1 - 25 of 77 results for author:"Green E.D." in Literature citations
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| Birth-and-death of KLK3 and KLK2 in primates: evolution driven by reproductive biology. Marques P.I., Bernardino R., Fernandes T., Green E.D., Hurle B., Quesada V., Seixas S. Genome Biol Evol 4:1331-1338(2012) · UniProtKB (5) |
| Gene therapy rescues cilia defects and restores olfactory function in a mammalian ciliopathy model. McIntyre J.C., Davis E.E., Joiner A., Williams C.L., Tsai I.C., Jenkins P.M., McEwen D.P., Zhang L., Escobado J., Thomas S. et al. Nat. Med. 18:1423-1428(2012) · Mapped (10) |
| Evolution of siglec-11 and siglec-16 genes in hominins. Wang X., Mitra N., Cruz P., Deng L., Varki N., Angata T., Green E.D., Mullikin J., Hayakawa T., Varki A. Mol. Biol. Evol. 29:2073-2086(2012) · UniProtKB (1) |
| Charcot-Marie-Tooth-linked mutant GARS is toxic to peripheral neurons independent of wild-type GARS levels. Motley W.W., Seburn K.L., Nawaz M.H., Miers K.E., Cheng J., Antonellis A., Green E.D., Talbot K., Yang X.L., Fischbeck K.H. et al. PLoS Genet. 7:e1002399-e1002399(2011) · Mapped (3) |
| TTC21B contributes both causal and modifying alleles across the ciliopathy spectrum. Davis E.E., Zhang Q., Liu Q., Diplas B.H., Davey L.M., Hartley J., Stoetzel C., Szymanska K., Ramaswami G., Logan C.V. et al. |
| A rare myelin protein zero (MPZ) variant alters enhancer activity in vitro and in vivo. Antonellis A., Dennis M.Y., Burzynski G., Huynh J., Maduro V., Hodonsky C.J., Khajavi M., Szigeti K., Mukkamala S., Bessling S.L. et al. PLoS ONE 5:e14346-e14346(2010) · Mapped (4) |
| CFTR transcription defects in pancreatic sufficient cystic fibrosis patients with only one mutation in the coding region of CFTR. Sheridan M.B., Hefferon T.W., Wang N., Merlo C., Milla C., Borowitz D., Green E.D., Mogayzel P.J. Jr., Cutting G.R. J. Med. Genet. 48:235-241(2011) · Mapped (45) |
| Balancing selection maintains a form of ERAP2 that undergoes nonsense-mediated decay and affects antigen presentation. Andres A.M., Dennis M.Y., Kretzschmar W.W., Cannons J.L., Lee-Lin S.Q., Hurle B., Schwartzberg P.L., Williamson S.H., Bustamante C.D., Nielsen R. et al. PLoS Genet. 6:e1001157-e1001157(2010) · Mapped (2) |
| Compound heterozygosity for loss-of-function lysyl-tRNA synthetase mutations in a patient with peripheral neuropathy. McLaughlin H.M., Sakaguchi R., Liu C., Igarashi T., Pehlivan D., Chu K., Iyer R., Cruz P., Cherukuri P.F., Hansen N.F. et al. Am. J. Hum. Genet. 87:560-566(2010) · UniProtKB (1) · Mapped (1) |
| 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 (1) |
| 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 (19) |
| 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 (15) |
| 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 (5) |
| 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 (4) |
| 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 (3) |
| 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 (9) |
| 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) |
| 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 (21) |