CATALOGO DEI PRODOTTI DELLA RICERCA

MOTTES, Monica
 Distribuzione geografica
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Continente #
NA - Nord America 4.447
EU - Europa 4.001
AS - Asia 2.356
OC - Oceania 22
SA - Sud America 10
AF - Africa 3
Continente sconosciuto - Info sul continente non disponibili 2
Totale 10.841
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Nazione #
US - Stati Uniti d'America 4.432
CN - Cina 2.176
GB - Regno Unito 1.561
IT - Italia 639
SE - Svezia 402
IE - Irlanda 349
FR - Francia 317
DE - Germania 259
FI - Finlandia 248
VN - Vietnam 106
UA - Ucraina 100
BE - Belgio 36
NL - Olanda 30
RU - Federazione Russa 22
AU - Australia 21
TR - Turchia 17
CA - Canada 13
IN - India 11
JP - Giappone 10
AT - Austria 8
DK - Danimarca 6
SG - Singapore 6
PK - Pakistan 5
CL - Cile 4
ES - Italia 4
HK - Hong Kong 4
KR - Corea 3
NO - Norvegia 3
RO - Romania 3
SA - Arabia Saudita 3
A2 - ???statistics.table.value.countryCode.A2??? 2
AR - Argentina 2
AZ - Azerbaigian 2
BR - Brasile 2
GR - Grecia 2
HR - Croazia 2
LV - Lettonia 2
PE - Perù 2
PL - Polonia 2
SK - Slovacchia (Repubblica Slovacca) 2
TH - Thailandia 2
AE - Emirati Arabi Uniti 1
AM - Armenia 1
BD - Bangladesh 1
CR - Costa Rica 1
CY - Cipro 1
EG - Egitto 1
HU - Ungheria 1
IL - Israele 1
IQ - Iraq 1
IR - Iran 1
JM - Giamaica 1
KE - Kenya 1
LU - Lussemburgo 1
MD - Moldavia 1
MN - Mongolia 1
NP - Nepal 1
NZ - Nuova Zelanda 1
RS - Serbia 1
TN - Tunisia 1
TW - Taiwan 1
UZ - Uzbekistan 1
Totale 10.841
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Città #
Southend 1.391
Jacksonville 848
Chandler 804
Woodbridge 400
Dublin 348
Verona 321
Ann Arbor 301
Ashburn 276
Houston 236
Beijing 152
New York 139
Wilmington 136
Princeton 128
Lawrence 127
Nanjing 126
Jinan 118
Shenyang 97
Sindelfingen 75
Hebei 73
Dong Ket 68
Helsinki 67
Tianjin 50
Boardman 49
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
Norwalk 22
Lanzhou 18
Lancaster 17
San Francisco 17
Redwood City 16
Sant'Ambrogio di Valpolicella 15
Auburn Hills 14
Philadelphia 13
Brisbane 12
Düsseldorf 12
Bologna 11
Toronto 11
Dearborn 10
Washington 10
Cagliari 8
Chicago 8
Fairfield 8
Vienna 8
London 7
Rome 7
Dallas 6
Detroit 6
Riva 6
Tombolo 6
Andover 5
Binetto 5
Los Angeles 5
Melbourne 5
Cambridge 4
Clearwater 4
Esslingen am Neckar 4
Florence 4
Leawood 4
Pomezia 4
Sala Di Cesenatico 4
Schio 4
Tokyo 4
Tomsk 4
Turin 4
Brescia 3
Buk-gu 3
Des Moines 3
Edinburgh 3
Ikast 3
Lappeenranta 3
Leeds 3
Madrid 3
Mansehra 3
Mantova 3
Oslo 3
Parma 3
Qingdao 3
Rieti 3
Riyadh 3
Singapore 3
St Petersburg 3
Udupi 3
Waanrode 3
Alezio 2
Amsterdam 2
Athens 2
Totale 7.264
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Nome #
CRISPR/Cas9 genome editing in melanoma cells: new insight of RUNT domain 1.185
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 142
Indagine sul coinvolgimento di gene LRP5 nella densità minerale ossea 130
Characterization and functional analysis of cis-acting elements of the human farnesyl diphosphate synthetase (FDPS) gene 5' flanking region. 128
A common beta hexosaminidase gene mutation in adult Sandhoff disease patients. 127
TREATMENT OF SKELETAL DISEASES WITH A NATURALLY DERIVED ANTIOXIDANT AND BISPHOSPHONATE EMBEDDED NANOPARTICLES 127
Association of CTR and COLIA1 alleles with BMD values in peri and postmenopausal women 123
Lack of expression of SERPINF1, the gene coding for pigment epithelium derived factor, causes progressively deforming Osteogenesis Imperfecta with normal type I collagen 117
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 116
Molecole, cellule e organismi 115
An integrated approach identifies new oncotargets in melanoma 114
Genetic testing for adult-type hypolactasia in Italian families 112
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 110
Splicing mutation causes infantile Sandhoff disease 107
A 931 +2T-C transition in one COL1A2 allele causes exon 16 skipping in pro alpha 2(I) mRNA and produces moderately severe OI 106
Can half-marathon affect overall health? The yin-yang of sport 106
Two novel frameshift mutations in the adrenoleukodystrophy gene in Italian patients 105
Linkage analysis for prenatal diagnosis in a familial case of Stickler syndrome 103
A novel mutation which represents the fifth non-pathogenic polymorphism in the coding sequence of the arylsulfatase A gene 102
