KILSTRUP-NIELSEN, CHARLOTTE
 Distribuzione geografica
Continente #
NA - Nord America 5.126
EU - Europa 3.336
AS - Asia 1.783
SA - Sud America 210
AF - Africa 27
OC - Oceania 12
Continente sconosciuto - Info sul continente non disponibili 3
AN - Antartide 1
Totale 10.498
Nazione #
US - Stati Uniti d'America 5.074
IT - Italia 1.665
SG - Singapore 648
UA - Ucraina 523
CN - Cina 346
DE - Germania 246
TR - Turchia 241
VN - Vietnam 236
SE - Svezia 227
HK - Hong Kong 209
BR - Brasile 180
FI - Finlandia 168
IE - Irlanda 149
GB - Regno Unito 122
RU - Federazione Russa 77
FR - Francia 45
JP - Giappone 36
CA - Canada 27
IN - India 23
NL - Olanda 21
BE - Belgio 19
MX - Messico 19
PL - Polonia 18
ES - Italia 14
AR - Argentina 13
AT - Austria 12
AU - Australia 12
GH - Ghana 10
CZ - Repubblica Ceca 8
BD - Bangladesh 7
ZA - Sudafrica 7
IR - Iran 6
IQ - Iraq 5
CL - Cile 4
EC - Ecuador 4
UZ - Uzbekistan 4
CO - Colombia 3
DK - Danimarca 3
EG - Egitto 3
EU - Europa 3
MA - Marocco 3
PT - Portogallo 3
RS - Serbia 3
AE - Emirati Arabi Uniti 2
BN - Brunei Darussalam 2
CH - Svizzera 2
EE - Estonia 2
ID - Indonesia 2
IL - Israele 2
JM - Giamaica 2
PH - Filippine 2
RO - Romania 2
TN - Tunisia 2
VE - Venezuela 2
AQ - Antartide 1
AZ - Azerbaigian 1
BG - Bulgaria 1
BH - Bahrain 1
DO - Repubblica Dominicana 1
DZ - Algeria 1
GR - Grecia 1
GY - Guiana 1
HN - Honduras 1
JO - Giordania 1
KE - Kenya 1
KR - Corea 1
KZ - Kazakistan 1
LB - Libano 1
LI - Liechtenstein 1
LT - Lituania 1
LV - Lettonia 1
MN - Mongolia 1
MT - Malta 1
MY - Malesia 1
NO - Norvegia 1
OM - Oman 1
PA - Panama 1
PE - Perù 1
PK - Pakistan 1
PS - Palestinian Territory 1
SA - Arabia Saudita 1
SR - Suriname 1
TT - Trinidad e Tobago 1
UY - Uruguay 1
Totale 10.498
Città #
Milan 1.080
Fairfield 473
Chandler 431
Jacksonville 403
Ashburn 358
Woodbridge 357
Singapore 343
Houston 339
Ann Arbor 243
Dearborn 233
Seattle 212
Hong Kong 207
Wilmington 188
Cambridge 168
Dallas 159
Beijing 157
Dublin 149
Princeton 146
Como 131
Izmir 109
Nyköping 105
New York 102
Dong Ket 92
Boardman 88
Rome 81
The Dalles 72
Los Angeles 67
Munich 59
Chicago 57
San Mateo 41
Buffalo 37
Kocaeli 36
Ogden 30
Tokyo 29
London 28
San Diego 27
Ho Chi Minh City 26
Santa Clara 25
Turku 25
Helsinki 24
Brussels 19
São Paulo 17
Turin 17
Warsaw 17
Brooklyn 16
Nanjing 16
Washington 16
Hanoi 15
Hefei 15
Orem 15
Kunming 14
Monza 14
Düsseldorf 13
Guangzhou 11
Melbourne 11
Stockholm 11
Toronto 11
Boston 10
Chennai 10
Jinan 10
Magnago 10
Phoenix 10
Verona 10
Amsterdam 9
Denver 9
Frankfurt am Main 9
Gallarate 9
Mexico City 9
Vienna 9
Ankara 8
Atlanta 8
Council Bluffs 8
Norwalk 8
Nuremberg 8
Ponte Lambro 8
Poplar 8
West Jordan 8
Redmond 7
Edinburgh 6
Kilburn 6
Montreal 6
Nanchang 6
Naples 6
Osaka 6
Rosdorf 6
Secaucus 6
Shenyang 6
Cavaria con Premezzo 5
Charlotte 5
Columbus 5
Detroit 5
Edgware 5
Haiphong 5
Johannesburg 5
Providence 5
Shanghai 5
Vancouver 5
Angri 4
Auburn Hills 4
Cattolica 4
Totale 7.486
Nome #
CDKL5 and shootin1 interact and concur in regulating neuronal polarization 248
Cannabidivarin completely rescues cognitive deficits and delays neurological and motor defects in male Mecp2 mutant mice 247
MeCP2 related studies benefit from the use of CD1 as genetic background 214
Rett syndrome and the urge of novel approaches to study MeCP2 functions and mechanisms of action 206
Methyl-CpG binding protein 2 (MeCP2) localizes at the centrosome and is required for proper mitotic spindle organization 198
A novel protein, Xenopus p20, influences the stability of MeCP2 through direct interaction 195
The neurosteroid pregnenolone reverts microtubule derangement induced by the loss of a functional CDKL5-IQGAP1 complex 194
CDKL5 belongs to the same molecular pathway of MeCP2 and it is responsible for the early-onset seizure variant of Rett syndrome 187
CDKL5 localizes at the centrosome and midbody and is required for faithful cell division 186
MeCP2 affects skeletal muscle growth and morphology through non cell-autonomous mechanisms 183
