Lopez C, Alseekh S, Martinez Rivas F, Fernie A, Prieto P, Alamillo J
J Exp Bot. 2024; 76(2):346-362.
PMID: 39387692
PMC: 11714751.
DOI: 10.1093/jxb/erae424.
Rashid I, Verma A, Tiwari P, DCruz S
J Bras Nefrol. 2022; 44(3):403-416.
PMID: 35635787
PMC: 9518620.
DOI: 10.1590/2175-8239-JBN-2021-0283en.
Kandpal R, Sandhu A, Kaur G, Kaur G, Athwal R
Cancer Genomics Proteomics. 2017; 14(2):93-101.
PMID: 28387649
PMC: 5369314.
DOI: 10.21873/cgp.20022.
Valaperta R, Rizzo V, Lombardi F, Verdelli C, Piccoli M, Ghiroldi A
BMC Nephrol. 2014; 15:102.
PMID: 24986359
PMC: 4094445.
DOI: 10.1186/1471-2369-15-102.
Marra G, Vercelloni P, Edefonti A, Manzoni G, Pavesi M, Fogazzi G
JIMD Rep. 2013; 5:45-8.
PMID: 23430916
PMC: 3509922.
DOI: 10.1007/8904_2011_92.
Adenine phosphoribosyltransferase deficiency in children.
Harambat J, Bollee G, Daudon M, Ceballos-Picot I, Bensman A
Pediatr Nephrol. 2012; 27(4):571-9.
PMID: 22212387
DOI: 10.1007/s00467-011-2037-0.
Ionizing radiation is a potent inducer of mitotic recombination in mouse embryonic stem cells.
Denissova N, Tereshchenko I, Cui E, Stambrook P, Shao C, Tischfield J
Mutat Res. 2011; 715(1-2):1-6.
PMID: 21802432
PMC: 3172342.
DOI: 10.1016/j.mrfmmm.2011.06.017.
Two families with compound heterozygosity for adenine phosphoribosyltransferase deficiency.
Iwaki T, Kusaka T, Ohashi I, Nishida T, Imai T, Itoh S
Pediatr Nephrol. 2010; 25(6):1173-6.
PMID: 20101413
DOI: 10.1007/s00467-009-1430-4.
APRT from erythrocytes of HGPRT deficient patients: kinetic, regulatory and thermostability properties.
Crespillo J, Llorente P, Argomaniz L, Montero C
Mol Cell Biochem. 2003; 254(1-2):359-63.
PMID: 14674717
DOI: 10.1023/a:1027323521969.
Embryonic stem cells and somatic cells differ in mutation frequency and type.
Cervantes R, Stringer J, Shao C, Tischfield J, Stambrook P
Proc Natl Acad Sci U S A. 2002; 99(6):3586-90.
PMID: 11891338
PMC: 122567.
DOI: 10.1073/pnas.062527199.
Detection of mutations in adenine phosphoribosyltransferase (APRT) deficiency using the LightCycler system.
Funato T, Nishiyama Y, Ioritani N, Matsuki R, Yoshida K, Kaku M
J Clin Lab Anal. 2001; 14(6):274-9.
PMID: 11138609
PMC: 6808163.
DOI: 10.1002/1098-2825(20001212)14:6<274::aid-jcla5>3.0.co;2-2.
Functional complementation by electroporation of human BACs into mammalian fibroblast cells.
Hejna J, Johnstone P, Kohler S, Bruun D, Reifsteck C, Olson S
Nucleic Acids Res. 1998; 26(4):1124-5.
PMID: 9461477
PMC: 147338.
DOI: 10.1093/nar/26.4.1124.
Loss of heterozygosity or: how I learned to stop worrying and love mitotic recombination.
Tischfield J
Am J Hum Genet. 1997; 61(5):995-9.
PMID: 9345110
PMC: 1716040.
DOI: 10.1086/301617.
Characterization of the biochemical basis of a complete deficiency of the adenine phosphoribosyl transferase (APRT).
Doppler W, Hirsch-Kauffmann M, Schabel F, Schweiger M
Hum Genet. 1981; 57(4):404-10.
PMID: 7286981
DOI: 10.1007/BF00281694.
Assignment to chromosome 16 of a gene necessary for the expression of human mitochondrial glutamate oxaloacetate transaminase (aspartate aminotransferase) (E.C. 2.6.1.1.).
Tolley E, Van Heyningen V, Brown R, Bobrow M, Craig I
Biochem Genet. 1980; 18(9-10):947-54.
PMID: 7225087
DOI: 10.1007/BF00500127.
Genetic instability at the adenine phosphoribosyltransferase locus in mouse L cells.
Tischfield J, Trill J, Lee Y, Coy K, Taylor M
Mol Cell Biol. 1982; 2(3):250-7.
PMID: 7110133
PMC: 369783.
DOI: 10.1128/mcb.2.3.250-257.1982.
Expression of human and mouse nonhistone chromosomal proteins in hybrid mouse erythroleukemia cells containing a single human chromosome.
Bode U, Deisseroth A, Hendrick D
Proc Natl Acad Sci U S A. 1981; 78(5):2815-9.
PMID: 6942405
PMC: 319448.
DOI: 10.1073/pnas.78.5.2815.
Interstitial deletion for a region in the long arm of chromosome 16.
Lin C, Lowry R, SNYDER F
Hum Genet. 1983; 65(2):134-8.
PMID: 6654327
DOI: 10.1007/BF00286649.
Suppression of vesicular stomatitis virus defective intefering particle generation by a function(s) associated with human chromosome 16.
Kang C, Weide L, Tischfield J
J Virol. 1981; 40(3):946-52.
PMID: 6275129
PMC: 256708.
DOI: 10.1128/JVI.40.3.946-952.1981.
Regional assignment of genes for human alpha-globin and phosphoglycollate phosphatase to the short arm of chromosome 16.
Koeffler H, Sparkes R, Stang H, Mohandas T
Proc Natl Acad Sci U S A. 1981; 78(11):7015-8.
PMID: 6273902
PMC: 349184.
DOI: 10.1073/pnas.78.11.7015.