statistiche ricercatore

PALLOTTI, FRANCESCO

Distribuzione geografica

Continente	#
NA - Nord America	9.193
EU - Europa	5.314
AS - Asia	3.567
SA - Sud America	350
AF - Africa	85
Continente sconosciuto - Info sul continente non disponibili	15
OC - Oceania	6
Totale	18.530

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Nazione	#
US - Stati Uniti d'America	9.107
IT - Italia	2.105
SG - Singapore	1.145
UA - Ucraina	992
CN - Cina	820
SE - Svezia	564
TR - Turchia	556
VN - Vietnam	499
HK - Hong Kong	382
FI - Finlandia	312
BR - Brasile	303
IE - Irlanda	277
GB - Regno Unito	268
DE - Germania	259
FR - Francia	244
RU - Federazione Russa	143
IN - India	55
NG - Nigeria	40
CA - Canada	38
MX - Messico	36
BD - Bangladesh	27
PL - Polonia	22
JP - Giappone	20
NL - Olanda	20
AR - Argentina	19
AT - Austria	18
BE - Belgio	18
ES - Italia	18
ZA - Sudafrica	16
CZ - Repubblica Ceca	14
IQ - Iraq	14
EU - Europa	13
LT - Lituania	10
BG - Bulgaria	8
CL - Cile	7
MA - Marocco	7
KE - Kenya	6
UZ - Uzbekistan	6
AE - Emirati Arabi Uniti	5
AU - Australia	5
EC - Ecuador	5
EG - Egitto	5
ET - Etiopia	5
ID - Indonesia	5
PH - Filippine	5
PK - Pakistan	5
CO - Colombia	4
PA - Panama	4
VE - Venezuela	4
BO - Bolivia	3
DK - Danimarca	3
GR - Grecia	3
HU - Ungheria	3
IL - Israele	3
RO - Romania	3
SA - Arabia Saudita	3
CH - Svizzera	2
GT - Guatemala	2
HR - Croazia	2
JM - Giamaica	2
KR - Corea	2
KZ - Kazakistan	2
MY - Malesia	2
PE - Perù	2
PY - Paraguay	2
AM - Armenia	1
AO - Angola	1
AZ - Azerbaigian	1
BA - Bosnia-Erzegovina	1
BH - Bahrain	1
BW - Botswana	1
BY - Bielorussia	1
CR - Costa Rica	1
DM - Dominica	1
DO - Repubblica Dominicana	1
DZ - Algeria	1
JO - Giordania	1
LB - Libano	1
LV - Lettonia	1
MD - Moldavia	1
MU - Mauritius	1
MW - Malawi	1
NI - Nicaragua	1
NZ - Nuova Zelanda	1
OM - Oman	1
PS - Palestinian Territory	1
QA - Qatar	1
RS - Serbia	1
SI - Slovenia	1
SS - ???statistics.table.value.countryCode.SS???	1
SY - Repubblica araba siriana	1
TL - Timor Orientale	1
TN - Tunisia	1
TW - Taiwan	1
UY - Uruguay	1
XK - ???statistics.table.value.countryCode.XK???	1
Totale	18.530

