-Philip J Mason Researcher Activity Profile

Research Author Detailed Information 

Philip J Mason Publication Rate By Year

Philip J Mason has published 1 paper(s) in 2006, 6 paper(s) in 2007, 3 paper(s) in 2008, for a total of 10 research publications in total.

Philip J Pj Mason Author Information

LAST NAME: mason

FIRST NAME: Philip J

INITIALS: pj

AFFILIATION:

Papers

Philip J Mason's Publication Record

1. A four base pair insertion in exon 1 of the RPS19 gene is a common polymorphism in African-Americans. Year Published: 2006
2. Cells depleted for RPS19, a protein associated with Diamond Blackfan Anemia, show defects in 18S ribosomal RNA synthesis and small ribosomal subunit production. Year Published: 2007
Department of Internal Medicine, Division of Hematology, Division of Laboratory Medicine, Washington University School of Medicine, 660 South Euclid Avenue, St. Louis, MO 63110, USA.
3. Dysfunctional telomeres and dyskeratosis congenita. Year Published: 2007
4. G6PD deficiency: the genotype-phenotype association. Year Published: 2007
Division of Hematology, Department of Internal Medicine, Washington University School of Medicine, Campus Box 8125, 660 South Euclid Avenue, St. Louis, MO 63110, USA. Pmason@im.wustl.edu
5. Telomerase reverse transcriptase haploinsufficiency and telomere length in individuals with 5p- syndrome. Year Published: 2007
Department of Internal Medicine, Washington Uiversity School of Medicine, 660 S Euclid Avenue, St. Louis, MO 63110, USA.
6. Telomerase reverse transcriptase haploinsufficiency and telomere length in individuals with 5p- syndrome. Year Published: 2007
Department of Internal Medicine, Washington Uiversity School of Medicine, 660 S Euclid Avenue, St. Louis, MO 63110, USA.
7. G6PD deficiency: the genotype-phenotype association. Year Published: 2007
Division of Hematology, Department of Internal Medicine, Washington University School of Medicine, Campus Box 8125, 660 South Euclid Avenue, St. Louis, MO 63110, USA. Pmason@im.wustl.edu
8. Complex inheritance pattern of dyskeratosis congenita in two families with 2 different mutations in the telomerase reverse transcriptase gene. Year Published: 2008
9. Identification of ATPases pontin and reptin as telomerase components essential for holoenzyme assembly. Year Published: 2008
Department of Medicine, Stanford School of Medicine, Stanford, CA 94305, USA.
10. Complex inheritance pattern of dyskeratosis congenita in two families with 2 different mutations in the telomerase reverse transcriptase gene. Year Published: 2008
Department of Internal Medicine, Washington University School of Medicine, St Louis, MO 63110, USA.