Haplotype analysis of collagen type I genes in the general population and in osteogenesis imperfecta families. 99
Allelic frequencies of FBN1 gene polymorphisms and genetic analysis of Italian families with Marfan syndrome 99
Clodronate as a Therapeutic Strategy against Osteoarthritis 99
The genetic background of osteoporosis in cystic fibrosis: association analysis with polymorphic markers in four candidate genes 98
Defects of SERPINF1 cause progressively deforming recessive osteogenesis imperfecta with normal Collagen I 97
Analisi di linkage di geni candidati per densità minerale 97
The Runt domain of RUNX2 induces the migration of melanoma cells to bone 96
Detection of mutations in the ALD gene (ABCD1) in seven Italian families: description of four novel mutations 95
Densità dei siti variabili in sequenze codificanti del gene COL1A1 con diversa rilevanza funzionale 94
Hypophosphatasia and mesenchymal stem cells: a therapeutic promise 94
Restoration by T4 ligase of DNA sequences sensitive to "flush" cleaving restriction enzyme 93
Four new cases of lethal Osteogenesis Imperfecta due to glycine substitutions in the COL1A1 and COL1A2 genes 93
A new type of EcoRI polymorphism of the human ribosomal DNA repeating unit revealed by analysis of cloned DNA fragments 92
Intarfamilial variable expressivity of osteogenesis imperfecta due to mosaicism for a lethal G382R substitution in the COL1A1 gene 92
Identificazione ed analisi della regione 5' del gene umano per l'enzima farnesil difosfato sintetasi (FDPS). 91
The recurrent causal mutation for osteogenesis imperfecta type V occurs at a highly methylated CpG dinucleotide within the IFITM5 gene 91
Segregation analysis of dominant osteogenesis imperfecta in Italy 89
Convergent transcription of the Escherichia coli hisG gene cloned in Bacillus subtilis stops in the vicinity of the attenuator 89
Effects of intense physical exercise on osteogenic commitment of mesenchymal progenitors 89
Bone histomorphometry in acromegaly patients with fragility vertebral fractures 89
Runx2 stimulates neoangiogenesis through the Runt domain in melanoma 89
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 87
Association of BK virus with human brain tumors and tumors of pancreatic islets 87
Osteogenesis Imperfecta: Practical treatment guidelines 87
Enhanced osteogenic differentiation in Zoledronate-treated osteoporotic patients 87
A potential role of RUNX2- RUNT domain in modulating the expression of genes involved in bone metastases: an in vitro study with melanoma cells 87
Autosomal dominant benign recurrent intrahepatic cholestasis (BRIC) unlinked to 18q21 and 2q24 86
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)) 85
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 85
Clodronate as a Therapeutic Strategy against Osteoarthritis 85
Two novel missense mutations causing adrenoleukodystrophy in Italian patients 84
Linkage analysis of LRP5 gene with bone mass density 83
Runx2 overexpression compromises bone quality in acromegalic patients 83
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 82
Osteogenesis Imperfecta: clinical, biochemical and molecular findings 82
New Insights into the Runt Domain of RUNX2 in Melanoma Cell Proliferation and Migration 82
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 81
Rapid and efficient genotype analysis of the COL1A1 Sp1 binding site dimorphism, a genetic marker for bone mineral density 81
Condrodisplasie e mucopolisaccaridosi. Fisipopatologia, Clinica e Terapia 81
Multiple forms of human dihydrofolate reductase messenger RNA. Cloning and expression in Escherichia coli of their DNA coding sequence 79
Effects of oral anticoagulant therapy on gene expression in crosstalk between osteogenic progenitor cells and endothelial cells 79
Expression of hepatitis B surface antigen in human cells by a recombinant BK virus DNA vector 78
Osteogenesis imperfecta and type-I collagen mutations. A lethal variant caused by a Gly910-->Ala substitution in the alpha 1 (I) chain 78
Relationship among VDR (BsmI and FokI), COL1A1, and CTR polymorphisms with bone mass, bone turnover markers, and sex hormones in men 78
Immunosenesscence and physical exercise: search for healthy ageing 78
