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Differentiation properties of pure populations of human dystrophic muscle cells.
- H. Blau, C. Webster, C. Chiu, S. Guttman, F. Chandler
- Biology, Medicine
- Experimental cell research
- 1 April 1983
The interpretation of the majority of studies of Duchenne muscular dystrophy (DMD) has been complicated by the heterogeneous composition of the cultures used. In addition to muscle cells, muscle… Expand
Mutator genes of baby hamster kidney cells.
Two mutator genes of mammalian cells were demonstrated. One was associated with the ribonucleoside diphosphate reductase, and the other was associated with an extreme adenosine sensitivity.
Properties of ts Cl mouse L cells which exhibit temperature-sensitive DNA synthesis.
Abstract ts Cl mouse L cells are temperature-sensitive (ts) in DNA synthesis. The protein involved undergoes inactivation at 38.5 °C, with an apparent half-life of 3–4 h. A variety of experimental… Expand
Semi-conservative and non-conservative replication of DNA in temperature-sensitive mouse L-cells.
The mode of DNA replication has been studied in wild-type mouse L-cells (WT-4) and in two subclones (TS A1S9 and ts C1 cells) which are temperature-sensitive in DNA synthesis. It has been… Expand
An adenosine kinase mutation in baby hamster kidney cells causing increased sensitivity to adenosine.
- P. Juranka, F. Meffe, S. Guttman, S. Archer, V. Chan
- Biology, Medicine
- Mutation research
- 1 December 1984
A class of arabinosyladenine (araA)-resistant mutants of baby hamster kidney (BHK 21/C13) cells exhibits multiple phenotypes: resistance to araA and deoxyadenosine, extreme sensitivity to adenosine… Expand
In Vitro Generation of Epstein-Barr Virus–Specific Cytotoxic T Cells in Patients Receiving Haplo-Identical Allogeneic Stem Cell Transplantation
Use of a partially mismatched related donor (PMRD) is an option for patients who require allogeneic transplantation but do not have a matched sibling or unrelated donor. Epstein-Barr virus… Expand
The pathogenicity of SLC38A8 in five families with foveal hypoplasia and congenital nystagmus.
PURPOSE A recently described subtype of foveal hypoplasia with congenital nystagmus and optic-nerve-decussation defects was found to be associated with mutations in the SLC38A8 gene. The aim of this… Expand
Codominant and recessive 9-β-D-arabinofuranosyladenine-resistant mutation of baby hamster cells
Abstract 9-β- D -Arabinosyladenine (araA)-resistant mutants of baby hamster kidney (BHK) cells can be classified into 3 classes. In order to gain a better understanding of the mechanism(s) of… Expand
Codominant and recessive 9-beta-D-arabinofuranosyladenine-resistant mutations of baby hamster cells.
9-beta-D-Arabinosyladenine (araA)-resistant mutants of baby hamster kidney (BHK) cells can be classified into 3 classes. In order to gain a better understanding of the mechanism(s) of resistance and… Expand