CATALOGO DEI PRODOTTI DELLA RICERCA

MOTTES, Monica
 Distribuzione geografica
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Continente #
NA - Nord America 4.513
EU - Europa 4.072
AS - Asia 2.566
OC - Oceania 22
SA - Sud America 13
AF - Africa 5
Continente sconosciuto - Info sul continente non disponibili 2
Totale 11.193
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Nazione #
US - Stati Uniti d'America 4.498
CN - Cina 2.208
GB - Regno Unito 1.564
IT - Italia 651
SE - Svezia 404
IE - Irlanda 349
FR - Francia 319
DE - Germania 260
FI - Finlandia 248
SG - Singapore 138
VN - Vietnam 106
UA - Ucraina 100
RU - Federazione Russa 61
BE - Belgio 36
NL - Olanda 33
JP - Giappone 27
KR - Corea 27
AU - Australia 21
TR - Turchia 19
CA - Canada 13
IN - India 11
AT - Austria 8
DK - Danimarca 6
CL - Cile 5
CZ - Repubblica Ceca 5
PK - Pakistan 5
ES - Italia 4
HK - Hong Kong 4
LV - Lettonia 3
NO - Norvegia 3
PL - Polonia 3
RO - Romania 3
SA - Arabia Saudita 3
A2 - ???statistics.table.value.countryCode.A2??? 2
AE - Emirati Arabi Uniti 2
AR - Argentina 2
AZ - Azerbaigian 2
BO - Bolivia 2
BR - Brasile 2
EG - Egitto 2
GR - Grecia 2
HR - Croazia 2
PE - Perù 2
SK - Slovacchia (Repubblica Slovacca) 2
TH - Thailandia 2
TW - Taiwan 2
UZ - Uzbekistan 2
AM - Armenia 1
BD - Bangladesh 1
CR - Costa Rica 1
CY - Cipro 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
LU - Lussemburgo 1
MA - Marocco 1
MD - Moldavia 1
MN - Mongolia 1
NP - Nepal 1
NZ - Nuova Zelanda 1
RS - Serbia 1
TN - Tunisia 1
Totale 11.193
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Città #
Southend 1.391
Jacksonville 848
Chandler 804
Woodbridge 400
Dublin 348
Verona 321
Ann Arbor 301
Ashburn 285
Houston 236
Beijing 165
New York 140
Wilmington 136
Princeton 128
Lawrence 127
Nanjing 126
Jinan 118
Shenyang 97
Singapore 91
Sindelfingen 75
Hebei 73
Dong Ket 68
Helsinki 67
Boardman 63
Tianjin 50
Hangzhou 48
Changsha 42
Ningbo 42
Haikou 41
Nanchang 40
Redmond 37
Taiyuan 35
Brussels 33
Jiaxing 33
Taizhou 31
Milan 30
Zhengzhou 29
Seattle 26
Falls Church 24
Fuzhou 24
Guangzhou 24
Seoul 24
Norwalk 22
San Francisco 22
Tokyo 21
Kent 19
Lanzhou 18
Lancaster 17
Redwood City 16
Sant'Ambrogio di Valpolicella 16
Auburn Hills 14
Philadelphia 13
Brisbane 12
Düsseldorf 12
Bologna 11
Los Angeles 11
Toronto 11
Dearborn 10
London 10
St Petersburg 10
Washington 10
Cagliari 8
Chicago 8
Fairfield 8
Vienna 8
Rome 7
Dallas 6
Des Moines 6
Detroit 6
Riva 6
Tombolo 6
Andover 5
Binetto 5
Melbourne 5
Amsterdam 4
Brno 4
Cambridge 4
Clearwater 4
Esslingen am Neckar 4
Florence 4
Leawood 4
Moscow 4
Naples 4
Phoenix 4
Pomezia 4
Sala Di Cesenatico 4
Schio 4
Tomsk 4
Turin 4
Brescia 3
Buk-gu 3
Edinburgh 3
Ikast 3
Lappeenranta 3
Leeds 3
Madrid 3
Mansehra 3
Mantova 3
Oslo 3
Parma 3
Qingdao 3
Totale 7.476
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Nome #
CRISPR/Cas9 genome editing in melanoma cells: new insight of RUNT domain 1.188
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 146
Indagine sul coinvolgimento di gene LRP5 nella densità minerale ossea 132
A common beta hexosaminidase gene mutation in adult Sandhoff disease patients. 131
TREATMENT OF SKELETAL DISEASES WITH A NATURALLY DERIVED ANTIOXIDANT AND BISPHOSPHONATE EMBEDDED NANOPARTICLES 131
Characterization and functional analysis of cis-acting elements of the human farnesyl diphosphate synthetase (FDPS) gene 5' flanking region. 130
Association of CTR and COLIA1 alleles with BMD values in peri and postmenopausal women 127
Lack of expression of SERPINF1, the gene coding for pigment epithelium derived factor, causes progressively deforming Osteogenesis Imperfecta with normal type I collagen 120
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 119
An integrated approach identifies new oncotargets in melanoma 118
Molecole, cellule e organismi 117
Genetic testing for adult-type hypolactasia in Italian families 113
Splicing mutation causes infantile Sandhoff disease 111
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 111
Can half-marathon affect overall health? The yin-yang of sport 110
A 931 +2T-C transition in one COL1A2 allele causes exon 16 skipping in pro alpha 2(I) mRNA and produces moderately severe OI 109
Hypophosphatasia and mesenchymal stem cells: a therapeutic promise 109
Two novel frameshift mutations in the adrenoleukodystrophy gene in Italian patients 108