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Città	#
Milan	1.516
Fairfield	876
Jacksonville	756
Ashburn	713
San Jose	702
Chandler	670
Singapore	599
Woodbridge	553
Houston	391
Hong Kong	373
Seattle	346
Izmir	341
Dallas	328
Cambridge	317
Wilmington	317
Dublin	277
Ann Arbor	270
Princeton	262
Dearborn	254
Nyköping	218
Beijing	175
Chicago	167
The Dalles	154
Boardman	147
Lauterbourg	118
New York	117
Rome	114
San Mateo	114
Dong Ket	112
Council Bluffs	91
Como	76
Los Angeles	75
San Diego	64
Ho Chi Minh City	62
London	61
Helsinki	57
Orem	48
Hanoi	47
Santa Clara	47
Guangzhou	44
Ogden	44
Abuja	39
Hefei	34
Munich	34
Washington	34
Nanjing	32
Kunming	30
São Paulo	29
Norwalk	25
Düsseldorf	24
Mexico City	24
Kocaeli	21
San Francisco	21
Philadelphia	20
Shenzhen	20
Shanghai	19
Tokyo	19
Brussels	18
Buffalo	18
Chennai	18
Warsaw	18
Zhengzhou	17
Hangzhou	16
Montreal	16
Atlanta	15
Frankfurt am Main	15
Jinan	15
Poplar	15
Phoenix	14
Johannesburg	13
Stockholm	13
Manchester	12
Tianjin	12
Turku	12
Denver	11
Haiphong	11
Mumbai	11
Redmond	11
Verona	11
Brooklyn	10
Nanchang	10
Redwood City	10
Brno	9
Changsha	9
Chengdu	9
Da Nang	9
Fuzhou	9
Shenyang	9
Amsterdam	8
Nuremberg	8
Rio de Janeiro	8
Vienna	8
Boston	7
Campinas	7
Paris	7
Sofia	7
Varese	7
Wuhan	7
Berlin	6
Biên Hòa	6
Totale	12.920

