1 - 25 of 33 results for author:"McBride K." in Literature citations
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| Cardiac teratogenicity in mouse maternal phenylketonuria: defining phenotype parameters and genetic background influences. Seagraves N.J., McBride K.L. Mol. Genet. Metab. 107:650-658(2012) · Mapped (5) |
| Coronary artery disease in a Werner syndrome-like form of progeria characterized by low levels of progerin, a splice variant of lamin A. Hisama F.M., Lessel D., Leistritz D., Friedrich K., McBride K.L., Pastore M.T., Gottesman G.S., Saha B., Martin G.M., Kubisch C. et al. Am. J. Med. Genet. A 155A:3002-3006(2011) · Mapped (11) |
| Association of common variants in ERBB4 with congenital left ventricular outflow tract obstruction defects. McBride K.L., Zender G.A., Fitzgerald-Butt S.M., Seagraves N.J., Fernbach S.D., Zapata G., Lewin M., Towbin J.A., Belmont J.W. Birth Defects Res. Part A Clin. Mol. Teratol. 91:162-168(2011) · Mapped (7) |
| Amino-terminal phosphorylation of activation-induced cytidine deaminase suppresses c-myc/IgH translocation. Gazumyan A., Timachova K., Yuen G., Siden E., Di Virgilio M., Woo E.M., Chait B.T., Reina San-Martin B., Nussenzweig M.C., McBride K.M. Mol. Cell. Biol. 31:442-449(2011) · Mapped (8) |
| Deep-sequencing identification of the genomic targets of the cytidine deaminase AID and its cofactor RPA in B lymphocytes. Yamane A., Resch W., Kuo N., Kuchen S., Li Z., Sun H.W., Robbiani D.F., McBride K., Nussenzweig M.C., Casellas R. Nat. Immunol. 12:62-69(2011) · Mapped (6) |
| NOTCH1 missense alleles associated with left ventricular outflow tract defects exhibit impaired receptor processing and defective EMT. Riley M.F., McBride K.L., Cole S.E. Biochim. Biophys. Acta 1812:121-129(2011) · Mapped (3) |
| Confirmation study of PTEN mutations among individuals with autism or developmental delays/mental retardation and macrocephaly. McBride K.L., Varga E.A., Pastore M.T., Prior T.W., Manickam K., Atkin J.F., Herman G.E. Autism Res 3:137-141(2010) · Mapped (3) |
| AID produces DNA double-strand breaks in non-Ig genes and mature B cell lymphomas with reciprocal chromosome translocations. Robbiani D.F., Bunting S., Feldhahn N., Bothmer A., Camps J., Deroubaix S., McBride K.M., Klein I.A., Stone G., Eisenreich T.R. et al. Mol. Cell 36:631-641(2009) · Mapped (18) |
| Significant contributions of the extraembryonic membranes and maternal genotype to the placental pathology in heterozygous Nsdhl deficient female embryos. Cunningham D., Talabere T., Bir N., Kennedy M., McBride K.L., Herman G.E. Hum. Mol. Genet. 19:364-373(2010) · Mapped (5) |
| The prevalence of PTEN mutations in a clinical pediatric cohort with autism spectrum disorders, developmental delay, and macrocephaly. Varga E.A., Pastore M., Prior T., Herman G.E., McBride K.L. Genet. Med. 11:111-117(2009) · Mapped (3) |
| The anti-neurodegeneration drug clioquinol inhibits the aging-associated protein CLK-1. Wang Y., Branicky R., Stepanyan Z., Carroll M., Guimond M.P., Hihi A., Hayes S., McBride K., Hekimi S. J. Biol. Chem. 284:314-323(2009) · Mapped (5) |
| Regulation of class switch recombination and somatic mutation by AID phosphorylation. McBride K.M., Gazumyan A., Woo E.M., Schwickert T.A., Chait B.T., Nussenzweig M.C. J. Exp. Med. 205:2585-2594(2008) · Mapped (3) |
