statistiche ricercatore

PALLOTTI, FRANCESCO

Distribuzione geografica

Continente	#
NA - Nord America	10.551
EU - Europa	5.403
AS - Asia	3.587
SA - Sud America	382
AF - Africa	88
Continente sconosciuto - Info sul continente non disponibili	61
OC - Oceania	8
Totale	20.080

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Nazione	#
US - Stati Uniti d'America	10.381
IT - Italia	2.157
SG - Singapore	1.150
UA - Ucraina	993
CN - Cina	823
SE - Svezia	567
TR - Turchia	556
VN - Vietnam	501
HK - Hong Kong	383
BR - Brasile	329
FI - Finlandia	313
GB - Regno Unito	285
IE - Irlanda	278
DE - Germania	259
FR - Francia	246
RU - Federazione Russa	145
CA - Canada	83
IN - India	55
NG - Nigeria	40
MX - Messico	37
BD - Bangladesh	33
PL - Polonia	23
NL - Olanda	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	11
CL - Cile	9
BG - Bulgaria	8
CR - Costa Rica	8
AU - Australia	7
MA - Marocco	7
CO - Colombia	6
GT - Guatemala	6
KE - Kenya	6
PK - Pakistan	6
UZ - Uzbekistan	6
AE - Emirati Arabi Uniti	5
CW - ???statistics.table.value.countryCode.CW???	5
EC - Ecuador	5
EG - Egitto	5
ET - Etiopia	5
ID - Indonesia	5
PH - Filippine	5
GP - Guadalupe	4
HN - Honduras	4
IL - Israele	4
JM - Giamaica	4
NI - Nicaragua	4
PA - Panama	4
SV - El Salvador	4
VE - Venezuela	4
BO - Bolivia	3
DK - Danimarca	3
DO - Repubblica Dominicana	3
GR - Grecia	3
HU - Ungheria	3
PR - Porto Rico	3
RO - Romania	3
SA - Arabia Saudita	3
TT - Trinidad e Tobago	3
CH - Svizzera	2
EE - Estonia	2
HR - Croazia	2
KR - Corea	2
KZ - Kazakistan	2
MY - Malesia	2
PE - Perù	2
PS - Palestinian Territory	2
PY - Paraguay	2
SC - Seychelles	2
AM - Armenia	1
AO - Angola	1
AZ - Azerbaigian	1
BA - Bosnia-Erzegovina	1
BH - Bahrain	1
BS - Bahamas	1
BW - Botswana	1
BY - Bielorussia	1
CG - Congo	1
DM - Dominica	1
DZ - Algeria	1
JO - Giordania	1
LB - Libano	1
LV - Lettonia	1
MD - Moldavia	1
MQ - Martinica	1
MU - Mauritius	1
MW - Malawi	1
NZ - Nuova Zelanda	1
OM - Oman	1
PT - Portogallo	1
QA - Qatar	1
RS - Serbia	1
Totale	20.031

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Città	#
Milan	1.518
Ashburn	1.081
Fairfield	876
San Jose	858
Jacksonville	756
Chandler	670
Singapore	601
Woodbridge	553
Houston	392
Hong Kong	374
Council Bluffs	370
Seattle	346
Izmir	341
Dallas	333
Wilmington	318
Cambridge	317
Dublin	277
Ann Arbor	270
Princeton	262
Dearborn	254
Nyköping	218
Beijing	178
Chicago	169
The Dalles	156
Boardman	147
New York	126
Rome	119
Lauterbourg	118
San Mateo	114
Dong Ket	112
Los Angeles	93
Como	76
San Diego	65
Ho Chi Minh City	63
London	63
Santa Clara	60
Helsinki	57
Washington	56
Orem	50
São Paulo	50
Hanoi	47
Guangzhou	44
Ogden	44
Abuja	39
Hefei	34
Munich	34
Nanjing	32
Kunming	30
Philadelphia	27
Toronto	26
Buffalo	25
Norwalk	25
Düsseldorf	24
Mexico City	24
Phoenix	22
San Francisco	22
Atlanta	21
Kocaeli	21
Shenzhen	20
Montreal	19
Shanghai	19
Tokyo	19
Brussels	18
Chennai	18
Warsaw	18
Zhengzhou	17
Hangzhou	16
Frankfurt am Main	15
Jinan	15
Poplar	15
Denver	14
Johannesburg	13
Manchester	13
Stockholm	13
Brooklyn	12
Tianjin	12
Turku	12
Haiphong	11
Mumbai	11
Redmond	11
Verona	11
Nanchang	10
Redwood City	10
Boston	9
Brno	9
Changsha	9
Chengdu	9
Da Nang	9
Fuzhou	9
Naples	9
Shenyang	9
Amsterdam	8
Brasília	8
Las Vegas	8
Nuremberg	8
Paris	8
Rio de Janeiro	8
San José	8
Vienna	8
Bologna	7
Totale	13.903

