1 - 25 of
667
results
for author:"Martin J."
in Literature Citations
| A dual role for HSP90 and HSP70 in the inflammatory myopathies: from muscle fiber protection to active invasion by macrophages. De Paepe B., Creus K.K., Martin J.J., Weis J., De Bleecker J.L. Ann. N. Y. Acad. Sci. 1173:463-469(2009) · Mapped (24) |
| Association of a NKG2D gene variant with SLE in two populations. Kabalak G., Thomas R., Martin J., Ortego-Centeno N., Jimenez-Alonso J., de Ramon E., Buyny S., Hamsen S., Gross W.L., Schnarr S. et al. Hum. Immunol. 0:0-0(2009) · Mapped (3) |
| Clinical heterogeneity in 3 unrelated families linked to VCP p.Arg159His. van der Zee J., Pirici D., Van Langenhove T., Engelborghs S., Vandenberghe R., Hoffmann M., Pusswald G., Van den Broeck M., Peeters K., Mattheijssens M. et al. Neurology 73:626-632(2009) · Mapped (6) |
| Tbx1 controls cardiac neural crest cell migration during arch artery development by regulating Gbx2 expression in the pharyngeal ectoderm. Calmont A., Ivins S., Van Bueren K.L., Papangeli I., Kyriakopoulou V., Andrews W.D., Martin J.F., Moon A.M., Illingworth E.A., Basson M.A. et al. Development 136:3173-3183(2009) · Mapped (45) |
| Nutrigenetics: links between genetic background and response to Mediterranean-type diets. Lairon D., Defoort C., Martin J.C., Amiot-Carlin M.J., Gastaldi M., Planells R. Public Health Nutr 12:1601-1606(2009) · Mapped (64) |
| Mutation of SHOC2 promotes aberrant protein N-myristoylation and causes Noonan-like syndrome with loose anagen hair. Cordeddu V., Di Schiavi E., Pennacchio L.A., Ma'ayan A., Sarkozy A., Fodale V., Cecchetti S., Cardinale A., Martin J., Schackwitz W. et al. |
| Targeted ablation of PINCH1 and PINCH2 from murine myocardium results in dilated cardiomyopathy and early postnatal lethality. Liang X., Sun Y., Ye M., Scimia M.C., Cheng H., Martin J., Wang G., Rearden A., Wu C., Peterson K.L. et al. Circulation 120:568-576(2009) · Mapped (5) |
| Potentiation of growth factor signaling by insulin-like growth factor-binding protein-3 in breast epithelial cells requires sphingosine kinase activity. Martin J.L., Lin M.Z., McGowan E.M., Baxter R.C. J. Biol. Chem. 284:25542-25552(2009) · Mapped (28) |
| Indirect regulation of PTH by estrogens may require FGF23. Carrillo-Lopez N., Roman-Garcia P., Rodriguez-Rebollar A., Fernandez-Martin J.L., Naves-Diaz M., Cannata-Andia J.B. J. Am. Soc. Nephrol. 20:2009-2017(2009) · Mapped (2) |
| Identification of a new putative functional IL18 gene variant through an association study in systemic lupus erythematosus. Sanchez E., Palomino-Morales R.J., Ortego-Centeno N., Jimenez-Alonso J., Gonzalez-Gay M.A., Lopez-Nevot M.A., Sanchez-Roman J., de Ramon E., Gonzalez-Escribano M.F., Pons-Estel B.A. et al. Hum. Mol. Genet. 18:3739-3748(2009) · Mapped (4) |
| Comparative genomics of MAP kinase and calcium-calcineurin signalling components in plant and human pathogenic fungi. Rispail N., Soanes D.M., Ant C., Czajkowski R., Grunler A., Huguet R., Perez-Nadales E., Poli A., Sartorel E., Valiante V. et al. Fungal Genet. Biol. 46:287-298(2009) · Mapped (11) |
| Molecular recognition of physiological substrate noradrenaline by the adrenaline-synthesizing enzyme PNMT and factors influencing its methyltransferase activity. Drinkwater N., Gee C.L., Puri M., Criscione K.R., McLeish M.J., Grunewald G.L., Martin J.L. Biochem. J. 422:463-471(2009) · Mapped (2) |
