statistiche per SANDRI, MARCO

Distribuzione geografica

Continente	#
NA - Nord America	10321
EU - Europa	913
AS - Asia	677
Continente sconosciuto - Info sul continente non disponibili	7
OC - Oceania	4
AF - Africa	2
SA - Sud America	1
Totale	11925

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Nazione	#
US - Stati Uniti d'America	10293
CN - Cina	560
IT - Italia	364
FI - Finlandia	132
SE - Svezia	125
UA - Ucraina	115
DE - Germania	102
VN - Vietnam	93
GB - Regno Unito	38
CA - Canada	28
FR - Francia	15
IN - India	15
NL - Olanda	9
EU - Europa	7
GR - Grecia	5
AU - Australia	4
RU - Federazione Russa	3
TR - Turchia	3
BG - Bulgaria	2
AR - Argentina	1
BD - Bangladesh	1
BY - Bielorussia	1
CH - Svizzera	1
ID - Indonesia	1
IE - Irlanda	1
IR - Iran	1
JP - Giappone	1
KR - Corea	1
NG - Nigeria	1
PH - Filippine	1
ZA - Sudafrica	1
Totale	11925

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Città	#
Fairfield	2485
Woodbridge	1494
Houston	1078
Ann Arbor	953
Seattle	918
Ashburn	882
Cambridge	805
Wilmington	754
Jacksonville	412
San Diego	182
Padova	160
Beijing	135
Nanjing	104
Dong Ket	93
Guangzhou	41
Shenyang	41
Hebei	38
Munich	36
Nanchang	34
Jinan	31
Falls Church	29
Jiaxing	22
Changsha	18
Ottawa	18
Redwood City	15
Tianjin	15
Concordia Sulla Secchia	13
Indiana	13
Milan	13
Norwalk	13
Zhengzhou	13
Dearborn	11
Hefei	11
Aprilia	10
Rome	10
Haikou	8
New York	8
Ningbo	8
Montréal	7
Bari	6
Kunming	6
Shanghai	5
Hangzhou	4
Lanzhou	4
Orange	4
Phoenix	4
Taiyuan	4
Chongqing	3
Redmond	3
Sommacampagna	3
Udine	3
Yenibosna	3
Brescia	2
Florence	2
Fuzhou	2
Las Vegas	2
Mcallen	2
Mountain View	2
Napoli	2
Perth	2
San Francisco	2
San Polo	2
Tricesimo	2
Vercelli	2
Yellow Springs	2
Aci Catena	1
Acireale	1
Athens	1
Augusta	1
Bagno A Ripoli	1
Belvedere Spinello	1
Borgomanero	1
Brivio	1
Cadoneghe	1
Camisano	1
Camisano Vicentino	1
Capua	1
Changping	1
Chengdu	1
Cittadella	1
Dallas	1
Dhaka	1
Edinburgh	1
Edmonton	1
Este	1
Ferrara	1
Formigine	1
Freiburg	1
Genova	1
Isola Vicentina	1
Lachine	1
Ladispoli	1
Langfang	1
Limbiate	1
London	1
Malo	1
Mestre	1
Michigan City	1
Monmouth Junction	1
Montenero Di Bisaccia	1
Totale	11044