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Nome	#
Analysis of three screening methods for the detection of calreticulin gene mutations	279
A wide range of 3243A>G/tRNALeu(UUR) (MELAS) mutation loads may segregate in offspring through the female germline bottleneck	249
Authors’ Reply to Crampe and Langabeer: Technical Issues Behind Molecular Monitoring in Chronic Myeloid Leukemia	236
Assessing Heteroplasmic Load in Leber's Hereditary Optic Neuropathy Mutation 3460G->A/MT-ND1 with A Real-Time PCR Quantitative Approach	235
ASSAY CONDITIONS FOR THE MITOCHONDRIAL NADH - COENZYME-Q OXIDOREDUCTASE	233
Matrix metalloproteinase 2 and tissue inhibitors of metalloproteinases regulate human aortic smooth muscle cell migration during in vitro aging	225
A new acute myeloid leukemia case with STAT5B-RARA gene fusion due to 17q21.2 interstitial deletion	225
THE FUNCTION OF COENZYME-Q IN MITOCHONDRIA	219
Biochemical-clinical correlation in patients with different loads of the mitochondrial DNA T8993G mutation	219
Biochemical analysis of respiratory function in cybrid cell lines harbouring mitochondrial DNA mutations	219
A particular case of AML patient with the polymorphism G105G (rs11554137) and the missense mutation R132C in IDH1 gene	214
Biological variation of procalcitonin in healthy individuals	213
JAK2, 46/1 haplotype and chronic myelogenous leukemia: diagnostic and therapeutic potential	209
Biological variation of procalcitonin in healthy individuals	208
Analysis of mtDNA deletions in muscle by in situ hybridization	201
AN UPDATING OF THE BIOCHEMICAL FUNCTION OF COENZYME-Q IN MITOCHONDRIA	200
Aortic smooth muscle cells migration and the role of metalloproteinases and hyaluronan.	198
Rescue of a mitochondrial deficiency causing Leber hereditary optic neuropathy	196
A stop-codon mutation in the human mtDNA cytochrome c oxidase I gene disrupts the functional structure of complex IV	196
JAK2 mutation and atypical chronic myeloid leukemia	195
UDP-Glucose dehydrogenase and its involvement in GAG synthesis	193
FTL gene mutation and persistent hyperferritinemia without iron deficiency anemia after phlebotomy	192
Differential cerebro spinal fluid proteome investigation of Leber hereditary optic neuropathy (LHON) and multiple sclerosis.	190
In vivo regulation of oxidative phosphorylation in cells harboring a stop-codon mutation in mitochondrial DNA-encoded cytochrome c oxidase subunit I	188
New insights into the pathobiology of Down syndrome - Hyaluronan synthase-2 overexpression is regulated by collagen VI α2 chain	188
Pure myopathy with enlarged mitochondria associated to a new mutation in MTND2 gene	187
Mitochondrial DNA nucleotide changes C14482G and C14482A in the ND6 gene are pathogenic for Leber's hereditary optic neuropathy	186
Biological variation of procalcitonin in healthy individuals	186
Steady-state kinetics of the reduction of coenzyme Q analogs by complex I (NADH:Ubiquinone oxidoreductase) in bovine heart mitochondria and submitochondrial particles	182
Isolation and subfractionation of mitochondria from animal cells and tissue culture lines.	182
Decorin from different bovine tissues: study of glycosaminoglycan chain by PAGEFS	182
Mitochondrial Complex I defects in aging	181
Identification of a novel mutation in Cu/Zn superoxide dismutase gene associated with familial amyotrophic lateral sclerosis	180
Hyaluronan and human endothelial cell behavior.	179
Mitochondrial DNA in platelets from aged subjects	177
The fate of human sperm-derived mtDNA in somatic cells	177
Mitochondrial abnormalities in muscle and other aging cells: Classification, causes, and effects	175
High frequency of migraine-only patients negative for the 3243 A>G tRNALeu mtDNA mutation in two MELAS families	175
Decrease of rotenone inhibition is a sensitive parameter of complex I damage in brain non-synaptic mitochondria of aged rats	174
New highlights on the synthesis of hyaluronan	172
UDP-glucose dehydrogenase and Hyaluronan synthesis	172
Isolation and subfractionation of mitochondria from animal cells and tissue culture lines.	170
Differential features of patients with mutations in two COX assembly genes, SURF-1 and SCO2	169
Technical Issues Behind Molecular Monitoring in Chronic Myeloid Leukemia	169
Pathogenesis of the deafness-associated A1555G mitochondrial DNA mutation	168
MODES OF COENZYME-Q FUNCTION IN ELECTRON-TRANSFER	168
UDP-Glucose Dehydrogenase and its involvement in glycosaminoglycan Synthesis	168
Pathogenesis of primary defects in mitochondrial ATP synthesis	168
Hyaluronan synthesis and human endothelial cell behaviour	166
Molecular control of the hyaluronan biosynthesis	165
Comparison of three strategies for myocardial protection during coronary artery bypass graft surgery based on markers of cardiac damage.	164