MeCP2 post-translational modifications: a mechanism to control its involvement in synaptic plasticity and homeostasis? 180
Characterization of PREP2, a paralog of PREP1, which defines a novel sub-family of the MEINOX TALE homeodomain transcription factors 179
The subcellular localization of PBX1 and EXD proteins depends on nuclear import and export signals and is modulated by association with PREP1 and HTH 173
A novel transcript of cyclin-dependent kinase-like 5 (CDKL5) has an alternative C-terminus and is the predominant transcript in brain. 173
CDKL5 influences RNA splicing activity by its association to the nuclear speckle molecular machinery. 170
CDKL5 expression is modulated during neuronal development and its subcellular distribution is tightly regulated by the C-terminal tail 168
What We Know and Would Like to Know about CDKL5 and Its Involvement in Epileptic Encephalopathy. 165
Synaptic synthesis, dephosphorylation and degradation: a novel paradigm for an activity-dependent neuronal control of CDKL5. 164
Characterization of CDKL5 transcript isoforms in human and mouse 164
PBX1 nuclear export is regulated independently of PBX-MEINOX interaction by PKA phosphorylation of the PBC-B domain 159
The antidepressant tianeptine reverts synaptic AMPA receptor defects caused by deficiency of CDKL5 156
Retinoic acid receptor a fusion to PML affects its transcriptional and chromatin-remodeling properties 155
CDKL5 ensures excitatory synapse stability by reinforcing NGL1-PSD95 interaction in the postsynaptic compartment and is impaired in patient iPSC-derived neurons 154
Defects During Mecp2 Null Embryonic Cortex Development Precede the Onset of Overt Neurological Symptoms 153
Spatio-temporal dynamics and localization of MeCP2 and pathological mutants in living cells 149
La cromatina e controllo dell'espressione genica. 147
The MeCP2/YY1 interaction regulates ANT1 expression at 4q35: novel hints for Rett syndrome pathogenesis 147
Brain phosphorylation of MeCP2 at serene 164 is developmentally regulated and globally alters its chromatin association 146
Methyl-CpG-binding protein 2 is phosphorylated by homeodomain-interacting protein kinase 2 and contributes to apoptosis 145
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. 144
Characterization of HIPK2 that, by Associating with MeCP2, Might Function as a Modifier Gene in Rett Syndrome 142
Extrasynaptic N-methyl-D-aspartate (NMDA) receptor stimulation induces cytoplasmic translocation of the CDKL5 kinase and its proteasomal degradation 141
CDKL5 belongs to the same molecular pathway of MeCP2 and is responsible for the early seizure variant of Rett Syndrome 134
Characterization of a novel MeCP2 interacting protein 133
DNA methylation and Rett syndrome 132
Genetics and mechanisms of disease in Rett Syndrome 129
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 129
Identification and Characterization of proteins that, interacting with MeCP2, could be involved in Rett Syndrome 126
Functional consequences of mutations in CDKL5, an X-linked gene involved in infantile spasms and mental retardation 126
Identification and characterization of proteins that, interacting with MeCP2, could be involved in Rett Syndrome 126
CDKL5 levels quickly respond to neuronal activity, reinforcing its involvement in synaptic plasticity 125
2nd European Working Group on Rett Syndrome 124
Pregnenolone and pregnenolone-methyl-ether rescue neuronal defects caused by dysfunctional CLIP170 in a neuronal model of CDKL5 Deficiency Disorder 124
The green tea polyphenol epigallocatechin-3-gallate (EGCG) restores CDKL5-dependent synaptic defects in vitro and in vivo 124
Functional Characterization of CDKL5, a Novel Gene Involved in The Onset of Rett Syndrome and Infantile Spasms. 123
CHARACTERIZATION OF THE CDKL5 GENE INVOLVED IN MENTAL RETARDATION AND INFANTILE SPASMS. 121
Spatio-temporal dynamics and localization of MeCP2 and pathological mutants in living cells 120
