Chen F - Search Results

1

Comparative sequence analysis of 634 kb of the mouse chromosome 16 region of conserved synteny with the human velocardiofacial syndrome region on chromosome 22q11.2.

Lund J, Chen F, Hua A, Roe B, Budarf M, Emanuel BS, Reeves RH. Lund J, et al. Among authors: chen f. Genomics. 2000 Feb 1;63(3):374-83. doi: 10.1006/geno.1999.6044. Genomics. 2000. PMID: 10704284 Free article.

2

Sequence-ready physical map of the mouse chromosome 16 region with conserved synteny to the human velocardiofacial syndrome region on 22q11.2.

Lund J, Roe B, Chen F, Budarf M, Galili N, Riblet R, Miller RD, Emanuel BS, Reeves RH. Lund J, et al. Among authors: chen f. Mamm Genome. 1999 May;10(5):438-43. doi: 10.1007/s003359901019. Mamm Genome. 1999. PMID: 10337614

3

Chromosome evolution: the junction of mammalian chromosomes in the formation of mouse chromosome 10.

Pletcher MT, Roe BA, Chen F, Do T, Do A, Malaj E, Reeves RH. Pletcher MT, et al. Among authors: chen f. Genome Res. 2000 Oct;10(10):1463-7. doi: 10.1101/gr.146600. Genome Res. 2000. PMID: 11042146 Free PMC article.

4

A transcription map of the DiGeorge and velo-cardio-facial syndrome minimal critical region on 22q11.

Gong W, Emanuel BS, Collins J, Kim DH, Wang Z, Chen F, Zhang G, Roe B, Budarf ML. Gong W, et al. Among authors: chen f. Hum Mol Genet. 1996 Jun;5(6):789-800. doi: 10.1093/hmg/5.6.789. Hum Mol Genet. 1996. PMID: 8776594

5

Disruption of the clathrin heavy chain-like gene (CLTCL) associated with features of DGS/VCFS: a balanced (21;22)(p12;q11) translocation.

Holmes SE, Riazi MA, Gong W, McDermid HE, Sellinger BT, Hua A, Chen F, Wang Z, Zhang G, Roe B, Gonzalez I, McDonald-McGinn DM, Zackai E, Emanuel BS, Budarf ML. Holmes SE, et al. Among authors: chen f. Hum Mol Genet. 1997 Mar;6(3):357-67. doi: 10.1093/hmg/6.3.357. Hum Mol Genet. 1997. PMID: 9147638

6

Characterization of CDC45L: a gene in the 22q11.2 deletion region expressed during murine and human development.

Shaikh TH, Gottlieb S, Sellinger B, Chen F, Roe BA, Oakey RJ, Emanuel BS, Budarf ML. Shaikh TH, et al. Among authors: chen f. Mamm Genome. 1999 Mar;10(3):322-6. doi: 10.1007/s003359900996. Mamm Genome. 1999. PMID: 10051334 No abstract available.

7

Analysis of the cat eye syndrome critical region in humans and the region of conserved synteny in mice: a search for candidate genes at or near the human chromosome 22 pericentromere.

Footz TK, Brinkman-Mills P, Banting GS, Maier SA, Riazi MA, Bridgland L, Hu S, Birren B, Minoshima S, Shimizu N, Pan H, Nguyen T, Fang F, Fu Y, Ray L, Wu H, Shaull S, Phan S, Yao Z, Chen F, Huan A, Hu P, Wang Q, Loh P, Qi S, Roe BA, McDermid HE. Footz TK, et al. Among authors: chen f. Genome Res. 2001 Jun;11(6):1053-70. doi: 10.1101/gr.154901. Genome Res. 2001. PMID: 11381032 Free PMC article.

8

DQX1, an RNA-dependent ATPase homolog with a novel DEAQ box: expression pattern and genomic sequence comparison of the human and mouse genes.

Ji W, Chen F, Do T, Do A, Roe BA, Meisler MH. Ji W, et al. Among authors: chen f. Mamm Genome. 2001 Jun;12(6):456-61. doi: 10.1007/s003350020032. Mamm Genome. 2001. PMID: 11353393 Free article.

9

A novel complex locus UGT1 encodes human bilirubin, phenol, and other UDP-glucuronosyltransferase isozymes with identical carboxyl termini.

Ritter JK, Chen F, Sheen YY, Tran HM, Kimura S, Yeatman MT, Owens IS. Ritter JK, et al. Among authors: chen f. J Biol Chem. 1992 Feb 15;267(5):3257-61. J Biol Chem. 1992. PMID: 1339448 Free article.

10

Coding defect and a TATA box mutation at the bilirubin UDP-glucuronosyltransferase gene cause Crigler-Najjar type I disease.

Ciotti M, Chen F, Rubaltelli FF, Owens IS. Ciotti M, et al. Among authors: chen f. Biochim Biophys Acta. 1998 Jul 1;1407(1):40-50. doi: 10.1016/s0925-4439(98)00030-1. Biochim Biophys Acta. 1998. PMID: 9639672 Free article.

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