statistiche ricercatore

PALLOTTI, FRANCESCO

Distribuzione geografica

Continente	#
NA - Nord America	8.872
EU - Europa	5.304
AS - Asia	3.555
SA - Sud America	350
AF - Africa	85
Continente sconosciuto - Info sul continente non disponibili	15
OC - Oceania	6
Totale	18.187

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Nazione	#
US - Stati Uniti d'America	8.794
IT - Italia	2.103
SG - Singapore	1.139
UA - Ucraina	992
CN - Cina	817
SE - Svezia	564
TR - Turchia	556
VN - Vietnam	499
HK - Hong Kong	382
FI - Finlandia	312
BR - Brasile	303
IE - Irlanda	277
GB - Regno Unito	266
DE - Germania	259
FR - Francia	244
RU - Federazione Russa	140
IN - India	55
NG - Nigeria	40
MX - Messico	36
CA - Canada	31
BD - Bangladesh	26
PL - Polonia	22
NL - Olanda	20
AR - Argentina	19
JP - Giappone	19
AT - Austria	18
BE - Belgio	18
ES - Italia	18
ZA - Sudafrica	16
CZ - Repubblica Ceca	14
IQ - Iraq	14
EU - Europa	13
LT - Lituania	10
BG - Bulgaria	8
CL - Cile	7
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
DK - Danimarca	3
GR - Grecia	3
HU - Ungheria	3
IL - Israele	3
RO - Romania	3
SA - Arabia Saudita	3
GT - Guatemala	2
HR - Croazia	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
CR - Costa Rica	1
DM - Dominica	1
DO - Repubblica Dominicana	1
DZ - Algeria	1
JM - Giamaica	1
JO - Giordania	1
KR - Corea	1
LB - Libano	1
LV - Lettonia	1
MU - Mauritius	1
MW - Malawi	1
NI - Nicaragua	1
NZ - Nuova Zelanda	1
OM - Oman	1
PS - Palestinian Territory	1
QA - Qatar	1
RS - Serbia	1
SI - Slovenia	1
SS - ???statistics.table.value.countryCode.SS???	1
SY - Repubblica araba siriana	1
TL - Timor Orientale	1
TN - Tunisia	1
TW - Taiwan	1
UY - Uruguay	1
XK - ???statistics.table.value.countryCode.XK???	1
Totale	18.187

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Città	#
Milan	1.516
Fairfield	876
Jacksonville	756
Ashburn	705
Chandler	670
Singapore	598
San Jose	583
Woodbridge	553
Houston	389
Hong Kong	373
Seattle	346
Izmir	341
Dallas	323
Cambridge	317
Wilmington	317
Dublin	277
Ann Arbor	270
Princeton	262
Dearborn	254
Nyköping	218
Beijing	175
Chicago	165
The Dalles	153
Boardman	147
Lauterbourg	118
San Mateo	114
Rome	113
Dong Ket	112
New York	111
Como	76
Los Angeles	73
San Diego	63
Ho Chi Minh City	62
London	60
Helsinki	57
Hanoi	47
Orem	46
Santa Clara	45
Guangzhou	44
Ogden	44
Abuja	39
Hefei	34
Munich	34
Washington	33
Nanjing	32
Kunming	30
São Paulo	29
Norwalk	25
Düsseldorf	24
Mexico City	24
Kocaeli	21
Council Bluffs	20
Philadelphia	20
Shenzhen	20
Shanghai	19
Tokyo	19
Brussels	18
Buffalo	18
Chennai	18
Warsaw	18
Zhengzhou	17
Hangzhou	16
San Francisco	16
Frankfurt am Main	15
Jinan	15
Poplar	15
Montreal	14
Johannesburg	13
Phoenix	13
Stockholm	13
Atlanta	12
Manchester	12
Tianjin	12
Turku	12
Denver	11
Haiphong	11
Mumbai	11
Redmond	11
Verona	11
Nanchang	10
Redwood City	10
Brno	9
Brooklyn	9
Changsha	9
Chengdu	9
Da Nang	9
Fuzhou	9
Shenyang	9
Amsterdam	8
Nuremberg	8
Rio de Janeiro	8
Vienna	8
Boston	7
Campinas	7
Paris	7
Sofia	7
Varese	7
Wuhan	7
Berlin	6
Biên Hòa	6
Totale	12.683