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Nome	#
Age-Associated Loss of OPA1 in Muscle Impacts Muscle Mass, Metabolic Homeostasis, Systemic Inflammation, and Epithelial Senescence	226
Patologia generale del tessuto muscolare scheletrico.	197
Glycolytic-to-oxidative fiber-type switch and mTOR signaling activation are early-onset features of SBMA muscle modified by high-fat diet	145
The Opa1-Dependent Mitochondrial Cristae Remodeling Pathway Controls Atrophic, Apoptotic and Ischemic Tissue Damage	136
Glycolytic-to-oxidative fiber-type switch and mTOR signaling activation are early-onset features of SBMA muscle modified by high-fat diet	124
The mitochondrial calcium uniporter controls skeletal muscle trophism in vivo.	123
Lifelong physical exercise delays age-associated skeletal muscle decline.	119
Epigenetic targeting of bromodomain protein BRD4 counteracts cancer cachexia and prolongs survival	119
Skeletal Muscle Is a Primary Target of SOD1(G93A)-Mediated Toxicity	117
Lysosomal calcium signalling regulates autophagy through calcineurin and TFEB.	114
A new two-step precipitation method removes free-SDS and Thiol reagents from diluted solutions, and then allows recovery and quantitation of proteins	113
Transcription Factor EB Controls Metabolic Flexibility during Exercise	112
Inducible activation of Akt increases skeletal muscle mass and force without satellite cell activation.	110
Physical exercise stimulates autophagy in normal skeletal muscles but is detrimental for collagen VI deficient muscles.	109
SELECTIVE REMOVAL OF FREE DODECYL-SULFATE FROM 2- MERCAPTOETHANOL SDS-SOLUBILIZED PROTEINS BEFORE KDS PROTEIN PRECIPITATION	108
Autophagy is not required to sustain exercise and PRKAA1/AMPK activity but is important to prevent mitochondrial damage during physical activity.	108
Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition)	108
Apoptosis, DNA damage and ubiquitin expression in normal and mdx muscle fibers after exercise.	105
Differential expression of perilipin 2 and 5 in human skeletal muscle during aging and their association with atrophy-related genes.	103
Content of mitochondrial calcium uniporter (MCU) in cardiomyocytes is regulated by microRNA-1 in physiologic and pathologic hypertrophy	103
Functional in vivo gene transfer into the myofibers of adult skeletal muscle	102
New findings of lysosomal proteolysis in skeletal muscle	101
Autophagy is defective in collagen VI muscular dystrophies, and its reactivation rescues myofiber degeneration.	100
Mitochondrial DNA and TLR9 drive muscle inflammation upon Opa1 deficiency	99
Autophagy dysregulation in Danon disease	98
Transcriptomic Analysis of Single Isolated Myofibers Identifies miR-27a-3p and miR-142-3p as Regulators of Metabolism in Skeletal Muscle	98
DRP1-mediated mitochondrial shape controls calcium homeostasis and muscle mass	98
Autophagy maintains stemness by preventing senescence	96
Autophagy is required to maintain muscle mass.	95
FoxO-dependent atrogenes vary among catabolic conditions and play a key role in muscle atrophy induced by hindlimb suspension.	92
Dystrophin deficient myotubes undergo apoptosis in mouse primary muscle cell culture after DNA damage.	90
Food Restriction Reverses the Hyper-Muscular Phenotype and Force Generation Capacity Deficit of the Myostatin Null Mouse	90
Smad2 and 3 transcription factors control muscle mass in adulthood	89
Neuromuscular junction degeneration in muscle wasting.	89
Autophagy inhibition induces atrophy and myopathy in adult skeletal muscles	88
Effect of thalidomide on the skeletal muscle in experimental heart failure	87
JunB transcription factor maintains skeletal muscle mass and promotes hypertrophy	86
Cellular prion protein promotes regeneration of adult muscle tissue.	85
Long-term high-level exercise promotes muscle reinnervation with age.	85
Macrophage-derived glutamine boosts satellite cells and muscle regeneration	85
Autophagy in health and disease. 3. Involvement of autophagy in muscle atrophy	84
Akt activation prevents the force drop induced by eccentric contractions in dystrophin-deficient skeletal muscle	84
FoxO3 controls autophagy in skeletal muscle in vivo.	84
In mammalian skeletal muscle, phosphorylation of TOMM22 by protein kinase CSNK2/CK2 controls mitophagy.	84
Multimodal label-free ex vivo imaging using a dual-wavelength microscope with axial chromatic aberration compensation	83
Polyglutamine-Expanded Androgen Receptor Alteration of Skeletal Muscle Homeostasis and Myonuclear Aggregation Are Affected by Sex, Age and Muscle Metabolism	83
TFE3 regulates whole-body energy metabolism in cooperation with TFEB.	82
FGF21 as Modulator of Metabolism in Health and Disease	82
Loss of Dystrophin and Some Dystrophin-Associated Proteins with Concomitant Signs of Apoptosis in Rat Leg Muscle Overworked in Extension	81
Autophagy activation in COL6 myopathic patients by a low-protein-diet pilot trial	81
Skeletal Muscle-Specific Methyltransferase METTL21C Trimethylates p97 and Regulates Autophagy-Associated Protein Breakdown.	81
Activity-dependent signaling pathways controlling muscle diversity and plasticity	79
The role of alterations in mitochondrial dynamics and PGC-1α over-expression in fast muscle atrophy following hindlimb unloading.	79
