19 results for author:"Jones L.A." in Literature citations
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| B cell TLR7 expression drives anti-RNA autoantibody production and exacerbates disease in systemic lupus erythematosus-prone mice. Hwang S.H., Lee H., Yamamoto M., Jones L.A., Dayalan J., Hopkins R., Zhou X.J., Yarovinsky F., Connolly J.E., Curotto de Lafaille M.A. et al. J. Immunol. 189:5786-5796(2012) · Mapped (4) |
| Spitzenkorper, exocyst, and polarisome components in Candida albicans hyphae show different patterns of localization and have distinct dynamic properties. Jones L.A., Sudbery P.E. Eukaryotic Cell 9:1455-1465(2010) · Mapped (4) |
| Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls. Wellcome Trust Case Control Consortium Nature 464:713-720(2010) · Mapped (3) |
| IL-33 receptor (T1/ST2) signalling is necessary to prevent the development of encephalitis in mice infected with Toxoplasma gondii. Jones L.A., Roberts F., Nickdel M.B., Brombacher F., McKenzie A.N., Henriquez F.L., Alexander J., Roberts C.W. Eur. J. Immunol. 40:426-436(2010) · Mapped (6) |
| CD54 is a surrogate marker of antigen presenting cell activation. Sheikh N.A., Jones L.A. Cancer Immunol. Immunother. 57:1381-1390(2008) · Mapped (9) |
| Candidate gene and locus analysis of myopia. Mutti D.O., Cooper M.E., O'Brien S., Jones L.A., Marazita M.L., Murray J.C., Zadnik K. Mol. Vis. 13:1012-1019(2007) · Mapped (18) |
| Association of p53 mutations and a codon 72 single nucleotide polymorphism with lower overall survival and responsiveness to adjuvant radiotherapy in endometrioid endometrial carcinomas. Saffari B., Bernstein L., Hong D.C., Sullivan-Halley J., Runnebaum I.B., Grill H.J., Jones L.A., El-Naggar A., Press M.F. Int. J. Gynecol. Cancer 15:952-963(2005) · Mapped (32) |
| Polymorphisms in the MAOA, MAOB, and COMT genes and aggressive behavior in schizophrenia. Zammit S., Jones G., Jones S.J., Norton N., Sanders R.D., Milham C., McCarthy G.M., Jones L.A., Cardno A.G., Gray M. et al. Am. J. Med. Genet. B Neuropsychiatr. Genet. 128B:19-20(2004) · Mapped (19) |
| Aggressive behaviour in patients with schizophrenia is associated with catechol-O-methyltransferase genotype. Jones G., Zammit S., Norton N., Hamshere M.L., Jones S.J., Milham C., Sanders R.D., McCarthy G.M., Jones L.A., Cardno A.G. et al. Br J Psychiatry 179:351-355(2001) · Mapped (7) |
| No evidence for association between a non-synonymous polymorphism in the gene encoding human metabotropic glutamate receptor 7 and schizophrenia. Bray N.J., Williams N.M., Bowen T., Cardno A.G., Gray M., Jones L.A., Murphy K.C., Sanders R.D., Spurlock G., Odonovan M.C. et al. Psychiatr. Genet. 10:83-86(2000) · Mapped (5) |
| No evidence for allelic association between schizophrenia and a functional variant of the human dopamine beta-hydroxylase gene (DBH). Williams H.J., Bray N., Murphy K.C., Cardno A.G., Jones L.A., Owen M.J. Am. J. Med. Genet. 88:557-559(1999) · UniProtKB (1) |
| Further support for an association between a polymorphic CAG repeat in the hKCa3 gene and schizophrenia. Bowen T., Guy C.A., Craddock N., Cardno A.G., Williams N.M., Spurlock G., Murphy K.C., Jones L.A., Gray M., Sanders R.D. et al. Mol. Psychiatry 3:266-269(1998) · Mapped (9) |
| Linked polymorphisms upstream of exons 1 and 2 of the human cholecystokinin gene are not associated with schizophrenia or bipolar disorder. Bowen T., Norton N., Jacobsen N.J., Guy C., Daniels J.K., Sanders R.D., Cardno A.G., Jones L.A., Murphy K.C., McGuffin P. et al. Mol. Psychiatry 3:67-71(1998) · Mapped (2) |
| Association between schizophrenia and a microsatellite polymorphism at the dopamine D5 receptor gene. Williams N.M., Cardno A.G., Murphy K.C., Jones L.A., Asherson P., McGuffin P., Owen M.J. Psychiatr. Genet. 7:83-85(1997) · Mapped (1) |
| WAF1/Cip1 gene polymorphism and expression in carcinomas of the breast, ovary, and endometrium. Lukas J., Groshen S., Saffari B., Niu N., Reles A., Wen W.H., Felix J., Jones L.A., Hall F.L., Press M.F. Am. J. Pathol. 150:167-175(1997) · Mapped (1) |
| Two transthyretin mutations (Glu42Gly, His90Asn) in an Italian family with amyloidosis. Skare J.C., Jones L.A., Myles N., Kane K., Milunsky A., Cohen A.S., Skinner M. Clin. Genet. 45:281-284(1994) · UniProtKB (1) |
| Proline at position 36: a new transthyretin mutation associated with familial amyloidotic polyneuropathy. Jones L.A., Skare J.C., Harding J.A., Cohen A.S., Milunsky A., Skinner M. Am. J. Hum. Genet. 48:979-982(1991) · Mapped (6) |
| Familial amyloidotic polyneuropathy: a new transthyretin position 30 mutation (alanine for valine) in a family of German descent. Jones L.A., Skare J.C., Cohen A.S., Harding J.A., Milunsky A., Skinner M. Clin. Genet. 41:70-73(1992) · UniProtKB (1) |
| A new transthyretin mutation associated with amyloidotic vitreous opacities. Asparagine for isoleucine at position 84. Skinner M., Harding J., Skare I., Jones L.A., Cohen A.S., Milunsky A., Skare J. Ophthalmology 99:503-508(1992) · Mapped (6) |