statistiche ricercatore

PALLOTTI, FRANCESCO

Distribuzione geografica

Continente	#
NA - Nord America	7.916
EU - Europa	5.087
AS - Asia	2.844
SA - Sud America	321
AF - Africa	33
Continente sconosciuto - Info sul continente non disponibili	15
OC - Oceania	5
Totale	16.221

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Nazione	#
US - Stati Uniti d'America	7.845
IT - Italia	2.089
UA - Ucraina	991
SG - Singapore	987
SE - Svezia	563
TR - Turchia	556
CN - Cina	483
VN - Vietnam	363
HK - Hong Kong	353
BR - Brasile	288
IE - Irlanda	277
FI - Finlandia	276
DE - Germania	256
GB - Regno Unito	254
RU - Federazione Russa	138
FR - Francia	108
IN - India	36
MX - Messico	35
CA - Canada	26
AT - Austria	18
BD - Bangladesh	18
BE - Belgio	18
ES - Italia	18
JP - Giappone	17
PL - Polonia	17
AR - Argentina	16
NL - Olanda	16
CZ - Repubblica Ceca	14
EU - Europa	13
ZA - Sudafrica	13
LT - Lituania	10
BG - Bulgaria	8
IQ - Iraq	7
MA - Marocco	5
AU - Australia	4
CL - Cile	4
EC - Ecuador	4
ET - Etiopia	4
KE - Kenya	4
PA - Panama	4
UZ - Uzbekistan	4
AE - Emirati Arabi Uniti	3
DK - Danimarca	3
HU - Ungheria	3
IL - Israele	3
PK - Pakistan	3
RO - Romania	3
VE - Venezuela	3
CO - Colombia	2
EG - Egitto	2
GR - Grecia	2
GT - Guatemala	2
HR - Croazia	2
PE - Perù	2
PH - Filippine	2
AM - Armenia	1
AO - Angola	1
BW - Botswana	1
CR - Costa Rica	1
DM - Dominica	1
DO - Repubblica Dominicana	1
JM - Giamaica	1
KR - Corea	1
KZ - Kazakistan	1
LB - Libano	1
LV - Lettonia	1
MU - Mauritius	1
MW - Malawi	1
NZ - Nuova Zelanda	1
OM - Oman	1
PS - Palestinian Territory	1
PY - Paraguay	1
RS - Serbia	1
SA - Arabia Saudita	1
SI - Slovenia	1
SS - ???statistics.table.value.countryCode.SS???	1
TL - Timor Orientale	1
TN - Tunisia	1
TW - Taiwan	1
UY - Uruguay	1
XK - ???statistics.table.value.countryCode.XK???	1
Totale	16.221

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Città	#
Milan	1.515
Fairfield	876
Jacksonville	756
Chandler	670
Ashburn	614
Woodbridge	553
Singapore	549
Houston	389
Hong Kong	352
Seattle	346
Izmir	341
Dallas	320
Cambridge	317
Wilmington	317
Dublin	277
Ann Arbor	270
Princeton	262
Dearborn	254
Nyköping	218
Beijing	156
Boardman	147
San Mateo	114
Dong Ket	112
Rome	112
New York	99
Chicago	91
Como	76
Los Angeles	72
San Diego	62
The Dalles	62
London	58
Ogden	44
Santa Clara	42
Munich	34
Hefei	33
Nanjing	32
Washington	32
Kunming	30
São Paulo	26
Norwalk	25
Düsseldorf	24
Mexico City	23
Helsinki	21
Kocaeli	21
Orem	21
Ho Chi Minh City	20
Philadelphia	20
Brussels	18
Buffalo	18
Tokyo	17
Jinan	15
San Francisco	15
Poplar	14
Zhengzhou	14
Frankfurt am Main	13
Guangzhou	13
Montreal	13
Warsaw	13
Johannesburg	12
Phoenix	12
Stockholm	12
Turku	12
Atlanta	11
Hanoi	11
Redmond	11
Verona	11
Council Bluffs	10
Denver	10
Nanchang	10
Redwood City	10
Brno	9
Chengdu	9
Shenyang	9
Brooklyn	8
Chennai	8
Fuzhou	8
Rio de Janeiro	8
Vienna	8
Campinas	7
Manchester	7
Mumbai	7
Nuremberg	7
Sofia	7
Varese	7
Berlin	6
Boston	6
Brasília	6
Changsha	6
Wuhan	6
Belo Horizonte	5
Guarulhos	5
Hangzhou	5
Hebei	5
Hounslow	5
Porto Alegre	5
Seveso	5
Acton	4
Amsterdam	4
Bologna	4
Curitiba	4
Totale	11.290