Phosphorylation of NBR1 by GSK3 modulates protein aggregation.	79
Effective recovery by KCl precipitation of highly diluted muscle proteins solubilized with sodium dodecyl sulfate	78
Histone deacetylase 6 is a FoxO transcription factor-dependent effector in skeletal muscle atrophy.	78
Perilipin 2 and Age-Related Metabolic Diseases: A New Perspective.	78
Phosphoinositide 3-Kinase Gamma Inhibition Protects from Anthracycline Cardiotoxicity and Reduces Tumor Growth	78
Cardiac sympathetic neurons provide trophic signal to the heart via β2- adrenoceptor dependent regulation of proteolysis.	77
Autophagy controls neonatal myogenesis by regulating the GH-IGF1 system through a NFE2L2- and DDIT3-mediated mechanism	77
Protective Role of Testicular Hormone INSL3 From Atrophy and Weakness in Skeletal Muscle	77
The role of autophagy in neonatal tissues - Just a response to amino acid starvation?	76
Exercise training attenuates the hypermuscular phenotype and restores skeletal muscle function in the myostatin null mouse	76
Normal myogenesis and increased apoptosis in myotonic dystrophy type-1 muscle cells.	75
Bone and morphogenetic protein signalling and muscle mass.	75
Symmorphosis through dietary regulation: a combinatorial role for proteolysis, autophagy and protein synthesis in normalising muscle metabolism and function of hypertrophic mice after acute starvation.	75
Sarcopenia: Aging-Related Loss of Muscle Mass and Function.	75
Study of Muscle Autophagy and Atrophy Markers in Different Phenotypes of Pompe Disease	74
Oxidative damage and autophagy in the human trabecular meshwork as related with ageing.	74
Mitochondrial quality control: Cell-type-dependent responses to pathological mutant mitochondrial DNA.	74
Autophagy activation in COL6 myopathic patients by a low-protein-diet pilot trial	74
Effects of short-to-long term enzyme replacement therapy (ERT) on skeletal muscle tissue in late onset Pompe disease (LOPD).	74
Inhibition of the Fission Machinery Mitigates OPA1 Impairment in Adult Skeletal Muscles	73
Skeletal muscle mTORC1 regulates neuromuscular junction stability	73
Beneficial effects on skeletal muscle of the angiotensin II type 1 receptor blocker irbesartan in experimental heart failure	72
Memory or amnesia: the dilemma of stem cell therapy in muscular dystrophies.	72
Autophagy in skeletal muscle	71
Atrophy/hypertrophy cell signaling in muscles of young athletes trained with vibrational-proprioceptive stimulation.	71
Defects of Vps15 in skeletal muscles lead to autophagic vacuolar myopathy and lysosomal disease	71
The time course of the adaptations of human muscle proteome to bed rest and the underlying mechanisms	70
Aggresome-autophagy involvement in a sarcopenic patient with rigid spine syndrome and a p.C150R mutation in FHL1 gene	70
Mitochondrial quality control and muscle mass maintenance	70
Caspase 3 expression correlates with skeletal muscle apoptosis in Duchenne and facio-scapulo human muscular dystrophy. A potential target for pharmacological treatment?	69
Role of autophagy, SQSTM1, SH3GLB1, and TRIM63 in the turnover of nicotinic acetylcholine receptors.	69
Muscle-specific Perilipin2 down-regulation affects lipid metabolism and induces myofiber hypertrophy.	69
Mitochondrial fission and remodelling contributes to muscle atrophy	68
Increasing Cardiomyocyte Atrogin-1 Reduces Aging-Associated Fibrosis and Regulates Remodeling in Vivo.	68
Autophagy induction rescues muscular dystrophy	67
Autophagy as a new therapeutic target in Duchenne muscular dystrophy.	67
Apoptotic signaling in skeletal muscle fibers during atrophy.	67
Exercise induces myonuclear ubiquitination and apoptosis in dystrophin deficient muscle of mice	66
The role of autophagy in the pathogenesis of glycogen storage disease type II (GSDII).	66
Regulation of autophagy and the ubiquitin-proteasome system by the FoxO transcriptional network during muscle atrophy	66
Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition)	66
S6 kinase deletion suppresses muscle growth adaptations to nutrient availability by activating AMP kinase	65
L-Carnitine: a potential treatment for blocking apoptosis and preventing skeletal muscle myopathy in heart failure	65
FOXOphagy path to inducing stress resistance and cell survival	64
Physical exercise in aging human skeletal muscle increases mitochondrial calcium uniporter expression levels and affects mitochondria dynamics	64
FoxO3 coordinately activates protein degradation by the Autophagic/Lysosomal and proteasomal pathways in atrophying muscle cells	62
BMP signaling controls muscle mass.	62
Totale	8766

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Categoria	#
all - tutte	12133
article - articoli	11876
book - libri	0
conference - conferenze	0
curatela - curatele	0
other - altro	0
patent - brevetti	9
selected - selezionate	0
volume - volumi	218
Totale	24236

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	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2016/2017	90	0	0	0	0	0	0	0	0	0	0	20	70
2017/2018	1364	385	736	10	37	7	17	26	16	19	8	102	1
2018/2019	1619	4	7	105	9	5	3	14	72	20	295	593	492
2019/2020	3569	433	154	48	210	405	280	383	451	429	395	241	140
2020/2021	3023	128	174	120	292	267	294	105	268	417	342	404	212
2021/2022	2149	76	280	427	226	160	146	142	323	115	58	196	0
Totale													12133