia coli hisG gene cloned in Bacillus subtilis stops in the vicinity of the attenuator 97
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 96
Enhanced osteogenic differentiation in Zoledronate-treated osteoporotic patients 96
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 95
Clodronate as a Therapeutic Strategy against Osteoarthritis 95
Osteogenesis Imperfecta: Practical treatment guidelines 94
Immunosenesscence and physical exercise: search for healthy ageing 94
New Insights into the Runt Domain of RUNX2 in Melanoma Cell Proliferation and Migration 94
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)) 93
Linkage analysis of LRP5 gene with bone mass density 93
Runx2 overexpression compromises bone quality in acromegalic patients 93
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 92
Two novel missense mutations causing adrenoleukodystrophy in Italian patients 92
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 92
Osteogenesi Imperfetta 91
Condrodisplasie e mucopolisaccaridosi. Fisipopatologia, Clinica e Terapia 91
Molecular screening in OI patients at Verona reference center: typical mutations 90
Osteogenesis Imperfecta: clinical, biochemical and molecular findings 90
Effects of oral anticoagulant therapy on gene expression in crosstalk between osteogenic progenitor cells and endothelial cells 90
Osteogenesis imperfecta and type-I collagen mutations. A lethal variant caused by a Gly910-->Ala substitution in the alpha 1 (I) chain 88
Rapid and efficient genotype analysis of the COL1A1 Sp1 binding site dimorphism, a genetic marker for bone mineral density 87
Expression of hepatitis B surface antigen in human cells by a recombinant BK virus DNA vector 86
Association study of Estrogen receptor-alpha gene with mineral bone density in a group of unrelated Italian females 86
Studio di associazione del gene per il recettore alpha degli estrogeni con densità minerale ossea in donne italiane 85
Osteogenic differentiation in healthy and pathological conditions 85
Possible hyperattenuation of transcription in the Escherichia coli hisG gene cloned in Bacillus subtilis 84
Different specific activities of the monomeric and oligomeric forms of plasmid DNA in transformation of B. subtilis and E. coli 84
Multiple forms of human dihydrofolate reductase messenger RNA. Cloning and expression in Escherichia coli of their DNA coding sequence 84
Relationship among VDR (BsmI and FokI), COL1A1, and CTR polymorphisms with bone mass, bone turnover markers, and sex hormones in men 84
No osteonecrosis of the jaw in children and adolescents treated with Neridronate for osteogenesis imperfecta. 84
Physical activity prevents cartilage degradation: a metabolomics study pinpoints the involvement of vitamin B6 84
BEL β‐Trefoil Reduces the Migration Ability of RUNX2 Expressing Melanoma Cells in Xenotransplanted Zebrafish 84
Linkage analysis of three candidate gene polymorphisms with bone density in a sample of Italian families 83
A novel 4-bp deletion creates a premature stop codon and dramatically decreases HEXB mRNA levels in a severe case of Sandhoff disease 83
Paternal mosaicism for a COL1A1 dominant mutation (alpha 1 Ser-415) causes recurrent osteogenesis imperfecta 82
Circulating progenitor stem cells are important biomarkers of chondrogenesis and osteogenesis: employment in diagnosis and treatment follow up 82
Type I collagen molecular map lends insights into the domain structure of the fibril and the genotype-phenotype relationship for some collagen mutations 81
Specific pattern of instability of Escherichia coli HisG gene cloned in Bacillus subtilis via the Staphylococcus aureus plasmid pCS194 79
Osteogenesis Imperfecta at the beginning of bone and joint decade 79
Cellular stress due to impairment of collagen prolyl hydroxylation complex is rescued by the chaperone 4-phenylbutyrate 78
Haplotype frequencies of the collagen type-I genes in the Italian population 76
A novel intragenic polymorphism within the COL1A1 locus which can be detected by Taq I restriction of amplified genomic DNA 76
Deficiency of CRTAP in non-lethal recessive osteogenesis imperfecta reduces collagen deposition into matrix 75
osteoporosis in (beta) - Thalassemia: Clinical and Genetic Aspect 74
Two novel C-terminus RUNX2 mutations in two cleidocranial dysplasia (CCD) patients impairing p53 expression 74
Molecular defects and cellular dysfunctions in restricted growth conditions 72
Physical Exercise Modulates miR-21-5p, miR-129-5p, miR-378-5p, and miR-188-5p Expression in Progenitor Cells Promoting Osteogenesis 72
Severe (type III) osteogenesis imperfecta due to glycine substitutions in the central domain of the collagen triple helix 71
Malattie dell'osso e del tessuto connettivo 71
Association study of Estrogen receptor-alpha gene with mineral bone density in a group of unrelated Italian females 71
Increased Gene Expression of RUNX2 and SOX9 in Mesenchymal Circulating Progenitors Is Associated with Autophagy during Physical Activity 71
Relationship between vertebral fractures, bone mineral density, and osteometabolic profile in HIV and Hepatitis B and C-infected patients treated with ART 71
Gly85 to Val substitution in pro alpha 1(I) chain causes mild osteogenesis imperfecta and introduces a susceptibility to protease digestion 70
A potential role for astaxanthin in the treatment of bone diseases (Review) 70
Current and emerging treatments for the management of osteogenesis imperfecta 69
Role of autophagy in bone and muscle biology 67
Role of microRNAs in progenitor cell commitment and osteogenic differentiation in health and disease (Review) 67
Totale 10.756
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Categoria #
all - tutte 38.055
article - articoli 28.804
book - libri 0
conference - conferenze 6.746
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 2.505
Totale 76.110
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020952 0 0 0 0 161 139 117 103 67 157 50 158
2020/20211.357 132 185 82 170 145 137 24 94 92 17 139 140
2021/20221.160 143 373 22 62 29 37 10 59 36 25 89 275
2022/20232.379 162 236 222 404 202 564 25 151 304 12 52 45
2023/20242.355 42 92 136 140 180 1.246 108 104 2 56 169 80
2024/20251.117 167 204 134 470 142 0 0 0 0 0 0 0
Totale 12.411