statistiche ricercatore

PALLOTTI, FRANCESCO

Distribuzione geografica

Continente	#
NA - Nord America	6.856
EU - Europa	4.671
AS - Asia	1.247
Continente sconosciuto - Info sul continente non disponibili	13
OC - Oceania	5
SA - Sud America	2
Totale	12.794

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Nazione	#
US - Stati Uniti d'America	6.852
IT - Italia	2.049
UA - Ucraina	989
SE - Svezia	553
TR - Turchia	549
VN - Vietnam	306
CN - Cina	292
IE - Irlanda	277
FI - Finlandia	255
DE - Germania	207
GB - Regno Unito	177
FR - Francia	97
SG - Singapore	78
CZ - Repubblica Ceca	13
EU - Europa	13
IN - India	10
NL - Olanda	10
BE - Belgio	9
BG - Bulgaria	7
RU - Federazione Russa	6
JP - Giappone	5
AU - Australia	4
ES - Italia	4
DK - Danimarca	3
HU - Ungheria	3
RO - Romania	3
AT - Austria	2
CA - Canada	2
HR - Croazia	2
PA - Panama	2
AE - Emirati Arabi Uniti	1
AM - Armenia	1
AR - Argentina	1
BD - Bangladesh	1
CL - Cile	1
GR - Grecia	1
HK - Hong Kong	1
KZ - Kazakistan	1
LT - Lituania	1
LV - Lettonia	1
NZ - Nuova Zelanda	1
PH - Filippine	1
RS - Serbia	1
SI - Slovenia	1
TW - Taiwan	1
Totale	12.794

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Città	#
Milan	1.509
Fairfield	876
Jacksonville	754
Chandler	670
Woodbridge	553
Ashburn	475
Houston	387
Izmir	341
Seattle	340
Cambridge	317
Wilmington	314
Dublin	277
Ann Arbor	270
Princeton	262
Dearborn	254
Nyköping	218
Boardman	146
San Mateo	114
Dong Ket	112
Rome	108
Como	76
Singapore	75
Chicago	71
New York	67
San Diego	62
Beijing	57
Ogden	44
Hefei	33
Nanjing	32
Washington	32
Kunming	30
Norwalk	25
Santa Clara	25
Düsseldorf	24
Kocaeli	21
Philadelphia	20
Dallas	17
Los Angeles	17
London	16
Jinan	14
Helsinki	13
Zhengzhou	12
Redmond	11
Verona	11
Nanchang	10
Redwood City	10
Brno	9
Brussels	9
Chengdu	9
Guangzhou	9
Shenyang	9
Fuzhou	8
Frankfurt am Main	7
Sofia	7
Berlin	6
Wuhan	6
Changsha	5
Hangzhou	5
Hebei	5
Phoenix	5
San Francisco	5
Tokyo	5
Varese	5
Acton	4
Bologna	4
Hounslow	4
Munich	4
Baotou	3
Budapest	3
Chiswick	3
Chongqing	3
Copenhagen	3
Edinburgh	3
Madrid	3
Marano di Napoli	3
Paris	3
Segrate	3
Shaoxing	3
Southwark	3
Sydney	3
Xian	3
Amsterdam	2
Atlanta	2
Auburn Hills	2
Bergamo	2
Boston	2
Desio	2
Ferrara	2
Islington	2
Istanbul	2
Kilburn	2
Lanzhou	2
Panama City	2
Pioltello	2
Prague	2
Pune	2
Quzhou	2
Rimini	2
Roncello	2
Seveso	2
Totale	9.332

