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64 in total

1. Identification of a single nucleotide substitution in the coding sequence of in vitro amplified cDNA from a patient with partial HPRT deficiency (HPRTBRISBANE).

Authors: R B Gordon; D G Sculley; P A Dawson; I R Beacham; B T Emmerson
Journal: J Inherit Metab Dis Date: 1990 Impact factor: 4.982

2. Hypomutability in Fanconi anemia cells is associated with increased deletion frequency at the HPRT locus.

Authors: D Papadopoulo; C Guillouf; H Mohrenweiser; E Moustacchi
Journal: Proc Natl Acad Sci U S A Date: 1990-11 Impact factor: 11.205

3. Characterization of three new deletions at the 5' end of the HPRT structural gene.

Authors: M Wehnert; F H Herrmann
Journal: J Inherit Metab Dis Date: 1990 Impact factor: 4.982

Review 4. Towards in vivo amplification: Overcoming hurdles in the use of hematopoietic stem cells in transplantation and gene therapy.

Authors: Murtaza S Nagree; Lucía López-Vásquez; Jeffrey A Medin
Journal: World J Stem Cells Date: 2015-12-26 Impact factor: 5.326

5. Falling from grace: HPRT is not suitable as an endogenous control for cancer-related studies.

Authors: Michelle H Townsend; Abigail M Felsted; Zac E Ence; Stephen R Piccolo; Richard A Robison; Kim L O'Neill
Journal: Mol Cell Oncol Date: 2019-02-26

6. Nuclease sensitivity of the mouse HPRT gene promoter region: differential sensitivity on the active and inactive X chromosomes.

Authors: T P Yang; C T Caskey
Journal: Mol Cell Biol Date: 1987-08 Impact factor: 4.272

7. Combined preconditioning and in vivo chemoselection with 6-thioguanine alone achieves highly efficient reconstitution of normal hematopoiesis with HPRT-deficient bone marrow.

Authors: Katrin Hacke; Akos Szakmary; Andrew R Cuddihy; Nora Rozengurt; Nathan A Lemp; Jiri Aubrecht; Gregory W Lawson; Nagesh P Rao; Gay M Crooks; Robert H Schiestl; Noriyuki Kasahara
Journal: Exp Hematol Date: 2011-10-12 Impact factor: 3.084

8. Lesch-Nyhan syndrome: molecular investigation of three French Canadian families using a hypoxanthine-guanine phosphoribosyltransferase cDNA probe.

Authors: D Sinnett; L Lavergne; S B Melançon; L Dallaire; M Potier; D Labuda
Journal: Hum Genet Date: 1988-12 Impact factor: 4.132

Review 9. The mutational spectrum of single base-pair substitutions causing human genetic disease: patterns and predictions.

Authors: D N Cooper; M Krawczak
Journal: Hum Genet Date: 1990-06 Impact factor: 4.132

10. Characterization of a family of gamma-ray-induced CHO mutants demonstrates that the ldlA locus is diploid and encodes the low-density lipoprotein receptor.

Authors: R D Sege; K F Kozarsky; M Krieger
Journal: Mol Cell Biol Date: 1986-09 Impact factor: 4.272