1 - 25 of
71
results
for author:"Green E.D."
in Literature Citations
| A common variant associated with dyslexia reduces expression of the KIAA0319 gene. Dennis M.Y., Paracchini S., Scerri T.S., Prokunina-Olsson L., Knight J.C., Wade-Martins R., Coggill P., Beck S., Green E.D., Monaco A.P. PLoS Genet. 5:e1000436-e1000436(2009) · Mapped (2) |
| Gpnmb is a melanoblast-expressed, MITF-dependent gene. Loftus S.K., Antonellis A., Matera I., Renaud G., Baxter L.L., Reid D., Wolfsberg T.G., Chen Y., Wang C., Prasad M.K. et al. Pigment Cell Melanoma Res 22:99-110(2009) · Mapped (21) |
| Comparative sequence analysis of primate subtelomeres originating from a chromosome fission event. Rudd M.K., Endicott R.M., Friedman C., Walker M., Young J.M., Osoegawa K., de Jong P.J., Green E.D., Trask B.J. Genome Res. 19:33-41(2009) · UniProtKB (1) |
| Disruption of an AP-2alpha binding site in an IRF6 enhancer is associated with cleft lip. Rahimov F., Marazita M.L., Visel A., Cooper M.E., Hitchler M.J., Rubini M., Domann F.E., Govil M., Christensen K., Bille C. et al. Nat. Genet. 40:1341-1347(2008) · Mapped (21) |
| Identification of neural crest and glial enhancers at the mouse Sox10 locus through transgenesis in zebrafish. Antonellis A., Huynh J.L., Lee-Lin S.Q., Vinton R.M., Renaud G., Loftus S.K., Elliot G., Wolfsberg T.G., Green E.D., McCallion A.S. et al. PLoS Genet. 4:e1000174-e1000174(2008) · Mapped (4) |
| Identification of pendrin as a common mediator for mucus production in bronchial asthma and chronic obstructive pulmonary disease. Nakao I., Kanaji S., Ohta S., Matsushita H., Arima K., Yuyama N., Yamaya M., Nakayama K., Kubo H., Watanabe M. et al. J. Immunol. 180:6262-6269(2008) · Mapped (5) |
| Regulatory divergence modifies limb length between mammals. Cretekos C.J., Wang Y., Green E.D., Martin J.F., Rasweiler J.J., Behringer R.R. |
| Reduced ENaC protein abundance contributes to the lower blood pressure observed in pendrin-null mice. Kim Y.H., Pech V., Spencer K.B., Beierwaltes W.H., Everett L.A., Green E.D., Shin W., Verlander J.W., Sutliff R.L., Wall S.M. Am. J. Physiol. Renal Physiol. 293:F1314-24(2007) · Mapped (4) |
| Comparative sequence analyses reveal rapid and divergent evolutionary changes of the WFDC locus in the primate lineage. NISC comparative sequencing program Genome Res. 17:276-286(2007) · UniProtKB (123) |
| Lack of pendrin HCO3- transport elevates vestibular endolymphatic [Ca2+] by inhibition of acid-sensitive TRPV5 and TRPV6 channels. Nakaya K., Harbidge D.G., Wangemann P., Schultz B.D., Green E.D., Wall S.M., Marcus D.C. Am. J. Physiol. Renal Physiol. 292:F1314-21(2007) · Mapped (2) |
| Macrophage invasion contributes to degeneration of stria vascularis in Pendred syndrome mouse model. Jabba S.V., Oelke A., Singh R., Maganti R.J., Fleming S., Wall S.M., Everett L.A., Green E.D., Wangemann P. BMC Med 4:37-37(2006) · Mapped (3) |
| Further evidence that the KIAA0319 gene confers susceptibility to developmental dyslexia. Harold D., Paracchini S., Scerri T., Dennis M., Cope N., Hill G., Moskvina V., Walter J., Richardson A.J., Owen M.J. et al. Mol. Psychiatry 11:1085-91, 2006:1061-1061(2006) · Mapped (4) |