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Nome	#
Analysis of three screening methods for the detection of calreticulin gene mutations	204
THE FUNCTION OF COENZYME-Q IN MITOCHONDRIA	166
Authors’ Reply to Crampe and Langabeer: Technical Issues Behind Molecular Monitoring in Chronic Myeloid Leukemia	164
FTL gene mutation and persistent hyperferritinemia without iron deficiency anemia after phlebotomy	162
ASSAY CONDITIONS FOR THE MITOCHONDRIAL NADH - COENZYME-Q OXIDOREDUCTASE	157
JAK2, 46/1 haplotype and chronic myelogenous leukemia: diagnostic and therapeutic potential	153
Differential cerebro spinal fluid proteome investigation of Leber hereditary optic neuropathy (LHON) and multiple sclerosis.	151
Assessing Heteroplasmic Load in Leber's Hereditary Optic Neuropathy Mutation 3460G->A/MT-ND1 with A Real-Time PCR Quantitative Approach	149
Rescue of a mitochondrial deficiency causing Leber hereditary optic neuropathy	147
Biochemical-clinical correlation in patients with different loads of the mitochondrial DNA T8993G mutation	146
New insights into the pathobiology of Down syndrome - Hyaluronan synthase-2 overexpression is regulated by collagen VI α2 chain	146
A wide range of 3243A>G/tRNALeu(UUR) (MELAS) mutation loads may segregate in offspring through the female germline bottleneck	145
A new acute myeloid leukemia case with STAT5B-RARA gene fusion due to 17q21.2 interstitial deletion	145
Biological variation of procalcitonin in healthy individuals	140
Technical Issues Behind Molecular Monitoring in Chronic Myeloid Leukemia	140
A particular case of AML patient with the polymorphism G105G (rs11554137) and the missense mutation R132C in IDH1 gene	140
Biological variation of procalcitonin in healthy individuals	139
In vivo regulation of oxidative phosphorylation in cells harboring a stop-codon mutation in mitochondrial DNA-encoded cytochrome c oxidase subunit I	138
Isolation and subfractionation of mitochondria from animal cells and tissue culture lines.	138
Identification of a novel mutation in Cu/Zn superoxide dismutase gene associated with familial amyotrophic lateral sclerosis	137
Mitochondrial DNA nucleotide changes C14482G and C14482A in the ND6 gene are pathogenic for Leber's hereditary optic neuropathy	136
JAK2 mutation and atypical chronic myeloid leukemia	134
Steady-state kinetics of the reduction of coenzyme Q analogs by complex I (NADH:Ubiquinone oxidoreductase) in bovine heart mitochondria and submitochondrial particles	133
Biochemical analysis of respiratory function in cybrid cell lines harbouring mitochondrial DNA mutations	133
AN UPDATING OF THE BIOCHEMICAL FUNCTION OF COENZYME-Q IN MITOCHONDRIA	132
Differential features of patients with mutations in two COX assembly genes, SURF-1 and SCO2	130
A stop-codon mutation in the human mtDNA cytochrome c oxidase I gene disrupts the functional structure of complex IV	130
Mitochondrial Complex I defects in aging	130
Mitochondrial abnormalities in muscle and other aging cells: Classification, causes, and effects	129
Decorin from different bovine tissues: study of glycosaminoglycan chain by PAGEFS	129
Isolation and subfractionation of mitochondria from animal cells and tissue culture lines.	127
High frequency of migraine-only patients negative for the 3243 A>G tRNALeu mtDNA mutation in two MELAS families	126
Mitochondrial DNA in platelets from aged subjects	125
MODES OF COENZYME-Q FUNCTION IN ELECTRON-TRANSFER	125
Biological variation of procalcitonin in healthy individuals	124
Decrease of rotenone inhibition is a sensitive parameter of complex I damage in brain non-synaptic mitochondria of aged rats	123
Analysis of mtDNA deletions in muscle by in situ hybridization	121
Aortic smooth muscle cells migration and the role of metalloproteinases and hyaluronan.	121
Pathogenesis of primary defects in mitochondrial ATP synthesis	121
The fate of human sperm-derived mtDNA in somatic cells	120
Hyaluronan synthesis and human endothelial cell behaviour	120
Exercise intolerance due to mutations in the cytochrome b gene of mitochondrial DNA	119
Hyaluronan and human endothelial cell behavior.	119
Molecular control of the hyaluronan biosynthesis	119
Pure myopathy with enlarged mitochondria associated to a new mutation in MTND2 gene	119
Mitochondrial dysfunction and brain disorders	114
Pathogenesis of the deafness-associated A1555G mitochondrial DNA mutation	113
Phosphorus MR spectroscopy shows a tissue specific in vivo distribution of biochemical expression of the G3460A mutation in Leber's hereditary optic neuropathy	113
Matrix metalloproteinase 2 and tissue inhibitors of metalloproteinases regulate human aortic smooth muscle cell migration during in vitro aging	113
Histomorphometric studies in rat cerebral cortex: Normal aging and cell loss	112
