102 related articles for article (PubMed ID: 1339400)
1. Alpha-1-antichymotrypsin variant detected by PCR-single strand conformation polymorphism (PCR-SSCP) and direct sequencing.
Tsuda M; Sei Y; Matsumoto M; Kamiguchi H; Yamamoto M; Shinohara Y; Igarashi T; Yamamura M
Hum Genet; 1992 Dec; 90(4):467-8. PubMed ID: 1339400
[TBL] [Abstract][Full Text] [Related]
2. Detection of a new mutant alpha-1-antichymotrypsin in patients with occlusive-cerebrovascular disease.
Tsuda M; Sei Y; Yamamura M; Yamamoto M; Shinohara Y
FEBS Lett; 1992 Jun; 304(1):66-8. PubMed ID: 1618300
[TBL] [Abstract][Full Text] [Related]
3. Genetic variation in alpha(1)-antichymotrypsin and its association with Alzheimer's disease.
Wang X; DeKosky ST; Luedecking-Zimmer E; Ganguli M; Kamboh MI
Hum Genet; 2002 Apr; 110(4):356-65. PubMed ID: 11941486
[TBL] [Abstract][Full Text] [Related]
4. The molecular basis of alpha 1-antichymotrypsin deficiency in a heterozygote with liver and lung disease.
Faber JP; Poller W; Olek K; Baumann U; Carlson J; Lindmark B; Eriksson S
J Hepatol; 1993 Jul; 18(3):313-21. PubMed ID: 8228125
[TBL] [Abstract][Full Text] [Related]
5. Direct cycle sequencing of mutated alleles detected by PCR single-strand conformation polymorphism analysis.
Mok SC; Lo KW; Tsao SW
Biotechniques; 1993 May; 14(5):790-4. PubMed ID: 8512704
[TBL] [Abstract][Full Text] [Related]
6. The defective secretion of a naturally occurring alpha-1-antichymotrypsin variant with a frameshift mutation.
Tsuda M; Sei Y; Ohkubo T; Yamamura M; Kamiguchi H; Akatsuka A; Tsuda T; Tachikawa H; Yamamoto M; Shinohara Y
Eur J Biochem; 1996 Feb; 235(3):821-7. PubMed ID: 8654434
[TBL] [Abstract][Full Text] [Related]
7. A leucine-to-proline substitution causes a defective alpha 1-antichymotrypsin allele associated with familial obstructive lung disease.
Poller W; Faber JP; Weidinger S; Tief K; Scholz S; Fischer M; Olek K; Kirchgesser M; Heidtmann HH
Genomics; 1993 Sep; 17(3):740-3. PubMed ID: 8244391
[TBL] [Abstract][Full Text] [Related]
8. Mutation of tumor suppressor gene p53 is frequently found in vulvar carcinoma cells.
Hietanen SH; Kurvinen K; Syrjänen K; Grénman S; Carey T; McClatchey K; Syrjänen S
Am J Obstet Gynecol; 1995 Nov; 173(5):1477-82. PubMed ID: 7503188
[TBL] [Abstract][Full Text] [Related]
9. A novel porcine gene, alpha-1-antichymotrypsin 2 (SERPINA3-2): sequence, genomic organization, polymorphism and mapping.
Stratil A; Peelman LJ; Mattheeuws M; Van Poucke M; Reiner G; Geldermann H
Gene; 2002 Jun; 292(1-2):113-9. PubMed ID: 12119105
[TBL] [Abstract][Full Text] [Related]
10. Genetic basis and carrier detection of hemophilia B of Chinese origin.
Lin SW; Shen MC
Thromb Haemost; 1993 Mar; 69(3):247-52. PubMed ID: 8470048
[TBL] [Abstract][Full Text] [Related]
11. Molecular scanning of insulin-responsive glucose transporter (GLUT4) gene in NIDDM subjects.
Choi WH; O'Rahilly S; Buse JB; Rees A; Morgan R; Flier JS; Moller DE
Diabetes; 1991 Dec; 40(12):1712-8. PubMed ID: 1756912
[TBL] [Abstract][Full Text] [Related]
12. Characterization of genetic defects of hemophilia A in patients of Chinese origin.
Lin SW; Lin SR; Shen MC
Genomics; 1993 Dec; 18(3):496-504. PubMed ID: 8307558
[TBL] [Abstract][Full Text] [Related]
13. Search for mutations in the beta 1 GABAA receptor subunit gene in patients with schizophrenia.
Coon H; Sobell J; Heston L; Sommer S; Hoff M; Holik J; Umar F; Robertson M; Reimherr F; Wender P
Am J Med Genet; 1994 Mar; 54(1):12-20. PubMed ID: 8178835
[TBL] [Abstract][Full Text] [Related]
14. Detection of a single base substitution of the gene for prothrombin Tokushima. The application of PCR-SSCP for the genetic and molecular analysis of dysprothrombinemia.
Iwahana H; Yoshimoto K; Shigekiyo T; Shirakami A; Saito S; Itakura M
Int J Hematol; 1992 Feb; 55(1):93-100. PubMed ID: 1349838
[TBL] [Abstract][Full Text] [Related]
15. Mutational analysis by a combined application of the multiple restriction fragment-single strand conformation polymorphism and the direct linear amplification DNA sequencing protocols.
Lee HH; Lo WJ; Choo KB
Anal Biochem; 1992 Sep; 205(2):289-93. PubMed ID: 1443575
[TBL] [Abstract][Full Text] [Related]
16. Double strand conformation polymorphism (DSCP) detects two point mutations at codon 280 (AAC-->ATC) and at codon 431 (TAC-->AAC) of the blood coagulation factor VIII gene.
Pieneman WC; Reitsma PH; Briët E
Thromb Haemost; 1993 May; 69(5):473-5. PubMed ID: 8322269
[TBL] [Abstract][Full Text] [Related]
17. Detection of p53 gene mutations in human ovarian and endometrial cancers by polymerase chain reaction-single strand conformation polymorphism analysis.
Naito M; Satake M; Sakai E; Hirano Y; Tsuchida N; Kanzaki H; Ito Y; Mori T
Jpn J Cancer Res; 1992 Oct; 83(10):1030-6. PubMed ID: 1333465
[TBL] [Abstract][Full Text] [Related]
18. Mutations in the p53 gene in human astrocytomas: detection by single-strand conformation polymorphism analysis and direct DNA sequencing.
Hunter SB; Bandea C; Swan D; Abbott K; Varma VA
Mod Pathol; 1993 Jul; 6(4):442-5. PubMed ID: 8415589
[TBL] [Abstract][Full Text] [Related]
19. Microsatellite polymorphism of the alpha 1-antichymotrypsin gene locus associated with sporadic Alzheimer's disease.
Morgan K; Morgan L; Carpenter K; Lowe J; Lam L; Cave S; Xuereb J; Wischik C; Harrington C; Kalsheker NA
Hum Genet; 1997 Jan; 99(1):27-31. PubMed ID: 9003488
[TBL] [Abstract][Full Text] [Related]
20. A rapid method for detection of mutations in the lacI gene using PCR-single strand conformation polymorphism analysis: demonstration of its high sensitivity.
Ushijima T; Hosoya Y; Suzuki T; Sofuni T; Sugimura T; Nagao M
Mutat Res; 1995 Jun; 334(3):283-92. PubMed ID: 7753092
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
