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Find link is a tool written by Edward Betts.searching for UBE3A 15 found (50 total)
alternate case: uBE3A
Small nucleolar RNA SNORD64
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intron of the large paternally-expressed transcription unit (SNURF-SNRNP-UBE3A AS) along with several other snoRNAs HBII-436, HBII-437, HBII-438A/B andSmall nuclear ribonucleoprotein polypeptide N (1,220 words) [view diff] exact match in snippet view article find links to article
fluorescent-in-situ-hybridization has confirmed the presence of either SNRPN or UBE3A (a neighboring gene that is also imprinted), the methylation test (of SNRPN)Artificial transcription factor (1,698 words) [view diff] exact match in snippet view article find links to article
of UBE3A-AS gene, the gene that causes repression of the paternal UBE3A gene. Zinc finger ATF TAT-S1 acts as a strong repressor against the UBE3A-AS geneSNRPN upstream reading frame protein (935 words) [view diff] exact match in snippet view article find links to article
host for multiple small nucleolar RNA species and as an antisense RNA for UBE3A". Human Molecular Genetics. 10 (23): 2687–700. doi:10.1093/hmg/10.23.2687Arthur Beaudet (1,097 words) [view diff] exact match in snippet view article find links to article
of which has since been shown to occur. His group co-discovered that the UBE3A gene was inactivated as the cause of Angelman syndrome, and that deletionPhospholipid-transporting ATPase VA (590 words) [view diff] exact match in snippet view article find links to article
Human Aminophospholipid-Transporting ATPase Gene ATP10C Maps Adjacent to UBE3A and Exhibits Similar Imprinted Expression". Am. J. Hum. Genet. 68 (6): 1501–5Nihar Ranjan Jana (892 words) [view diff] case mismatch in snippet view article find links to article
Shekhar, Shashi; Sharma, Ankit; Jana, Nihar Ranjan (15 October 2017). "Ube3a deficiency inhibits amyloid plaque formation in APPswe/PS1δE9 mouse modelEpigenetics of autism (6,263 words) [view diff] exact match in snippet view article find links to article
regulation of expression in 15q11-13. Altered (decreased) expression of UBE3A and GABRB3 is observed in MeCP2 deficient mice and ASD patients. This effectIsodicentric 15 (2,370 words) [view diff] case mismatch in snippet view article find links to article
extra copies of just a single gene present in the 15q11.2-q13.1 region, Ube3a, into mice to model the gene copy number expressed in the brain in idic(15)Neurodevelopmental disorder (4,625 words) [view diff] exact match in snippet view article find links to article
neurodevelopmental disorders: MECP2 deficiency causes reduced expression of UBE3A and GABRB3". Human Molecular Genetics. 14 (4): 483–492. doi:10.1093/hmg/ddi045Causes of autism (15,822 words) [view diff] exact match in snippet view article find links to article
neurodevelopmental disorders: MECP2 deficiency causes reduced expression of UBE3A and GABRB3". Human Molecular Genetics. 14 (4): 483–492. doi:10.1093/hmg/ddi045Papillomaviridae (7,242 words) [view diff] exact match in snippet view article find links to article
PMC 3072458. PMID 11077444. "iHOP information Hyperlinked over Proteins UBE3A". Archived from the original on 2007-09-27. Retrieved 2007-05-01. "BiochemistryBrenda Bloodgood (1,492 words) [view diff] case mismatch in snippet view article find links to article
Greenberg, M. E. (2010). The AngelmanSyndrome-associated ubiquitin ligase Ube3a regulates synapse development and function through the ubiquination of ArcHERC1 (1,525 words) [view diff] exact match in snippet view article find links to article
1201170. PMID 9233772. "Entrez Gene: HERC1 hect (homologous to the E6-AP (UBE3A) carboxyl terminus) domain and RCC1 (CHC1)-like domain (RLD) 1". WassefCarl H. Johnson (2,506 words) [view diff] case mismatch in snippet view article find links to article
PMID 26982486. Shi, S.; Bichell, T.J.; Ihrie, R.A.; Johnson, C.H. (2015). "Ube3a Imprinting Impairs Circadian Robustness in Angelman Syndrome Models". Current