1 - 25 of 40 results for author:"McDermott D." in Literature citations
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| Complete genome sequence of a tenth human polyomavirus. Buck C.B., Phan G.Q., Raiji M.T., Murphy P.M., McDermott D.H., McBride A.A. J. Virol. 86:10887-10887(2012) · UniProtKB (5) |
| WHIM syndrome caused by a single amino acid substitution in the carboxy-tail of chemokine receptor CXCR4. Liu Q., Chen H., Ojode T., Gao X., Anaya-O'Brien S., Turner N.A., Ulrick J., DeCastro R., Kelly C., Cardones A.R. et al. Blood 120:181-189(2012) · Mapped (2) |
| The CXCR4 antagonist plerixafor corrects panleukopenia in patients with WHIM syndrome. McDermott D.H., Liu Q., Ulrick J., Kwatemaa N., Anaya-O'Brien S., Penzak S.R., Filho J.O., Priel D.A., Kelly C., Garofalo M. et al. Blood 118:4957-4962(2011) · Mapped (5) |
| Genetic deletion of chemokine receptor Ccr6 decreases atherogenesis in ApoE-deficient mice. Wan W., Lim J.K., Lionakis M.S., Rivollier A., McDermott D.H., Kelsall B.L., Farber J.M., Murphy P.M. Circ. Res. 109:374-381(2011) · Mapped (17) |
| Comparison of four early posttherapy imaging changes (EPTIC; RECIST 1.0, tumor shrinkage, computed tomography tumor density, Choi criteria) in assessing outcome to vascular endothelial growth factor-targeted therapy in patients with advanced renal cell carcinoma. Krajewski K.M., Guo M., Van den Abbeele A.D., Yap J., Ramaiya N., Jagannathan J., Heng D.Y., Atkins M.B., McDermott D.F., Schutz F.A. et al. Eur. Urol. 59:856-862(2011) · Mapped (7) |
| AMD3100 is a potent antagonist at CXCR4(R334X) , a hyperfunctional mutant chemokine receptor and cause of WHIM syndrome. McDermott D.H., Lopez J., Deng F., Liu Q., Ojode T., Chen H., Ulrick J., Kwatemaa N., Kelly C., Anaya-O'Brien S. et al. J. Cell. Mol. Med. 15:2071-2081(2011) · Mapped (2) |
| Severe congenital neutropenia resulting from G6PC3 deficiency with increased neutrophil CXCR4 expression and myelokathexis. McDermott D.H., De Ravin S.S., Jun H.S., Liu Q., Priel D.A., Noel P., Takemoto C.M., Ojode T., Paul S.M., Dunsmore K.P. et al. |
| Lack of glucose recycling between endoplasmic reticulum and cytoplasm underlies cellular dysfunction in glucose-6-phosphatase-beta-deficient neutrophils in a congenital neutropenia syndrome. Jun H.S., Lee Y.M., Cheung Y.Y., McDermott D.H., Murphy P.M., De Ravin S.S., Mansfield B.C., Chou J.Y. Blood 116:2783-2792(2010) · Mapped (2) |
| Donor and recipient chemokine receptor CCR5 genotype is associated with survival after bone marrow transplantation. McDermott D.H., Conway S.E., Wang T., Ricklefs S.M., Agovi M.A., Porcella S.F., Tran H.T., Milford E., Spellman S., Abdi R. Blood 115:2311-2318(2010) · Mapped (22) |
| CCR5 deficiency is a risk factor for early clinical manifestations of West Nile virus infection but not for viral transmission. Lim J.K., McDermott D.H., Lisco A., Foster G.A., Krysztof D., Follmann D., Stramer S.L., Murphy P.M. J. Infect. Dis. 201:178-185(2010) · Mapped (22) |
| Autosomal dominant epidermodysplasia verruciformis lacking a known EVER1 or EVER2 mutation. McDermott D.F., Gammon B., Snijders P.J., Mbata I., Phifer B., Howland Hartley A., Lee C.C., Murphy P.M., Hwang S.T. Pediatr Dermatol 26:306-310(2009) · Mapped (10) |
| Genetic variation in OAS1 is a risk factor for initial infection with West Nile virus in man. Lim J.K., Lisco A., McDermott D.H., Huynh L., Ward J.M., Johnson B., Johnson H., Pape J., Foster G.A., Krysztof D. et al. PLoS Pathog. 5:e1000321-e1000321(2009) · Mapped (5) |
