Dinucleotide repeat polymorphism in the human glucagon gene (GCG)

Por Wu, S., Xiang, K., Bell, G.I.
Publicado em 1991

BamHI RFLP at the insulin-like growth factor II (IGF2) locus on chromosome 11.

Por Xiang, K, Karam, J H, Bell, G I
Publicado em 1987

Apa I and Sst I RFLPs at the insulin-like growth factor II (IGF2) locus on chromosome 11.

Por Xiang, K, Cox, N J, Bell, G I
Publicado em 1988

Gene regulatory networks generating the phenomena of additivity, dominance and epistasis.

Por Omholt, S W, Plahte, E, Oyehaug, L, Xiang, K
Publicado em 2000

Linkage disequilibrium in the human insulin/insulin-like growth factor II region of human chromosome II.

Por Cox, N J, Bell, G I, Xiang, K S
Publicado em 1988

Dinucleotide repeat polymorphism in Gs-α subunit gene (GNAS1) on chromosome 20

Por Granqvist, M., Xiang, K., Seino, M., Bell, G.I.
Publicado em 1991

Dinucleotide repeat polymorphism in D20S17 (CRI-L127)

Por Iwasaki, N., Xiang, K., Seino, M., Bell, G.I.
Publicado em 1991

Microsatellite polymorphism in human insulin receptor gene (INSR) on chromosome 19

Por Xiang, K., Granqvist, M., Seino, M., Seino, S., Bell, G.I.
Publicado em 1991

Multiple Taq I RFLPs at the human manganese superoxide dismutase (S0D2) locus on chromosome 6.

Por Xiang, K, Cox, N J, Hallewell, R A, Bell, G I
Publicado em 1987

Bgl II RFLP at the human erythrocyte/HepG2-type glucose transporter (GLUT) locus on chromosome 1.

Por Xiang, K, Cox, N J, Karam, J H, Bell, G I
Publicado em 1987

Dinucleotide repeat polymorphism in human GLUT2/liver facilitative glucose transporter gene on chromosome 3

Por Granqvist, M., Xiang, K., Seino, M., Fukumoto, H., Bell, G.I.
Publicado em 1991

Dinucleotide repeat polymorphism in the human SRC gene on chromosome 20

Por Xiang, K., Phillippe, G., Seino, M., Bonham, K., Fugita, D.J., Bell, G.I.
Publicado em 1991

A common variant of NOS1AP is associated with QT interval duration in a Chinese population with Type 2 diabetes

Por Lu, J., Hu, C., Hu, W., Zhang, R., Wang, C., Qin, W., Yu, W., Xiang, K., Jia, W.
Publicado em 2010

Functional analyses of the mutation nt-128 T→G in the hepatocyte nuclear factor-1α promoter region in Chinese diabetes pedigrees

Por Fang, Q., Chen, S., Wang, Y., Jiang, S., Zhang, R., Hu, C., Wang, C., Liu, F., Xiang, K., Jia, W.
Publicado em 2012

Gene for non-insulin-dependent diabetes mellitus (maturity-onset diabetes of the young subtype) is linked to DNA polymorphism on human chromosome 20q.

Por Bell, G I, Xiang, K S, Newman, M V, Wu, S H, Wright, L G, Fajans, S S, Spielman, R S, Cox, N J
Publicado em 1991

Usefulness of DWI in preoperative assessment of deep myometrial invasion in patients with endometrial carcinoma: a systematic review and meta-analysis

Por Das, Sushant K, Niu, Xiang K, Wang, Jing L, Zeng, Li C, Wang, Wen X, Bhetuwal, Anup, Yang, Han F
Publicado no Cancer Imaging (2014)

A yeast artificial chromosome-based map of the region of chromosome 20 containing the diabetes-susceptibility gene, MODY1, and a myeloid leukemia related gene.

Por Stoffel, M, Le Beau, M M, Espinosa, R, Bohlander, S F, Le Paslier, D, Cohen, D, Xiang, K S, Cox, N J, Fajans, S S, Bell, C I
Publicado em 1996

Genome-wide association study in a Chinese population identifies a susceptibility locus for type 2 diabetes at 7q32 near PAX4

Por Ma, R. C. W., Hu, C., Tam, C. H., Zhang, R., Kwan, P., Leung, T. F., Thomas, G. N., Go, M. J., Hara, K., Sim, X., Ho, J. S. K., Wang, C., Li, H., Lu, L., Wang, Y., Li, J. W., Wang, Y., Lam, V. K. L., Wang, J., Yu, W., Kim, Y. J., Ng, D. P., Fujita, H., Panoutsopoulou, K., Day-Williams, A. G., Lee, H. M., Ng, A. C. W., Fang, Y-J., Kong, A. P. S., Jiang, F., Ma, X., Hou, X., Tang, S., Lu, J., Yamauchi, T., Tsui, S. K. W., Woo, J., Leung, P. C., Zhang, X., Tang, N. L. S., Sy, H. Y., Liu, J., Wong, T. Y., Lee, J. Y., Maeda, S., Xu, G., Cherny, S. S., Chan, T. F., Ng, M. C. Y., Xiang, K., Morris, A. P., Keildson, S., Hu, R., Ji, L., Lin, X., Cho, Y. S., Kadowaki, T., Tai, E. S., Zeggini, E., McCarthy, M. I., Hon, K. L., Baum, L., Tomlinson, B., So, W. Y., Bao, Y., Chan, J. C. N., Jia, W.
Publicado em 2013