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Cytogenetics and Cell Genetics

Volumn 92, Issue 1-2, 2001, Pages 149-152

Analysis of DEXI/Dexi refines the organization of the mouse 7C and human 15q11 → q13 imprinting clusters

(3) Kelly, M a Edgar, A J b Wevrick, Rachel a,c

a UNIVERSITY OF ALBERTA (Canada)

b IMPERIAL COLLEGE SCHOOL OF MEDICINE (United Kingdom)

c 842 Medical Sciences Building ^* (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CHROMOSOME 15Q; CHROMOSOME 16; DNA FLANKING REGION; GENE DELETION; GENE LOCATION; GENOME IMPRINTING; HUMAN; MOUSE; NONHUMAN; NUCLEOTIDE SEQUENCE; POLYMERASE CHAIN REACTION; PRADER WILLI SYNDROME; PRIORITY JOURNAL; SEQUENCE HOMOLOGY;

ANGELMAN SYNDROME; ANIMALS; CHROMOSOMES, HUMAN, PAIR 15; DEXAMETHASONE; EVOLUTION, MOLECULAR; EXPRESSED SEQUENCE TAGS; GENOMIC IMPRINTING; HUMANS; MICE; MICE, INBRED C57BL; MICE, INBRED STRAINS; MOLECULAR SEQUENCE DATA; MULTIGENE FAMILY; OPEN READING FRAMES; PHYSICAL CHROMOSOME MAPPING; PRADER-WILLI SYNDROME; RNA, MESSENGER; TRANSCRIPTION, GENETIC;

EID: 0035044937 PISSN: 03010171 EISSN: None Source Type: Journal
DOI: None Document Type: Article

Times cited : (1)

References (10)

1
- 17544385914
- The human gene for the poly(A)-specific ribonuclease (PARN) maps to 16p13 and has a truncated copy in the Prader-Willi/Angelman syndrome region on 15q11 → q13
- (1999) Cytogenet Cell Genet , vol.87 , pp. 125-131
- Buiting, K.¹ Korner, C.² Ulrich, B.³ Wahle, E.⁴ Horsthemke, B.⁵

2
- 0028939902
- Inherited microdeletions in the Angelman and Prader-Willi syndromes define an imprinting centre on human chromosome 15
- (1995) Nature Genet , vol.9 , pp. 395-400
- Buiting, K.¹ Saitoh, S.² Gross, S.³ Dittrich, B.⁴ Schwartz, S.⁵ Nicholls, R.D.⁶ Horsthemke, B.⁷

3
- 0027017879
- A candidate mouse model for Prader-Willi syndrome which shows an absence of Snrpn expression
- (1992) Nature Genet , vol.2 , pp. 270-274
- Cattanach, B.M.¹ Barr, J.A.² Evans, E.P.³ Burtenshaw, M.⁴ Beechey, C.V.⁵ Leff, S.E.⁶ Brannan, C.I.⁷ Copeland, N.G.⁸ Jenkins, N.A.⁹ Jones, J.¹⁰

4
- 0032971379
- Large genomic duplicons map to sites of instability in the Prader-Willi/Angelman syndrome chromosome region (15q11 → q13)
- (1999) Hum Mol Genet , vol.8 , pp. 1025-1037
- Christian, S.L.¹ Fantes, J.A.² Mewbom, S.K.³ Huang, B.⁴ Ledbetter, D.H.⁵

5
- 4243316264
- A novel dexamethasone-induced gene MYLE is upregulated in emphysema
- (2000) Am J Respir Crit Care Med , vol.580
- Edgar, A.J.¹ Yacoub, M.H.² Polak, J.M.³

6
- 0032922431
- Repetitive conundrums of centromere structure and function
- (1999) Hum Mol Genet , vol.8 , pp. 151-155
- Eichler, E.E.¹

7
- 0033016617
- The ancestral gene for transcribed low-copy repeats in the Prader-Willi/Angelman region encodes a large protein implicated in protein trafficking which is deficient in mice with neuromuscular and spermiogenic abnormalities
- (1999) Hum Mol Genet , vol.8 , pp. 533-542
- Ji, Y.¹ Walkowicz, M.J.² Buiting, K.³ Johnson, D.K.⁴ Tarvin, R.E.⁵ Rinchik, E.M.⁶ Horsthemke, B.⁷ Stubbs, L.⁸ Nicholls, R.D.⁹

8
- 0033942565
- Identification of novel imprinted transcripts in the Prader-Willi/Angelman syndrome deletion region: Further evidence for regional imprinting control
- (2000) Am J hum Genet , vol.66 , pp. 848-858
- Lee, S.¹ Wevrick, R.²

9
- 0033997450
- The impact of genomic imprinting for neurobehavioral and developmental disorders
- (2000) J Clin Invest , vol.105 , pp. 413-418
- Nicholls, R.D.¹

10
- 0031747932
- A mouse model for Prader-Willi syndrome imprinting-centre mutations
- (1998) Nature Genet , vol.19 , pp. 25-31
- Yang, T.¹ Adamson, T.E.² Resnick, J.L.³ Leff, S.⁴ Wevrick, R.⁵ Francke, U.⁶ Jenkins, N.A.⁷ Copeland, N.G.⁸ Brannan, C.I.⁹

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.