Possible hyperattenuation of transcription in the Escherichia coli hisG gene cloned in Bacillus subtilis 77
Different specific activities of the monomeric and oligomeric forms of plasmid DNA in transformation of B. subtilis and E. coli 77
Association study of Estrogen receptor-alpha gene with mineral bone density in a group of unrelated Italian females 77
Circulating progenitor stem cells are important biomarkers of chondrogenesis and osteogenesis: employment in diagnosis and treatment follow up 76
Molecular screening in OI patients at Verona reference center: typical mutations 75
Studio di associazione del gene per il recettore alpha degli estrogeni con densità minerale ossea in donne italiane 75
A novel 4-bp deletion creates a premature stop codon and dramatically decreases HEXB mRNA levels in a severe case of Sandhoff disease 74
Paternal mosaicism for a COL1A1 dominant mutation (alpha 1 Ser-415) causes recurrent osteogenesis imperfecta 74
Linkage analysis of three candidate gene polymorphisms with bone density in a sample of Italian families 73
Osteogenic differentiation in healthy and pathological conditions 73
Osteogenesi Imperfetta 72
Type I collagen molecular map lends insights into the domain structure of the fibril and the genotype-phenotype relationship for some collagen mutations 72
Specific pattern of instability of Escherichia coli HisG gene cloned in Bacillus subtilis via the Staphylococcus aureus plasmid pCS194 71
Haplotype frequencies of the collagen type-I genes in the Italian population 70
No osteonecrosis of the jaw in children and adolescents treated with Neridronate for osteogenesis imperfecta. 70
Physical activity prevents cartilage degradation: a metabolomics study pinpoints the involvement of vitamin B6 70
BEL β‐Trefoil Reduces the Migration Ability of RUNX2 Expressing Melanoma Cells in Xenotransplanted Zebrafish 70
Deficiency of CRTAP in non-lethal recessive osteogenesis imperfecta reduces collagen deposition into matrix 69
osteoporosis in (beta) - Thalassemia: Clinical and Genetic Aspect 68
A novel intragenic polymorphism within the COL1A1 locus which can be detected by Taq I restriction of amplified genomic DNA 68
Osteogenesis Imperfecta at the beginning of bone and joint decade 67
Molecular defects and cellular dysfunctions in restricted growth conditions 66
Type VI Osteogenesis imperfecta: effect of plasma transfusion on bone metabolism 65
Association study of Estrogen receptor-alpha gene with mineral bone density in a group of unrelated Italian females 62
Gly85 to Val substitution in pro alpha 1(I) chain causes mild osteogenesis imperfecta and introduces a susceptibility to protease digestion 61
Role of autophagy in bone and muscle biology 61
Increased Gene Expression of RUNX2 and SOX9 in Mesenchymal Circulating Progenitors Is Associated with Autophagy during Physical Activity 61
Three novel polymorphic sequence variants in the type I collagen gene COL1A1, the main disease locus for Osteogenesis Imperfecta 60
Current and emerging treatments for the management of osteogenesis imperfecta 60
Role of microRNAs in progenitor cell commitment and osteogenic differentiation in health and disease (Review) 60
Severe (type III) osteogenesis imperfecta due to glycine substitutions in the central domain of the collagen triple helix 59
Physical Exercise Modulates miR-21-5p, miR-129-5p, miR-378-5p, and miR-188-5p Expression in Progenitor Cells Promoting Osteogenesis 59
Mutation producing alternative splicing of exon 26 in the COL1A2 gene causes type IV osteogenesis imperfecta with intrafamilial clinical variability 58
Cellular stress due to impairment of collagen prolyl hydroxylation complex is rescued by the chaperone 4-phenylbutyrate 58
Two novel C-terminus RUNX2 mutations in two cleidocranial dysplasia (CCD) patients impairing p53 expression 58
Molecular and lifestyle factors modulating obesity disease 57
Totale 9.648
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Categoria #
all - tutte 28.787
article - articoli 21.454
book - libri 0
conference - conferenze 5.450
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 1.883
Totale 57.574
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/201997 0 0 0 0 0 0 0 0 0 17 35 45
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
2023/20242.064 42 92 136 140 180 1.246 108 104 2 14 0 0
Totale 11.003