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Nome	#
Analysis of three screening methods for the detection of calreticulin gene mutations	247
ASSAY CONDITIONS FOR THE MITOCHONDRIAL NADH - COENZYME-Q OXIDOREDUCTASE	207
Authors’ Reply to Crampe and Langabeer: Technical Issues Behind Molecular Monitoring in Chronic Myeloid Leukemia	206
Assessing Heteroplasmic Load in Leber's Hereditary Optic Neuropathy Mutation 3460G->A/MT-ND1 with A Real-Time PCR Quantitative Approach	203
A new acute myeloid leukemia case with STAT5B-RARA gene fusion due to 17q21.2 interstitial deletion	201
A wide range of 3243A>G/tRNALeu(UUR) (MELAS) mutation loads may segregate in offspring through the female germline bottleneck	198
Biochemical-clinical correlation in patients with different loads of the mitochondrial DNA T8993G mutation	197
Biological variation of procalcitonin in healthy individuals	189
A particular case of AML patient with the polymorphism G105G (rs11554137) and the missense mutation R132C in IDH1 gene	189
THE FUNCTION OF COENZYME-Q IN MITOCHONDRIA	187
Biological variation of procalcitonin in healthy individuals	182
JAK2, 46/1 haplotype and chronic myelogenous leukemia: diagnostic and therapeutic potential	182
Biochemical analysis of respiratory function in cybrid cell lines harbouring mitochondrial DNA mutations	179
FTL gene mutation and persistent hyperferritinemia without iron deficiency anemia after phlebotomy	177
Analysis of mtDNA deletions in muscle by in situ hybridization	174
Differential cerebro spinal fluid proteome investigation of Leber hereditary optic neuropathy (LHON) and multiple sclerosis.	173
A stop-codon mutation in the human mtDNA cytochrome c oxidase I gene disrupts the functional structure of complex IV	172
Aortic smooth muscle cells migration and the role of metalloproteinases and hyaluronan.	172
New insights into the pathobiology of Down syndrome - Hyaluronan synthase-2 overexpression is regulated by collagen VI α2 chain	171
JAK2 mutation and atypical chronic myeloid leukemia	169
Rescue of a mitochondrial deficiency causing Leber hereditary optic neuropathy	168
AN UPDATING OF THE BIOCHEMICAL FUNCTION OF COENZYME-Q IN MITOCHONDRIA	168
Biological variation of procalcitonin in healthy individuals	162
In vivo regulation of oxidative phosphorylation in cells harboring a stop-codon mutation in mitochondrial DNA-encoded cytochrome c oxidase subunit I	159
Identification of a novel mutation in Cu/Zn superoxide dismutase gene associated with familial amyotrophic lateral sclerosis	156
Mitochondrial DNA nucleotide changes C14482G and C14482A in the ND6 gene are pathogenic for Leber's hereditary optic neuropathy	155
Isolation and subfractionation of mitochondria from animal cells and tissue culture lines.	154
Technical Issues Behind Molecular Monitoring in Chronic Myeloid Leukemia	154
Steady-state kinetics of the reduction of coenzyme Q analogs by complex I (NADH:Ubiquinone oxidoreductase) in bovine heart mitochondria and submitochondrial particles	153
Mitochondrial Complex I defects in aging	152
Decorin from different bovine tissues: study of glycosaminoglycan chain by PAGEFS	152
Isolation and subfractionation of mitochondria from animal cells and tissue culture lines.	149
The fate of human sperm-derived mtDNA in somatic cells	149
Differential features of patients with mutations in two COX assembly genes, SURF-1 and SCO2	148
Mitochondrial DNA in platelets from aged subjects	148
High frequency of migraine-only patients negative for the 3243 A>G tRNALeu mtDNA mutation in two MELAS families	148
Mitochondrial abnormalities in muscle and other aging cells: Classification, causes, and effects	147
Hyaluronan synthesis and human endothelial cell behaviour	147
Matrix metalloproteinase 2 and tissue inhibitors of metalloproteinases regulate human aortic smooth muscle cell migration during in vitro aging	147
Decrease of rotenone inhibition is a sensitive parameter of complex I damage in brain non-synaptic mitochondria of aged rats	147
Pathogenesis of the deafness-associated A1555G mitochondrial DNA mutation	146
Hyaluronan and human endothelial cell behavior.	146
Pure myopathy with enlarged mitochondria associated to a new mutation in MTND2 gene	146
MODES OF COENZYME-Q FUNCTION IN ELECTRON-TRANSFER	144
Molecular control of the hyaluronan biosynthesis	142
Comparison of three strategies for myocardial protection during coronary artery bypass graft surgery based on markers of cardiac damage.	141
Pathogenesis of primary defects in mitochondrial ATP synthesis	139
Exercise intolerance due to mutations in the cytochrome b gene of mitochondrial DNA	138
UDP-glucose dehydrogenase and Hyaluronan synthesis	136
Mitochondrial dysfunction and brain disorders	135
Histomorphometric studies in rat cerebral cortex: Normal aging and cell loss	134
