| A novel role for reciprocal CD30-CD30L signaling in the cross-talk between natural killer and dendritic cells. Simhadri V.L., Hansen H.P., Simhadri V.R., Reiners K.S., Bessler M., Engert A., von Strandmann E.P.
Biol. Chem. 393:101-106(2012) · Mapped (7) |
| 3'UTR-truncated Hmga2 cDNA causes MPN-like hematopoiesis by conferring a clonal growth advantage at the level of HSC in mice. Ikeda K., Mason P.J., Bessler M.
Blood 117:5860-5869(2011) · Mapped (7) |
| SnoRNA microarray analysis reveals changes in H/ACA and C/D RNA levels caused by dyskerin ablation in mouse liver. Ge J., Crosby S.D., Heinz M.E., Bessler M., Mason P.J.
Biochem. J. 429:33-41(2010) · Mapped (8) |
| Dyskerin ablation in mouse liver inhibits rRNA processing and cell division. Ge J., Rudnick D.A., He J., Crimmins D.L., Ladenson J.H., Bessler M., Mason P.J.
Mol. Cell. Biol. 30:413-422(2010) · Mapped (8) |
| Anomalous electrophoretic migration of newly synthesized ribosomal RNAs and their precursors from cells with DKC1 mutations. Gu B.W., Zhao C., Fan J.M., Dai Q., Bessler M., Mason P.J.
FEBS Lett. 583:3086-3090(2009) · Mapped (8) |
| Variable expression of Dkc1 mutations in mice. He J., Gu B.W., Ge J., Mochizuki Y., Bessler M., Mason P.J.
Genesis 47:366-373(2009) · Mapped (8) |
| TINF2 mutations in children with severe aplastic anemia. Du H.Y., Mason P.J., Bessler M., Wilson D.B.
Pediatr Blood Cancer 52:687-687(2009) · Mapped (5) |
| The role of human ribosomal proteins in the maturation of rRNA and ribosome production. Robledo S., Idol R.A., Crimmins D.L., Ladenson J.H., Mason P.J., Bessler M.
RNA 14:1918-1929(2008) |
| A pathogenic dyskerin mutation impairs proliferation and activates a DNA damage response independent of telomere length in mice. Gu B.W., Bessler M., Mason P.J.
Proc. Natl. Acad. Sci. U.S.A. 105:10173-10178(2008) · Mapped (24) |
| Complex inheritance pattern of dyskeratosis congenita in two families with 2 different mutations in the telomerase reverse transcriptase gene. Du H.Y., Pumbo E., Manley P., Field J.J., Bayliss S.J., Wilson D.B., Mason P.J., Bessler M.
Blood 111:1128-1130(2008) · UniProtKB (1) |
| A four base pair insertion in exon 1 of the RPS19 gene is a common polymorphism in African-Americans. Huang Q., Robledo S., Wilson D.B., Bessler M., Mason P.J.
Br. J. Haematol. 135:745-746(2006) · Mapped (3) |
| G-CSF induced progenitor mobilization in mice with PIGA- blood cells. Han B., Unsinger J., Liu F., Link D.C., Bessler M.
Hematol. J. 5:347-352(2004) · Mapped (6) |
| Mutations of the SBDS gene are present in most patients with Shwachman-Diamond syndrome. Woloszynek J.R., Rothbaum R.J., Rawls A.S., Minx P.J., Wilson R.K., Mason P.J., Bessler M., Link D.C.
Blood 104:3588-3590(2004) · Mapped (1) |
| Mouse dyskerin mutations affect accumulation of telomerase RNA and small nucleolar RNA, telomerase activity, and ribosomal RNA processing. Mochizuki Y., He J., Kulkarni S., Bessler M., Mason P.J.
Proc. Natl. Acad. Sci. U.S.A. 101:10756-10761(2004) · UniProtKB (1) · Mapped (7) |
| The effect of GPI-anchor deficiency on apoptosis in mice carrying a Piga gene mutation in hematopoietic cells. Kulkarni S., Bessler M.
J. Leukoc. Biol. 72:1228-1233(2002) · Mapped (6) |
| Targeted disruption of Dkc1, the gene mutated in X-linked dyskeratosis congenita, causes embryonic lethality in mice. He J., Navarrete S., Jasinski M., Vulliamy T., Dokal I., Bessler M., Mason P.J.
Oncogene 21:7740-7744(2002) · Mapped (8) |
| Plasma from patients undergoing major open surgery stimulates in vitro tumor growth: Lower insulin-like growth factor binding protein 3 levels may, in part, account for this change. Kirman I., Cekic V., Poltaratskaia N., Asi Z., Bessler M., Huang E.H., Forde K.A., Whelan R.L.
Surgery 132:186-192(2002) · Mapped (17) |
| Glycosylphosphatidylinositol-linked proteins are required for maintenance of a normal peripheral lymphoid compartment but not for lymphocyte development. Bessler M., Rosti V., Peng Y., Cattoretti G., Notaro R., Ohsako S., Elkon K.B., Luzzatto L.
Eur. J. Immunol. 32:2607-2616(2002) · Mapped (3) |
| GATA1-Cre mediates Piga gene inactivation in the erythroid/megakaryocytic lineage and leads to circulating red cells with a partial deficiency in glycosyl phosphatidylinositol-linked proteins (paroxysmal nocturnal hemoglobinuria type II cells). Jasinski M., Keller P., Fujiwara Y., Orkin S.H., Bessler M.
Blood 98:2248-2255(2001) · Mapped (7) |
| FES-Cre targets phosphatidylinositol glycan class A (PIGA) inactivation to hematopoietic stem cells in the bone marrow. Keller P., Payne J.L., Tremml G., Greer P.A., Gaboli M., Pandolfi P.P., Bessler M.
J. Exp. Med. 194:581-589(2001) · Mapped (7) |
| Increased sensitivity to complement and a decreased red blood cell life span in mice mosaic for a nonfunctional Piga gene. Tremml G., Dominguez C., Rosti V., Zhang Z., Pandolfi P.P., Keller P., Bessler M.
Blood 94:2945-2954(1999) · Mapped (7) |
| X inactivation and somatic cell selection rescue female mice carrying a Piga-null mutation. Keller P., Tremml G., Rosti V., Bessler M.
Proc. Natl. Acad. Sci. U.S.A. 96:7479-7483(1999) · Mapped (7) |
| The spectrum of somatic mutations in the PIG-A gene in paroxysmal nocturnal hemoglobinuria includes large deletions and small duplications. Nafa K., Bessler M., Castro-Malaspina H., Jhanwar S., Luzzatto L.
Blood Cells Mol. Dis. 24:370-384(1998) · UniProtKB (1) |
| Murine embryonic stem cells without pig-a gene activity are competent for hematopoiesis with the PNH phenotype but not for clonal expansion. Rosti V., Tremml G., Soares V., Pandolfi P.P., Luzzatto L., Bessler M.
J. Clin. Invest. 100:1028-1036(1997) · Mapped (7) |
| Paroxysmal nocturnal haemoglobinuria (PNH) is caused by somatic mutations in the PIG-A gene. Bessler M., Mason P.J., Hilmen P., Miyata T., Yamada N., Takeda J., Luzzato L., Kinoshita T.
EMBO J. 13:110-117(1994) · UniProtKB (1) |
