-Monica Bessler Researcher Activity Profile

Research Author Detailed Information 

Monica Bessler Publication Rate By Year

Monica Bessler has published 1 paper(s) in 2006, 7 paper(s) in 2007, 4 paper(s) in 2008, for a total of 12 research publications in total.

Monica M Bessler Author Information

LAST NAME: bessler

FIRST NAME: monica

INITIALS: M

AFFILIATION:

Papers

Monica Bessler'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. 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.
5. Effect of the complement inhibitor eculizumab on thromboembolism in patients with paroxysmal nocturnal hemoglobinuria. Year Published: 2007
6. Effect of the complement inhibitor eculizumab on thromboembolism in patients with paroxysmal nocturnal hemoglobinuria. Year Published: 2007
Leeds General Infirmary, Leeds, United Kingdom. peter.hillmen@nhs.net
7. 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.
8. Effect of the complement inhibitor eculizumab on thromboembolism in patients with paroxysmal nocturnal hemoglobinuria. Year Published: 2007
Leeds General Infirmary, Leeds, United Kingdom. peter.hillmen@nhs.net
9. Complex inheritance pattern of dyskeratosis congenita in two families with 2 different mutations in the telomerase reverse transcriptase gene. Year Published: 2008
10. Multicenter phase 3 study of the complement inhibitor eculizumab for the treatment of patients with paroxysmal nocturnal hemoglobinuria. Year Published: 2008
11. Multicenter phase 3 study of the complement inhibitor eculizumab for the treatment of patients with paroxysmal nocturnal hemoglobinuria. Year Published: 2008
Johns Hopkins School of Medicine, Baltimore, MD 21205, USA. brodsro@jhmi.edu
12. 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.