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Nome	#
Analysis of three screening methods for the detection of calreticulin gene mutations	267
A wide range of 3243A>G/tRNALeu(UUR) (MELAS) mutation loads may segregate in offspring through the female germline bottleneck	234
Authors’ Reply to Crampe and Langabeer: Technical Issues Behind Molecular Monitoring in Chronic Myeloid Leukemia	230
Assessing Heteroplasmic Load in Leber's Hereditary Optic Neuropathy Mutation 3460G->A/MT-ND1 with A Real-Time PCR Quantitative Approach	226
ASSAY CONDITIONS FOR THE MITOCHONDRIAL NADH - COENZYME-Q OXIDOREDUCTASE	223
A new acute myeloid leukemia case with STAT5B-RARA gene fusion due to 17q21.2 interstitial deletion	217
Biochemical analysis of respiratory function in cybrid cell lines harbouring mitochondrial DNA mutations	213
Biochemical-clinical correlation in patients with different loads of the mitochondrial DNA T8993G mutation	211
THE FUNCTION OF COENZYME-Q IN MITOCHONDRIA	209
A particular case of AML patient with the polymorphism G105G (rs11554137) and the missense mutation R132C in IDH1 gene	206
Biological variation of procalcitonin in healthy individuals	205
Biological variation of procalcitonin in healthy individuals	204
JAK2, 46/1 haplotype and chronic myelogenous leukemia: diagnostic and therapeutic potential	203
Matrix metalloproteinase 2 and tissue inhibitors of metalloproteinases regulate human aortic smooth muscle cell migration during in vitro aging	202
AN UPDATING OF THE BIOCHEMICAL FUNCTION OF COENZYME-Q IN MITOCHONDRIA	190
Analysis of mtDNA deletions in muscle by in situ hybridization	189
Aortic smooth muscle cells migration and the role of metalloproteinases and hyaluronan.	189
JAK2 mutation and atypical chronic myeloid leukemia	188
Rescue of a mitochondrial deficiency causing Leber hereditary optic neuropathy	186
A stop-codon mutation in the human mtDNA cytochrome c oxidase I gene disrupts the functional structure of complex IV	186
FTL gene mutation and persistent hyperferritinemia without iron deficiency anemia after phlebotomy	186
Differential cerebro spinal fluid proteome investigation of Leber hereditary optic neuropathy (LHON) and multiple sclerosis.	182
New insights into the pathobiology of Down syndrome - Hyaluronan synthase-2 overexpression is regulated by collagen VI α2 chain	182
Biological variation of procalcitonin in healthy individuals	179
Mitochondrial DNA nucleotide changes C14482G and C14482A in the ND6 gene are pathogenic for Leber's hereditary optic neuropathy	175
In vivo regulation of oxidative phosphorylation in cells harboring a stop-codon mutation in mitochondrial DNA-encoded cytochrome c oxidase subunit I	173
Isolation and subfractionation of mitochondria from animal cells and tissue culture lines.	172
Identification of a novel mutation in Cu/Zn superoxide dismutase gene associated with familial amyotrophic lateral sclerosis	171
Pure myopathy with enlarged mitochondria associated to a new mutation in MTND2 gene	171
Steady-state kinetics of the reduction of coenzyme Q analogs by complex I (NADH:Ubiquinone oxidoreductase) in bovine heart mitochondria and submitochondrial particles	170
Mitochondrial Complex I defects in aging	168
Decorin from different bovine tissues: study of glycosaminoglycan chain by PAGEFS	168
Mitochondrial abnormalities in muscle and other aging cells: Classification, causes, and effects	167
The fate of human sperm-derived mtDNA in somatic cells	167
Hyaluronan and human endothelial cell behavior.	165
Mitochondrial DNA in platelets from aged subjects	164
High frequency of migraine-only patients negative for the 3243 A>G tRNALeu mtDNA mutation in two MELAS families	164
Technical Issues Behind Molecular Monitoring in Chronic Myeloid Leukemia	164
Decrease of rotenone inhibition is a sensitive parameter of complex I damage in brain non-synaptic mitochondria of aged rats	163
Differential features of patients with mutations in two COX assembly genes, SURF-1 and SCO2	162
Isolation and subfractionation of mitochondria from animal cells and tissue culture lines.	161
MODES OF COENZYME-Q FUNCTION IN ELECTRON-TRANSFER	161
UDP-glucose dehydrogenase and Hyaluronan synthesis	161
Hyaluronan synthesis and human endothelial cell behaviour	158
Molecular cloning and characterization of UDP-glucose dehydrogenase from the amphibian xenopus laevis and its involvement in hyaluronan synthesis	158
Pathogenesis of primary defects in mitochondrial ATP synthesis	158
Pathogenesis of the deafness-associated A1555G mitochondrial DNA mutation	157
Comparison of three strategies for myocardial protection during coronary artery bypass graft surgery based on markers of cardiac damage.	156
Molecular control of the hyaluronan biosynthesis	156
G1HYALURONAN CONTENT OF UMBILICAL CORDS OF HEALTHY AND DOWN SYNDROME FETUSES	153
Exercise intolerance due to mutations in the cytochrome b gene of mitochondrial DNA	152
Mitochondrial dysfunction and brain disorders	152
Hyaluronan metabolism in human breast cancer cell line 8701BC	151
UDP-Glucose Dehydrogenase and its involvement in glycosaminoglycan Synthesis	150
