X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (2576) 2576
Publication (366) 366
Book Chapter (54) 54
Book Review (26) 26
Conference Proceeding (11) 11
Dissertation (7) 7
Reference (4) 4
Magazine Article (3) 3
Book / eBook (2) 2
Paper (1) 1
Streaming Video (1) 1
Web Resource (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (1794) 1794
angelman syndrome (1153) 1153
female (1026) 1026
male (1004) 1004
angelman syndrome - genetics (858) 858
index medicus (846) 846
genetics & heredity (838) 838
angelman-syndrome (651) 651
animals (584) 584
child (572) 572
prader-willi syndrome - genetics (557) 557
prader-willi syndrome (508) 508
genomic imprinting (473) 473
child, preschool (449) 449
dna methylation (417) 417
phenotype (396) 396
mice (395) 395
adult (364) 364
prader-willi-syndrome (358) 358
adolescent (348) 348
chromosomes, human, pair 15 (333) 333
neurosciences (318) 318
biochemistry & molecular biology (285) 285
angelman syndrome - diagnosis (283) 283
autism (283) 283
mutation (283) 283
infant (273) 273
chromosomes, human, pair 15 - genetics (272) 272
clinical neurology (262) 262
gene (250) 250
deletion (248) 248
epilepsy (246) 246
chromosome deletion (244) 244
genetics (244) 244
ube3a (236) 236
ubiquitin-protein ligases - genetics (232) 232
pediatrics (230) 230
uniparental disomy (229) 229
children (227) 227
genetic aspects (208) 208
research (208) 208
congenital, hereditary, and neonatal diseases and abnormalities (201) 201
mutations (199) 199
diagnosis (189) 189
methylation (188) 188
article (185) 185
gene expression (183) 183
analysis (180) 180
in situ hybridization, fluorescence (177) 177
genes (176) 176
expression (165) 165
chromosome 15 (159) 159
angelman syndrome - physiopathology (158) 158
chromosome mapping (150) 150
mouse model (149) 149
imprinting (148) 148
molecular sequence data (148) 148
prader-willi syndrome - diagnosis (148) 148
alleles (146) 146
base sequence (144) 144
mental retardation (140) 140
region (140) 140
pedigree (139) 139
disease models, animal (138) 138
cell biology (135) 135
prader-willi (134) 134
chromosome-15 (132) 132
genomic imprinting - genetics (132) 132
angelman syndrome - complications (127) 127
seizures (127) 127
angelman-syndromes (126) 126
chromosomes (126) 126
intellectual disability - genetics (126) 126
brain (125) 125
mental-retardation (124) 124
ubiquitin (124) 124
ubiquitin-protein ligases - metabolism (120) 120
electroencephalography (119) 119
fragile-x-syndrome (119) 119
chromosome aberrations (118) 118
gene deletion (117) 117
psychiatry (115) 115
beckwith-wiedemann-syndrome (114) 114
genetic disorders (114) 114
parental origin (114) 114
rett-syndrome (108) 108
rehabilitation (105) 105
intellectual disability (102) 102
behavior (101) 101
genotype (101) 101
mice, inbred c57bl (101) 101
angelman syndrome - pathology (100) 100
ubiquitin-protein ligase (100) 100
pregnancy (99) 99
ubiquitin ligase (99) 99
polymerase chain reaction (98) 98
research article (98) 98
epigenetics (96) 96
proteins (96) 96
karyotyping (93) 93
more...
Library Location Library Location
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (2420) 2420
Spanish (52) 52
French (26) 26
German (25) 25
Japanese (23) 23
Chinese (13) 13
Portuguese (10) 10
Italian (9) 9
Czech (8) 8
Polish (8) 8
Korean (7) 7
Russian (7) 7
Swedish (4) 4
Danish (3) 3
Hungarian (3) 3
Norwegian (3) 3
Slovak (3) 3
Serbian (2) 2
Afrikaans (1) 1
Croatian (1) 1
Dutch (1) 1
Finnish (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Biological Psychiatry, ISSN 0006-3223, 05/2019, Volume 85, Issue 9, pp. e45 - e46
Journal Article
Neurobiology of Disease, ISSN 0969-9961, 12/2019, Volume 132, p. 104585
Angelman syndrome (AS) is a severe neurodevelopmental disorder caused by maternal mutation and paternal imprinting of the gene encoding UBE3A, an E3 ubiquitin... 
SILAM | Proteome | Angelman syndrome | UBE3A | autophagy | HAP1
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 08/2015, Volume 112, Issue 32, pp. 9872 - 9877
Journal Article
Progress in neurobiology, ISSN 0301-0082, 08/2019, p. 101676
Angelman syndrome (AS) is a neurodevelopmental disorder caused by the loss of function of the maternal copy of the UBE3A gene. Previous studies reported an... 
Journal Article
Zdorovʹe Rebenka, ISSN 2224-0551, 10/2015, Volume 10, Issue 7.67, pp. 81 - 87
The article discusses the problem of differential diagnosis and treatment of patients with Angelman syndrome (AS). It provides the most common syndromes with... 
Angelman syndrome
Journal Article
Zdorovʹe Rebenka, ISSN 2224-0551, 08/2015, Volume 10, Issue 5.65, pp. 83 - 92
В статье приведены современные представления о механизмах генетических изменений при синдроме Ангельмана. Статья содержит данные о частоте встречаемости и... 
Angelman syndrome
Journal Article
Nature Reviews Genetics, ISSN 1471-0056, 2014, Volume 15, Issue 8, pp. 517 - 530
Journal Article
Epileptic Disorders, ISSN 1294-9361, 12/2015, Volume 17, Issue 4, pp. 496 - 496
Journal Article
2008, Clinics in developmental medicine, ISBN 1898683557, Volume no. 177, ix, 181
Book
Human Molecular Genetics, ISSN 0964-6906, 1995, Volume 4, Issue 5, pp. 801 - 806
Journal Article
Journal of Virology, ISSN 0022-538X, 2015, Volume 89, Issue 1, pp. 784 - 798
Journal Article