[an error occurred while processing this directive] ����Ƥ���Բ�ѧ��־ 0, () 302-304 DOI:     ISSN: 2096-5540 CN: 32-1880/R

����Ŀ¼ | ����Ŀ¼ | ������� | �߼�����                                                            [��ӡ��ҳ]   [�ر�]
����
��չ����
������Ϣ
Supporting info
PDFȫ��
[HTMLȫ��]
�����
�����뷴��
�ѱ����Ƽ�������
�����ҵ����
�������ù�����
����
Email Alert
���·���
���������Ϣ
���Ĺؼ����������
ɫ�س����쳣
�����Ŵ�ѧ
����ͻ��
���������������
����
�����
PubMed
Article by
Article by

�Ŵ��ԶԳ���ɫ���쳣֢�����Ŵ�ѧ�о���չ

����, �����

�Ͼ�ҽ�ƴ�ѧ���������ڶ�ҽԺƤ���ơ������еڶ�����ҽԺƤ����, ��������214002

ժҪ��

�Ŵ��ԶԳ���ɫ���쳣֢��һ�ֽ�Ϊ�ټ��ij�Ⱦɫ�������Ŵ���Ƥ�������������ò��ķ����Ŵ�ѧ�о�ȡ���˺ܴ�Ľ�չ,�²�������ȷ��Ϊ1q11-q21�ϵ�ADAR����,�����IJ���ΪRNA�����������ʺ������Ѱ�ø�������ò����²�����λ��ADAR����Ľṹ���������IJ�������Լ�����ͻ���뼲������֮��Ĺ�ϵ��

�ؼ����� ɫ�س����쳣   �����Ŵ�ѧ   ����ͻ��  

Abstract:

Keywords:
�ո����� 2004-09-22 �޻�����  ����淢������  
DOI:
������Ŀ:

ͨѶ����:
���߼��:

