statistiche ricercatore

PALLOTTI, FRANCESCO

Distribuzione geografica

Continente	#
NA - Nord America	9.426
EU - Europa	5.334
AS - Asia	3.579
SA - Sud America	357
AF - Africa	85
Continente sconosciuto - Info sul continente non disponibili	56
OC - Oceania	6
Totale	18.843

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Nazione	#
US - Stati Uniti d'America	9.329
IT - Italia	2.113
SG - Singapore	1.150
UA - Ucraina	992
CN - Cina	822
SE - Svezia	567
TR - Turchia	556
VN - Vietnam	499
HK - Hong Kong	383
FI - Finlandia	313
BR - Brasile	307
IE - Irlanda	277
GB - Regno Unito	269
DE - Germania	259
FR - Francia	245
RU - Federazione Russa	143
IN - India	55
NG - Nigeria	40
CA - Canada	39
MX - Messico	37
BD - Bangladesh	31
NL - Olanda	22
PL - Polonia	22
AR - Argentina	21
ES - Italia	20
JP - Giappone	20
BE - Belgio	19
AT - Austria	18
ZA - Sudafrica	16
CZ - Repubblica Ceca	14
IQ - Iraq	14
EU - Europa	13
LT - Lituania	10
BG - Bulgaria	8
CL - Cile	8
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
CR - Costa Rica	3
DK - Danimarca	3
GR - Grecia	3
GT - Guatemala	3
HU - Ungheria	3
IL - Israele	3
JM - Giamaica	3
RO - Romania	3
SA - Arabia Saudita	3
CH - Svizzera	2
DO - Repubblica Dominicana	2
HR - Croazia	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
DM - Dominica	1
DZ - Algeria	1
HN - Honduras	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
PR - Porto Rico	1
PS - Palestinian Territory	1
PT - Portogallo	1
QA - Qatar	1
RS - Serbia	1
SI - Slovenia	1
SS - ???statistics.table.value.countryCode.SS???	1
SV - El Salvador	1
SY - Repubblica araba siriana	1
TL - Timor Orientale	1
TN - Tunisia	1
TT - Trinidad e Tobago	1
TW - Taiwan	1
UY - Uruguay	1
Totale	18.801

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Città	#
Milan	1.517
Fairfield	876
Jacksonville	756
Ashburn	732
San Jose	711
Chandler	670
Singapore	601
Woodbridge	553
Houston	391
Hong Kong	374
Seattle	346
Izmir	341
Dallas	329
Cambridge	317
Wilmington	317
Dublin	277
Ann Arbor	270
Princeton	262
Dearborn	254
Council Bluffs	221
Nyköping	218
Beijing	177
Chicago	167
The Dalles	156
Boardman	147
Lauterbourg	118
New York	118
Rome	114
San Mateo	114
Dong Ket	112
Como	76
Los Angeles	75
San Diego	64
Ho Chi Minh City	62
London	62
Helsinki	57
Santa Clara	53
Orem	48
Hanoi	47
Guangzhou	44
Ogden	44
Abuja	39
Hefei	34
Munich	34
Washington	34
Nanjing	32
Kunming	30
São Paulo	30
Norwalk	25
Düsseldorf	24
Mexico City	24
Kocaeli	21
Philadelphia	21
San Francisco	21
Shenzhen	20
Shanghai	19
Tokyo	19
Brussels	18
Buffalo	18
Chennai	18
Warsaw	18
Zhengzhou	17
Hangzhou	16
Montreal	16
Phoenix	16
Atlanta	15
Frankfurt am Main	15
Jinan	15
Poplar	15
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
Paris	8
Rio de Janeiro	8
Vienna	8
Boston	7
Brasília	7
Campinas	7
Sofia	7
Varese	7
Wuhan	7
Berlin	6
Totale	13.101

