CATALOGO DEI PRODOTTI DELLA RICERCA

SANGALLI, Antonella
 Distribuzione geografica
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Continente #
NA - Nord America 1.444
EU - Europa 1.325
AS - Asia 346
OC - Oceania 2
SA - Sud America 2
AF - Africa 1
Totale 3.120
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Nazione #
US - Stati Uniti d'America 1.434
GB - Regno Unito 581
CN - Cina 329
IT - Italia 149
SE - Svezia 137
FR - Francia 114
IE - Irlanda 101
FI - Finlandia 90
DE - Germania 82
UA - Ucraina 30
BE - Belgio 15
NL - Olanda 14
CA - Canada 10
RU - Federazione Russa 7
KR - Corea 4
VN - Vietnam 4
IN - India 3
AU - Australia 2
CL - Cile 2
JP - Giappone 2
AT - Austria 1
CY - Cipro 1
CZ - Repubblica Ceca 1
ES - Italia 1
LK - Sri Lanka 1
LV - Lettonia 1
NG - Nigeria 1
RO - Romania 1
SA - Arabia Saudita 1
SG - Singapore 1
Totale 3.120
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Città #
Southend 530
Jacksonville 273
Chandler 227
Ann Arbor 146
Woodbridge 118
Ashburn 113
Dublin 100
Verona 75
Houston 71
Beijing 52
New York 50
Wilmington 46
Lawrence 40
Princeton 40
Nanjing 36
Jinan 32
Shenyang 27
Sindelfingen 27
Helsinki 26
Hebei 22
Boardman 19
Haikou 16
Tianjin 16
Changsha 14
Brussels 13
Jiaxing 12
Taiyuan 11
Hangzhou 10
Nanchang 10
Ningbo 9
Redmond 9
Zhengzhou 9
Milan 8
Seattle 7
Taizhou 7
Toronto 7
Auburn Hills 6
Düsseldorf 6
Lanzhou 6
Norwalk 6
Fuzhou 5
Guangzhou 5
San Francisco 5
Dong Ket 4
Falls Church 4
Seoul 4
Washington 4
Brescia 3
Detroit 3
Leeds 3
Lonigo 3
Los Angeles 3
Parma 3
Redwood City 3
Riva 3
Bologna 2
Chions 2
Dearborn 2
Edinburgh 2
Malcesine 2
Meppel 2
Montréal 2
Philadelphia 2
Qingdao 2
Senigallia 2
Turin 2
Waanrode 2
Bassano Del Grappa 1
Brno 1
Cambridge 1
Carini 1
Caserta 1
Cento 1
Charlotte 1
Chicago 1
Clearwater 1
Colombo 1
Costa Mesa 1
Crotone 1
Delhi 1
Dongguan 1
Eden Prairie 1
Elora 1
Fairfield 1
Falkenstein 1
Giarre 1
Gunzenhausen 1
Kyiv 1
Lagos 1
Lancaster 1
Leawood 1
Lodi 1
Lunano 1
Macerata 1
Madrid 1
Melbourne 1
Mumbai 1
Napoli 1
Nicosia 1
Padova 1
Totale 2.364
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Nome #
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
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
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
Haplotype analysis of collagen type I genes in the general population and in osteogenesis imperfecta families. 99
The genetic background of osteoporosis in cystic fibrosis: association analysis with polymorphic markers in four candidate genes 98
Analisi di linkage di geni candidati per densità minerale 97
Densità dei siti variabili in sequenze codificanti del gene COL1A1 con diversa rilevanza funzionale 94
Identificazione ed analisi della regione 5' del gene umano per l'enzima farnesil difosfato sintetasi (FDPS). 91
Autosomal dominant benign recurrent intrahepatic cholestasis (BRIC) unlinked to 18q21 and 2q24 86
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
Linkage analysis of LRP5 gene with bone mass density 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
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
Transduced fibroblasts and metachromatic leukodystrophy lymphocytes transfer arylsulfatase A to myelinating glia and deficient cells in vitro. 79
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
Association study of Estrogen receptor-alpha gene with mineral bone density in a group of unrelated Italian females 77
Association of variant -765G>C in the PTGS2 gene promoter with melanoma in Italian patients and its relation to gene expression in dermal fibroblasts. 76
Studio di associazione del gene per il recettore alpha degli estrogeni con densità minerale ossea in donne italiane 75
Identification of a novelABCD1 mutation in a family with Adrenoleukodistrophy 74
Linkage analysis of three candidate gene polymorphisms with bone density in a sample of Italian families 73
Sex-specific effect of RNASEL rs486907 and miR-146a rs2910164 polymorphisms' interaction as a susceptibility factor for melanoma skin cancer 72
osteoporosis in (beta) - Thalassemia: Clinical and Genetic Aspect 68
Association study of Estrogen receptor-alpha gene with mineral bone density in a group of unrelated Italian females 62
Association of promoter polymorphism -765G>C in the PTGS2 gene with malignant melanoma in Italian patients and its correlation to gene expression in dermal fibroblasts. 62
Lack of association of metastasis-associated lung adenocarcinoma transcript 1 variants with melanoma skin cancer risk 58
Studio di procedure per l’aggiustamento delle genotipizzazioni condotte su un elevato numero di famiglie 54
Stickler syndrome and vitreoretinal degeneration: correlation between locus mitation and vitreous phenotype. Apropos of a case 52
A novel mutation in ABCD1 unveils different clinical phenotypes in a family with adrenoleukodystrophy 51
Enhancer of zeste 2 polycomb repressive complex 2 subunit polymorphisms in melanoma skin cancer risk 51
RNA-binding proteins RBM20 and PTBP1 regulate the alternative splicing of FHOD3 49
Wound repair capability in EDS fibroblasts can be retrieved by exogenous type Vcollagen. 45
Whole-exome sequencing in patients with protein aggregate myopathies reveals causative mutations associated with novel atypical phenotypes 45
HLA-C stability and AIDS progression 43
Rescue of Migratory Defects of Ehlers-Danlos Syndrome Fibroblasts In Vitro byType V Collagen but not Insulin-Like Binding Protein-1. 42
Melanoma risk alleles are associated with down-regulation of the MTAP gene and hyper-methylation of a CpG Island upstream of the gene in dermal fibroblasts 40
Increased prevalence of unstable HLA-C variants in HIV-1 rapid-progressor patients 20
Totale 3.154
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Categoria #
all - tutte 8.876
article - articoli 6.040
book - libri 0
conference - conferenze 2.836
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 17.752
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/201925 0 0 0 0 0 0 0 0 0 0 14 11
2019/2020427 48 7 6 32 70 47 42 37 26 39 19 54
2020/2021376 39 63 20 46 44 36 7 33 28 3 43 14
2021/2022329 44 89 3 18 12 14 6 22 13 3 26 79
2022/2023742 52 82 66 116 68 173 9 55 101 3 8 9
2023/2024333 16 21 37 54 54 65 34 45 0 7 0 0
Totale 3.154