Molecular cloning and characterization of UDP-glucose dehydrogenase from the amphibian xenopus laevis and its involvement in hyaluronan synthesis	108
UDP-glucose dehydrogenase and Hyaluronan synthesis	108
Oxidative stress, antioxidant defences and aging	105
Comparison of three strategies for myocardial protection during coronary artery bypass graft surgery based on markers of cardiac damage.	103
UDP-Glucose Dehydrogenase and its involvement in glycosaminoglycan Synthesis	102
UDP-Glucose dehydrogenase and its involvement in GAG synthesis	101
LACK OF MAJOR MITOCHONDRIAL BIOENERGETIC CHANGES IN CULTURED SKIN FIBROBLASTS FROM AGED INDIVIDUALS	99
G1HYALURONAN CONTENT OF UMBILICAL CORDS OF HEALTHY AND DOWN SYNDROME FETUSES	99
UDP-glucose dehydrogenase from Xenopus laevis and its involvement in hyaluronan synthesis	99
Regulation of Hyaluronan synthesis in human endothelial cells	98
Mitochondrial activities of rat heart during ageing	96
Heteroplasmic 24-base pair deletion in the mitochondrial cytochrome b gene in a patient with isolated myopathy	95
Comparison of clinical features in patients with COX assembly gene mutations	93
The search of the stool and blood K-ras mutations in patients with pancreatic mass	91
Haplogroup effects and recombination of mitochondrial DNA: novel clues from the analysis of Leber hereditary optic neuropathy pedigrees.	91
New highlights on the synthesis of hyaluronan	90
Structure and function of hyaluronan	90
New electrophoretic and chromatographic tecniques for analysis of heparin and heparan sulphate.	89
Gene therapy with the ND4 subunit gene recoded in the universal genetic code reverses a mitochondrial deficiency causing Leber hereditary optic neuropathy (LHON)	88
Biochemical analysis of mitochondrial function in cybrid cell lines harboring mtDNA mutations	88
Hyaluronan synthesis and human endothelial cell behaviour	88
Hyaluronan in human umbilical cord	88
Hyaluronan metabolism in human breast cancer cell line 8701BC	88
Hyaluronan synthesis in human endothelial cells and its involvement during “in vitro” inflammation	86
L’attivita’ della MMP2 come regolatore della migrazione di cellule umane muscolari lisce	86
Carcinoma breast cancer cells modulates HA metabolism of fibroblasts	86
Osservazioni metodologiche nel dosaggio della NADH Coenzima Q ossidoreduttasi mitocondriale	86
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	85
Hyaluronan content of umbilical cords of healthy and Down Syndrome fetuses	85
Hyaluronan synthesis in human endothelial cells and its involvement during in vitro inflammation	82
Evidence that specific mtDNA point mutations may not accumulate in skeletal muscle during normal human aging	81
Analysis of fluorophore labeled glycosaminoglycan disaccharides using polyacrylamide gel electroforesis and HPLC	79
Glicosamminoglicani prodotti in coltura cellulari umane	79
Experimental isovolemic hemodilution. Study of tissue perfusion with Hb 3% in swine	79
HYALURONAN CONTENT AND SYNTHASE GENE EXPRESSION BY REAL TIME –PCR IN UMBILICAL CORDS OF HEALTHY AND DOWN SYNDROME FETUSES	77
Hyaluronan content of umbilical cords of healthy and Down Syndrome fetuses	77
Hyaluronan content of umbilical cords of healthy and Down Syndrome fetuses.	77
Quantificazione della mutazione 3460 G>A/ND1 (LHON) mediante Real Time PCR quantitativa	76
Hyaluronan synthesis and human endothelial cell behaviour	74
Regulation of hyaluronan synthesis in human endothelial cells	74
INVOLVEMENT OF HYALURONAN DURING IN VITRO ANGIOGENESIS OF ENDOTHELIAL CELLS	73
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	73
Hyaluronan content and gene expression for hyaluronan synthases and hyaluronidases inthe umbilical cord of healthy and Down syndrome fetuses	71
Hyaluronan content of umbilical cords of healthy and Down Syndrome fetuses	70
Involvement of Hyaluronan during in vitro angiogenesis of endothelial cells	70
Hyaluronan metabolism in human breast carcinoma	70
Alteration of mitochondrial membrane inner potential in three Italian patients with megaconial congenital muscular dystrophy carrying new mutations in CHKB gene	70
Hyaluronan metabolism in in vitro culture of endothelial cells.	69
Hyaluronan metabolism in in vitro culture of endothelial cells	68
Involvement of Hyaluronan during in vitro angiogenesis of endothelial cells	67
Totale	10.984

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Categoria	#
all - tutte	47.141
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	47.141

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	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2019/2020	2.116	0	0	0	413	118	279	415	315	146	201	30	199
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	383	6	22	355	0	0	0	0	0	0	0	0	0
Totale													12.829