| Dietary Cl(-) restriction upregulates pendrin expression within the apical plasma membrane of type B intercalated cells. Verlander J.W., Kim Y.H., Shin W., Pham T.D., Hassell K.A., Beierwaltes W.H., Green E.D., Everett L., Matthews S.W., Wall S.M. Am. J. Physiol. Renal Physiol. 291:F833-9(2006) · Mapped (2) |
| Mutations in TRIOBP, which encodes a putative cytoskeletal-organizing protein, are associated with nonsyndromic recessive deafness. Riazuddin S., Khan S.N., Ahmed Z.M., Ghosh M., Caution K., Nazli S., Kabra M., Zafar A.U., Chen K., Naz S. et al. Am. J. Hum. Genet. 78:137-143(2006) · UniProtKB (2) · Mapped (7) |
| Deletion of long-range sequences at Sox10 compromises developmental expression in a mouse model of Waardenburg-Shah (WS4) syndrome. Antonellis A., Bennett W.R., Menheniott T.R., Prasad A.B., Lee-Lin S.Q., Green E.D., Paisley D., Kelsh R.N., Pavan W.J., Ward A. Hum. Mol. Genet. 15:259-271(2006) · Mapped (6) |
| Evaluation of the RET regulatory landscape reveals the biological relevance of a HSCR-implicated enhancer. Grice E.A., Rochelle E.S., Green E.D., Chakravarti A., McCallion A.S. Hum. Mol. Genet. 14:3837-3845(2005) · Mapped (16) |
| Intercalated cell H+/OH- transporter expression is reduced in Slc26a4 null mice. Kim Y.H., Verlander J.W., Matthews S.W., Kurtz I., Shin W., Weiner I.D., Everett L.A., Green E.D., Nielsen S., Wall S.M. Am. J. Physiol. Renal Physiol. 289:F1262-72(2005) · Mapped (10) |
| Phenotype-genotype correlation in Hirschsprung disease is illuminated by comparative analysis of the RET protein sequence. Kashuk C.S., Stone E.A., Grice E.A., Portnoy M.E., Green E.D., Sidow A., Chakravarti A., McCallion A.S. Proc. Natl. Acad. Sci. U.S.A. 102:8949-8954(2005) · Mapped (16) |
| A common sex-dependent mutation in a RET enhancer underlies Hirschsprung disease risk. Emison E.S., McCallion A.S., Kashuk C.S., Bush R.T., Grice E., Lin S., Portnoy M.E., Cutler D.J., Green E.D., Chakravarti A. Nature 434:857-863(2005) · Mapped (16) |
| Isolation and analysis of candidate myeloid tumor suppressor genes from a commonly deleted segment of 7q22. Curtiss N.P., Bonifas J.M., Lauchle J.O., Balkman J.D., Kratz C.P., Emerling B.M., Green E.D., Le Beau M.M., Shannon K.M. Genomics 85:600-607(2005) · UniProtKB (2) |
| Large-scale sequencing of the CD33-related Siglec gene cluster in five mammalian species reveals rapid evolution by multiple mechanisms. Angata T., Margulies E.H., Green E.D., Varki A. Proc. Natl. Acad. Sci. U.S.A. 101:13251-13256(2004) · UniProtKB (1) · Mapped (31) |
| Loss of KCNJ10 protein expression abolishes endocochlear potential and causes deafness in Pendred syndrome mouse model. Wangemann P., Itza E.M., Albrecht B., Wu T., Jabba S.V., Maganti R.J., Lee J.H., Everett L.A., Wall S.M., Royaux I.E. et al. BMC Med 2:30-30(2004) · Mapped (2) |
| Mechanism of iodide/chloride exchange by pendrin. Yoshida A., Hisatome I., Taniguchi S., Sasaki N., Yamamoto Y., Miake J., Fukui H., Shimizu H., Okamura T., Okura T. et al. Endocrinology 145:4301-4308(2004) · Mapped (5) |
| Genome sequence of the Brown Norway rat yields insights into mammalian evolution. Gibbs R.A., Weinstock G.M., Metzker M.L., Muzny D.M., Sodergren E.J., Scherer S., Scott G., Steffen D., Worley K.C., Burch P.E. et al. |
| Comparative sequence analysis of a single-gene conserved segment in mouse and human. Thomas J.W., Green E.D. Mamm. Genome 14:673-678(2003) · Mapped (16) |
