SCOPUS 정보 검색 플랫폼

Neurobiology of Aging

Volumn 35, Issue 4, 2014, Pages 935.e1-935.e2

DNAJ mutations are rare in Chinese Parkinson's disease patients and controls

(7) Foo, Jia Nee a Liany, Herty a Tan, Louis C b Au, Wing Lok b Prakash, Kumar M b Liu, Jianjun a Tan, Eng King b,c

a GENOME INSTITUTE OF SINGAPORE (Singapore)

b SINGAPORE GENERAL HOSPITAL (Singapore)

c DUKE NUS MEDICAL SCHOOL (Singapore)

Author keywords

Association; Chinese population; DNAJ family; Mutation; Parkinson's disease

Indexed keywords

ADULT; AGED; ARTICLE; CHINESE; CONTROLLED STUDY; DISEASE ASSOCIATION; DNAJC13 GENE; DNAJC5 GENE; DNAJC6 GENE; FEMALE; GENE; GENE FREQUENCY; GENE IDENTIFICATION; GENE MUTATION; GENE SEQUENCE; GENETIC ASSOCIATION; GENETIC VARIABILITY; GENOTYPE; HUMAN; MAJOR CLINICAL STUDY; MALE; MIDDLE AGED; NUCLEOTIDE SEQUENCE; ONSET AGE; PARKINSON DISEASE; PRIORITY JOURNAL; RISK FACTOR;

ASSOCIATION; CHINESE POPULATION; DNAJ FAMILY; MUTATION; PARKINSON'S DISEASE;

AGED; ASIAN CONTINENTAL ANCESTRY GROUP; EXONS; GENOTYPE; HSP40 HEAT-SHOCK PROTEINS; HUMANS; MALE; MEMBRANE PROTEINS; MIDDLE AGED; MOLECULAR CHAPERONES; MUTATION, MISSENSE; PARKINSON DISEASE;

EID: 85058205841 PISSN: 01974580 EISSN: 15581497 Source Type: Journal
DOI: 10.1016/j.neurobiolaging.2013.09.018 Document Type: Article

Times cited : (22)

References (4)

1
- 84881376726
- Advances in the genetics of Parkinson disease
- Epub 2013 Jul 16
- Trinh J., Farrer M. Advances in the genetics of Parkinson disease. Nat Rev Neurol. 2013 Aug, 9:445-454. Epub 2013 Jul 16.
- (2013) Nat Rev Neurol. , vol.9 , pp. 445-454
- Trinh, J.¹ Farrer, M.²

2
- 84860487766
- Adeleterious mutation in DNAJC6 encoding the neuronal-specific clathrin- uncoating co-chaperone auxilin, is associated with juvenile parkinsonism
- Edvardson S., Cinnamon Y., Ta-Shma A., Shaag A., Yim Y.I., Zenvirt S., Jalas C., Lesage S., Brice A., Taraboulos A., Kaestner K.H., Greene L.E., Elpeleg O. Adeleterious mutation in DNAJC6 encoding the neuronal-specific clathrin- uncoating co-chaperone auxilin, is associated with juvenile parkinsonism. PLoS ONE 2012, 7:e36458.
- (2012) PLoS ONE , vol.7
- Edvardson, S.¹ Cinnamon, Y.² Ta-Shma, A.³ Shaag, A.⁴ Yim, Y.I.⁵ Zenvirt, S.⁶ Jalas, C.⁷ Lesage, S.⁸ Brice, A.⁹ Taraboulos, A.¹⁰ Kaestner, K.H.¹¹ Greene, L.E.¹² Elpeleg, O.¹³

3
- 84876789790
- Recurrent mutations in DNAJC5 cause autosomal dominant Kufs disease
- Epub 2012 Nov 7
- Cadieux-Dion M., Andermann E., Lachance-Touchette P., Ansorge O., Meloche C., Barnabé A., Kuzniecky R.I., Andermann F., Faught E., Leonberg S., Damiano J.A., Berkovic S.F., Rouleau G.A., Cossette P. Recurrent mutations in DNAJC5 cause autosomal dominant Kufs disease. Clin Genet. 2013 Jun, 83:571-575. Epub 2012 Nov 7.
- (2013) Clin Genet. , vol.83 , pp. 571-575
- Cadieux-Dion, M.¹ Andermann, E.² Lachance-Touchette, P.³ Ansorge, O.⁴ Meloche, C.⁵ Barnabé, A.⁶ Kuzniecky, R.I.⁷ Andermann, F.⁸ Faught, E.⁹ Leonberg, S.¹⁰ Damiano, J.A.¹¹ Berkovic, S.F.¹² Rouleau, G.A.¹³ Cossette, P.¹⁴

4
- 0043122919
- SIFT: predicting amino acid changes that affect protein function
- Ng P.C., Henikoff S. SIFT: predicting amino acid changes that affect protein function. Nucleic Acids Res. 2013, 31:3812-3814.
- (2013) Nucleic Acids Res. , vol.31 , pp. 3812-3814
- Ng, P.C.¹ Henikoff, S.²

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.