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11 results for author:"Moyzis R.K."Drop in Literature Citations

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Molecular genetic contribution to the developmental course of attention-deficit hyperactivity disorder.

Langley K., Fowler T.A., Grady D.L., Moyzis R.K., Holmans P.A., van den Bree M.B., Owen M.J., O'Donovan M.C., Thapar A.

Eur Child Adolesc Psychiatry 18:26-32(2009) · Mapped (60)

The sequence and analysis of duplication-rich human chromosome 16.

Martin J., Han C., Gordon L.A., Terry A., Prabhakar S., She X., Xie G., Hellsten U., Chan Y.M., Altherr M. et al.

Nature 432:988-994(2004) · UniProtKB (629)

High prevalence of rare dopamine receptor D4 alleles in children diagnosed with attention-deficit hyperactivity disorder.

Grady D.L., Chi H.C., Ding Y.C., Smith M., Wang E., Schuck S., Flodman P., Spence M.A., Swanson J.M., Moyzis R.K.

Mol. Psychiatry 8:536-545(2003) · Mapped (59)

Evidence of positive selection acting at the human dopamine receptor D4 gene locus.

Ding Y.C., Chi H.C., Grady D.L., Morishima A., Kidd J.R., Kidd K.K., Flodman P., Spence M.A., Schuck S., Swanson J.M. et al.

Proc. Natl. Acad. Sci. U.S.A. 99:309-314(2002) · UniProtKB (42) · Mapped (17)

Construction of an approximately 700-kb transcript map around the familial Mediterranean fever locus on human chromosome 16p13.3.

Centola M., Chen X., Sood R., Deng Z., Aksentijevich I., Blake T., Ricke D.O., Chen X., Wood G., Zaks N. et al.

Genome Res. 8:1172-1191(1998) · UniProtKB (2)

Centromeric protein B null mice are viable with no apparent abnormalities.

Perez-Castro A.V., Shamanski F.L., Meneses J.J., Lovato T.L., Vogel K.G., Moyzis R.K., Pedersen R.

Dev. Biol. 201:135-143(1998) · Mapped (2)

Ancient missense mutations in a new member of the RoRet gene family are likely to cause familial Mediterranean fever.

Aksentijevich I., Centola M., Deng Z., Sood R., Balow J.E. Jr., Wood G., Zaks N., Mansfield E., Chen X., Eisenberg S. et al.

Cell 90:797-807(1997) · UniProtKB (1)

Genomic structure and complete nucleotide sequence of the Batten disease gene, CLN3.

Mitchison H.M., Munroe P.B., O'Rawe A.M., Taschner P.E.M., de Vos N., Kremmidiotis G., Lensink I., Munk A.C., D'Arigo K.L., Anderson J.W. et al.

Genomics 40:346-350(1997) · UniProtKB (1)

Associations of UBE2I with RAD52, UBL1, p53, and RAD51 proteins in a yeast two-hybrid system.

Shen Z., Pardington-Purtymun P.E., Comeaux J.C., Moyzis R.K., Chen D.J.

Genomics 37:183-186(1996) · Mapped (4)

UBL1, a human ubiquitin-like protein associating with human RAD51/RAD52 proteins.

Shen Z., Pardington-Purtymun P.E., Comeaux J.C., Moyzis R.K., Chen D.J.

Genomics 36:271-279(1996) · UniProtKB (1) · Mapped (1)

Multiple opsin mRNA species in bovine retina.

Kuo C.-H., Yamagata K., Moyzis R.K., Bitensky M.W., Miki N.

Brain Res. 387:251-260(1986) · UniProtKB (1)

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