statistiche ricercatore

PALLOTTI, FRANCESCO

Distribuzione geografica

Continente	#
NA - Nord America	7.103
EU - Europa	4.971
AS - Asia	1.986
SA - Sud America	217
AF - Africa	17
Continente sconosciuto - Info sul continente non disponibili	13
OC - Oceania	5
Totale	14.312

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Nazione	#
US - Stati Uniti d'America	7.079
IT - Italia	2.087
UA - Ucraina	991
SE - Svezia	556
TR - Turchia	555
SG - Singapore	422
HK - Hong Kong	323
VN - Vietnam	315
CN - Cina	314
IE - Irlanda	277
FI - Finlandia	273
DE - Germania	252
BR - Brasile	206
GB - Regno Unito	191
RU - Federazione Russa	138
FR - Francia	99
IN - India	20
BE - Belgio	18
AT - Austria	17
CA - Canada	15
NL - Olanda	15
CZ - Repubblica Ceca	14
EU - Europa	13
ES - Italia	12
BD - Bangladesh	8
JP - Giappone	8
BG - Bulgaria	7
LT - Lituania	6
ZA - Sudafrica	6
AR - Argentina	5
MX - Messico	5
AU - Australia	4
IQ - Iraq	4
AE - Emirati Arabi Uniti	3
DK - Danimarca	3
HU - Ungheria	3
IL - Israele	3
KE - Kenya	3
MA - Marocco	3
RO - Romania	3
UZ - Uzbekistan	3
CL - Cile	2
EG - Egitto	2
GR - Grecia	2
HR - Croazia	2
PA - Panama	2
PH - Filippine	2
PL - Polonia	2
VE - Venezuela	2
AM - Armenia	1
AO - Angola	1
BW - Botswana	1
DO - Repubblica Dominicana	1
GT - Guatemala	1
KZ - Kazakistan	1
LB - Libano	1
LV - Lettonia	1
MU - Mauritius	1
NZ - Nuova Zelanda	1
OM - Oman	1
PK - Pakistan	1
PY - Paraguay	1
RS - Serbia	1
SI - Slovenia	1
TW - Taiwan	1
UY - Uruguay	1
Totale	14.312

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Città	#
Milan	1.515
Fairfield	876
Jacksonville	756
Chandler	670
Woodbridge	553
Ashburn	489
Houston	387
Seattle	344
Izmir	341
Hong Kong	322
Cambridge	317
Wilmington	314
Dublin	277
Ann Arbor	270
Princeton	262
Dearborn	254
Nyköping	218
Singapore	202
Boardman	147
San Mateo	114
Dong Ket	112
Rome	112
Chicago	81
Como	76
New York	75
Beijing	72
San Diego	62
Ogden	44
The Dalles	37
Munich	34
Hefei	33
Nanjing	32
Washington	32
Kunming	30
Santa Clara	30
Los Angeles	28
Norwalk	25
Düsseldorf	24
Helsinki	21
Kocaeli	21
Philadelphia	20
Brussels	18
Dallas	18
London	17
São Paulo	15
Jinan	14
San Francisco	14
Zhengzhou	13
Redmond	11
Verona	11
Guangzhou	10
Nanchang	10
Redwood City	10
Brno	9
Chengdu	9
Frankfurt am Main	9
Shenyang	9
Turku	9
Fuzhou	8
Tokyo	8
Vienna	8
Campinas	7
Nuremberg	7
Sofia	7
Varese	7
Berlin	6
Brasília	6
Hanoi	6
Rio de Janeiro	6
Wuhan	6
Atlanta	5
Changsha	5
Hangzhou	5
Hebei	5
Hounslow	5
Johannesburg	5
Montreal	5
Phoenix	5
Seveso	5
Stockholm	5
Acton	4
Belo Horizonte	4
Bologna	4
Brooklyn	4
Des Moines	4
Istanbul	4
Missaglia	4
Amsterdam	3
Baotou	3
Birmingham	3
Boston	3
Budapest	3
Cagliari	3
Campo Grande	3
Chiswick	3
Chongqing	3
Copenhagen	3
Edinburgh	3
Goiânia	3
Guarulhos	3
Totale	10.034

