| Isolation and biochemical characterization of two lipases from a metagenomic library of China Holstein cow rumen. Liu K., Wang J., Bu D., Zhao S., McSweeney C., Yu P., Li D.
Biochem. Biophys. Res. Commun. 385:605-611(2009) · UniProtKB (34) |
| A novel missense mutation in the SLC6A19 gene in a Chinese family with Hartnup disorder. Zheng Y., Zhou C., Huang Y., Bu D., Zhu X., Jiang W.
Int. J. Dermatol. 48:388-392(2009) · Mapped (3) |
| Role of hydrogen sulfide in the development of atherosclerotic lesions in apolipoprotein E knockout mice. Wang Y., Zhao X., Jin H., Wei H., Li W., Bu D., Tang X., Ren Y., Tang C., Du J.
Arterioscler. Thromb. Vasc. Biol. 29:173-179(2009) · Mapped (9) |
| Urotensin II is an autocrine/paracrine growth factor for aortic adventitia of rat. Zhang Y., Li Y., Wei R., Wang Z., Bu D., Zhao J., Pang Y., Tang C.
Regul. Pept. 151:88-94(2008) · Mapped (1) |
| DNA methylation in benign breast epithelium in relation to age and breast cancer risk. Euhus D.M., Bu D., Milchgrub S., Xie X.J., Bian A., Leitch A.M., Lewis C.M.
Cancer Epidemiol. Biomarkers Prev. 17:1051-1059(2008) · Mapped (32) |
| Vascular and inflammatory stresses mediate atherosclerosis via RAGE and its ligands in apoE-/- mice. Harja E., Bu D.X., Hudson B.I., Chang J.S., Shen X., Hallam K., Kalea A.Z., Lu Y., Rosario R.H., Oruganti S. et al.
J. Clin. Invest. 118:183-194(2008) · Mapped (54) |
| Genotyping of HLA-I and HLA-II alleles in Chinese patients with paraneoplastic pemphigus. Liu Q., Bu D.F., Li D., Zhu X.J.
Br. J. Dermatol. 158:587-591(2008) · Mapped (3,040) |
| Urotensin II accelerates cardiac fibrosis and hypertrophy of rats induced by isoproterenol. Zhang Y.G., Li Y.G., Liu B.G., Wei R.H., Wang D.M., Tan X.R., Bu D.F., Pang Y.Z., Tang C.S.
Acta Pharmacol. Sin. 28:36-43(2007) · Mapped (2) |
| Induction of neutrophil gelatinase-associated lipocalin in vascular injury via activation of nuclear factor-kappaB. Bu D.X., Hemdahl A.L., Gabrielsen A., Fuxe J., Zhu C., Eriksson P., Yan Z.Q.
Am. J. Pathol. 169:2245-2253(2006) · Mapped (1) |
| An intronic polymorphism associated with increased XRCC1 expression, reduced apoptosis and familial breast cancer. Bu D., Tomlinson G., Lewis C.M., Zhang C., Kildebeck E., Euhus D.M.
Breast Cancer Res. Treat. 99:257-265(2006) · Mapped (5) |
| Alteration of vascular urotensin II receptor in mice with apolipoprotein E gene knockout. Wang Z.J., Shi L.B., Xiong Z.W., Zhang L.F., Meng L., Bu D.F., Tang C.S., Ding W.H.
Peptides 27:858-863(2006) · Mapped (9) |
| Leukotriene B4 signaling through NF-kappaB-dependent BLT1 receptors on vascular smooth muscle cells in atherosclerosis and intimal hyperplasia. Back M., Bu D.X., Branstrom R., Sheikine Y., Yan Z.Q., Hansson G.K.
Proc. Natl. Acad. Sci. U.S.A. 102:17501-17506(2005) · Mapped (2) |
| Compound heterozygosity for new splice site mutations in the plakophilin 1 gene (PKP1) in a Chinese case of ectodermal dysplasia-skin fragility syndrome. Zheng R., Bu D.F., Zhu X.J.
Acta Derm. Venereol. 85:394-399(2005) · Mapped (3) |
| Association between familial febrile convulsions and HCN2 gene. Ma Y.N., Chen Z.Y., Zou L.P., Zhang Y., Niu S.L., Xu Y.F., Pei P., Bu D.F., Qi Y.
Zhonghua Yi Xue Za Zhi 85:663-666(2005) · Mapped (2) |
| The genomes of Oryza sativa: a history of duplications. Yu J., Wang J., Lin W., Li S., Li H., Zhou J., Ni P., Dong W., Hu S., Zeng C. et al.
PLoS Biol. 3:266-281(2005) · UniProtKB (72,815) |
| Five single nucleotide polymorphisms of casein kinase I gamma 2 gene in children with familial febrile convulsions. Ma Y.N., Hao L., Niu S.L., Xu Y.F., Zhang Y., Pei P., Bu D.F., Qi Y.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi 21:347-350(2004) · Mapped (3) |
| Mutations in SCN9A, encoding a sodium channel alpha subunit, in patients with primary erythermalgia. Yang Y., Wang Y., Li S., Xu Z., Li H., Ma L., Fan J., Bu D., Liu B., Fan Z. et al.
J. Med. Genet. 41:171-174(2004) · UniProtKB (1) · Mapped (2) |
| Changes of adrenomedullin and receptor activity modifying protein 2 (RAMP2) in myocardium and aorta in rats with isoproterenol-induced myocardial ischemia. Qi Y.F., Shi Y.R., Bu D.F., Pang Y.Z., Tang C.S.
Peptides 24:463-468(2003) · Mapped (2) |
| A novel splice site mutation in collagen type VII gene in a Chinese family with dominant dystrophic epidermolysis bullosa pruriginosa. Jiang W., Bu D., Yang Y., Zhu X.
Acta Derm. Venereol. 82:187-191(2002) · Mapped (2) |
| Impaired lung branching morphogenesis in the absence of functional EGF receptor. Miettinen P.J., Warburton D., Bu D., Zhao J.S., Berger J.E., Minoo P., Koivisto T., Allen L., Dobbs L., Werb Z. et al.
Dev. Biol. 186:224-236(1997) · Mapped (6) |
| Abrogation of transforming growth factor-beta type II receptor stimulates embryonic mouse lung branching morphogenesis in culture. Zhao J., Bu D., Lee M., Slavkin H.C., Hall F.L., Warburton D.
Dev. Biol. 180:242-257(1996) · Mapped (7) |
| The exon-intron organization of the genes (GAD1 and GAD2) encoding two human glutamate decarboxylases (GAD67 and GAD65) suggests that they derive from a common ancestral GAD. Bu D.-F., Tobin A.J.
Genomics 21:222-228(1994) · UniProtKB (2) |
| Abnormal lung development and cleft palate in mice lacking TGF-beta 3 indicates defects of epithelial-mesenchymal interaction. Kaartinen V., Voncken J.W., Shuler C., Warburton D., Bu D., Heisterkamp N., Groffen J.
Nat. Genet. 11:415-421(1995) · Mapped (6) |
| Two human glutamate decarboxylases, 65-kDa GAD and 67-kDa GAD, are each encoded by a single gene. Bu D.-F., Erlander M.G., Hitz B.C., Tillakaratne N.J., Kaufman D.L., Wagner-Mcpherson C.B., Evans G.A., Tobin A.J.
Proc. Natl. Acad. Sci. U.S.A. 89:2115-2119(1992) · UniProtKB (2) · Mapped (1) |
in Literature Citations
