Genomic Rearrangements Resulting in PLP1 Deletion Occur by Nonhomologous End Joining and Cause Different Dysmyelinating Phenotypes in Males and Females
Inoue, Ken, Osaka, Hitoshi, Thurston, Virginia C., Clarke, Joe T.R., Yoneyama, Akira, Rosenbarker, Lisa, Bird, Thomas D., Hodes, M.E., Shaffer, Lisa G., Lupski, James R.
Published in American journal of human genetics (01.10.2002)
Published in American journal of human genetics (01.10.2002)
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Properties and Tissue Distribution of Mouse Monomeric Carbonyl Reductase
ISHIKURA, Shuhei, YAMAMOTO, Yutaka, MATSUURA, Kazuya, WEI, Jianjun, HODES, M.E., HARA, Akira
Published in Biological & pharmaceutical bulletin (01.08.1998)
Published in Biological & pharmaceutical bulletin (01.08.1998)
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Heterogeneous Duplications in Patients with Pelizaeus-Merzbacher Disease Suggest a Mechanism of Coupled Homologous and Nonhomologous Recombination
Woodward, Karen J., Cundall, Maria, Sperle, Karen, Sistermans, Erik A., Ross, Mark, Howell, Gareth, Gribble, Susan M., Burford, Deborah C., Carter, Nigel P., Hobson, Donald L., Garbern, James Y., Kamholz, John, Heng, Henry, Hodes, M.E., Malcolm, Sue, Hobson, Grace M.
Published in American journal of human genetics (01.12.2005)
Published in American journal of human genetics (01.12.2005)
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Evaluation of psychological symptoms among presymptomatic HD gene carriers as measured by selected MMPI scales
Close Kirkwood, Sandra, Siemers, Eric, Viken, Richard J, Hodes, M.E, Conneally, P.Michael, Christian, Joe C, Foroud, Tatiana
Published in Journal of psychiatric research (01.11.2002)
Published in Journal of psychiatric research (01.11.2002)
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Additional Copies of the Proteolipid Protein Gene Causing Pelizaeus-Merzbacher Disease Arise by Separate Integration into the X Chromosome
Hodes, M.E., Woodward, Karen, Spinner, Nancy B., Emanuel, Beverly S., Enrico-Simon, Agnes, Kamholz, John, Stambolian, Dwight, Zackai, Elaine H., Pratt, Victoria M., Thomas, I.T., Crandall, Kerry, Dlouhy, Stephen R., Malcolm, Sue
Published in American journal of human genetics (01.07.2000)
Published in American journal of human genetics (01.07.2000)
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The weaver mutation changes the ion selectivity of the affected inwardly rectifying potassium channel GIRK2
Tong, Yanhe, Wei, Jianjun, Zhang, Shengwen, Strong, Judith A., Dlouhy, Stephen R., Hodes, M.E., Ghetti, Bernardino, Yu, Lei
Published in FEBS letters (15.07.1996)
Published in FEBS letters (15.07.1996)
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Confirmation of linkage of limb-girdle muscular dystrophy, type 2, to chromosome 15
Young, K., Foroud, T., Williams, P., Jackson, C.E., Beckmann, J.S., Cohen, D., Conneally, P.M., Tischfield, J., Hodes, M.E.
Published in Genomics (San Diego, Calif.) (01.08.1992)
Published in Genomics (San Diego, Calif.) (01.08.1992)
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AhaII polymorphism in human X-linked proteolipid protein gene (PLP)
Trofatter, J A, Pratt, V M, Dlouhy, S R, Hodes, M E
Published in Nucleic acids research (11.11.1991)
Published in Nucleic acids research (11.11.1991)
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Linkage of a new mutation in the proteolipid protein (PLP) gene to Pelizaeus-Merzbacher disease (PMD) in a large Finnish kindred
PRATT, V. M, KIEFER, J. R, LÄHDETIE, J, SCHLEUTKER, J, HODES, M. E, DLOUHY, S. R
Published in American journal of human genetics (01.06.1993)
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Published in American journal of human genetics (01.06.1993)
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