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.
79 related articles for article (PubMed ID: 1976239)
1. Disruption of phase during PCR amplification and cloning of heterozygous target sequences. Jansen R; Ledley FD Nucleic Acids Res; 1990 Sep; 18(17):5153-6. PubMed ID: 1976239 [TBL] [Abstract][Full Text] [Related]
2. Cloning of full-length methylmalonyl-CoA mutase from a cDNA library using the polymerase chain reaction. Jansen R; Kalousek F; Fenton WA; Rosenberg LE; Ledley FD Genomics; 1989 Feb; 4(2):198-205. PubMed ID: 2567699 [TBL] [Abstract][Full Text] [Related]
3. Heterozygous mutations at the mut locus in fibroblasts with mut0 methylmalonic acidemia identified by polymerase-chain-reaction cDNA cloning. Jansen R; Ledley FD Am J Hum Genet; 1990 Nov; 47(5):808-14. PubMed ID: 1977311 [TBL] [Abstract][Full Text] [Related]
4. Structure of the human methylmalonyl-CoA mutase (MUT) locus. Nham SU; Wilkemeyer MF; Ledley FD Genomics; 1990 Dec; 8(4):710-6. PubMed ID: 1980486 [TBL] [Abstract][Full Text] [Related]
5. Mutation eliminating mitochondrial leader sequence of methylmalonyl-CoA mutase causes muto methylmalonic acidemia. Ledley FD; Jansen R; Nham SU; Fenton WA; Rosenberg LE Proc Natl Acad Sci U S A; 1990 Apr; 87(8):3147-50. PubMed ID: 1970180 [TBL] [Abstract][Full Text] [Related]
6. Mapping of human methylmalonyl CoA mutase (MUT) locus on chromosome 6. Ledley FD; Lumetta MR; Zoghbi HY; VanTuinen P; Ledbetter SA; Ledbetter DH Am J Hum Genet; 1988 Jun; 42(6):839-46. PubMed ID: 2897160 [TBL] [Abstract][Full Text] [Related]
7. Inherited methylmalonyl CoA mutase apoenzyme deficiency in human fibroblasts: evidence for allelic heterogeneity, genetic compounds, and codominant expression. Willard HF; Rosenberg LE J Clin Invest; 1980 Mar; 65(3):690-8. PubMed ID: 6101601 [TBL] [Abstract][Full Text] [Related]
8. Cloning and structural characterization of the genes coding for adenosylcobalamin-dependent methylmalonyl-CoA mutase from Propionibacterium shermanii. Marsh EN; McKie N; Davis NK; Leadlay PF Biochem J; 1989 Jun; 260(2):345-52. PubMed ID: 2569861 [TBL] [Abstract][Full Text] [Related]
9. Molecular cloning of L-methylmalonyl-CoA mutase: gene transfer and analysis of mut cell lines. Ledley FD; Lumetta M; Nguyen PN; Kolhouse JF; Allen RH Proc Natl Acad Sci U S A; 1988 May; 85(10):3518-21. PubMed ID: 2453061 [TBL] [Abstract][Full Text] [Related]
10. Restriction fragment length polymorphisms at the methylmalonyl CoA mutase locus in normal Chinese. Wang TR; Hou JW; Tsai HM Zhonghua Min Guo Xiao Er Ke Yi Xue Hui Za Zhi; 1990; 31(5):275-9. PubMed ID: 1979711 [TBL] [Abstract][Full Text] [Related]
11. Perspectives on methylmalonic acidemia resulting from molecular cloning of methylmalonyl CoA mutase. Ledley FD Bioessays; 1990 Jul; 12(7):335-40. PubMed ID: 1975493 [TBL] [Abstract][Full Text] [Related]
12. Characterization and rapid analysis of the highly polymorphic VNTR locus D4S125 (YNZ32), closely linked to the Huntington disease gene. Richards B; Horn GT; Merrill JJ; Klinger KW Genomics; 1991 Feb; 9(2):235-40. PubMed ID: 1672295 [TBL] [Abstract][Full Text] [Related]
13. Localization of the murine methylmalonyl CoA mutase (Mut) locus on chromosome 17 by in situ hybridization. Threadgill DW; Wilkmeyer M; Womack JE; Ledley FD Cytogenet Cell Genet; 1990; 53(2-3):112-4. PubMed ID: 1973376 [TBL] [Abstract][Full Text] [Related]
14. Amplification of human polymorphic sites in the X-chromosomal region q21.33 to q24: DXS17, DXS87, DXS287, and alpha-galactosidase A. Kornreich R; Astrin KH; Desnick RJ Genomics; 1992 May; 13(1):70-4. PubMed ID: 1349583 [TBL] [Abstract][Full Text] [Related]
15. Molecular basis for dysfunction of some mutant forms of methylmalonyl-CoA mutase: deductions from the structure of methionine synthase. Drennan CL; Matthews RG; Rosenblatt DS; Ledley FD; Fenton WA; Ludwig ML Proc Natl Acad Sci U S A; 1996 May; 93(11):5550-5. PubMed ID: 8643613 [TBL] [Abstract][Full Text] [Related]
16. Thiopurine methyltransferase pharmacogenetics: human gene cloning and characterization of a common polymorphism. Szumlanski C; Otterness D; Her C; Lee D; Brandriff B; Kelsell D; Spurr N; Lennard L; Wieben E; Weinshilboum R DNA Cell Biol; 1996 Jan; 15(1):17-30. PubMed ID: 8561894 [TBL] [Abstract][Full Text] [Related]
17. Effects of ionizing radiation on a plant genome: analysis of two Arabidopsis transparent testa mutations. Shirley BW; Hanley S; Goodman HM Plant Cell; 1992 Mar; 4(3):333-47. PubMed ID: 1354004 [TBL] [Abstract][Full Text] [Related]
19. Detection of a new polymorphism of the human prothrombin (F2) gene by combination of PASA and mutated primer-mediated PCR-RFLP. Iwahana H; Mizusawa N; Yoshimoto K; Itakura M Hum Genet; 1992 Nov; 90(3):325-6. PubMed ID: 1362561 [TBL] [Abstract][Full Text] [Related]
20. PCR-based cloning and segregation analysis of functional gene homologues in Beta vulgaris. Schneider K; Borchardt DC; Schäfer-Pregl R; Nagl N; Glass C; Jeppsson A; Gebhardt C; Salamini F Mol Gen Genet; 1999 Oct; 262(3):515-24. PubMed ID: 10589840 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]