Molecular cloning and characterization of UDP-glucose dehydrogenase from the amphibian xenopus laevis and its involvement in hyaluronan synthesis	164
Hyaluronan metabolism in human breast cancer cell line 8701BC	164
Exercise intolerance due to mutations in the cytochrome b gene of mitochondrial DNA	162
G1HYALURONAN CONTENT OF UMBILICAL CORDS OF HEALTHY AND DOWN SYNDROME FETUSES	161
Biochemical analysis of mitochondrial function in cybrid cell lines harboring mtDNA mutations	160
Phosphorus MR spectroscopy shows a tissue specific in vivo distribution of biochemical expression of the G3460A mutation in Leber's hereditary optic neuropathy	159
Histomorphometric studies in rat cerebral cortex: Normal aging and cell loss	158
Mitochondrial dysfunction and brain disorders	158
UDP-glucose dehydrogenase from Xenopus laevis and its involvement in hyaluronan synthesis	158
New electrophoretic and chromatographic tecniques for analysis of heparin and heparan sulphate.	158
Mitochondrial activities of rat heart during ageing	157
Analysis of fluorophore labeled glycosaminoglycan disaccharides using polyacrylamide gel electroforesis and HPLC	156
Alteration of mitochondrial membrane inner potential in three Italian patients with megaconial congenital muscular dystrophy carrying new mutations in CHKB gene	156
Carcinoma breast cancer cells modulates HA metabolism of fibroblasts	155
Oxidative stress, antioxidant defences and aging	153
LACK OF MAJOR MITOCHONDRIAL BIOENERGETIC CHANGES IN CULTURED SKIN FIBROBLASTS FROM AGED INDIVIDUALS	147
Regulation of Hyaluronan synthesis in human endothelial cells	146
Heteroplasmic 24-base pair deletion in the mitochondrial cytochrome b gene in a patient with isolated myopathy	143
Comparison of clinical features in patients with COX assembly gene mutations	141
Haplogroup effects and recombination of mitochondrial DNA: novel clues from the analysis of Leber hereditary optic neuropathy pedigrees.	141
Archaeogenomics in Caravate and Cittiglio (Lombardy): from the excavation of ancient human bones to the study of DNA	140
Glicosamminoglicani prodotti in coltura cellulari umane	139
COLLAGEN TYPE I CARBOXY-TERMINAL PROPETIDE AND TELOPEPTIDE MEASUREMENT IN PLASMA OF PATIENTS WITH ESSENTIAL HYPERTENSION BY RIA AND EIA METHODS	137
Quantificazione della mutazione 3460 G>A/ND1 (LHON) mediante Real Time PCR quantitativa	137
Structure and function of hyaluronan	136
Gene therapy with the ND4 subunit gene recoded in the universal genetic code reverses a mitochondrial deficiency causing Leber hereditary optic neuropathy (LHON)	135
Hyaluronan in human umbilical cord	133
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	132
Hyaluronan metabolism in breast cancer cell line	132
The search of the stool and blood K-ras mutations in patients with pancreatic mass	131
L’attivita’ della MMP2 come regolatore della migrazione di cellule umane muscolari lisce	130
Evidence that specific mtDNA point mutations may not accumulate in skeletal muscle during normal human aging	129
Hyaluronan metabolism in in vitro culture of endothelial cells	129
Osservazioni metodologiche nel dosaggio della NADH Coenzima Q ossidoreduttasi mitocondriale	129
Hyaluronan content and gene expression for hyaluronan synthases and hyaluronidases inthe umbilical cord of healthy and Down syndrome fetuses	127
Serum amyloid A: Biology and clinical application [La siero amiloide A: Biologia ed applicazioni cliniche]	126
Hyaluronan synthesis in human endothelial cells and its involvement during “in vitro” inflammation	124
Changes in different mitochondrial populations from cerebral cortex of aged rats	124
Hyaluronan synthesis in human endothelial cells and its involvement during in vitro inflammation	120
Hyaluronan content of umbilical cords of healthy and Down Syndrome fetuses	120
Hyaluronan content of umbilical cords of healthy and Down Syndrome fetuses	119
Regulation of hyaluronan metabolism in human endothelial cells.	119
Hyaluronan synthesis and human endothelial cell behaviour	119
Involvement of Hyaluronan during in vitro angiogenesis of endothelial cells	115
Hyaluronan metabolism in in vitro culture of endothelial cells.	115
INVOLVEMENT OF HYALURONAN DURING IN VITRO ANGIOGENESIS OF ENDOTHELIAL CELLS	115
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	114
HYALURONAN CONTENT AND SYNTHASE GENE EXPRESSION BY REAL TIME –PCR IN UMBILICAL CORDS OF HEALTHY AND DOWN SYNDROME FETUSES	113
Regulation of hyaluronan synthesis in human endothelial cells	113
Totale	16.611

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Categoria	#
all - tutte	81.484
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	81.484

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	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2021/2022	809	0	0	0	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	1.494	72	209	696	517	0	0	0	0	0	0	0	0
Totale													20.080