A microarray screen for novel candidate genes in coeliac disease pathogenesis
Diosdado, B, Wapenaar, M C, Franke, L, Duran, K J, Goerres, M J, Hadithi, M, Crusius, J B A, Meijer, J W R, Duggan, D J, Mulder, C J J, Holstege, F C P, Wijmenga, C
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Published in Gut (01.07.2004)
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Mutations in the Sarcoglycan Genes in Patients with Myopathy
Duggan, David J, Gorospe, J. Rafael, Fanin, Marina, Hoffman, Eric P, Angelini, Corrado, Pegoraro, E, Noguchi, S, Ozawa, E, Pendlebury, W, Waclawik, A.J, Duenas, D.A, Hausmanowa-Petrusewicz, I, Fidzianska, A, Bean, S.C, Haller, J.S, Bodensteiner, J, Greco, C.M, Pestronk, A, Berardinelli, A, Gelinas, D.F, Abram, H, Kuncl, R.W
Published in The New England journal of medicine (27.02.1997)
Published in The New England journal of medicine (27.02.1997)
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The clinical spectrum of sarcoglycanopathies
Angelini, C, Fanin, M, Freda, M P, Duggan, D J, Siciliano, G, Hoffman, E P
Published in Neurology (01.01.1999)
Published in Neurology (01.01.1999)
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β-sarcoglycan (A3b) mutations cause autosomal recessive muscular dystrophy with loss of the sarcoglycan complex
Bönnemann, Carsten G, Yoshida, Mikiharu, Mizuno, Yuji, McNally, Elizabeth M, Duggan, David J, Modi, Raju, Noguchi, Satoru, Angelini, Corrado, Kunkel, Louis M, Hoffman, Eric P, Gussoni, Emanuela, Ozawa, Eijiro
Published in Nature genetics (01.11.1995)
Published in Nature genetics (01.11.1995)
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Caveolin-3 in Muscular Dystrophy
McNally, Elizabeth M., de Sá Moreira, Eloisa, Duggan, David J., Bönnemann, Carsten G., Lisanti, Michael P., Lidov, Hart G.W., Vainzof, Mariz, Rita Passos-Bueno, M., Hoffman, Eric P., Zatz, Mayana, Kunkel, Louis M.
Published in Human molecular genetics (01.05.1998)
Published in Human molecular genetics (01.05.1998)
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Genetic epidemiology of muscular dystrophies resulting from sarcoglycan gene mutations
Fanin, M, Duggan, D J, Mostacciuolo, M L, Martinello, F, Freda, M P, Sorarù, G, Trevisan, C P, Hoffman, E P, Angelini, C
Published in Journal of medical genetics (01.12.1997)
Published in Journal of medical genetics (01.12.1997)
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MYB oncogene amplification in hereditary BRCA1 breast cancer
KAURANIEMI, Päivikki, HEDENFALK, Ingrid, PERSSON, Karin, DUGGAN, David J, TANNER, Minna, JOHANNSSON, Oskar, OLSSON, Hakan, TRENT, Jeffrey M, ISOLA, Jorma, BORG, Ake
Published in Cancer research (Chicago, Ill.) (01.10.2000)
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Published in Cancer research (Chicago, Ill.) (01.10.2000)
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Homozygous α-sarcoglycan mutation in two siblings: One asymptomatic and one steroid-responsive mild limb-girdle muscular dystrophy patient
Angelini, Corrado, Fanin, Marina, Menegazzo, Elisabetta, Freda, Maria Pia, Duggan, David J., Hoffman, Eric P.
Published in Muscle & nerve (01.06.1998)
Published in Muscle & nerve (01.06.1998)
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Heart involvement in muscular dystrophies due to sarcoglycan gene mutations
Melacini, P., Fanin, M., Duggan, D.J., Freda, M.P., Berardinelli, A., Danieli, G.A., Barchitta, A., Hoffman, E.P., Volta, S. Dalla, Angelini, C.
Published in Muscle & nerve (01.04.1999)
Published in Muscle & nerve (01.04.1999)
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Human prostate cancer and benign prostatic hyperplasia : Molecular dissection by gene expression profiling
JUN LUO, DUGGAN, David J, YIDONG CHEN, SAUVAGEOT, Jurga, EWING, Charles M, BITTNER, Michael L, TRENT, Jeffrey M, ISAACS, William B
Published in Cancer research (Chicago, Ill.) (15.06.2001)
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Published in Cancer research (Chicago, Ill.) (15.06.2001)
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A dystrophin missense mutation showing persistence of dystrophin and dystrophin-associated proteins yet a severe phenotype
Goldberg, L R, Hausmanowa-Petrusewicz, I, Fidzianska, A, Duggan, D J, Steinberg, L S, Hoffman, E P
Published in Annals of neurology (01.12.1998)
Published in Annals of neurology (01.12.1998)
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α-Sarcoglycan (adhalin) deficiency: complete deficiency patients are 5% of childhood-onset dystrophin-normal muscular dystrophy and most partial deficiency patients do not have gene mutations
Duggan, David J., Fanin, Marina, Pegoraro, Elena, Angelini, Corrado, Hoffman, Eric P.
Published in Journal of the neurological sciences (01.09.1996)
Published in Journal of the neurological sciences (01.09.1996)
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Journal Article
Heart involvement in muscular dystrophies due to sarcoglycan gene mutations
Melacini, P., Fanin, M., Duggan, D.J., Freda, M.P., Berardinelli, A., Danieli, G.A., Barchitta, A., Hoffman, E.P., Volta, S. Dalla, Angelini, C.
Published in Muscle & nerve (01.04.1999)
Published in Muscle & nerve (01.04.1999)
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Rapid Construction of Integrated Maps Using Inner Product Mapping: YAC Coverage of Human Chromosome 11
Perlin, Mark W., Duggan, David J., Davis, Katya, Farr, Joan E., Findler, Robert B., Higgins, Michael J., Nowak, Norma J., Evans, Glen A., Qin, Shizhen, Zhang, Jialu, Shows, Thomas B., James, Michael R., Richard, Charles W.
Published in Genomics (San Diego, Calif.) (20.07.1995)
Published in Genomics (San Diego, Calif.) (20.07.1995)
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Mutations in the delta-sarcoglycan gene are a rare cause of autosomal recessive limb-girdle muscular dystrophy (LGMD2)
Duggan, D J, Manchester, D, Stears, K P, Mathews, D J, Hart, C, Hoffman, E P
Published in Neurogenetics (01.05.1997)
Published in Neurogenetics (01.05.1997)
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