Overweight modulates APOE and APOA5 alleles on the risk of severe hypertriglyceridemia
Lee, Ming-Jen, Chien, Kuo-Liong, Chen, Ming-Fong, Stephenson, Dennis A., Su, Ta-Chen
Published in Clinica chimica acta (01.02.2013)
Published in Clinica chimica acta (01.02.2013)
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The proto-oncogene c-kit encoding a transmembrane tyrosine kinase receptor maps to the mouse W locus
Chabot, B, Stephenson, D A, Chapman, V M, Besmer, P, Bernstein, A
Published in Nature (London) (01.09.1988)
Published in Nature (London) (01.09.1988)
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Disrupted SOX10 function causes spongiform neurodegeneration in gray tremor mice
Anderson, Sarah R, Lee, Inyoul, Ebeling, Christine, Stephenson, Dennis A, Schweitzer, Kelsey M, Baxter, David, Moon, Tara M, LaPierre, Sarah, Jaques, Benjamin, Silvius, Derek, Wegner, Michael, Hood, Leroy E, Carlson, George, Gunn, Teresa M
Published in Mammalian genome (01.02.2015)
Published in Mammalian genome (01.02.2015)
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Characterization of a familial case with primary erythromelalgia from Taiwan
LEE, Ming-Jen, YU, Hsin-Su, HSIEH, Sung-Tsang, STEPHENSON, Dennis A, LU, Chien-Jung, YANG, Chih-Chao
Published in Journal of neurology (01.02.2007)
Published in Journal of neurology (01.02.2007)
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Identification of forty-five novel and twenty-three known NF1 mutations in Chinese patients with neurofibromatosis type 1
Lee, Ming-Jen, Su, Yi-Ning, You, Huey-Ling, Chiou, Shinn-Chong, Lin, Li-Chu, Yang, Chih-Chao, Lee, Wang-Chao, Hwu, Wu-Liang, Hsieh, Fon-Jou, Stephenson, Dennis A., Yu, Chia-Li
Published in Human mutation (01.08.2006)
Published in Human mutation (01.08.2006)
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Journal Article
Hereditary sensory neuropathy is caused by a mutation in the delta subunit of the cytosolic chaperonin-containing t-complex peptide-1 (Cct4 ) gene
Lee, Ming-Jen, Stephenson, Dennis A., Groves, Michael J., Sweeney, Mary G., Davis, Mary B., An, Shu-Fang, Houlden, Henry, Salih, Mustafa A. M., Timmerman, Vincent, de Jonghe, Peter, Auer-Grumbach, Michaela, Di Maria, Emilio, Scaravilli, Francesco, Wood, Nicholas W., Reilly, Mary M.
Published in Human molecular genetics (01.08.2003)
Published in Human molecular genetics (01.08.2003)
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Spinocerebellar Ataxia Types 1, 2, 3 and 6: the Clinical Spectrum of Ataxia and Morphometric Brainstem and Cerebellar Findings
Jacobi, Heike, Hauser, Till-Karsten, Giunti, Paola, Globas, Christoph, Bauer, Peter, Schmitz-Hübsch, Tanja, Baliko, László, Filla, Alessandro, Mariotti, Caterina, Rakowicz, Maria, Charles, Perine, Ribai, Pascale, Szymanski, Sandra, Infante, Jon, van de Warrenburg, Bart P. C., Dürr, Alexandra, Timmann, Dagmar, Boesch, Sylvia, Fancellu, Roberto, Rola, Rafal, Depondt, Chantal, Schöls, Ludger, Zdzienicka, Elzbieta, Kang, Jun-Suk, Ratzka, Susanne, Kremer, Berry, Stephenson, Dennis A., Melegh, Béla, Pandolfo, Massimo, du Montcel, Sophie Tezenas, Borkert, Johannes, Schulz, Jörg B., Klockgether, Thomas
Published in Cerebellum (London, England) (01.03.2012)
Published in Cerebellum (London, England) (01.03.2012)
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Identification of forty-five novel and twenty-three knownNF1 mutations in Chinese patients with neurofibromatosis type 1
Lee, Ming-Jen, Su, Yi-Ning, You, Huey-Ling, Chiou, Shinn-Chong, Lin, Li-Chu, Yang, Chih-Chao, Lee, Wang-Chao, Hwu, Wu-Liang, Hsieh, Fon-Jou, Stephenson, Dennis A., Yu, Chia-Li
Published in Human mutation (01.08.2006)
Published in Human mutation (01.08.2006)
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P2-016 Penetrance of a new mutant allele of the voltage gated calcium channel gene CACNA1A is dependent on amyloid precursor protein (APP) concentration
Mellem, Jerald E., Toxopeus, Corike, Stephenson, Dennis A., Turner, Sherry, Peterson, Dionne, Gilchrist, Julie, Carlson, George A.
Published in Neurobiology of aging (01.07.2004)
Published in Neurobiology of aging (01.07.2004)
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Platelet-Derived Growth Factor Receptor α-Subunit Gene (Pdgfra) is Deleted in the Mouse Patch (Ph) Mutation
Stephenson, Dennis A., Mercola, Mark, Anderson, Elizabeth, Wang, Chiayeng, Stiles, Charles D., Bowen-Pope, Daniel F., Chapman, Verne M.
Published in Proceedings of the National Academy of Sciences - PNAS (01.01.1991)
Published in Proceedings of the National Academy of Sciences - PNAS (01.01.1991)
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Multilocus molecular mapping of the mouse X chromosome
Mullins, Linda J., Grant, Stephen G., Stephenson, Dennis A., Chapman, Verne M.
Published in Genomics (San Diego, Calif.) (01.10.1988)
Published in Genomics (San Diego, Calif.) (01.10.1988)
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