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Nome	#
Analysis of three screening methods for the detection of calreticulin gene mutations	264
A wide range of 3243A>G/tRNALeu(UUR) (MELAS) mutation loads may segregate in offspring through the female germline bottleneck	233
Assessing Heteroplasmic Load in Leber's Hereditary Optic Neuropathy Mutation 3460G->A/MT-ND1 with A Real-Time PCR Quantitative Approach	224
Authors’ Reply to Crampe and Langabeer: Technical Issues Behind Molecular Monitoring in Chronic Myeloid Leukemia	224
ASSAY CONDITIONS FOR THE MITOCHONDRIAL NADH - COENZYME-Q OXIDOREDUCTASE	223
A new acute myeloid leukemia case with STAT5B-RARA gene fusion due to 17q21.2 interstitial deletion	217
Biochemical-clinical correlation in patients with different loads of the mitochondrial DNA T8993G mutation	209
Biochemical analysis of respiratory function in cybrid cell lines harbouring mitochondrial DNA mutations	209
THE FUNCTION OF COENZYME-Q IN MITOCHONDRIA	207
A particular case of AML patient with the polymorphism G105G (rs11554137) and the missense mutation R132C in IDH1 gene	206
Biological variation of procalcitonin in healthy individuals	201
JAK2, 46/1 haplotype and chronic myelogenous leukemia: diagnostic and therapeutic potential	201
Biological variation of procalcitonin in healthy individuals	199
Matrix metalloproteinase 2 and tissue inhibitors of metalloproteinases regulate human aortic smooth muscle cell migration during in vitro aging	197
Analysis of mtDNA deletions in muscle by in situ hybridization	188
AN UPDATING OF THE BIOCHEMICAL FUNCTION OF COENZYME-Q IN MITOCHONDRIA	188
Aortic smooth muscle cells migration and the role of metalloproteinases and hyaluronan.	188
Rescue of a mitochondrial deficiency causing Leber hereditary optic neuropathy	184
A stop-codon mutation in the human mtDNA cytochrome c oxidase I gene disrupts the functional structure of complex IV	184
FTL gene mutation and persistent hyperferritinemia without iron deficiency anemia after phlebotomy	184
JAK2 mutation and atypical chronic myeloid leukemia	183
Differential cerebro spinal fluid proteome investigation of Leber hereditary optic neuropathy (LHON) and multiple sclerosis.	181
New insights into the pathobiology of Down syndrome - Hyaluronan synthase-2 overexpression is regulated by collagen VI α2 chain	177
Biological variation of procalcitonin in healthy individuals	176
Mitochondrial DNA nucleotide changes C14482G and C14482A in the ND6 gene are pathogenic for Leber's hereditary optic neuropathy	173
Isolation and subfractionation of mitochondria from animal cells and tissue culture lines.	171
In vivo regulation of oxidative phosphorylation in cells harboring a stop-codon mutation in mitochondrial DNA-encoded cytochrome c oxidase subunit I	170
Identification of a novel mutation in Cu/Zn superoxide dismutase gene associated with familial amyotrophic lateral sclerosis	169
Steady-state kinetics of the reduction of coenzyme Q analogs by complex I (NADH:Ubiquinone oxidoreductase) in bovine heart mitochondria and submitochondrial particles	169
Pure myopathy with enlarged mitochondria associated to a new mutation in MTND2 gene	168
Mitochondrial Complex I defects in aging	166
The fate of human sperm-derived mtDNA in somatic cells	166
Decorin from different bovine tissues: study of glycosaminoglycan chain by PAGEFS	166
Mitochondrial abnormalities in muscle and other aging cells: Classification, causes, and effects	163
Hyaluronan and human endothelial cell behavior.	163
High frequency of migraine-only patients negative for the 3243 A>G tRNALeu mtDNA mutation in two MELAS families	163
Technical Issues Behind Molecular Monitoring in Chronic Myeloid Leukemia	163
Differential features of patients with mutations in two COX assembly genes, SURF-1 and SCO2	162
Mitochondrial DNA in platelets from aged subjects	162
Decrease of rotenone inhibition is a sensitive parameter of complex I damage in brain non-synaptic mitochondria of aged rats	161
UDP-glucose dehydrogenase and Hyaluronan synthesis	160
Isolation and subfractionation of mitochondria from animal cells and tissue culture lines.	159
MODES OF COENZYME-Q FUNCTION IN ELECTRON-TRANSFER	159
Hyaluronan synthesis and human endothelial cell behaviour	158
Pathogenesis of the deafness-associated A1555G mitochondrial DNA mutation	156
Comparison of three strategies for myocardial protection during coronary artery bypass graft surgery based on markers of cardiac damage.	156
Pathogenesis of primary defects in mitochondrial ATP synthesis	156
Molecular control of the hyaluronan biosynthesis	155
G1HYALURONAN CONTENT OF UMBILICAL CORDS OF HEALTHY AND DOWN SYNDROME FETUSES	151
Exercise intolerance due to mutations in the cytochrome b gene of mitochondrial DNA	150
Molecular cloning and characterization of UDP-glucose dehydrogenase from the amphibian xenopus laevis and its involvement in hyaluronan synthesis	150
