SCOPUS 정보 검색 플랫폼

Volumn 2, Issue 1, 2007, Pages

Design of an improved set of oligonucleotide primers for genotyping MeCP2tm1.1Bird KO mice by PCR

Author keywords

[No Author keywords available]

Indexed keywords

ANIMALIA; AVES; MUS;

EID: 35348865132 PISSN: None EISSN: 17501326 Source Type: Journal
DOI: 10.1186/1750-1326-2-16 Document Type: Article

Times cited : (16)

References (11)

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- Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2
- Amir RE, Van den Veyver IB, Wan M, Tran CQ, Francke U, Zoghbi HY: Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2. Nat Genet 1999, 23(2): 185-188.
- (1999) Nat Genet , vol.23 , Issue.2 , pp. 185-188
- Amir, R.E.¹ Van den Veyver, I.B.² Wan, M.³ Tran, C.Q.⁴ Francke, U.⁵ Zoghbi, H.Y.⁶

2
- 0035094767
- A mouse Mecp2null mutation causes neurological symptoms that mimic Rett syndrome
- Guy J, Hendrich B, Holmes M, Martin JE, Bird A: A mouse Mecp2null mutation causes neurological symptoms that mimic Rett syndrome. Not Genet 2001, 27(3):322-326.
- (2001) Not Genet , vol.27 , Issue.3 , pp. 322-326
- Guy, J.¹ Hendrich, B.² Holmes, M.³ Martin, J.E.⁴ Bird, A.⁵

3
- 0035093830
- Deficiency of methylCpG binding protein-2 in CNS neurons results in a Rett-like phenotype in mice
- Chen RZ, Akbarian S, Tudor M, Jaenisch R: Deficiency of methylCpG binding protein-2 in CNS neurons results in a Rett-like phenotype in mice. Not Genet 2001, 27(3):327-331.
- (2001) Not Genet , vol.27 , Issue.3 , pp. 327-331
- Chen, R.Z.¹ Akbarian, S.² Tudor, M.³ Jaenisch, R.⁴

4
- 0037130455
- Mice with truncated MeCP2 recapitulate many Rett syndrome features and display hyperacetylation of histone H3
- Shahbazian M, Young J, Yuva-Paylor L, Spencer C, Antalffy B, Noebels J, Armstrong D, Paylor R, Zoghbi H: Mice with truncated MeCP2 recapitulate many Rett syndrome features and display hyperacetylation of histone H3. Neuron 2002, 35(2):243-254.
- (2002) Neuron , vol.35 , Issue.2 , pp. 243-254
- Shahbazian, M.¹ Young, J.² Yuva-Paylor, L.³ Spencer, C.⁴ Antalffy, B.⁵ Noebels, J.⁶ Armstrong, D.⁷ Paylor, R.⁸ Zoghbi, H.⁹

5
- 33744550950
- Breeding and maintenance of an Mecp2-deficient mouse model of Rett syndrome
- Jugloff DG, Logan R, Eubanks JH: Breeding and maintenance of an Mecp2-deficient mouse model of Rett syndrome. J Neurosa Methods 2006, 154(1-2):89-95.
- (2006) J Neurosa Methods , vol.154 , Issue.1-2 , pp. 89-95
- Jugloff, D.G.¹ Logan, R.² Eubanks, J.H.³

6
- 23844525077
- Repbase Update, a database of eukaryotic repetitive elements
- Jurka J, Kapitonov W, Pavlicek A, Klonowski P, Kohany O, Walichiewicz J: Repbase Update, a database of eukaryotic repetitive elements. Cytogenet Genome Res 2005, 110(1-4):462-467.
- (2005) Cytogenet Genome Res , vol.110 , Issue.1-4 , pp. 462-467
- Jurka, J.¹ Kapitonov, W.² Pavlicek, A.³ Klonowski, P.⁴ Kohany, O.⁵ Walichiewicz, J.⁶

7
- 0025877323
- Male development of chromosomally female mice transgenic for Sry
- Koopman P, Gubbay J, Vivian N, Goodfellow P, Lovell-Badge R: Male development of chromosomally female mice transgenic for Sry. Noture 1991, 351 (6322): 117-121.
- (1991) Noture , vol.351 , Issue.6322 , pp. 117-121
- Koopman, P.¹ Gubbay, J.² Vivian, N.³ Goodfellow, P.⁴ Lovell-Badge, R.⁵

8
- 35348918994
- 3
- Primer3 [http://biotools.umassmed.edu/bioapps/ primer3 www.cgi]
- Primer¹

9
- 35348816319
- GeneFisher [http://bibiserv.techfak.uni-bielefeld.de/ genefisher/]
- GeneFisher¹

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.