�ο����ף�
[1] Oyama M, Shimizu H, Ohata Y, et al. Dyschromatosis symmetrica hereditaria (reticulate acropigmentation of Dohi):report of a Japanese family with the condition and a literature review of 185cases. Br J Dermatol, 1999,140:491-496.
[2] Urabe K, Hori Y. Dyschromatosis. Semin Cutan Med Surg, 1997,16:81-85.
[3] Alfadley A, Al Ajlan A, Hainau B, et al. Reticulate acropigmentation of Dohi:a case report of autosomal recessive inheritance. J Am Acad Derm, 2000, 43:113-117.
[4] He PP, He CD, Cui Y, et al. Refined localization of dyschromatosis symmetrica hereditaria gene to a 9.4--cM region at 1q21-22 and a literature review of 136 cases reported in China. Br J Dermatol,2004, 150:633-639.
[5] Patrizi A, Manneschi V, Pini A, et al. Dyschromatosis symmetrica hereditaria associated with idiopathic torsion dystonia. A case report. Acta Derm Venereol, 1994, 74:135-137.
[6] Kono M, Miyamura Y, Matsunaga J, et al. Exclusion of linkage between dyschromatosis symmetrica hereditaria and chromosome 9. J Dermatol Sci, 2000, 22:88-95.
[7] Zhang XJ, Gao M, Li M, et al. Identification of a locus for dyschromatosis symmetrica hereditaria at chromosome 1q11-1q21. J Invest Dermatol, 2003, 120:776-780.
[8] Xing QH, Wang MT, Chen XD, et al. A gene locus responsible for dyschromatosis symmetrica hereditaria (DSH) maps to chromosome 6q24.2-q25.2. Am J Hum Genet, 2003, 73:377-382.
[9] Miyamura Y, Suzuki T, Kono M, et al. Mutations of the RNA-specific adenosine deaminase gene (DSRAD) are involved in dyschromatosis symmetrica hereditaria. Am J Hum Genet, 2003, 73:693.
[10] Schade M, Turner CJ, Kuhne R, et al. The solution structure of the Zalpha domain of the human RNA editing enzyme ADAR1 reveals a prepositioned binding surface for Z-DNA. Proc Natl Acad Sci USA,1999, 96:12465-12470.
[11] Kim U, Wang Y, Sanford T, et al. Molecular cloning of cDNA for double-stranded RNA adenosine deaminase, a candidate enzyme for nuclear RNA editing. Proc Nat Acad Sci USA, 1994,91:11457-11461.
[12] Patterson JB, Samuel CE. Expression and regulation by interferon of a double-stranded-RNA-specific adenosine deaminase from human cells:evidence for two forms of the deaminase. Molec Cell Biol,1995,15:5376-5388.
[13] Weier HUG, George CX, Greulich KM, et al. The interferon-inducible, double-stranded RNA-specific adenosine deaminase gene(DSRAD) maps to human chromosome 1q21.1-21.2. Genomics,1995,30:372-375.
[14] O Connell MA, Krause S, Higuchi M, et al. Cloning of cDNAs encoding mammalian double-stranded RNA-specific adenosine deaminase. Molec Cell Biol, 1995, 15:1389-1397.
[15] Bass BL, Weintraub H. An unwinding activity that covalently modifies its double-stranded RNA substrate. Cell, 1988, 55:1089-1098.
[16] Morse DP. Identification of substrates for adenosine deaminases that act on RNA. Methods Mol Biol, 2004,265:199-218.
[17] Wang Q, Khillan J, Gadue P, et al. Requirement of the RNA editing deaminase ADAR1 gene for embryonic erythropoiesis. Science,2000, 290:1765-1768.
[18] Kawahara Y, Ito K,Sun H, et al. Regulation of glutamate receptor RNA editing and ADAR mRNA expression in developing human normal and Down's syndrome brains. Brain Res Dev, 2004, 148:151-155.
[19] Liu Q, Liu W, Jiang L, et al. Novel mutations of the RNA-specific adenosine deaminase gene (DSRAD) in Chinese families with dyschromatosis symmetrica hereditaria. J Invest Dermatol, 2004,122:896-899.
[20] Zhang XJ, He PP, Li M, et al. Seven novel mutations of the ADAR gene in Chinese families and sporadic patients with dyschromatosis symmetrica hereditaria (DSH). Hum Mutat, 2004, 23:629-630.
[21] Li M, Jiang YX, Liu JB, et al. A novel mutation of the DSRAD gene in a Chinese family with Dyschromatosis symmetrica hereditaria.Clin Exp Dermatol, 2004, 29:533-535.
�������������
1���¾�, ������.����ţ��ɫ��[J]. ����Ƥ���Բ�ѧ��־, 0,(): 357-359
2�����ٷ� ��Ϧ�� ��С�� �˺�.QY-520��Q����YAG��������ɫ����Ƥ������Ч�۲�[J]. ����Ƥ���Բ�ѧ��־, 2006,32(4): 264-264
3������, �����.�Ŵ��ԶԳ���ɫ���쳣֢�����Ŵ�ѧ�о���չ[J]. ����Ƥ���Բ�ѧ��־, 0,(): 302-304
4���¾�, ������.����ţ��ɫ��[J]. ����Ƥ���Բ�ѧ��־, 2007,33(6): 357-359
5������, �����.�Ŵ��ԶԳ���ɫ���쳣֢�����Ŵ�ѧ�о���չ[J]. ����Ƥ���Բ�ѧ��־, 2005,31(5): 302-304
6������, �����.������״ɫ���쳣�о���չ[J]. ����Ƥ���Բ�ѧ��־, 2007,33(3): 165-167

�������� (��ע��:��վʵ�������Ը�, �벻Ҫ������ѧ���޹ص�����!�������ݲ�����վ�۵�.)

Copyright 2008 by ����Ƥ���Բ�ѧ��־