UDP-Glucose Dehydrogenase and its involvement in glycosaminoglycan Synthesis	134
Phosphorus MR spectroscopy shows a tissue specific in vivo distribution of biochemical expression of the G3460A mutation in Leber's hereditary optic neuropathy	132
UDP-glucose dehydrogenase from Xenopus laevis and its involvement in hyaluronan synthesis	132
G1HYALURONAN CONTENT OF UMBILICAL CORDS OF HEALTHY AND DOWN SYNDROME FETUSES	131
Carcinoma breast cancer cells modulates HA metabolism of fibroblasts	131
Analysis of fluorophore labeled glycosaminoglycan disaccharides using polyacrylamide gel electroforesis and HPLC	130
Molecular cloning and characterization of UDP-glucose dehydrogenase from the amphibian xenopus laevis and its involvement in hyaluronan synthesis	129
Hyaluronan metabolism in human breast cancer cell line 8701BC	129
Biochemical analysis of mitochondrial function in cybrid cell lines harboring mtDNA mutations	128
UDP-Glucose dehydrogenase and its involvement in GAG synthesis	128
Oxidative stress, antioxidant defences and aging	126
Regulation of Hyaluronan synthesis in human endothelial cells	122
New electrophoretic and chromatographic tecniques for analysis of heparin and heparan sulphate.	121
Alteration of mitochondrial membrane inner potential in three Italian patients with megaconial congenital muscular dystrophy carrying new mutations in CHKB gene	121
Mitochondrial activities of rat heart during ageing	121
LACK OF MAJOR MITOCHONDRIAL BIOENERGETIC CHANGES IN CULTURED SKIN FIBROBLASTS FROM AGED INDIVIDUALS	120
COLLAGEN TYPE I CARBOXY-TERMINAL PROPETIDE AND TELOPEPTIDE MEASUREMENT IN PLASMA OF PATIENTS WITH ESSENTIAL HYPERTENSION BY RIA AND EIA METHODS	120
Heteroplasmic 24-base pair deletion in the mitochondrial cytochrome b gene in a patient with isolated myopathy	117
Comparison of clinical features in patients with COX assembly gene mutations	113
Archaeogenomics in Caravate and Cittiglio (Lombardy): from the excavation of ancient human bones to the study of DNA	112
New highlights on the synthesis of hyaluronan	111
Hyaluronan in human umbilical cord	111
Glicosamminoglicani prodotti in coltura cellulari umane	110
Structure and function of hyaluronan	110
L’attivita’ della MMP2 come regolatore della migrazione di cellule umane muscolari lisce	110
Haplogroup effects and recombination of mitochondrial DNA: novel clues from the analysis of Leber hereditary optic neuropathy pedigrees.	109
Gene therapy with the ND4 subunit gene recoded in the universal genetic code reverses a mitochondrial deficiency causing Leber hereditary optic neuropathy (LHON)	107
The search of the stool and blood K-ras mutations in patients with pancreatic mass	107
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	105
Hyaluronan synthesis in human endothelial cells and its involvement during “in vitro” inflammation	105
Osservazioni metodologiche nel dosaggio della NADH Coenzima Q ossidoreduttasi mitocondriale	103
Hyaluronan content and gene expression for hyaluronan synthases and hyaluronidases inthe umbilical cord of healthy and Down syndrome fetuses	101
Hyaluronan content of umbilical cords of healthy and Down Syndrome fetuses	101
Hyaluronan metabolism in in vitro culture of endothelial cells	100
Hyaluronan synthesis and human endothelial cell behaviour	100
Evidence that specific mtDNA point mutations may not accumulate in skeletal muscle during normal human aging	99
Hyaluronan content of umbilical cords of healthy and Down Syndrome fetuses	99
Quantificazione della mutazione 3460 G>A/ND1 (LHON) mediante Real Time PCR quantitativa	98
Hyaluronan content of umbilical cords of healthy and Down Syndrome fetuses.	98
Hyaluronan content of umbilical cords of healthy and Down Syndrome fetuses	97
Hyaluronan metabolism in breast cancer cell line	97
HYALURONAN CONTENT AND SYNTHASE GENE EXPRESSION BY REAL TIME –PCR IN UMBILICAL CORDS OF HEALTHY AND DOWN SYNDROME FETUSES	96
Hyaluronan metabolism in in vitro culture of endothelial cells.	96
Hyaluronan synthesis in human endothelial cells and its involvement during in vitro inflammation	96
INVOLVEMENT OF HYALURONAN DURING IN VITRO ANGIOGENESIS OF ENDOTHELIAL CELLS	93
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	93
Experimental isovolemic hemodilution. Study of tissue perfusion with Hb 3% in swine	92
Regulation of hyaluronan synthesis in human endothelial cells	91
Involvement of Hyaluronan during in vitro angiogenesis of endothelial cells	90
Totale	13.807

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Categoria	#
all - tutte	67.172
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	67.172

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	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2020/2021	1.472	0	0	0	0	0	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	2.064	306	270	264	566	406	252	0	0	0	0	0	0
Totale													16.262