These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
Pubmed for Handhelds
PUBMED FOR HANDHELDS
Journal Abstract Search
186 related items for PubMed ID: 16814390
1. Screening of alpha-1-antitrypsin gene by denaturing gradient gel electrophoresis (DGGE). Ljujic M, Nikolic A, Divac A, Djordjevic V, Radojkovic D. J Biochem Biophys Methods; 2006 Oct 31; 68(3):167-73. PubMed ID: 16814390 [Abstract] [Full Text] [Related]
2. Mutation detection in the alpha-1 antitrypsin gene (PI) using denaturing gradient gel electrophoresis. Lodewyckx L, Vandevyver C, Vandervorst C, Van Steenbergen W, Raus J, Michiels L. Hum Mutat; 2001 Sep 31; 18(3):243-50. PubMed ID: 11524735 [Abstract] [Full Text] [Related]
3. Denaturing gradient gel electrophoresis of the alpha 1-antitrypsin gene: application to prenatal diagnosis. Dubel JR, Finwick R, Hejtmancik JF. Am J Med Genet; 1991 Oct 01; 41(1):39-43. PubMed ID: 1951462 [Abstract] [Full Text] [Related]
4. Isoelectric focusing phenotyping and denaturing gradient gel electrophoresis genotyping: a comparison of two methods in detection of alpha-1-antitrypsin variants. Ljujic M, Topic A, Divac A, Nikolic A, Petrovic-Stanojevic N, Surlan M, Mitic-Milikic M, Radojkovic D. Transl Res; 2008 May 01; 151(5):255-9. PubMed ID: 18433707 [Abstract] [Full Text] [Related]
5. Detection of the common alpha-1-antitrypsin variants by denaturing gradient gel electrophoresis. Johnson PH, Cadiou H, Hopkinson DA. Ann Hum Genet; 1991 Jul 01; 55(3):183-98. PubMed ID: 1684891 [Abstract] [Full Text] [Related]
6. Single-step DGGE-based mutation scanning of the p53 gene: application to genetic diagnosis of colorectal cancer. Guldberg P, Nedergaard T, Nielsen HJ, Olsen AC, Ahrenkiel V, Zeuthen J. Hum Mutat; 1997 Jul 01; 9(4):348-55. PubMed ID: 9101296 [Abstract] [Full Text] [Related]
7. Immunohistochemical and genetic characterization of the M Cagliari alpha-1-antitrypsin molecule (M-like alpha-1-antitrypsin deficiency). Sergi C, Consalez GG, Fabbretti G, Brisigotti M, Faa G, Costa V, Romeo G, Callea F. Lab Invest; 1994 Jan 01; 70(1):130-3. PubMed ID: 8302013 [Abstract] [Full Text] [Related]
8. Mutation detection by denaturing gradient gel electrophoresis (DGGE). Fodde R, Losekoot M. Hum Mutat; 1994 Jan 01; 3(2):83-94. PubMed ID: 8199599 [Abstract] [Full Text] [Related]
9. Rapid and inexpensive detection of alpha1-antitrypsin deficiency-related alleles S and Z by a real-time polymerase chain reaction suitable for a large-scale population-based screening. Kaczor MP, Sanak M, Szczeklik A. J Mol Diagn; 2007 Feb 01; 9(1):99-104. PubMed ID: 17251342 [Abstract] [Full Text] [Related]
10. Ribonuclease A cleavage combined with the polymerase chain reaction for detection of the Z mutation of the alpha-1-antitrypsin gene. Abe T, Takahashi H, Holmes MD, Curiel DT, Crystal RG. Am J Respir Cell Mol Biol; 1989 Oct 01; 1(4):329-34. PubMed ID: 2624766 [Abstract] [Full Text] [Related]
11. An alpha-1 antitrypsin genetic variant from India. Shasany AK, Shukla AK, Darokar MP, Saraiya M, Chaturvedi N, Tewari L, Khanuja SP. Indian J Biochem Biophys; 2007 Jun 01; 44(3):176-8. PubMed ID: 17650587 [Abstract] [Full Text] [Related]
12. Assessing high-resolution melt curve analysis for accurate detection of gene variants in complex DNA fragments. Tindall EA, Petersen DC, Woodbridge P, Schipany K, Hayes VM. Hum Mutat; 2009 Jun 01; 30(6):876-83. PubMed ID: 19280649 [Abstract] [Full Text] [Related]
13. Rapid and efficient molecular analysis of gyrate atrophy using denaturing gradient gel electrophoresis. Mashima Y, Shiono T, Inana G. Invest Ophthalmol Vis Sci; 1994 Mar 01; 35(3):1065-70. PubMed ID: 8125717 [Abstract] [Full Text] [Related]
14. Genetic control of human alpha-1-antitrypsin. Sifers RN, Shen RF, Woo SL. Mol Biol Med; 1989 Apr 01; 6(2):127-35. PubMed ID: 2693888 [Abstract] [Full Text] [Related]
15. Correcting the PiZ defect in the alpha 1-antitrypsin gene of human cells by targeted homologous recombination. Savransky E, Hytiroglou P, Harpaz N, Thung SN, Johnson EM. Lab Invest; 1994 May 01; 70(5):676-83. PubMed ID: 8196364 [Abstract] [Full Text] [Related]
16. Use of the denaturing gradient gel electrophoresis (DGGE) method for mutational screening of patients with familial hypercholesterolaemia (FH) and Familial defective apolipoprotein B100 (FDB). Azian M, Hapizah MN, Khalid BA, Khalid Y, Rosli A, Jamal R. Malays J Pathol; 2006 Jun 01; 28(1):7-15. PubMed ID: 17694954 [Abstract] [Full Text] [Related]
17. Alport syndrome. Molecular genetic aspects. Hertz JM. Dan Med Bull; 2009 Aug 01; 56(3):105-52. PubMed ID: 19728970 [Abstract] [Full Text] [Related]
18. Analysis of TP53 gene mutations in human lung cancer: comparison of capillary electrophoresis single strand conformation polymorphism assay with denaturing gradient gel electrophoresis and direct sequencing. Holmila R, Husgafvel-Pursiainen K. Cancer Detect Prev; 2006 Aug 01; 30(1):1-6. PubMed ID: 16458448 [Abstract] [Full Text] [Related]
19. Misclassification of an apparent alpha 1-antitrypsin "Z" deficiency variant by melting analysis. Greene DN, Procter M, Grenache DG, Lyon E, Bornhorst JA, Mao R. Clin Chim Acta; 2011 Jul 15; 412(15-16):1454-6. PubMed ID: 21497588 [Abstract] [Full Text] [Related]