MeSH Review:
Chromosomes, Artificial, P1 Bacteriophage
- Mutations in SLC19A2 cause thiamine-responsive megaloblastic anaemia associated with diabetes mellitus and deafness. Labay, V., Raz, T., Baron, D., Mandel, H., Williams, H., Barrett, T., Szargel, R., McDonald, L., Shalata, A., Nosaka, K., Gregory, S., Cohen, N. Nat. Genet. (1999)
- Mutations in ATP2A2, encoding a Ca2+ pump, cause Darier disease. Sakuntabhai, A., Ruiz-Perez, V., Carter, S., Jacobsen, N., Burge, S., Monk, S., Smith, M., Munro, C.S., O'Donovan, M., Craddock, N., Kucherlapati, R., Rees, J.L., Owen, M., Lathrop, G.M., Monaco, A.P., Strachan, T., Hovnanian, A. Nat. Genet. (1999)
- Identification and functional characterization of the promoter region of the human organic anion transporting polypeptide gene. Kullak-Ublick, G.A., Beuers, U., Fahney, C., Hagenbuch, B., Meier, P.J., Paumgartner, G. Hepatology (1997)
- A microinjected COL7A1-PAC vector restores synthesis of intact procollagen VII in a dystrophic epidermolysis bullosa keratinocyte cell line. Mecklenbeck, S., Compton, S.H., Mejía, J.E., Cervini, R., Hovnanian, A., Bruckner-Tuderman, L., Barrandon, Y. Hum. Gene Ther. (2002)
- Genomic organization of the dysferlin gene and novel mutations in Miyoshi myopathy. Aoki, M., Liu, J., Richard, I., Bashir, R., Britton, S., Keers, S.M., Oeltjen, J., Brown, H.E., Marchand, S., Bourg, N., Beley, C., McKenna-Yasek, D., Arahata, K., Bohlega, S., Cupler, E., Illa, I., Majneh, I., Barohn, R.J., Urtizberea, J.A., Fardeau, M., Amato, A., Angelini, C., Bushby, K., Beckmann, J.S., Brown, R.H. Neurology (2001)
- Autistic disorder and chromosome 15q11-q13: construction and analysis of a BAC/PAC contig. Maddox, L.O., Menold, M.M., Bass, M.P., Rogala, A.R., Pericak-Vance, M.A., Vance, J.M., Gilbert, J.R. Genomics (1999)
- Physical mapping and evolution of the centromeric class I gene-containing region of the rat MHC. Walter, L., Günther, E. Immunogenetics (2000)
- Use of PCR to screen for promoter elements in genomic DNA library clones. Poppe, M., Hahm, B., Eickelbaum, W., Arand, M., Paweletz, N., Knehr, M. BioTechniques (1999)
- Structural and functional organization of the gene encoding the human thyrotropin-releasing hormone receptor. Matre, V., Høvring, P.I., Orstavik, S., Frengen, E., Rian, E., Velickovic, Z., Murray-McIntosh, R.P., Gautvik, K.M. J. Neurochem. (1999)
- Chromosomal localization, structure, single-nucleotide polymorphisms, and expression of the human H-protein gene of the glycine cleavage system (GCSH), a candidate gene for nonketotic hyperglycinemia. Kure, S., Kojima, K., Kudo, T., Kanno, K., Aoki, Y., Suzuki, Y., Shinka, T., Sakata, Y., Narisawa, K., Matsubara, Y. J. Hum. Genet. (2001)
- Structure of the human acyl-CoA:cholesterol acyltransferase-2 (ACAT-2) gene and its relation to dyslipidemia. Katsuren, K., Tamura, T., Arashiro, R., Takata, K., Matsuura, T., Niikawa, N., Ohta, T. Biochim. Biophys. Acta (2001)
- Identification, characterization and cytogenetic mapping of a yeast Vps54 homolog in rat and mouse. Walter, L., Stark, S., Helou, K., Flügge, P., Levan, G., Günther, E. Gene (2002)
- Five new families with resistance to thyroid hormone not caused by mutations in the thyroid hormone receptor beta gene. Pohlenz, J., Weiss, R.E., Macchia, P.E., Pannain, S., Lau, I.T., Ho, H., Refetoff, S. J. Clin. Endocrinol. Metab. (1999)