A novel mutation which represents the fifth non-pathogenic polymorphism in the coding sequence of the arylsulfatase A gene 103
Linkage analysis for prenatal diagnosis in a familial case of Stickler syndrome 103
Haplotype analysis of collagen type I genes in the general population and in osteogenesis imperfecta families. 103
Defects of SERPINF1 cause progressively deforming recessive osteogenesis imperfecta with normal Collagen I 102
Clodronate as a Therapeutic Strategy against Osteoarthritis 101
The genetic background of osteoporosis in cystic fibrosis: association analysis with polymorphic markers in four candidate genes 100
Allelic frequencies of FBN1 gene polymorphisms and genetic analysis of Italian families with Marfan syndrome 100
Analisi di linkage di geni candidati per densità minerale 98
Detection of mutations in the ALD gene (ABCD1) in seven Italian families: description of four novel mutations 97
The Runt domain of RUNX2 induces the migration of melanoma cells to bone 97
Densità dei siti variabili in sequenze codificanti del gene COL1A1 con diversa rilevanza funzionale 96
Identificazione ed analisi della regione 5' del gene umano per l'enzima farnesil difosfato sintetasi (FDPS). 95
Four new cases of lethal Osteogenesis Imperfecta due to glycine substitutions in the COL1A1 and COL1A2 genes 95
Restoration by T4 ligase of DNA sequences sensitive to "flush" cleaving restriction enzyme 94
A new type of EcoRI polymorphism of the human ribosomal DNA repeating unit revealed by analysis of cloned DNA fragments 93
Intarfamilial variable expressivity of osteogenesis imperfecta due to mosaicism for a lethal G382R substitution in the COL1A1 gene 93
The recurrent causal mutation for osteogenesis imperfecta type V occurs at a highly methylated CpG dinucleotide within the IFITM5 gene 93
Segregation analysis of dominant osteogenesis imperfecta in Italy 92
Effects of intense physical exercise on osteogenic commitment of mesenchymal progenitors 92
Bone histomorphometry in acromegaly patients with fragility vertebral fractures 92
Runx2 stimulates neoangiogenesis through the Runt domain in melanoma 92
Convergent transcription of the Escherichia coli hisG gene cloned in Bacillus subtilis stops in the vicinity of the attenuator 91
Association of BK virus with human brain tumors and tumors of pancreatic islets 90
A potential role of RUNX2- RUNT domain in modulating the expression of genes involved in bone metastases: an in vitro study with melanoma cells 90
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 89
Osteogenesis Imperfecta: Practical treatment guidelines 89
Clodronate as a Therapeutic Strategy against Osteoarthritis 89
Autosomal dominant benign recurrent intrahepatic cholestasis (BRIC) unlinked to 18q21 and 2q24 88
Enhanced osteogenic differentiation in Zoledronate-treated osteoporotic patients 88
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)) 87
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 87
Runx2 overexpression compromises bone quality in acromegalic patients 87
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 85
Two novel missense mutations causing adrenoleukodystrophy in Italian patients 85
Linkage analysis of LRP5 gene with bone mass density 85
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 84
Rapid and efficient genotype analysis of the COL1A1 Sp1 binding site dimorphism, a genetic marker for bone mineral density 84
Condrodisplasie e mucopolisaccaridosi. Fisipopatologia, Clinica e Terapia 84
New Insights into the Runt Domain of RUNX2 in Melanoma Cell Proliferation and Migration 84
Type VI Osteogenesis imperfecta: effect of plasma transfusion on bone metabolism 83
Osteogenesis Imperfecta: clinical, biochemical and molecular findings 83
Immunosenesscence and physical exercise: search for healthy ageing 83
Effects of oral anticoagulant therapy on gene expression in crosstalk between osteogenic progenitor cells and endothelial cells 82
Multiple forms of human dihydrofolate reductase messenger RNA. Cloning and expression in Escherichia coli of their DNA coding sequence 80
Relationship among VDR (BsmI and FokI), COL1A1, and CTR polymorphisms with bone mass, bone turnover markers, and sex hormones in men 80
Expression of hepatitis B surface antigen in human cells by a recombinant BK virus DNA vector 79