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Nome	#
Analysis of three screening methods for the detection of calreticulin gene mutations	270
A wide range of 3243A>G/tRNALeu(UUR) (MELAS) mutation loads may segregate in offspring through the female germline bottleneck	238
Authors’ Reply to Crampe and Langabeer: Technical Issues Behind Molecular Monitoring in Chronic Myeloid Leukemia	232
Assessing Heteroplasmic Load in Leber's Hereditary Optic Neuropathy Mutation 3460G->A/MT-ND1 with A Real-Time PCR Quantitative Approach	227
ASSAY CONDITIONS FOR THE MITOCHONDRIAL NADH - COENZYME-Q OXIDOREDUCTASE	224
A new acute myeloid leukemia case with STAT5B-RARA gene fusion due to 17q21.2 interstitial deletion	219
Biochemical analysis of respiratory function in cybrid cell lines harbouring mitochondrial DNA mutations	215
Biochemical-clinical correlation in patients with different loads of the mitochondrial DNA T8993G mutation	212
THE FUNCTION OF COENZYME-Q IN MITOCHONDRIA	211
A particular case of AML patient with the polymorphism G105G (rs11554137) and the missense mutation R132C in IDH1 gene	208
Biological variation of procalcitonin in healthy individuals	206
Matrix metalloproteinase 2 and tissue inhibitors of metalloproteinases regulate human aortic smooth muscle cell migration during in vitro aging	206
Biological variation of procalcitonin in healthy individuals	205
JAK2, 46/1 haplotype and chronic myelogenous leukemia: diagnostic and therapeutic potential	204
Analysis of mtDNA deletions in muscle by in situ hybridization	193
AN UPDATING OF THE BIOCHEMICAL FUNCTION OF COENZYME-Q IN MITOCHONDRIA	193
Aortic smooth muscle cells migration and the role of metalloproteinases and hyaluronan.	193
JAK2 mutation and atypical chronic myeloid leukemia	190
A stop-codon mutation in the human mtDNA cytochrome c oxidase I gene disrupts the functional structure of complex IV	189
FTL gene mutation and persistent hyperferritinemia without iron deficiency anemia after phlebotomy	188
Rescue of a mitochondrial deficiency causing Leber hereditary optic neuropathy	187
New insights into the pathobiology of Down syndrome - Hyaluronan synthase-2 overexpression is regulated by collagen VI α2 chain	184
Differential cerebro spinal fluid proteome investigation of Leber hereditary optic neuropathy (LHON) and multiple sclerosis.	183
Pure myopathy with enlarged mitochondria associated to a new mutation in MTND2 gene	183
Biological variation of procalcitonin in healthy individuals	182
Mitochondrial DNA nucleotide changes C14482G and C14482A in the ND6 gene are pathogenic for Leber's hereditary optic neuropathy	178
Isolation and subfractionation of mitochondria from animal cells and tissue culture lines.	175
In vivo regulation of oxidative phosphorylation in cells harboring a stop-codon mutation in mitochondrial DNA-encoded cytochrome c oxidase subunit I	174
Identification of a novel mutation in Cu/Zn superoxide dismutase gene associated with familial amyotrophic lateral sclerosis	172
Steady-state kinetics of the reduction of coenzyme Q analogs by complex I (NADH:Ubiquinone oxidoreductase) in bovine heart mitochondria and submitochondrial particles	172
Mitochondrial Complex I defects in aging	170
Decorin from different bovine tissues: study of glycosaminoglycan chain by PAGEFS	169
Mitochondrial abnormalities in muscle and other aging cells: Classification, causes, and effects	168
The fate of human sperm-derived mtDNA in somatic cells	168
Hyaluronan and human endothelial cell behavior.	168
Mitochondrial DNA in platelets from aged subjects	167
High frequency of migraine-only patients negative for the 3243 A>G tRNALeu mtDNA mutation in two MELAS families	167
Technical Issues Behind Molecular Monitoring in Chronic Myeloid Leukemia	165
Isolation and subfractionation of mitochondria from animal cells and tissue culture lines.	164
UDP-glucose dehydrogenase and Hyaluronan synthesis	164
Differential features of patients with mutations in two COX assembly genes, SURF-1 and SCO2	163
Decrease of rotenone inhibition is a sensitive parameter of complex I damage in brain non-synaptic mitochondria of aged rats	163
MODES OF COENZYME-Q FUNCTION IN ELECTRON-TRANSFER	162
Pathogenesis of the deafness-associated A1555G mitochondrial DNA mutation	159
Hyaluronan synthesis and human endothelial cell behaviour	159
Pathogenesis of primary defects in mitochondrial ATP synthesis	159
Comparison of three strategies for myocardial protection during coronary artery bypass graft surgery based on markers of cardiac damage.	158
Molecular cloning and characterization of UDP-glucose dehydrogenase from the amphibian xenopus laevis and its involvement in hyaluronan synthesis	158
Molecular control of the hyaluronan biosynthesis	158
G1HYALURONAN CONTENT OF UMBILICAL CORDS OF HEALTHY AND DOWN SYNDROME FETUSES	155
