statistiche ricercatore

KILSTRUP-NIELSEN, CHARLOTTE

Distribuzione geografica

Continente	#
NA - Nord America	5.799
EU - Europa	3.477
AS - Asia	2.339
SA - Sud America	221
AF - Africa	51
OC - Oceania	26
Continente sconosciuto - Info sul continente non disponibili	3
AN - Antartide	1
Totale	11.917

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Nazione	#
US - Stati Uniti d'America	5.737
IT - Italia	1.679
SG - Singapore	788
CN - Cina	537
UA - Ucraina	526
VN - Vietnam	354
DE - Germania	250
TR - Turchia	247
HK - Hong Kong	246
SE - Svezia	227
BR - Brasile	185
FI - Finlandia	182
IE - Irlanda	149
FR - Francia	132
GB - Regno Unito	131
RU - Federazione Russa	77
IN - India	43
JP - Giappone	43
CA - Canada	27
AU - Australia	26
MX - Messico	26
NL - Olanda	23
GH - Ghana	21
BE - Belgio	20
PL - Polonia	19
BD - Bangladesh	17
ES - Italia	17
AR - Argentina	15
AT - Austria	12
IR - Iran	12
ZA - Sudafrica	10
CZ - Repubblica Ceca	8
IQ - Iraq	8
UZ - Uzbekistan	7
EC - Ecuador	5
ID - Indonesia	5
MA - Marocco	5
PH - Filippine	5
CL - Cile	4
CO - Colombia	4
EG - Egitto	4
PT - Portogallo	4
TN - Tunisia	4
DK - Danimarca	3
EU - Europa	3
IL - Israele	3
JM - Giamaica	3
JO - Giordania	3
MY - Malesia	3
NG - Nigeria	3
PK - Pakistan	3
RS - Serbia	3
AE - Emirati Arabi Uniti	2
BN - Brunei Darussalam	2
BO - Bolivia	2
CH - Svizzera	2
DO - Repubblica Dominicana	2
EE - Estonia	2
GR - Grecia	2
HN - Honduras	2
KE - Kenya	2
OM - Oman	2
RO - Romania	2
VE - Venezuela	2
AQ - Antartide	1
AZ - Azerbaigian	1
BG - Bulgaria	1
BH - Bahrain	1
DZ - Algeria	1
GA - Gabon	1
GY - Guiana	1
KR - Corea	1
KZ - Kazakistan	1
LB - Libano	1
LI - Liechtenstein	1
LT - Lituania	1
LV - Lettonia	1
MD - Moldavia	1
MN - Mongolia	1
MT - Malta	1
NO - Norvegia	1
PA - Panama	1
PE - Perù	1
PS - Palestinian Territory	1
SA - Arabia Saudita	1
SR - Suriname	1
SY - Repubblica araba siriana	1
TT - Trinidad e Tobago	1
UY - Uruguay	1
Totale	11.917

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Città	#
Milan	1.082
Fairfield	473
Singapore	445
Chandler	431
Ashburn	425
Jacksonville	403
San Jose	388
Woodbridge	358
Houston	339
Ann Arbor	243
Hong Kong	241
Dearborn	233
Seattle	212
Wilmington	188
Beijing	175
Cambridge	168
Dallas	160
Dublin	149
Princeton	146
Como	131
The Dalles	128
Izmir	111
Chicago	109
Nyköping	105
New York	104
Dong Ket	92
Boardman	89
Rome	81
Lauterbourg	75
Ho Chi Minh City	74
Los Angeles	71
Munich	59
Council Bluffs	41
San Mateo	41
Hanoi	39
Helsinki	38
Buffalo	37
Kocaeli	36
Tokyo	32
London	30
Ogden	30
Santa Clara	29
Orem	27
San Diego	27
Turku	25
Guangzhou	23
Brussels	19
São Paulo	19
Turin	18
Brooklyn	17
Chennai	17
Warsaw	17
Hefei	16
Mexico City	16
Nanjing	16
Washington	16
Kunming	14
Melbourne	14
Monza	14
Düsseldorf	13
Da Nang	12
Accra	11
Amsterdam	11
Atlanta	11
Frankfurt am Main	11
Phoenix	11
Stockholm	11
Toronto	11
Boston	10
Jinan	10
Magnago	10
Shanghai	10
Shenzhen	10
Verona	10
Denver	9
Gallarate	9
Vienna	9
Ankara	8
Mumbai	8
Norwalk	8
Nuremberg	8
Ponte Lambro	8
Poplar	8
West Jordan	8
Haiphong	7
Hangzhou	7
Redmond	7
Shenyang	7
Edinburgh	6
Johannesburg	6
Kilburn	6
Manchester	6
Montreal	6
Nanchang	6
Naples	6
Osaka	6
Rosdorf	6
Secaucus	6
Tashkent	6
Varese	6
Totale	8.501