Possible hyperattenuation of transcription in the Escherichia coli hisG gene cloned in Bacillus subtilis 79
Osteogenesis imperfecta and type-I collagen mutations. A lethal variant caused by a Gly910-->Ala substitution in the alpha 1 (I) chain 79
Studio di associazione del gene per il recettore alpha degli estrogeni con densità minerale ossea in donne italiane 79
Different specific activities of the monomeric and oligomeric forms of plasmid DNA in transformation of B. subtilis and E. coli 78
Molecular screening in OI patients at Verona reference center: typical mutations 78
Osteogenesi Imperfetta 78
Association study of Estrogen receptor-alpha gene with mineral bone density in a group of unrelated Italian females 78
No osteonecrosis of the jaw in children and adolescents treated with Neridronate for osteogenesis imperfecta. 77
Circulating progenitor stem cells are important biomarkers of chondrogenesis and osteogenesis: employment in diagnosis and treatment follow up 77
Linkage analysis of three candidate gene polymorphisms with bone density in a sample of Italian families 76
A novel 4-bp deletion creates a premature stop codon and dramatically decreases HEXB mRNA levels in a severe case of Sandhoff disease 76
Paternal mosaicism for a COL1A1 dominant mutation (alpha 1 Ser-415) causes recurrent osteogenesis imperfecta 76
Osteogenic differentiation in healthy and pathological conditions 76
Type I collagen molecular map lends insights into the domain structure of the fibril and the genotype-phenotype relationship for some collagen mutations 75
Physical activity prevents cartilage degradation: a metabolomics study pinpoints the involvement of vitamin B6 74
BEL β‐Trefoil Reduces the Migration Ability of RUNX2 Expressing Melanoma Cells in Xenotransplanted Zebrafish 74
Specific pattern of instability of Escherichia coli HisG gene cloned in Bacillus subtilis via the Staphylococcus aureus plasmid pCS194 73
Haplotype frequencies of the collagen type-I genes in the Italian population 71
osteoporosis in (beta) - Thalassemia: Clinical and Genetic Aspect 70
A novel intragenic polymorphism within the COL1A1 locus which can be detected by Taq I restriction of amplified genomic DNA 70
Deficiency of CRTAP in non-lethal recessive osteogenesis imperfecta reduces collagen deposition into matrix 70
Molecular defects and cellular dysfunctions in restricted growth conditions 69
Osteogenesis Imperfecta at the beginning of bone and joint decade 68
Increased Gene Expression of RUNX2 and SOX9 in Mesenchymal Circulating Progenitors Is Associated with Autophagy during Physical Activity 65
Association study of Estrogen receptor-alpha gene with mineral bone density in a group of unrelated Italian females 64
Gly85 to Val substitution in pro alpha 1(I) chain causes mild osteogenesis imperfecta and introduces a susceptibility to protease digestion 64
Cellular stress due to impairment of collagen prolyl hydroxylation complex is rescued by the chaperone 4-phenylbutyrate 64
Current and emerging treatments for the management of osteogenesis imperfecta 63
Physical Exercise Modulates miR-21-5p, miR-129-5p, miR-378-5p, and miR-188-5p Expression in Progenitor Cells Promoting Osteogenesis 63
Three novel polymorphic sequence variants in the type I collagen gene COL1A1, the main disease locus for Osteogenesis Imperfecta 62
Role of autophagy in bone and muscle biology 62
Role of microRNAs in progenitor cell commitment and osteogenic differentiation in health and disease (Review) 62
Two novel C-terminus RUNX2 mutations in two cleidocranial dysplasia (CCD) patients impairing p53 expression 62
Severe (type III) osteogenesis imperfecta due to glycine substitutions in the central domain of the collagen triple helix 60
Mutation producing alternative splicing of exon 26 in the COL1A2 gene causes type IV osteogenesis imperfecta with intrafamilial clinical variability 59
A potential role for astaxanthin in the treatment of bone diseases (Review) 59
Totale 9.927
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Categoria #
all - tutte 32.136
article - articoli 24.073
book - libri 0
conference - conferenze 5.921
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 2.142
Totale 64.272
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20201.234 145 22 15 100 161 139 117 103 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
2024/202561 61 0 0 0 0 0 0 0 0 0 0 0
Totale 11.355