Intragenic loss of function mutations demonstrate the primary role of FMR1 in fragile X syndrome
Lugenbeel, Kellie A, Peier, Andrea M, Carson, Nancy L, Chudley, Albert E, Nelson, David L
Published in Nature genetics (01.08.1995)
Published in Nature genetics (01.08.1995)
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Journal Article
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, type II
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.
Published in Molecular genetics and metabolism (01.12.2007)
Published in Molecular genetics and metabolism (01.12.2007)
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Journal Article
Mechanical properties of adult feline ventricular myocytes in culture
Pollack, P S, Carson, N L, Nuss, H B, Marino, T A, Houser, S R
Published in The American journal of physiology (01.01.1991)
Published in The American journal of physiology (01.01.1991)
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Journal Article
Preliminary assessment of captopril sonography in screening for renal artery stenosis
Gottlieb, R H, Lieberman, J L, Ghaed, V N, Grossman, E B, Waldman, D L, Azodo, M V, Watt, G H, Robinette, W B, Carson, N L
Published in Academic radiology (01.01.1996)
Published in Academic radiology (01.01.1996)
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Journal Article
The beta subunit locus of the human fibronectin receptor: DNA restriction fragment length polymorphism and linkage mapping studies
Wu, J S, Giuffra, L A, Goodfellow, P J, Myers, S, Carson, N L, Anderson, L, Hoyle, L S, Simpson, N E, Kidd, K K
Published in Human genetics (01.11.1989)
Published in Human genetics (01.11.1989)
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Journal Article
2420Effects of a selective small-molecule formyl peptide receptor 2 agonist on post myocardial inflammation and left ventricular structure-function relationships
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
Published in European heart journal (01.10.2019)
Published in European heart journal (01.10.2019)
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Journal Article
Norepinephrine-induced cardiac hypertrophy of the cat heart
Marino, T A, Cassidy, M, Marino, D R, Carson, N L, Houser, S
Published in The Anatomical record (01.04.1991)
Published in The Anatomical record (01.04.1991)
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Journal Article
The genetic defect in multiple endocrine neoplasia type 2A maps next to the centromere of chromosome 10
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
Published in American journal of human genetics (01.03.1990)
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Published in American journal of human genetics (01.03.1990)
Journal Article
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
Drouin, Jeanne, Carson, Nancy L., Laneuville, Odette
Published in American journal of hematology (01.01.2005)
Published in American journal of hematology (01.01.2005)
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Journal Article
The ACE D/D genotype is protective against the development of idiopathic deep vein thrombosis and pulmonary embolism
Wells, Philip S, Rodger, Marc A, Forgie, Melissa A, Langlois, Nicole J, Armstrong, Linlea, Carson, Nancy L, Jaffey, James
Published in Thrombosis and haemostasis (01.11.2003)
Published in Thrombosis and haemostasis (01.11.2003)
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Journal Article
Congenital club foot with survival of motor neuron 1, telomeric (SMN1) gene deletion
Echenne, Bernard, Rivier, François, Roubertie, Agathe, Carson, Nancy L
Published in Journal of child neurology (01.03.2004)
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Published in Journal of child neurology (01.03.2004)
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