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Nome	#
Cannabidivarin completely rescues cognitive deficits and delays neurological and motor defects in male Mecp2 mutant mice	272
CDKL5 and shootin1 interact and concur in regulating neuronal polarization	260
MeCP2 related studies benefit from the use of CD1 as genetic background	235
A novel protein, Xenopus p20, influences the stability of MeCP2 through direct interaction	221
Methyl-CpG binding protein 2 (MeCP2) localizes at the centrosome and is required for proper mitotic spindle organization	219
Rett syndrome and the urge of novel approaches to study MeCP2 functions and mechanisms of action	216
The neurosteroid pregnenolone reverts microtubule derangement induced by the loss of a functional CDKL5-IQGAP1 complex	211
CDKL5 belongs to the same molecular pathway of MeCP2 and it is responsible for the early-onset seizure variant of Rett syndrome	207
MeCP2 post-translational modifications: a mechanism to control its involvement in synaptic plasticity and homeostasis?	207
CDKL5 localizes at the centrosome and midbody and is required for faithful cell division	204
Characterization of PREP2, a paralog of PREP1, which defines a novel sub-family of the MEINOX TALE homeodomain transcription factors	203
CDKL5 expression is modulated during neuronal development and its subcellular distribution is tightly regulated by the C-terminal tail	202
MeCP2 affects skeletal muscle growth and morphology through non cell-autonomous mechanisms	196
Spatio-temporal dynamics and localization of MeCP2 and pathological mutants in living cells	187
CDKL5 influences RNA splicing activity by its association to the nuclear speckle molecular machinery.	187
A novel transcript of cyclin-dependent kinase-like 5 (CDKL5) has an alternative C-terminus and is the predominant transcript in brain.	184
What We Know and Would Like to Know about CDKL5 and Its Involvement in Epileptic Encephalopathy.	184
The subcellular localization of PBX1 and EXD proteins depends on nuclear import and export signals and is modulated by association with PREP1 and HTH	183
Synaptic synthesis, dephosphorylation and degradation: a novel paradigm for an activity-dependent neuronal control of CDKL5.	182
PBX1 nuclear export is regulated independently of PBX-MEINOX interaction by PKA phosphorylation of the PBC-B domain	176
Characterization of CDKL5 transcript isoforms in human and mouse	176
The antidepressant tianeptine reverts synaptic AMPA receptor defects caused by deficiency of CDKL5	175
Functional consequences of mutations in CDKL5, an X-linked gene involved in infantile spasms and mental retardation	174
Retinoic acid receptor a fusion to PML affects its transcriptional and chromatin-remodeling properties	170
Defects During Mecp2 Null Embryonic Cortex Development Precede the Onset of Overt Neurological Symptoms	168
The MeCP2/YY1 interaction regulates ANT1 expression at 4q35: novel hints for Rett syndrome pathogenesis	167
CDKL5 ensures excitatory synapse stability by reinforcing NGL1-PSD95 interaction in the postsynaptic compartment and is impaired in patient iPSC-derived neurons	165
Brain phosphorylation of MeCP2 at serene 164 is developmentally regulated and globally alters its chromatin association	160
Methyl-CpG-binding protein 2 is phosphorylated by homeodomain-interacting protein kinase 2 and contributes to apoptosis	160
La cromatina e controllo dell'espressione genica.	158
Characterization of HIPK2 that, by Associating with MeCP2, Might Function as a Modifier Gene in Rett Syndrome	157
A Novel Mecp2Y120D Knock-in Model Displays Similar Behavioral Traits But Distinct Molecular Features Compared to the Mecp2-Null Mouse Implying Precision Medicine for the Treatment of Rett Syndrome.	156
The functional role of CDKL5 at the inhibitory synapse and its interaction with the cytoplasmatic collybistin-gephyrin complex	154
CDKL5 belongs to the same molecular pathway of MeCP2 and is responsible for the early seizure variant of Rett Syndrome	152
Extrasynaptic N-methyl-D-aspartate (NMDA) receptor stimulation induces cytoplasmic translocation of the CDKL5 kinase and its proteasomal degradation	152
The green tea polyphenol epigallocatechin-3-gallate (EGCG) restores CDKL5-dependent synaptic defects in vitro and in vivo	151
Characterization of a novel MeCP2 interacting protein	150
Genetics and mechanisms of disease in Rett Syndrome	148
DNA methylation and Rett syndrome	144
Rescue of prepulse inhibition deficit and brain mitochondrial dysfunction by pharmacological stimulation of the central serotonin receptor 7 in a mouse model of CDKL5 Deficiency Disorder	144
Microtubules: A Key to Understand and Correct Neuronal Defects in CDKL5 Deficiency Disorder?	143
