Works matching IS 14345161 AND DT 1999 AND VI 44 AND IP 5
Results: 17
Polymorphic forms of the protein L-isoaspartate (D-aspartate) O-methyltrans-ferase involved in the repair of age-damaged proteins.
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- Journal of Human Genetics, 1999, v. 44, n. 5, p. 275, doi. 10.1007/s100380050161
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Spermatogenic ability is different among males in different Y chromosome lineage.
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- Journal of Human Genetics, 1999, v. 44, n. 5, p. 289, doi. 10.1007/s100380050162
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Transitional change in interaction between HIF-1 and HNF-4 in response to hypoxia.
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- Journal of Human Genetics, 1999, v. 44, n. 5, p. 293, doi. 10.1007/s100380050163
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Molecular cloning, expression, and mapping of a novel human cDNA, GRP17, highly homologous to human gadd45 and murine MyD118.
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- Journal of Human Genetics, 1999, v. 44, n. 5, p. 300, doi. 10.1007/s100380050164
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Rapid mass screening method and counseling for the 1555A⇾G mitochondrial mutation.
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- Journal of Human Genetics, 1999, v. 44, n. 5, p. 304, doi. 10.1007/s100380050165
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No association between atopic asthma and a coding variant of FcεR1β in a Japanese population.
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- Journal of Human Genetics, 1999, v. 44, n. 5, p. 308, doi. 10.1007/s100380050166
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Molecular analysis of Japanese patients with steroid 21-hydroxylase deficiency.
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- Journal of Human Genetics, 1999, v. 44, n. 5, p. 312, doi. 10.1007/s100380050167
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Preferential transmission of maternal allele with DQA1[sup *] 0301-DQB1[sup *] 0302 haplotype to affected offspring in families with type 1 diabetes.
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- Journal of Human Genetics, 1999, v. 44, n. 5, p. 318, doi. 10.1007/s100380050168
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Mutation analysis of a Japanese patient with fucosidosis.
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- Journal of Human Genetics, 1999, v. 44, n. 5, p. 323, doi. 10.1007/s100380050169
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A clinical and molecular study of a patient with Simpson-Golabi-Behmel syndrome.
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- Journal of Human Genetics, 1999, v. 44, n. 5, p. 327, doi. 10.1007/s100380050170
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Complete cDNA sequence and genomic organization of a human pancreas-specific gene homologous to Caenorhabditis elegans sel-1.
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- Journal of Human Genetics, 1999, v. 44, n. 5, p. 330, doi. 10.1007/s100380050171
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Cloning and characterization of human and mouse PROSC (proline synthetase co-transcribed) genes.
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- Journal of Human Genetics, 1999, v. 44, n. 5, p. 337, doi. 10.1007/s100380050172
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Isolation and localization of an IDDMK1,2-22-related human endogenous retroviral gene, and identification of a CA repeat marker at its locus.
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- Journal of Human Genetics, 1999, v. 44, n. 5, p. 343, doi. 10.1007/s100380050173
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Isolation, characterization, and mapping of four novel polymorphic markers and an H3.3B pseudogene to chromosome 9p21-22.
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- Journal of Human Genetics, 1999, v. 44, n. 5, p. 348, doi. 10.1007/s100380050174
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Isolation and radiation hybrid mapping of a highly polymorphic CA repeat sequence at the SREBP cleavage-activating protein (SCAP) locus.
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- Journal of Human Genetics, 1999, v. 44, n. 5, p. 350, doi. 10.1007/s100380050175
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Novel polymorphism in the 5′-untranslated region of the interleukin-4 gene.
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- Journal of Human Genetics, 1999, v. 44, n. 5, p. 352, doi. 10.1007/s100380050176
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Two single nucleotide polymorphisms of the hSNF5/INI1 gene.
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- Journal of Human Genetics, 1999, v. 44, n. 5, p. 354, doi. 10.1007/s100380050177
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