| Association of PTPN22 gene functional variants with development of pulmonary tuberculosis in Moroccan population. Lamsyah H., Rueda B., Baassi L., Elaouad R., Bottini N., Sadki K., Martin J. Tissue Antigens 74:228-232(2009) · Mapped (8) |
| Hsp27 inhibits sublethal, Src-mediated renal epithelial cell injury. Havasi A., Wang Z., Gall J.M., Spaderna M., Suri V., Canlas E., Martin J.L., Schwartz J.H., Borkan S.C. Am. J. Physiol. Renal Physiol. 297:F760-8(2009) · Mapped (4) |
| Association between toll-like receptor 4 gene polymorphism and biopsy-proven giant cell arteritis. Palomino-Morales R., Torres O., Vazquez-Rodriguez T.R., Morado I.C., Castaneda S., Callejas-Rubio J.L., Miranda-Filloy J.A., Fernandez-Gutierrez B., Martin J., Gonzalez-Gay M.A. J. Rheumatol. 36:1501-1506(2009) · Mapped (1) |
| Improved discrimination of autopsy-confirmed Alzheimer's disease (AD) from non-AD dementias using CSF P-tau(181P). Koopman K., Le Bastard N., Martin J.J., Nagels G., De Deyn P.P., Engelborghs S. Neurochem. Int. 55:214-218(2009) · Mapped (5) |
| The influence of class II transactivator and interleukin-6 polymorphisms on the production of antibodies to donor human leucocyte antigen mismatches in renal allograft recipients. Martin J., Worthington J., Harris S., Martin S. Int. J. Immunogenet. 36:235-239(2009) · Mapped (15) |
| Association of ATG16L1 and IRGM genes polymorphisms with inflammatory bowel disease: a meta-analysis approach. Palomino-Morales R.J., Oliver J., Gomez-Garcia M., Lopez-Nevot M.A., Rodrigo L., Nieto A., Alizadeh B.Z., Martin J. Genes Immun. 10:356-364(2009) · Mapped (11) |
| Structure and activity of the N-terminal substrate recognition domains in proteasomal ATPases. Djuranovic S., Hartmann M.D., Habeck M., Ursinus A., Zwickl P., Martin J., Lupas A.N., Zeth K. |
| Investigation of TLR5 and TLR7 as candidate genes for susceptibility to systemic lupus erythematosus. Sanchez E., Callejas-Rubio J.L., Sabio J.M., Gonzalez-Gay M.A., Jimenez-Alonso J., Mico L., de Ramon E., Camps M., Suarez A., Gutierrez C. et al. Clin. Exp. Rheumatol. 27:267-271(2009) · Mapped (5) |
| Prevalence and clinical features of LRRK2 mutations in patients with Parkinson's disease in southern Spain. Gao L., Gomez-Garre P., Diaz-Corrales F.J., Carrillo F., Carballo M., Palomino A., Diaz-Martin J., Mejias R., Vime P.J., Lopez-Barneo J. et al. Eur. J. Neurol. 16:957-960(2009) · Mapped (18) |
| Novel association of the interleukin 2-interleukin 21 region with inflammatory bowel disease. Marquez A., Orozco G., Martinez A., Palomino-Morales R., Fernandez-Arquero M., Mendoza J.L., Taxonera C., Diaz-Rubio M., Gomez-Garcia M., Nieto A. et al. Am. J. Gastroenterol. 104:1968-1975(2009) · Mapped (22) |
| An ENU-induced mutation in mouse glycyl-tRNA synthetase (GARS) causes peripheral sensory and motor phenotypes creating a model of Charcot-Marie-Tooth type 2D peripheral neuropathy. Achilli F., Bros-Facer V., Williams H.P., Banks G.T., AlQatari M., Chia R., Tucci V., Groves M., Nickols C.D., Seburn K.L. et al. Dis Model Mech 2:359-373(2009) · Mapped (2) |
| Efficient pyramidal arrangement of an ordered cosmid library: Rapid screening of genes of the tacrolimus-producer Streptomyces sp. ATCC 55098. Martinez-Castro M., Solera E., Martin J.F., Barreiro C. J. Microbiol. Methods 78:150-154(2009) · UniProtKB (4) |
| The TRAF1-C5 region on chromosome 9q33 is associated with multiple autoimmune diseases. Kurreeman F.S., Alizadeh B.Z., Goulielmos G.N., Rueda B., Houwing-Duistermaat J., Sanchez E., Bevova M., Radstake T.R., Vonk M.C., Galanakis E. et al. Ann. Rheum. Dis. 0:0-0(2009) · Mapped (3) |