Identification and Characterization of proteins that, interacting with MeCP2, could be involved in Rett Syndrome	142
MECP2 mutations affect ciliogenesis: a novel perspective for Rett syndrome and related disorders	142
CDKL5 levels quickly respond to neuronal activity, reinforcing its involvement in synaptic plasticity	140
Identification and characterization of proteins that, interacting with MeCP2, could be involved in Rett Syndrome	139
CHARACTERIZATION OF THE CDKL5 GENE INVOLVED IN MENTAL RETARDATION AND INFANTILE SPASMS.	138
Pregnenolone and pregnenolone-methyl-ether rescue neuronal defects caused by dysfunctional CLIP170 in a neuronal model of CDKL5 Deficiency Disorder	138
Spatio-temporal dynamics and localization of MeCP2 and pathological mutants in living cells	137
2nd European Working Group on Rett Syndrome	136
Functional Characterization of CDKL5, a Novel Gene Involved in The Onset of Rett Syndrome and Infantile Spasms.	132
Loss of CDKL5 Causes Synaptic GABAergic Defects That Can Be Restored with the Neuroactive Steroid Pregnenolone-Methyl-Ether	130
Functional Characterization of CDKL5, an X-Linked Gene Involved in Mental Retardation and Epileptic Crisis.	128
Characterization of HIPK2 that, by Associating with MeCP2, Might Function as a Modifier Gene in Rett Syndrome.	125
Disruption of the Cellular Regulation of CDKL5 Might be Relevant for Rett Syndrome	121
Molecular characterization of CDKL5, a novel kinase involved in Rett syndrome and infantile spasms	121
Pregnenolone-methyl-ether enhances CLIP170 and microtubule functions improving spine maturation and hippocampal deficits related to CDKL5 deficiency	120
Disruption of the Cellular Regulation of CDKL5 Might be Relevant for Rett Syndrome	119
Molecular characterization of CDKL5, a novel kinase involved in Rett syndrome and infantile spasms	117
Functional characterization of CDKL5, a novel gene involved in the onset of Rett Syndrome	117
DNA methylation in the control of gene silencing during development and human disorders (DisChrom)	115
Functional Characterization of CDKL5, a novel gene involved in the onset of Rett syndrome	115
Functional characterization of CDKL5, a novel gene involved in Rett syndrome and infantile spams associated with mental retardation	115
Characterization of the molecular mechanism underlying GABAA-receptor defects in CDKL5 deficiency disorder	113
Disruption of the Cellular Regulation of CDKL5 Might be Relevant for Rett Syndrome	112
European Working Group on Rett Syndrome	112
Revealing a novel and unexpected function of MeCP2, possibly involved in RTT pathophysiology	112
CDKL5 interacts with inhibitory postsynaptic scaffolding proteins and regulates synaptic GABAA receptor levels	110
Molecular characterization of the CDKL5 gene involved in mental retardation and infantile spams	108
Functional characterization of CDKL5, a novel gene involved in Rett Syndrome and infantile spams	107
Therapeutic potential of pregnenolone and pregnenolone methyl ether on depressive and CDKL5 deficiency disorders: Focus on microtubule targeting	107
Identification and characterization of proteins that interacting with MeCP2, could be involved in Rett Syndrome	104
Functional characterizationof CDKL5, a novel gene involved in the onset of Rett Syndrome	102
Molecular and functional characterization of CDKL5, a novel X-linked kinase, mainly involved in female mental retardation	101
Functional characterization of CDKL5, a novel kinase involved in Rett syndrome and infantile spasms	99
Molecular genetics of Rett syndrome: when epigenetic signals go unrecognized	96
Cromatina e controllo dell'espressione genica	91
The functional role of CDKL5 at the inhibitory synapse and its interaction with the cytoplasmatic collybistin-gephyrin complex	81
Identification and characterization of proteins that interacting with MECP2, could be involved in Rett Syndrome	81
Novel role of CDKL5 in the inhibitory synapse and a possible therapeutic strategy for CDKL5-related defects	79
The functional role of CDKL5 at the inhibitory synapse and its interaction with the cytoplasmatic collybistin-gephyrin complex	76
Rett syndrome: from the involved gene(s) to treatment	43
Totale	11.981

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Categoria	#
all - tutte	45.398
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	45.398

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	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2020/2021	365	0	0	0	0	0	0	0	0	0	95	116	154
2021/2022	669	87	92	50	33	23	21	26	32	36	100	80	89
2022/2023	1.082	107	82	56	114	70	227	9	149	131	38	50	49
2023/2024	1.829	282	261	293	289	322	181	20	47	59	29	12	34
2024/2025	1.318	7	38	238	36	93	72	55	34	161	117	148	319
2025/2026	2.973	268	203	170	420	305	257	659	201	356	134	0	0
Totale													11.981