GW3965, a synthetic liver X receptor (LXR) agonist, reduces angiotensin II‐mediated pressor responses in Sprague–Dawley rats von Leik, C E, Carson, N L, Hennan, J K, Basso, M D, Liu, Q‐Y, Crandall, D L, Nambi, P

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Intragenic loss of function mutations demonstrate the primary role of FMR1 in fragile X syndrome von Lugenbeel, Kellie A, Peier, Andrea M, Carson, Nancy L, Chudley, Albert E, Nelson, David L

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Development of a clinical assay for detection of GAA mutations and characterization of the GAA mutation spectrum in a Canadian cohort of individuals with glycogen storage disease,... von McCready, M.E., Carson, N.L., Chakraborty, P., Clarke, J.T.R., Callahan, J.W., Skomorowski, M.A., Chan, A.K.J., Bamforth, F., Casey, R., Rupar, C.A., Geraghty, M.T.

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2420Effects of a selective small-molecule formyl peptide receptor 2 agonist on post myocardial inflammation and left ventricular structure-function relationships von Garcia, R A, Lupisella, J A, Zhang, R, Carson, N L, Wang, Z, Hsu, M Y, Fernando, G, Ryan, C S, Dierks, E, Asahina, Y, Kohno, Y, Wurtz, N R, Ostrowski, J, Ito, B R, Villarreal, F J

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Mechanical properties of adult feline ventricular myocytes in culture von Pollack, P. S, Carson, N. L, Nuss, H. B, Marino, T. A, Houser, S. R

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A physical map of human chromosome 10 and a comparison with an existing genetic map von Carson, Nancy L., Simpson, Nancy E.

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Preliminary assessment of captopril sonography in screening for renal artery stenosis von Gottlieb, Ronald H., Lieberman, Jeffrey L., Ghaed, Victor N., Grossman, Eric B., Waldman, David L., Azodo, Michael V.U., Watt, Graeme H., Robinette, William B., Carson, Nancy L.

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The β subunit locus of the human fibronectin receptor: DNA restriction fragment length polymorphism and linkage mapping studies von JINGSHI WU, GIUFFRA, L. A, GOODFELLOW, P. J, MYERS, S, CARSON, N. L, ANDERSON, L, HOYLE, L. S, SIMPSON, N. E, KIDD, K. K

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Interstitial 4p deletion in a child with an Angelman syndrome-like phenotype von Innes, Am, Chudley, Ae, Carson, Nl, Dawson, Aj

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Transmission of the FRAXA haplotype from three nonpenetrant brothers to their affected grandsons: An update with AGG interspersion analysis von Mogk, R.L., Carson, N.L., Chudley, A.E., Dawson, A.J.

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A Pvull RFLP detected by pOB231 at CDC2 on human chromosome 10 von CARSON, N. L, MYERS, S, SIMPSON, N. E

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The genetic defect in multiple endocrine neoplasia type 2A maps next to the centromere of chromosome 10 von Wu, J S, Carson, N L, Myers, S, Pakstis, A J, Kidd, J R, Castiglione, C M, Anderson, L, Hoyle, L S, Genel, M, Verdy, M

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Norepinephrine‐induced cardiac hypertrophy of the cat heart von Marino, Thomas A., Cassidy, Michael, Marino, Deborah R., Carson, Nancy L., Houser, Steven

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A PvuII RFLP detected by pOB231 at CDC2 on human chromosome 10 von Carson, N L, Myers, S, Simpson, N E

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The ACE D/D genotype is protective against the development of idiopathic deep vein thrombosis and pulmonary embolism von Wells, Philip S., Rodger, Marc A., Forgie, Melissa A., Langlois, Nicole J., Armstrong, Linlea, Carson, Nancy L., Jaffey, James

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Compound heterozygosity for a novel nine‐nucleotide deletion and the Asn45Ser missense mutation in the glycoprotein IX gene in a patient with Bernard‐Soulier syndrome von Drouin, Jeanne, Carson, Nancy L., Laneuville, Odette

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The mutation for medullary thyroid carcinoma with parathyroid tumors (MTC with PTs) is closely linked to the centromeric region of chromosome 10 von Carson, N L, Wu, J S, Jackson, C E, Kidd, K K, Simpson, N E

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Congenital club foot with survival of motor neuron 1, telomeric (SMN1) gene deletion von Echenne, Bernard, Rivier, François, Roubertie, Agathe, Carson, Nancy L

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Two HinfI RFLPs detected by p alpha 10RP8 at D10Z1 von Carson, N L, Simpson, N E

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Two HinfI RFLPs detected by pα 10RP8 at D10Z1 von CARSON, N. L, SIMPSON, N. E

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