Phosphorus MR spectroscopy shows a tissue specific in vivo distribution of biochemical expression of the G3460A mutation in Leber's hereditary optic neuropathy	149
Carcinoma breast cancer cells modulates HA metabolism of fibroblasts	149
UDP-glucose dehydrogenase from Xenopus laevis and its involvement in hyaluronan synthesis	148
Mitochondrial activities of rat heart during ageing	148
Biochemical analysis of mitochondrial function in cybrid cell lines harboring mtDNA mutations	147
Analysis of fluorophore labeled glycosaminoglycan disaccharides using polyacrylamide gel electroforesis and HPLC	146
UDP-Glucose dehydrogenase and its involvement in GAG synthesis	146
Histomorphometric studies in rat cerebral cortex: Normal aging and cell loss	145
Oxidative stress, antioxidant defences and aging	145
Alteration of mitochondrial membrane inner potential in three Italian patients with megaconial congenital muscular dystrophy carrying new mutations in CHKB gene	140
New electrophoretic and chromatographic tecniques for analysis of heparin and heparan sulphate.	137
Regulation of Hyaluronan synthesis in human endothelial cells	136
Archaeogenomics in Caravate and Cittiglio (Lombardy): from the excavation of ancient human bones to the study of DNA	133
LACK OF MAJOR MITOCHONDRIAL BIOENERGETIC CHANGES IN CULTURED SKIN FIBROBLASTS FROM AGED INDIVIDUALS	133
COLLAGEN TYPE I CARBOXY-TERMINAL PROPETIDE AND TELOPEPTIDE MEASUREMENT IN PLASMA OF PATIENTS WITH ESSENTIAL HYPERTENSION BY RIA AND EIA METHODS	132
Heteroplasmic 24-base pair deletion in the mitochondrial cytochrome b gene in a patient with isolated myopathy	131
Glicosamminoglicani prodotti in coltura cellulari umane	129
New highlights on the synthesis of hyaluronan	128
Comparison of clinical features in patients with COX assembly gene mutations	127
The search of the stool and blood K-ras mutations in patients with pancreatic mass	125
Hyaluronan in human umbilical cord	125
L’attivita’ della MMP2 come regolatore della migrazione di cellule umane muscolari lisce	124
Haplogroup effects and recombination of mitochondrial DNA: novel clues from the analysis of Leber hereditary optic neuropathy pedigrees.	122
Structure and function of hyaluronan	122
Hyaluronan metabolism in breast cancer cell line	122
Gene therapy with the ND4 subunit gene recoded in the universal genetic code reverses a mitochondrial deficiency causing Leber Hereditary optic neuropathy. 54Th Annual Meeting of the America Academy of Neurology. Denver (USA) 15-20 aprile 2002	121
Gene therapy with the ND4 subunit gene recoded in the universal genetic code reverses a mitochondrial deficiency causing Leber hereditary optic neuropathy (LHON)	120
Hyaluronan content and gene expression for hyaluronan synthases and hyaluronidases inthe umbilical cord of healthy and Down syndrome fetuses	120
Hyaluronan metabolism in in vitro culture of endothelial cells	117
Hyaluronan synthesis in human endothelial cells and its involvement during “in vitro” inflammation	116
Evidence that specific mtDNA point mutations may not accumulate in skeletal muscle during normal human aging	115
Hyaluronan content of umbilical cords of healthy and Down Syndrome fetuses	115
Osservazioni metodologiche nel dosaggio della NADH Coenzima Q ossidoreduttasi mitocondriale	114
Hyaluronan content of umbilical cords of healthy and Down Syndrome fetuses	112
Hyaluronan synthesis in human endothelial cells and its involvement during in vitro inflammation	111
Hyaluronan synthesis and human endothelial cell behaviour	109
Hyaluronan content of umbilical cords of healthy and Down Syndrome fetuses	109
Involvement of Hyaluronan during in vitro angiogenesis of endothelial cells	108
HYALURONAN CONTENT AND SYNTHASE GENE EXPRESSION BY REAL TIME –PCR IN UMBILICAL CORDS OF HEALTHY AND DOWN SYNDROME FETUSES	108
Quantificazione della mutazione 3460 G>A/ND1 (LHON) mediante Real Time PCR quantitativa	108
Hyaluronan metabolism in in vitro culture of endothelial cells.	108
INVOLVEMENT OF HYALURONAN DURING IN VITRO ANGIOGENESIS OF ENDOTHELIAL CELLS	106
Hyaluronan content of umbilical cords of healthy and Down Syndrome fetuses.	106
Migration in senescent cells: the role of cell-extracellular matrix interface	105
Regulation of hyaluronan synthesis in human endothelial cells	105
Evaluation of white blood cell, procalcitonin, C-reactive protein and serum amyloid as a marker to predict Ventilator associated pneumonia severity in brain injured patients	105
Totale	15.502

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Categoria	#
all - tutte	74.467
article - articoli	0
book - libri	0
conference - conferenze	0
curatela - curatele	0
other - altro	0
patent - brevetti	0
selected - selezionate	0
volume - volumi	0
Totale	74.467

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	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2020/2021	355	0	0	0	0	0	0	0	0	0	0	0	355
2021/2022	1.214	173	112	120	105	42	51	33	61	51	202	80	184
2022/2023	1.737	158	92	145	184	127	389	0	227	242	76	56	41
2023/2024	2.487	411	392	400	453	469	197	24	32	60	14	6	29
2024/2025	1.752	6	22	357	36	48	96	63	121	211	103	192	497
2025/2026	4.373	306	270	264	566	406	308	1.029	251	438	299	150	86
Totale													18.571