Microtubules: A Key to Understand and Correct Neuronal Defects in CDKL5 Deficiency Disorder? 119
The functional role of CDKL5 at the inhibitory synapse and its interaction with the cytoplasmatic collybistin-gephyrin complex 118
MECP2 mutations affect ciliogenesis: a novel perspective for Rett syndrome and related disorders 113
Characterization of HIPK2 that, by Associating with MeCP2, Might Function as a Modifier Gene in Rett Syndrome. 112
Functional Characterization of CDKL5, an X-Linked Gene Involved in Mental Retardation and Epileptic Crisis. 111
Molecular characterization of CDKL5, a novel kinase involved in Rett syndrome and infantile spasms 111
Disruption of the Cellular Regulation of CDKL5 Might be Relevant for Rett Syndrome 109
DNA methylation in the control of gene silencing during development and human disorders (DisChrom) 107
Functional characterization of CDKL5, a novel gene involved in the onset of Rett Syndrome 107
Loss of CDKL5 Causes Synaptic GABAergic Defects That Can Be Restored with the Neuroactive Steroid Pregnenolone-Methyl-Ether 105
Molecular characterization of CDKL5, a novel kinase involved in Rett syndrome and infantile spasms 104
Disruption of the Cellular Regulation of CDKL5 Might be Relevant for Rett Syndrome 102
European Working Group on Rett Syndrome 102
Pregnenolone-methyl-ether enhances CLIP170 and microtubule functions improving spine maturation and hippocampal deficits related to CDKL5 deficiency 101
Functional Characterization of CDKL5, a novel gene involved in the onset of Rett syndrome 99
Molecular characterization of the CDKL5 gene involved in mental retardation and infantile spams 99
Disruption of the Cellular Regulation of CDKL5 Might be Relevant for Rett Syndrome 98
Functional characterization of CDKL5, a novel gene involved in Rett syndrome and infantile spams associated with mental retardation 95
Functional characterizationof CDKL5, a novel gene involved in the onset of Rett Syndrome 95
Revealing a novel and unexpected function of MeCP2, possibly involved in RTT pathophysiology 95
Functional characterization of CDKL5, a novel gene involved in Rett Syndrome and infantile spams 94
Functional characterization of CDKL5, a novel kinase involved in Rett syndrome and infantile spasms 92
Identification and characterization of proteins that interacting with MeCP2, could be involved in Rett Syndrome 87
Molecular and functional characterization of CDKL5, a novel X-linked kinase, mainly involved in female mental retardation 87
Characterization of the molecular mechanism underlying GABAA-receptor defects in CDKL5 deficiency disorder 86
Molecular genetics of Rett syndrome: when epigenetic signals go unrecognized 86
CDKL5 interacts with inhibitory postsynaptic scaffolding proteins and regulates synaptic GABAA receptor levels 83
Therapeutic potential of pregnenolone and pregnenolone methyl ether on depressive and CDKL5 deficiency disorders: Focus on microtubule targeting 78
Identification and characterization of proteins that interacting with MECP2, could be involved in Rett Syndrome 72
Cromatina e controllo dell'espressione genica 70
Novel role of CDKL5 in the inhibitory synapse and a possible therapeutic strategy for CDKL5-related defects 66
The functional role of CDKL5 at the inhibitory synapse and its interaction with the cytoplasmatic collybistin-gephyrin complex 53
The functional role of CDKL5 at the inhibitory synapse and its interaction with the cytoplasmatic collybistin-gephyrin complex 51
Rett syndrome: from the involved gene(s) to treatment 27
Totale 10.562
Categoria #
all - tutte 42.955
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 42.955


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021791 0 0 0 0 0 103 57 80 186 95 116 154
2021/2022669 87 92 50 33 23 21 26 32 36 100 80 89
2022/20231.082 107 82 56 114 70 227 9 149 131 38 50 49
2023/20241.829 282 261 293 289 322 181 20 47 59 29 12 34
2024/20251.318 7 38 238 36 93 72 55 34 161 117 148 319
2025/20261.554 268 203 170 420 305 188 0 0 0 0 0 0
Totale 10.562