Mitochondrial dysfunction and brain disorders	149
Hyaluronan metabolism in human breast cancer cell line 8701BC	149
UDP-Glucose Dehydrogenase and its involvement in glycosaminoglycan Synthesis	148
Carcinoma breast cancer cells modulates HA metabolism of fibroblasts	148
Phosphorus MR spectroscopy shows a tissue specific in vivo distribution of biochemical expression of the G3460A mutation in Leber's hereditary optic neuropathy	147
Oxidative stress, antioxidant defences and aging	145
Biochemical analysis of mitochondrial function in cybrid cell lines harboring mtDNA mutations	145
UDP-glucose dehydrogenase from Xenopus laevis and its involvement in hyaluronan synthesis	145
Mitochondrial activities of rat heart during ageing	145
Analysis of fluorophore labeled glycosaminoglycan disaccharides using polyacrylamide gel electroforesis and HPLC	144
UDP-Glucose dehydrogenase and its involvement in GAG synthesis	144
Histomorphometric studies in rat cerebral cortex: Normal aging and cell loss	143
Alteration of mitochondrial membrane inner potential in three Italian patients with megaconial congenital muscular dystrophy carrying new mutations in CHKB gene	139
Regulation of Hyaluronan synthesis in human endothelial cells	134
New electrophoretic and chromatographic tecniques for analysis of heparin and heparan sulphate.	134
Archaeogenomics in Caravate and Cittiglio (Lombardy): from the excavation of ancient human bones to the study of DNA	131
COLLAGEN TYPE I CARBOXY-TERMINAL PROPETIDE AND TELOPEPTIDE MEASUREMENT IN PLASMA OF PATIENTS WITH ESSENTIAL HYPERTENSION BY RIA AND EIA METHODS	131
LACK OF MAJOR MITOCHONDRIAL BIOENERGETIC CHANGES IN CULTURED SKIN FIBROBLASTS FROM AGED INDIVIDUALS	129
Heteroplasmic 24-base pair deletion in the mitochondrial cytochrome b gene in a patient with isolated myopathy	129
Glicosamminoglicani prodotti in coltura cellulari umane	124
New highlights on the synthesis of hyaluronan	124
Comparison of clinical features in patients with COX assembly gene mutations	123
Hyaluronan in human umbilical cord	122
Haplogroup effects and recombination of mitochondrial DNA: novel clues from the analysis of Leber hereditary optic neuropathy pedigrees.	121
Structure and function of hyaluronan	121
L’attivita’ della MMP2 come regolatore della migrazione di cellule umane muscolari lisce	121
The search of the stool and blood K-ras mutations in patients with pancreatic mass	120
Hyaluronan metabolism in breast cancer cell line	120
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	119
Hyaluronan content and gene expression for hyaluronan synthases and hyaluronidases inthe umbilical cord of healthy and Down syndrome fetuses	118
Gene therapy with the ND4 subunit gene recoded in the universal genetic code reverses a mitochondrial deficiency causing Leber hereditary optic neuropathy (LHON)	117
Hyaluronan metabolism in in vitro culture of endothelial cells	116
Hyaluronan content of umbilical cords of healthy and Down Syndrome fetuses	113
Evidence that specific mtDNA point mutations may not accumulate in skeletal muscle during normal human aging	112
Hyaluronan synthesis in human endothelial cells and its involvement during “in vitro” inflammation	111
Osservazioni metodologiche nel dosaggio della NADH Coenzima Q ossidoreduttasi mitocondriale	111
Hyaluronan content of umbilical cords of healthy and Down Syndrome fetuses	109
Involvement of Hyaluronan during in vitro angiogenesis of endothelial cells	107
Hyaluronan synthesis and human endothelial cell behaviour	107
Hyaluronan synthesis in human endothelial cells and its involvement during in vitro inflammation	107
Hyaluronan content of umbilical cords of healthy and Down Syndrome fetuses	107
Hyaluronan metabolism in in vitro culture of endothelial cells.	106
HYALURONAN CONTENT AND SYNTHASE GENE EXPRESSION BY REAL TIME –PCR IN UMBILICAL CORDS OF HEALTHY AND DOWN SYNDROME FETUSES	104
INVOLVEMENT OF HYALURONAN DURING IN VITRO ANGIOGENESIS OF ENDOTHELIAL CELLS	104
Hyaluronan content of umbilical cords of healthy and Down Syndrome fetuses.	104
Quantificazione della mutazione 3460 G>A/ND1 (LHON) mediante Real Time PCR quantitativa	103
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	103
Migration in senescent cells: the role of cell-extracellular matrix interface	102
Experimental isovolemic hemodilution. Study of tissue perfusion with Hb 3% in swine	101
Totale	15.268

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Categoria	#
all - tutte	70.779
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	70.779

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	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2020/2021	690	0	0	0	0	0	0	0	0	0	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	4.030	306	270	264	566	406	308	1.029	251	438	192	0	0
Totale													18.228