Skip Header

 

14 results for author:"Dawson E."Drop in Literature Citations

Customize display Download...

Page 1 of 1

Alterations in oestrogen metabolism: implications for higher penetrance of familial pulmonary arterial hypertension in females.

Austin E.D., Cogan J.D., West J.D., Hedges L.K., Hamid R., Dawson E.P., Wheeler L.A., Parl F.F., Loyd J.E., Phillips J.A.

Eur. Respir. J. 34:1093-1099(2009) · Mapped (10)

Association of a CYP4A11 variant and blood pressure in black men.

Gainer J.V., Lipkowitz M.S., Yu C., Waterman M.R., Dawson E.P., Capdevila J.H., Brown N.J.

J. Am. Soc. Nephrol. 19:1606-1612(2008) · Mapped (5)

Chimeric constructs endow the human CFTR Cl- channel with the gating behavior of murine CFTR.

Scott-Ward T.S., Cai Z., Dawson E.S., Doherty A., Da Paula A.C., Davidson H., Porteous D.J., Wainwright B.J., Amaral M.D., Sheppard D.N. et al.

Proc. Natl. Acad. Sci. U.S.A. 104:16365-16370(2007) · Mapped (51)

Variations in the alpha2A-adrenergic receptor gene and their functional effects.

Kurnik D., Muszkat M., Li C., Sofowora G.G., Solus J., Xie H.G., Harris P.A., Jiang L., McMunn C., Ihrie P. et al.

Clin. Pharmacol. Ther. 79:173-185(2006) · Mapped (1)

Kidneys extract BNP and NT-proBNP in healthy young men.

Schou M., Dalsgaard M.K., Clemmesen O., Dawson E.A., Yoshiga C.C., Nielsen H.B., Gustafsson F., Hildebrandt P.R., Secher N.H.

J. Appl. Physiol. 99:1676-1680(2005) · Mapped (2)

Variation in the alpha2B-adrenergic receptor gene (ADRA2B) and its relationship to vascular response in vivo.

Muszkat M., Kurnik D., Solus J., Sofowora G.G., Xie H.G., Jiang L., McMunn C., Ihrie P., Harris J.R., Dawson E.P. et al.

Pharmacogenet. Genomics 15:407-414(2005) · Mapped (2)

Functional variant of CYP4A11 20-hydroxyeicosatetraenoic acid synthase is associated with essential hypertension.

Gainer J.V., Bellamine A., Dawson E.P., Womble K.E., Grant S.W., Wang Y., Cupples L.A., Guo C.-Y., Demissie S., O'Donnell C.J. et al.

Circulation 111:63-69(2005) · UniProtKB (2) · Mapped (3)

Genetic mutations in surfactant protein C are a rare cause of sporadic cases of IPF.

Lawson W.E., Grant S.W., Ambrosini V., Womble K.E., Dawson E.P., Lane K.B., Markin C., Renzoni E., Lympany P., Thomas A.Q. et al.

Thorax 59:977-980(2004) · Mapped (2)

Genetic variation in eleven phase I drug metabolism genes in an ethnically diverse population.

Solus J.F., Arietta B.J., Harris J.R., Sexton D.P., Steward J.Q., McMunn C., Ihrie P., Mehall J.M., Edwards T.L., Dawson E.P.

Pharmacogenomics 5:895-931(2004) · UniProtKB (11)

beta-1,3-Glucuronyltransferase-1 gene implicated as a candidate for a schizophrenia-like psychosis through molecular analysis of a balanced translocation.

Jeffries A.R., Mungall A.J., Dawson E., Halls K., Langford C.F., Murray R.M., Dunham I., Powell J.F.

Mol. Psychiatry 8:654-663(2003) · Mapped (3)

Characterization of genomic structure and polymorphisms in the human carbamyl phosphate synthetase I gene.

Summar M.L., Hall L.D., Eeds A.M., Hutcheson H.B., Kuo A.N., Willis A.S., Rubio V., Arvin M.K., Schofield J.P., Dawson E.P.

Gene 311:51-57(2003) · UniProtKB (1)

Characterization of the CYP4A11 gene, a second CYP4A gene in humans.

Bellamine A., Wang Y., Waterman M.R., Gainer J.V. III, Dawson E.P., Brown N.J., Capdevila J.H.

Arch. Biochem. Biophys. 409:221-227(2003) · UniProtKB (1) · Mapped (4)

The DNA sequence of human chromosome 22.

Dunham I., Hunt A.R., Collins J.E., Bruskiewich R., Beare D.M., Clamp M., Smink L.J., Ainscough R., Almeida J.P., Babbage A.K. et al.

Nature 402:489-495(1999) · UniProtKB (1,031) · Mapped (3)

An association study of debrisoquine hydroxylase (CYP2D6) polymorphisms in schizophrenia.

Dawson E., Powell J.F., Nothen M.M., Crocq M.A., Lanczik M., Korner J., Rietschel M., van Os J., Wright P., Gill M.

Psychiatr. Genet. 4:215-218(1994) · Mapped (1)

Page 1 of 1