Citations for
1TPI1
Sequencing and genotypic analysis of the triosephosphate isomerase (TPI1) locus in a large sample of long-lived Germans.
Ralser M, Nebel A, Kleindorp R, Krobitsch S, Lehrach H, Schreiber S, Reinhardt R, Timmermann B.
BMC Genet 9:38. 2008
2TPI1, TPI1D
Triosephosphate isomerase deficiency: facts and doubts.
Orosz F, Oláh J, Ovádi J.
IUBMB Life 58(12):703-15. Review.PMID: 17424909 [PubMed - indexed for MEDLINE] 2006
3TPI1, TPI1D
Triosephosphate isomerase deficiency: consequences of an inherited mutation at mRNA, protein and metabolic levels.
Oláh J, Orosz F, Puskás LG, Hackler L Jr, Horányi M, Polgár L, Hollán S, Ovádi J.
Biochem J 392(Pt 3):675-83. 2005
4TPI1, TPI1D
Identical germ-line mutations in the triosephosphate isomerase alleles of two brothers are associated with distinct clinical phenotypes.
Valentin C, Cohen-Solal M, Maquat L, Horanyi M, Inselt-Kovacs M, Hollan S.
C R Acad Sci III 323(3):245-50. 2000
5DST2, RNU7, RPL13B, TPI1
Large-scale sequencing in human chromosome 12p13 : experimental and computational gene structure determination.
Ansari-Lari MA, et al.
Genome Res 7(3):268-80 1997
6TPI1, TPI1D
Evidence for founder effect of the Glu104Asp substitution and identification of new mutations in triosephosphate isomerase deficiency.
Arya R, Lalloz MR, Bellingham AJ, Layton DM.
Hum Mutat 10(4):290-4. 1997
7TPI1, TPI1D
Molecular analysis of a series of alleles in humans with reduced activity at the triosephosphate isomerase locus.
Watanabe M, et al.
Am J Hum Genet 58 : 308-316. 1996
8C12orf57, CD4, EMG1, GNB3, GPR162, LEPREL2, LPCAT3, PHB2, SPSB2, TPI1, USP5
A gene-rich cluster between the CD4 and triosephosphate isomerase genes at human chromosome 12p13.
Ansari-Lari MA, Muzny DM, Lu J, Lu F, Lilley CE, Spanos S, Malley T, GibbsRA.
Genome Res 6(4):314-26. 1996
9TPI1, TPI1D
Triosephosphate isomerase deficiency : repetitive occurence of point mutation in amino acid 104 in multiple apparently unrelated families.
Schneider A, et al.
Am J Hematol 50 : 263-268. 1995
10TPI1
Molecular analysis of triosephosphate isomerase mutants with reduced enzyme activity in humans and Mice. (abstr)
Zingg BC, et al.
Am J Hum Genet 55 : A252. 1994
11TPI1
Human triosephosphate isomerase deficiency resulting from mutation of the Phe-240.
Chang ML, et al.
Am J Hum Genet 52 : 1260-1269. 1993
12TPI1
Human triosephosphate isomerase : substitution of Arg for Gly at position 122 in a thermolabile electromorph variant, TPI-Manchester.
Perry BA, et al.
Hum Genet 88 : 634-638. 1992
13TPI1
Human triose-phosphate isomerase deficiency : a single amino acid substitution results in a thermolabile enzyme.
Daar IO, et al.
Proc Natl Acad Sci U S A 83 : 7903-7907. 1986
14PEPB, SHMT2, TPI1
Regional assignment of human genes TPI1, GAPDH, LDHb, SHMT, and PEPB on chromosome 12.
Law ML, et al.
Cytogenet Cell Genet 24 : 102-104. 1979
15PEPB, SHMT2, TPI1
Regional assignment on human chromosome 12 of seven genes TPI1, TPI2, GAPD, LDHB, ENO2, SHMT, and PEPB.
Law ML, et al.
Cytogenet Cell Genet 25 : 179-180. 1979
16PEPB, TPI1, LDHB
Regional mapping of TPI, LDH-B, and Pep-B on chromosome 12 of man.
Jongsma APM, et al.
Cytogenet Cell Genet 14 : 189-191. 1975
17TPI1
Synteny relationships of four human genes: mannose phosphate isomerase to pyruvate kinase-3 and triose phosphate isomerase to lactate dehydrogenase-B.
Kucherlapati RS, et al.
Cytogenet Cell Genet 14 : 194-197. 1975
18PEPB, TPI1, LDHB
Evidence for synteny between the human loci for triose phosphate isomerase, lactase dehydrogenase-B, and peptidase-B and the regional mapping of these loci on chromosome 12.
Jongsma APM, et al.
Cytogenet Cell Genet 13 : 106-107. 1974
19TPI1, TPI1D
Hereditary hemolytic anemia with triosephosphate isomerase deficiency.
Schneider AS, et al.
N Engl J Med 272 : 229-235. 1965