| NOTCH1 mutations in individuals with left ventricular outflow tract malformations reduce ligand-induced signaling. McBride K.L., Riley M.F., Zender G.A., Fitzgerald-Butt S.M., Towbin J.A., Belmont J.W., Cole S.E. Hum. Mol. Genet. 17:2886-2893(2008) · Mapped (8) |
| MicroRNA-155 suppresses activation-induced cytidine deaminase-mediated Myc-Igh translocation. Dorsett Y., McBride K.M., Jankovic M., Gazumyan A., Thai T.H., Robbiani D.F., Di Virgilio M., Reina San-Martin B., Heidkamp G., Schwickert T.A. et al. Immunity 28:630-638(2008) · Mapped (3) |
| Expression of AID transgene is regulated in activated B cells but not in resting B cells and kidney. Shen H.M., Bozek G., Pinkert C.A., McBride K., Wang L., Kenter A., Storb U. Mol. Immunol. 45:1883-1892(2008) · Mapped (3) |
| Evolutionary conservation of drug action on lipoprotein metabolism-related targets. Hihi A.K., Beauchamp M.C., Branicky R., Desjardins A., Casanova I., Guimond M.P., Carroll M., Ethier M., Kianicka I., McBride K. et al. J. Lipid Res. 49:74-83(2008) · Mapped (1) |
| ATM prevents the persistence and propagation of chromosome breaks in lymphocytes. Callen E., Jankovic M., Difilippantonio S., Daniel J.A., Chen H.T., Celeste A., Pellegrini M., McBride K., Wangsa D., Bredemeyer A.L. et al. Cell 130:63-75(2007) · Mapped (28) |
| Gene copy-number variation and associated polymorphisms of complement component C4 in human systemic lupus erythematosus (SLE): low copy number is a risk factor for and high copy number is a protective factor against SLE susceptibility in European Americans. Yang Y., Chung E.K., Wu Y.L., Savelli S.L., Nagaraja H.N., Zhou B., Hebert M., Jones K.N., Shu Y., Kitzmiller K. et al. Am. J. Hum. Genet. 80:1037-1054(2007) · UniProtKB (2) · Mapped (45) |
| Regulation of hypermutation by activation-induced cytidine deaminase phosphorylation. McBride K.M., Gazumyan A., Woo E.M., Barreto V.M., Robbiani D.F., Chait B.T., Nussenzweig M.C. Proc. Natl. Acad. Sci. U.S.A. 103:8798-8803(2006) · Mapped (2) |
| Role of genomic instability and p53 in AID-induced c-myc-Igh translocations. Ramiro A.R., Jankovic M., Callen E., Difilippantonio S., Chen H.T., McBride K.M., Eisenreich T.R., Chen J., Dickins R.A., Lowe S.W. et al. Nature 440:105-109(2006) · Mapped (60) |
| STAT3 nuclear import is independent of tyrosine phosphorylation and mediated by importin-alpha3. Liu L., McBride K.M., Reich N.C. Proc. Natl. Acad. Sci. U.S.A. 102:8150-8155(2005) · UniProtKB (2) · Mapped (7) |
| Somatic hypermutation is limited by CRM1-dependent nuclear export of activation-induced deaminase. McBride K.M., Barreto V., Ramiro A.R., Stavropoulos P., Nussenzweig M.C. J. Exp. Med. 199:1235-1244(2004) · Mapped (4) |
| C-terminal deletion of AID uncouples class switch recombination from somatic hypermutation and gene conversion. Barreto V., Reina-San-Martin B., Ramiro A.R., McBride K.M., Nussenzweig M.C. Mol. Cell 12:501-508(2003) · Mapped (23) |
| The model B6dom1 minor histocompatibility antigen is encoded by a mouse homolog of the yeast STT3 gene. McBride K., Baron C., Picard S., Martin S., Boismenu D., Bell A., Bergeron J., Perreault C. Immunogenetics 54:562-569(2002) · UniProtKB (2) · Mapped (2) |
| Tumor necrosis factor receptor-associated factor (TRAF)2 represses the T helper cell type 2 response through interaction with NFAT-interacting protein (NIP45). Lieberson R., Mowen K.A., McBride K.D., Leautaud V., Zhang X., Suh W.-K., Wu L., Glimcher L.H. J. Exp. Med. 194:89-98(2001) · UniProtKB (2) |