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Nome	#
Analysis of three screening methods for the detection of calreticulin gene mutations	223
Authors’ Reply to Crampe and Langabeer: Technical Issues Behind Molecular Monitoring in Chronic Myeloid Leukemia	180
ASSAY CONDITIONS FOR THE MITOCHONDRIAL NADH - COENZYME-Q OXIDOREDUCTASE	177
THE FUNCTION OF COENZYME-Q IN MITOCHONDRIA	175
FTL gene mutation and persistent hyperferritinemia without iron deficiency anemia after phlebotomy	171
Assessing Heteroplasmic Load in Leber's Hereditary Optic Neuropathy Mutation 3460G->A/MT-ND1 with A Real-Time PCR Quantitative Approach	170
A new acute myeloid leukemia case with STAT5B-RARA gene fusion due to 17q21.2 interstitial deletion	168
Biochemical-clinical correlation in patients with different loads of the mitochondrial DNA T8993G mutation	166
Differential cerebro spinal fluid proteome investigation of Leber hereditary optic neuropathy (LHON) and multiple sclerosis.	165
JAK2, 46/1 haplotype and chronic myelogenous leukemia: diagnostic and therapeutic potential	164
A wide range of 3243A>G/tRNALeu(UUR) (MELAS) mutation loads may segregate in offspring through the female germline bottleneck	161
A particular case of AML patient with the polymorphism G105G (rs11554137) and the missense mutation R132C in IDH1 gene	158
Rescue of a mitochondrial deficiency causing Leber hereditary optic neuropathy	157
New insights into the pathobiology of Down syndrome - Hyaluronan synthase-2 overexpression is regulated by collagen VI α2 chain	157
Biological variation of procalcitonin in healthy individuals	156
Biological variation of procalcitonin in healthy individuals	155
JAK2 mutation and atypical chronic myeloid leukemia	150
Biochemical analysis of respiratory function in cybrid cell lines harbouring mitochondrial DNA mutations	149
Isolation and subfractionation of mitochondria from animal cells and tissue culture lines.	149
Technical Issues Behind Molecular Monitoring in Chronic Myeloid Leukemia	148
Identification of a novel mutation in Cu/Zn superoxide dismutase gene associated with familial amyotrophic lateral sclerosis	147
AN UPDATING OF THE BIOCHEMICAL FUNCTION OF COENZYME-Q IN MITOCHONDRIA	147
In vivo regulation of oxidative phosphorylation in cells harboring a stop-codon mutation in mitochondrial DNA-encoded cytochrome c oxidase subunit I	145
Steady-state kinetics of the reduction of coenzyme Q analogs by complex I (NADH:Ubiquinone oxidoreductase) in bovine heart mitochondria and submitochondrial particles	143
Mitochondrial DNA nucleotide changes C14482G and C14482A in the ND6 gene are pathogenic for Leber's hereditary optic neuropathy	142
A stop-codon mutation in the human mtDNA cytochrome c oxidase I gene disrupts the functional structure of complex IV	141
Isolation and subfractionation of mitochondria from animal cells and tissue culture lines.	140
Analysis of mtDNA deletions in muscle by in situ hybridization	140
Mitochondrial Complex I defects in aging	140
Decorin from different bovine tissues: study of glycosaminoglycan chain by PAGEFS	139
Decrease of rotenone inhibition is a sensitive parameter of complex I damage in brain non-synaptic mitochondria of aged rats	139
Aortic smooth muscle cells migration and the role of metalloproteinases and hyaluronan.	138
Differential features of patients with mutations in two COX assembly genes, SURF-1 and SCO2	137
Mitochondrial DNA in platelets from aged subjects	137
Biological variation of procalcitonin in healthy individuals	137
Mitochondrial abnormalities in muscle and other aging cells: Classification, causes, and effects	136
High frequency of migraine-only patients negative for the 3243 A>G tRNALeu mtDNA mutation in two MELAS families	135
The fate of human sperm-derived mtDNA in somatic cells	134
MODES OF COENZYME-Q FUNCTION IN ELECTRON-TRANSFER	134
Pure myopathy with enlarged mitochondria associated to a new mutation in MTND2 gene	133
Hyaluronan synthesis and human endothelial cell behaviour	132
Pathogenesis of primary defects in mitochondrial ATP synthesis	132
Molecular control of the hyaluronan biosynthesis	128
Exercise intolerance due to mutations in the cytochrome b gene of mitochondrial DNA	127
Hyaluronan and human endothelial cell behavior.	127
Pathogenesis of the deafness-associated A1555G mitochondrial DNA mutation	125
Mitochondrial dysfunction and brain disorders	125
Matrix metalloproteinase 2 and tissue inhibitors of metalloproteinases regulate human aortic smooth muscle cell migration during in vitro aging	125
UDP-glucose dehydrogenase and Hyaluronan synthesis	121
Histomorphometric studies in rat cerebral cortex: Normal aging and cell loss	120
Phosphorus MR spectroscopy shows a tissue specific in vivo distribution of biochemical expression of the G3460A mutation in Leber's hereditary optic neuropathy	118