| Genetic deficiency of chemokine receptor CCR5 is a strong risk factor for symptomatic West Nile virus infection: a meta-analysis of 4 cohorts in the US epidemic. Lim J.K., Louie C.Y., Glaser C., Jean C., Johnson B., Johnson H., McDermott D.H., Murphy P.M. J. Infect. Dis. 197:262-265(2008) · Mapped (22) |
| Role of beta3 integrin in acute renal allograft rejection in humans. Chandrakantan A., McDermott D.H., Tran H.T., Jurewicz M., Gallon L., Gaston R., Milford E., Abdi R. Clin J Am Soc Nephrol 2:1268-1273(2007) · Mapped (5) |
| Haploinsufficiency at the protein kinase A RI alpha gene locus leads to fertility defects in male mice and men. Burton K.A., McDermott D.A., Wilkes D., Poulsen M.N., Nolan M.A., Goldstein M., Basson C.T., McKnight G.S. Mol. Endocrinol. 20:2504-2513(2006) · Mapped (11) |
| CCR5 deficiency increases risk of symptomatic West Nile virus infection. Glass W.G., McDermott D.H., Lim J.K., Lekhong S., Yu S.F., Frank W.A., Pape J., Cheshier R.C., Murphy P.M. J. Exp. Med. 203:35-40(2006) · UniProtKB (1) |
| TBX5 genetic testing validates strict clinical criteria for Holt-Oram syndrome. McDermott D.A., Bressan M.C., He J., Lee J.S., Aftimos S., Brueckner M., Gilbert F., Graham G.E., Hannibal M.C., Innis J.W. et al. Pediatr. Res. 58:981-986(2005) |
| CCL2 polymorphisms are associated with serum monocyte chemoattractant protein-1 levels and myocardial infarction in the Framingham Heart Study. McDermott D.H., Yang Q., Kathiresan S., Cupples L.A., Massaro J.M., Keaney J.F. Jr., Larson M.G., Vasan R.S., Hirschhorn J.N., O'Donnell C.J. et al. Circulation 112:1113-1120(2005) · Mapped (4) |
| Mutations in the desmosomal protein plakophilin-2 are common in arrhythmogenic right ventricular cardiomyopathy. Gerull B., Heuser A., Wichter T., Paul M., Basson C.T., McDermott D.A., Lerman B.B., Markowitz S.M., Ellinor P.T., MacRae C.A. et al. |
| Comparative PRKAR1A genotype-phenotype analyses in humans with Carney complex and prkar1a haploinsufficient mice. Veugelers M., Wilkes D., Burton K., McDermott D.A., Song Y., Goldstein M.M., La Perle K., Vaughan C.J., O'Hagan A., Bennett K.R. et al. Proc. Natl. Acad. Sci. U.S.A. 101:14222-14227(2004) · UniProtKB (1) · Mapped (10) |
| Interleukin (IL)-15 and IL-2 reciprocally regulate expression of the chemokine receptor CX3CR1 through selective NFAT1- and NFAT2-dependent mechanisms. Barlic J., McDermott D.H., Merrell M.N., Gonzales J., Via L.E., Murphy P.M. J. Biol. Chem. 279:48520-48534(2004) · Mapped (79) |
| Mutation of perinatal myosin heavy chain associated with a Carney complex variant. Veugelers M., Bressan M., McDermott D.A., Weremowicz S., Morton C.C., Mabry C.C., Lefaivre J.-F., Zunamon A., Destree A., Chaudron J.-M. et al. N. Engl. J. Med. 351:460-469(2004) · UniProtKB (1) · Mapped (3) |
| Reciprocal changes of CD44 and GAP-43 expression in the dentate gyrus inner molecular layer after status epilepticus in mice. Borges K., McDermott D.L., Dingledine R. Exp. Neurol. 188:1-10(2004) · Mapped (10) |
| Role for CCR5Delta32 protein in resistance to R5, R5X4, and X4 human immunodeficiency virus type 1 in primary CD4+ cells. Agrawal L., Lu X., Qingwen J., VanHorn-Ali Z., Nicolescu I.V., McDermott D.H., Murphy P.M., Alkhatib G. J. Virol. 78:2277-2287(2004) · Mapped (22) |
| Molecular genetic analysis of PRKAG2 in sporadic Wolff-Parkinson-White syndrome. Vaughan C.J., Hom Y., Okin D.A., McDermott D.A., Lerman B.B., Basson C.T. J. Cardiovasc. Electrophysiol. 14:263-268(2003) · Mapped (3) |