Exercise intolerance due to mutations in the cytochrome b gene of mitochondrial DNA	154
Mitochondrial dysfunction and brain disorders	154
Hyaluronan metabolism in human breast cancer cell line 8701BC	154
UDP-Glucose Dehydrogenase and its involvement in glycosaminoglycan Synthesis	151
Phosphorus MR spectroscopy shows a tissue specific in vivo distribution of biochemical expression of the G3460A mutation in Leber's hereditary optic neuropathy	150
UDP-Glucose dehydrogenase and its involvement in GAG synthesis	150
Carcinoma breast cancer cells modulates HA metabolism of fibroblasts	150
Mitochondrial activities of rat heart during ageing	150
Biochemical analysis of mitochondrial function in cybrid cell lines harboring mtDNA mutations	149
UDP-glucose dehydrogenase from Xenopus laevis and its involvement in hyaluronan synthesis	149
Oxidative stress, antioxidant defences and aging	147
Analysis of fluorophore labeled glycosaminoglycan disaccharides using polyacrylamide gel electroforesis and HPLC	147
Histomorphometric studies in rat cerebral cortex: Normal aging and cell loss	146
New electrophoretic and chromatographic tecniques for analysis of heparin and heparan sulphate.	141
Alteration of mitochondrial membrane inner potential in three Italian patients with megaconial congenital muscular dystrophy carrying new mutations in CHKB gene	141
Regulation of Hyaluronan synthesis in human endothelial cells	138
Archaeogenomics in Caravate and Cittiglio (Lombardy): from the excavation of ancient human bones to the study of DNA	135
LACK OF MAJOR MITOCHONDRIAL BIOENERGETIC CHANGES IN CULTURED SKIN FIBROBLASTS FROM AGED INDIVIDUALS	134
COLLAGEN TYPE I CARBOXY-TERMINAL PROPETIDE AND TELOPEPTIDE MEASUREMENT IN PLASMA OF PATIENTS WITH ESSENTIAL HYPERTENSION BY RIA AND EIA METHODS	133
Heteroplasmic 24-base pair deletion in the mitochondrial cytochrome b gene in a patient with isolated myopathy	132
Glicosamminoglicani prodotti in coltura cellulari umane	132
New highlights on the synthesis of hyaluronan	130
Comparison of clinical features in patients with COX assembly gene mutations	129
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	127
The search of the stool and blood K-ras mutations in patients with pancreatic mass	126
Haplogroup effects and recombination of mitochondrial DNA: novel clues from the analysis of Leber hereditary optic neuropathy pedigrees.	126
Hyaluronan in human umbilical cord	126
L’attivita’ della MMP2 come regolatore della migrazione di cellule umane muscolari lisce	125
Hyaluronan metabolism in breast cancer cell line	124
Gene therapy with the ND4 subunit gene recoded in the universal genetic code reverses a mitochondrial deficiency causing Leber hereditary optic neuropathy (LHON)	123
Structure and function of hyaluronan	123
Hyaluronan content and gene expression for hyaluronan synthases and hyaluronidases inthe umbilical cord of healthy and Down syndrome fetuses	121
Hyaluronan metabolism in in vitro culture of endothelial cells	119
Hyaluronan synthesis in human endothelial cells and its involvement during “in vitro” inflammation	118
Evidence that specific mtDNA point mutations may not accumulate in skeletal muscle during normal human aging	116
Hyaluronan content of umbilical cords of healthy and Down Syndrome fetuses	116
Osservazioni metodologiche nel dosaggio della NADH Coenzima Q ossidoreduttasi mitocondriale	116
Hyaluronan content of umbilical cords of healthy and Down Syndrome fetuses	113
Hyaluronan synthesis in human endothelial cells and its involvement during in vitro inflammation	113
Hyaluronan synthesis and human endothelial cell behaviour	112
Quantificazione della mutazione 3460 G>A/ND1 (LHON) mediante Real Time PCR quantitativa	111
Hyaluronan metabolism in in vitro culture of endothelial cells.	110
Hyaluronan content of umbilical cords of healthy and Down Syndrome fetuses	110
Involvement of Hyaluronan during in vitro angiogenesis of endothelial cells	109
HYALURONAN CONTENT AND SYNTHASE GENE EXPRESSION BY REAL TIME –PCR IN UMBILICAL CORDS OF HEALTHY AND DOWN SYNDROME FETUSES	109
INVOLVEMENT OF HYALURONAN DURING IN VITRO ANGIOGENESIS OF ENDOTHELIAL CELLS	108
Regulation of hyaluronan synthesis in human endothelial cells	107
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	107
Hyaluronan content of umbilical cords of healthy and Down Syndrome fetuses.	107
Migration in senescent cells: the role of cell-extracellular matrix interface	106
Totale	15.701

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Categoria	#
all - tutte	76.957
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	76.957

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	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2021/2022	1.041	0	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	4.388	306	270	264	566	406	308	1.029	251	438	299	150	101
2026/2027	257	72	185	0	0	0	0	0	0	0	0	0	0
Totale													18.843