G1HYALURONAN CONTENT OF UMBILICAL CORDS OF HEALTHY AND DOWN SYNDROME FETUSES	117
Comparison of three strategies for myocardial protection during coronary artery bypass graft surgery based on markers of cardiac damage.	117
Oxidative stress, antioxidant defences and aging	116
Molecular cloning and characterization of UDP-glucose dehydrogenase from the amphibian xenopus laevis and its involvement in hyaluronan synthesis	116
UDP-Glucose Dehydrogenase and its involvement in glycosaminoglycan Synthesis	116
LACK OF MAJOR MITOCHONDRIAL BIOENERGETIC CHANGES IN CULTURED SKIN FIBROBLASTS FROM AGED INDIVIDUALS	111
UDP-Glucose dehydrogenase and its involvement in GAG synthesis	110
UDP-glucose dehydrogenase from Xenopus laevis and its involvement in hyaluronan synthesis	110
Regulation of Hyaluronan synthesis in human endothelial cells	109
Mitochondrial activities of rat heart during ageing	108
Carcinoma breast cancer cells modulates HA metabolism of fibroblasts	105
Heteroplasmic 24-base pair deletion in the mitochondrial cytochrome b gene in a patient with isolated myopathy	104
Haplogroup effects and recombination of mitochondrial DNA: novel clues from the analysis of Leber hereditary optic neuropathy pedigrees.	104
Comparison of clinical features in patients with COX assembly gene mutations	102
Biochemical analysis of mitochondrial function in cybrid cell lines harboring mtDNA mutations	101
Hyaluronan metabolism in human breast cancer cell line 8701BC	101
New electrophoretic and chromatographic tecniques for analysis of heparin and heparan sulphate.	100
Gene therapy with the ND4 subunit gene recoded in the universal genetic code reverses a mitochondrial deficiency causing Leber hereditary optic neuropathy (LHON)	99
The search of the stool and blood K-ras mutations in patients with pancreatic mass	99
New highlights on the synthesis of hyaluronan	99
L’attivita’ della MMP2 come regolatore della migrazione di cellule umane muscolari lisce	99
Structure and function of hyaluronan	98
Hyaluronan in human umbilical cord	97
Hyaluronan synthesis in human endothelial cells and its involvement during “in vitro” inflammation	96
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	95
Hyaluronan synthesis and human endothelial cell behaviour	95
Osservazioni metodologiche nel dosaggio della NADH Coenzima Q ossidoreduttasi mitocondriale	95
Analysis of fluorophore labeled glycosaminoglycan disaccharides using polyacrylamide gel electroforesis and HPLC	93
Hyaluronan content of umbilical cords of healthy and Down Syndrome fetuses	93
Evidence that specific mtDNA point mutations may not accumulate in skeletal muscle during normal human aging	90
Quantificazione della mutazione 3460 G>A/ND1 (LHON) mediante Real Time PCR quantitativa	90
Glicosamminoglicani prodotti in coltura cellulari umane	90
Hyaluronan synthesis in human endothelial cells and its involvement during in vitro inflammation	88
Hyaluronan content of umbilical cords of healthy and Down Syndrome fetuses	88
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	88
Alteration of mitochondrial membrane inner potential in three Italian patients with megaconial congenital muscular dystrophy carrying new mutations in CHKB gene	88
Hyaluronan content of umbilical cords of healthy and Down Syndrome fetuses.	87
Hyaluronan content of umbilical cords of healthy and Down Syndrome fetuses	86
Regulation of hyaluronan synthesis in human endothelial cells	85
Experimental isovolemic hemodilution. Study of tissue perfusion with Hb 3% in swine	85
HYALURONAN CONTENT AND SYNTHASE GENE EXPRESSION BY REAL TIME –PCR IN UMBILICAL CORDS OF HEALTHY AND DOWN SYNDROME FETUSES	83
Hyaluronan content and gene expression for hyaluronan synthases and hyaluronidases inthe umbilical cord of healthy and Down syndrome fetuses	82
INVOLVEMENT OF HYALURONAN DURING IN VITRO ANGIOGENESIS OF ENDOTHELIAL CELLS	82
Hyaluronan synthesis and human endothelial cell behaviour	82
COLLAGEN TYPE I CARBOXY-TERMINAL PROPETIDE AND TELOPEPTIDE MEASUREMENT IN PLASMA OF PATIENTS WITH ESSENTIAL HYPERTENSION BY RIA AND EIA METHODS	80
Hyaluronan metabolism in in vitro culture of endothelial cells.	79
Involvement of Hyaluronan during in vitro angiogenesis of endothelial cells	78
Hyaluronan metabolism in in vitro culture of endothelial cells	78
Hyaluronan metabolism in human breast carcinoma	78
Totale	12.155

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Categoria	#
all - tutte	59.926
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	59.926

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	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2020/2021	2.149	30	177	108	279	83	235	82	164	301	189	146	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	155	155	0	0	0	0	0	0	0	0	0	0	0
Totale													14.353