88 related articles for article (PubMed ID: 19068596)
1. [Relationship between mutation at 1 573 fragment of TNF receptor II gene and keloid].
Zhang G; Fu J; Luo S; Tang S; Liang L
Zhongguo Xiu Fu Chong Jian Wai Ke Za Zhi; 2008 Nov; 22(11):1311-3. PubMed ID: 19068596
[TBL] [Abstract][Full Text] [Related]
2. [The relationship between RUNX3 gene mutation and keloid].
Zhang G; Jiang JJ; Luo SJ; Tang SM; Liang J; Yu Q
Zhonghua Zheng Xing Wai Ke Za Zhi; 2008 May; 24(3):224-7. PubMed ID: 18717361
[TBL] [Abstract][Full Text] [Related]
3. [Correlation analysis between clinical phenotypes of keloids and polymorphism of p53 gene codon 72].
Liu Y; Gao J; Liu X; Lu F; Liu H
Zhongguo Xiu Fu Chong Jian Wai Ke Za Zhi; 2008 Dec; 22(12):1433-6. PubMed ID: 19137883
[TBL] [Abstract][Full Text] [Related]
4. [Experimental study on p53 gene mutation in keloid fibroblasts].
Liu W; Jiang YH; Li YL; Lin ZH; Jiang H; Tan Q; Zhang JL; Wang ZM
Zhonghua Shao Shang Za Zhi; 2004 Apr; 20(2):85-7. PubMed ID: 15312469
[TBL] [Abstract][Full Text] [Related]
5. Analyses of CDC2L1 gene mutations in keloid tissue.
Zhang G; Jiang J; Luo S; Tang S; Liang J; Yao P
Clin Exp Dermatol; 2012 Apr; 37(3):277-83. PubMed ID: 22188294
[TBL] [Abstract][Full Text] [Related]
6. [Mutations in A((8)) and A((9)) loci of exon 8 of retinoblastoma protein-interacting zinc finger gene of keloid patients].
Fu JL; Zhang G; Liang J; Mei XC
Zhonghua Shao Shang Za Zhi; 2018 Sep; 34(9):643-647. PubMed ID: 30293369
[No Abstract] [Full Text] [Related]
7. Alport syndrome. Molecular genetic aspects.
Hertz JM
Dan Med Bull; 2009 Aug; 56(3):105-52. PubMed ID: 19728970
[TBL] [Abstract][Full Text] [Related]
8. [Frequencies of CGT52TGT, GGC54GAC and GGA57GAA point mutations in MBL gene in Chinese Uyghur population].
Zhong CQ; Yu XP; Wang FY; Kurexijiang T; Chen ZL
Nan Fang Yi Ke Da Xue Xue Bao; 2006 Dec; 26(12):1764-7. PubMed ID: 17259116
[TBL] [Abstract][Full Text] [Related]
9. Genetic susceptibility to keloid disease: mutation screening of the TGFbeta3 gene.
Bayat A; Walter JM; Bock O; Mrowietz U; Ollier WE; Ferguson MW
Br J Plast Surg; 2005 Oct; 58(7):914-21. PubMed ID: 16043141
[TBL] [Abstract][Full Text] [Related]
10. Quantification of the mRNA encoding Tumor Necrosis Factor alpha (TNFalpha) and its receptors in human nasal polyps.
Rostkowska-Nadolska B; Kapral M; Mazurek U; Fraczek M; Ziolkowski P; Gamian E
Adv Med Sci; 2008; 53(2):263-9. PubMed ID: 19095579
[TBL] [Abstract][Full Text] [Related]
11. Association of estrogen receptor beta gene polymorphisms with susceptibility to adolescent idiopathic scoliosis.
Zhang HQ; Lu SJ; Tang MX; Chen LQ; Liu SH; Guo CF; Wang XY; Chen J; Xie L
Spine (Phila Pa 1976); 2009 Apr; 34(8):760-4. PubMed ID: 19337134
[TBL] [Abstract][Full Text] [Related]
12. [Study on poly A site gene mutation of transforming growth factor-beta1 receptor type II between multiple and single site keloid].
Cai JL; An G; Xu B; Zhu GY; Fan SQ; Yan HS
Zhonghua Zheng Xing Wai Ke Za Zhi; 2006 Jan; 22(1):41-3. PubMed ID: 16573164
[TBL] [Abstract][Full Text] [Related]
13. [Mutation analysis of the SCN1A gene in severe myoclonic epilepsy of infancy].
Sun H; Zhang Y; Liu X; Ma X; Wu H; Xu K; Qin J; Qi Y; Wu X
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Apr; 26(2):121-7. PubMed ID: 19350499
[TBL] [Abstract][Full Text] [Related]
14. [Establishment of immortal lymphoblastoid cell bank of keloids pedigree].
Song M; Gao JH; Yan X; Liu XJ; Chen Y
Zhonghua Zheng Xing Wai Ke Za Zhi; 2006 Nov; 22(6):445-7. PubMed ID: 17286005
[TBL] [Abstract][Full Text] [Related]
15. [Identification of an ideal noninvasive method to detect A3243G gene mutation in MELAS syndrome].
Ma YN; Fang F; Yang YL; Zhang Y; Wang ST; Xu YF; Pei P; Yuan Y; Bu DF; Qi Y
Zhonghua Yi Xue Za Zhi; 2008 Dec; 88(46):3250-3. PubMed ID: 19159547
[TBL] [Abstract][Full Text] [Related]
16. Possible association of tumor necrosis factor receptor 2 gene polymorphism with severe hypertension using the extreme discordant phenotype design.
Eguchi T; Maruyama T; Ohno Y; Morii T; Hirao K; Hirose H; Kawabe H; Saito I; Hayashi M; Saruta T
Hypertens Res; 2009 Sep; 32(9):775-9. PubMed ID: 19557004
[TBL] [Abstract][Full Text] [Related]
17. An apparent inconsistency in parent to offspring transmission of point mutations of LDLR gene in familial hypercholesterolemia.
Rabacchi C; Wunsch A; Ghisellini M; Marino M; Pisciotta L; Bertolini S; Calandra S
Clin Chim Acta; 2009 Aug; 406(1-2):75-80. PubMed ID: 19467224
[TBL] [Abstract][Full Text] [Related]
18. [Application of PCR-DGGE technique in G-6-PD deficiency].
Li CG; Chen XW; Chen YS; Wang Y; Zhao WL; Shi HS; Li CR
Zhongguo Dang Dai Er Ke Za Zhi; 2007 Dec; 9(6):529-32. PubMed ID: 18082031
[TBL] [Abstract][Full Text] [Related]
19. [Detection and analysis of Fas gene (exon 1-6) mutations in keloids].
Liu YB; Gao JH; Duan HJ
Di Yi Jun Yi Da Xue Xue Bao; 2002 Jan; 22(1):61-3. PubMed ID: 12390849
[TBL] [Abstract][Full Text] [Related]
20. [A novel point mutation in NADH-cytochrome b5 reductase gene].
Wang Y; Wu Y; Yang W
Zhonghua Xue Ye Xue Za Zhi; 1999 Oct; 20(10):521-3. PubMed ID: 11721397
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
