11
results
for author:"Herbrick J.-A."
in Literature Citations
| Human chromosome 7: DNA sequence and biology. Scherer S.W., Cheung J., MacDonald J.R., Osborne L.R., Nakabayashi K., Herbrick J.-A., Carson A.R., Parker-Katiraee L., Skaug J., Khaja R. et al. Science 300:767-772(2003) · UniProtKB (658) |
| Molecular genetic studies of human chromosome 7 in Russell-Silver syndrome. Nakabayashi K., Fernandez B.A., Teshima I., Shuman C., Proud V.K., Curry C.J., Chitayat D., Grebe T., Ming J., Oshimura M. et al. |
| Fusion of two novel genes, RBM15 and MKL1, in the t(1;22)(p13;q13) of acute megakaryoblastic leukemia. Ma Z., Morris S.W., Valentine V., Li M., Herbrick J.-A., Cui X., Bouman D., Li Y., Mehta P.K., Nizetic D. et al. Nat. Genet. 28:220-221(2001) · UniProtKB (2) |
| Identification of a novel gene on chromosome 7q31 that is interrupted by a translocation breakpoint in an autistic individual. Vincent J.B., Herbrick J.-A., Gurling H.M.D., Bolton P.F., Roberts W., Scherer S.W. Am. J. Hum. Genet. 67:510-514(2000) · UniProtKB (3) · Mapped (1) |
| Chromosomal localization of phospholipase A2 activating protein, an ets2 target gene, to 9p21. Beatty B., Qi S., Pienkowska M., Scherer S.W., Testa J.R., Cheng J.Q., Herbrick J.-A., Scheidl T., Zhang Z., Kola I. et al. Genomics 62:529-532(1999) · UniProtKB (1) |
| Human GBF1 is a ubiquitously expressed gene of the sec7 domain family mapping to 10q24. Mansour S.J., Herbrick J.-A., Scherer S.W., Melancon P. Genomics 54:323-327(1998) · UniProtKB (1) |
| Mutations in a gene encoding a novel protein tyrosine phosphatase cause progressive myoclonus epilepsy. Minassian B.A., Lee J.R., Herbrick J.-A., Huizenga J., Soder S., Mungall A.J., Dunham I., Gardner R., Fong C.G., Carpenter S. et al. Nat. Genet. 20:171-174(1998) · UniProtKB (1) |
| Structural characterization and mapping of the normal epithelial cell-specific 1 gene. Luo L.-Y., Herbrick J.A., Scherer S.W., Beatty B., Squire J., Diamandis E.P. Biochem. Biophys. Res. Commun. 247:580-586(1998) · UniProtKB (1) |
| Molecular analysis of the PDS gene in Pendred syndrome (sensorineural hearing loss and goitre). Coyle B., Reardon W., Herbrick J.-A., Tsui L.-C., Gausden E., Lee J., Coffey R., Grueters A., Grossman A., Phelps P.D. et al. Hum. Mol. Genet. 7:1105-1112(1998) · UniProtKB (1) |
| P450RAI (CYP26A1) maps to human chromosome 10q23-q24 and mouse chromosome 19C2-3. White J.A., Beckett B., Scherer S.W., Herbrick J.A., Petkovich M. Genomics 48:270-272(1998) · Mapped (1) |
| Cone-rod dystrophy due to mutations in a novel photoreceptor-specific homeobox gene (CRX) essential for maintenance of the photoreceptor. Freund C.L., Gregory-Evans C.Y., Furukawa T., Papaioannou M., Looser J., Ploder L., Bellingham J., Ng D., Herbrick J.-A.S., Duncan A. et al. |
