769 related articles for article (PubMed ID: 10514831)
1. Parental imprinting and Angelman syndrome.
Lalande M; Minassian BA; DeLorey TM; Olsen RW
Adv Neurol; 1999; 79():421-9. PubMed ID: 10514831
[TBL] [Abstract][Full Text] [Related]
2. Genetic imprinting: the paradigm of Prader-Willi and Angelman syndromes.
Gurrieri F; Accadia M
Endocr Dev; 2009; 14():20-8. PubMed ID: 19293572
[TBL] [Abstract][Full Text] [Related]
3. Imprinting center analysis in Prader-Willi and Angelman syndrome patients with typical and atypical phenotypes.
Camprubí C; Coll MD; Villatoro S; Gabau E; Kamli A; Martínez MJ; Poyatos D; Guitart M
Eur J Med Genet; 2007; 50(1):11-20. PubMed ID: 17095305
[TBL] [Abstract][Full Text] [Related]
4. Allele specificity of DNA replication timing in the Angelman/Prader-Willi syndrome imprinted chromosomal region.
Knoll JH; Cheng SD; Lalande M
Nat Genet; 1994 Jan; 6(1):41-6. PubMed ID: 8136833
[TBL] [Abstract][Full Text] [Related]
5. Genomic imprinting and uniparental disomy in Angelman and Prader-Willi syndromes: a review.
Nicholls RD
Am J Med Genet; 1993 Apr; 46(1):16-25. PubMed ID: 8388169
[TBL] [Abstract][Full Text] [Related]
6. Angelman syndrome due to a novel splicing mutation of the UBE3A gene.
Sartori S; Anesi L; Polli R; Toldo I; Casarin A; Drigo P; Murgia A
J Child Neurol; 2008 Aug; 23(8):912-5. PubMed ID: 18487518
[TBL] [Abstract][Full Text] [Related]
7. Electroclinical characteristics of seizures-comparing Prader--Willi syndrome with Angelman syndrome.
Wang PJ; Hou JW; Sue WC; Lee WT
Brain Dev; 2005 Mar; 27(2):101-7. PubMed ID: 15668048
[TBL] [Abstract][Full Text] [Related]
8. GABAA receptor beta3 subunit gene-deficient heterozygous mice show parent-of-origin and gender-related differences in beta3 subunit levels, EEG, and behavior.
Liljelund P; Handforth A; Homanics GE; Olsen RW
Brain Res Dev Brain Res; 2005 Jun; 157(2):150-61. PubMed ID: 15878204
[TBL] [Abstract][Full Text] [Related]
9. Just how happy is the happy puppet? An emotion signaling and kinship theory perspective on the behavioral phenotype of children with Angelman syndrome.
Brown WM; Consedine NS
Med Hypotheses; 2004; 63(3):377-85. PubMed ID: 15288352
[TBL] [Abstract][Full Text] [Related]
10. [The GABAA receptor beta 3-subunit gene (GABRB3) as a candidate responsible for central nerve disturbances in Angelman syndrome (AS)].
Saitoh S; Niikawa N
Nihon Rinsho; 1993 Sep; 51(9):2409-13. PubMed ID: 8411721
[TBL] [Abstract][Full Text] [Related]
11. The imprinting box of the Prader-Willi/Angelman syndrome domain.
Shemer R; Hershko AY; Perk J; Mostoslavsky R; Tsuberi B; Cedar H; Buiting K; Razin A
Nat Genet; 2000 Dec; 26(4):440-3. PubMed ID: 11101841
[TBL] [Abstract][Full Text] [Related]
12. Control elements within the PWS/AS imprinting box and their function in the imprinting process.
Kantor B; Makedonski K; Green-Finberg Y; Shemer R; Razin A
Hum Mol Genet; 2004 Apr; 13(7):751-62. PubMed ID: 14962980
[TBL] [Abstract][Full Text] [Related]
13. Phenotypic differences in Angelman syndrome patients: imprinting mutations show less frequently microcephaly and hypopigmentation than deletions.
Bürger J; Kunze J; Sperling K; Reis A
Am J Med Genet; 1996 Dec; 66(2):221-6. PubMed ID: 8958335
[TBL] [Abstract][Full Text] [Related]
14. Detection of a novel familial deletion of four genes between BP1 and BP2 of the Prader-Willi/Angelman syndrome critical region by oligo-array CGH in a child with neurological disorder and speech impairment.
Murthy SK; Nygren AO; El Shakankiry HM; Schouten JP; Al Khayat AI; Ridha A; Al Ali MT
Cytogenet Genome Res; 2007; 116(1-2):135-40. PubMed ID: 17268193
[TBL] [Abstract][Full Text] [Related]
15. The Prader-Willi syndrome and the Angelman syndrome.
Vogels A; Fryns JP
Genet Couns; 2002; 13(4):385-96. PubMed ID: 12558108
[TBL] [Abstract][Full Text] [Related]
16. DNA methylation patterns in human tissues of uniparental origin using a zinc-finger gene (ZNF127) from the Angelman/Prader-Willi region.
Mowery-Rushton PA; Driscoll DJ; Nicholls RD; Locker J; Surti U
Am J Med Genet; 1996 Jan; 61(2):140-6. PubMed ID: 8669440
[TBL] [Abstract][Full Text] [Related]
17. Rearrangements of chromosome 15 in epilepsy.
Torrisi L; Sangiorgi E; Russo L; Gurrieri F
Am J Med Genet; 2001; 106(2):125-8. PubMed ID: 11579432
[TBL] [Abstract][Full Text] [Related]
18. Physical mapping studies at D15S10: implications for candidate gene identification in the Angelman syndrome/Prader-Willi syndrome chromosome region of 15q11-q13.
Woodage T; Lindeman R; Deng ZM; Fimmel A; Smith A; Trent RJ
Genomics; 1994 Jan; 19(1):170-2. PubMed ID: 8188222
[TBL] [Abstract][Full Text] [Related]
19. [Epigenetic modification of the genetic material. Genomic imprinting and its significance for disease in human beings].
Brøndum-Nielsen K; Pedersen ML
Ugeskr Laeger; 2001 Jun; 163(23):3218-22. PubMed ID: 11421188
[TBL] [Abstract][Full Text] [Related]
20. Difference in methylation patterns within the D15S9 region of chromosome 15q11-13 in first cousins with Angelman syndrome and Prader-Willi syndrome.
Clayton-Smith J; Driscoll DJ; Waters MF; Webb T; Andrews T; Malcolm S; Pembrey ME; Nicholls RD
Am J Med Genet; 1993 Oct; 47(5):683-6. PubMed ID: 8266996
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
