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Items: 1 to 50 of 104

1.

Detailed analysis of a 17q21 microdissection library by sequence bioinformatics and isolation of region-specific clones.

Bentley KL, Li WL, VannBerg FO, Choi JY, Yu J, Kao FT, Ruaño G.

Somat Cell Mol Genet. 1997 Sep;23(5):353-65.

PMID:
9580249
2.

Stch maps to mouse chromosome 16, extending the conserved synteny with human chromosome 21.

Reeves RH, Rue E, Yu J, Kao FT.

Genomics. 1998 Apr 1;49(1):156-7. No abstract available.

PMID:
9570963
3.

Assignment of three human markers in chromosome 21q11 to mouse chromosome 16.

Yu J, Shen Y, Tong S, Kao FT.

Somat Cell Mol Genet. 1997 Sep;23(5):367-70.

PMID:
9546078
4.

Gene identification and DNA sequence analysis in the GC-poor 20 megabase region of human chromosome 21.

Yu J, Tong S, Shen Y, Kao FT.

Proc Natl Acad Sci U S A. 1997 Jun 24;94(13):6862-7.

5.

Assignment of the acute phase response factor (APRF) gene to 17q21 by microdissection clone sequencing and fluorescence in situ hybridization of a P1 clone.

Choi JY, Li WL, Kouri RE, Yu J, Kao FT, Ruano G.

Genomics. 1996 Oct 15;37(2):264-5. No abstract available.

PMID:
8921406
6.

Construction and characterization of three region-specific microdissection libraries for human chromosome 18.

Kao FT, Tong S, Shen Y, Yu J.

Somat Cell Mol Genet. 1996 May;22(3):191-9.

PMID:
8914604
7.

Molecular characterization of breakpoints in patients with holoprosencephaly and definition of the HPE2 critical region 2p21.

Schell U, Wienberg J, Köhler A, Bray-Ward P, Ward DE, Wilson WG, Allen WP, Lebel RR, Sawyer JR, Campbell PL, Aughton DJ, Punnett HH, Lammer EJ, Kao FT, Ward DC, Muenke M.

Hum Mol Genet. 1996 Feb;5(2):223-9.

PMID:
8824878
8.

Report and abstracts of the Fourth International Workshop on Human Chromosome 2 Mapping 1996.

Spur NK, Bashir R, Bushby K, Cox A, Cox S, Hilde Brandt F, Hill N, Kao FT, Krols L, Marzella R, Miller N, Nothwang HG, Rocchi M, Sarfarazi M, Stratakis CA, Wallgren-Petterson C, Naylor S.

Cytogenet Cell Genet. 1996;73(4):255-73. No abstract available.

PMID:
8751373
9.

Complete set of eleven region-specific microdissection libraries for human chromosome 2.

Kao FT, Tong S, Whittier A, Yu J.

Somat Cell Mol Genet. 1996 Jan;22(1):57-66.

PMID:
8643994
10.
11.

YAC contig mapping of six expressed sequences encoded by human chromosome 21.

Yu J, Cox M, Patterson D, Kao FT.

Somat Cell Mol Genet. 1995 Mar;21(2):133-7.

PMID:
7570185
12.
13.

Three dinucleotide repeat polymorphisms proximal to the D2S123 locus.

Leach FS, Nicolaides NC, Sistonen P, Yu JW, Kao FT, de la Chapelle A, Kinzler KW, Vogelstein B.

Hum Mol Genet. 1994 Nov;3(11):2082. No abstract available.

PMID:
7874140
14.

Isolation and refined regional mapping of expressed sequences from human chromosome 21.

Kao FT, Yu J, Tong S, Qi J, Patanjali SR, Weissman SM, Patterson D.

Genomics. 1994 Oct;23(3):700-3.

PMID:
7851901
15.
17.

Region-specific microdissection library and single-copy microclones for human chromosome 2p11-p13.

Yu J, Qi J, Kao FT.

Somat Cell Mol Genet. 1994 Mar;20(2):133-6.

PMID:
8009366
18.

Report and abstracts of the Third International Workshop on Human Chromosome 2 Mapping 1994. Aarhus, Denmark, June 24-26, 1994.

Spurr NK, Barton H, Bashir R, Bryson GM, Bushby K, Cox S, Gringrich JC, Hentati A, Hildebrandt F, Kao FT, et al.

Cytogenet Cell Genet. 1994;67(4):215-44. No abstract available.

PMID:
7924452
19.

Microdissection and microcloning of human chromosome regions in genome and genetic disease analysis.

Kao FT.

Bioessays. 1993 Feb;15(2):141-6. Review. No abstract available.

PMID:
8471059
20.
21.

Isolation, characterization, and regional mapping of microclones from a human chromosome 21 microdissection library.

Yu J, Hartz J, Xu Y, Gemmill RM, Korenberg JR, Patterson D, Kao FT.

Am J Hum Genet. 1992 Aug;51(2):263-72.

22.

Assignment of the human glycogen debrancher gene to chromosome 1p21.

Yang-Feng TL, Zheng K, Yu J, Yang BZ, Chen YT, Kao FT.

Genomics. 1992 Aug;13(4):931-4.

PMID:
1505983
23.

Localization of the human urate oxidase gene (UOX) to 1p22.

Yeldandi AV, Patel YD, Liao M, Kao FT, Rao MS, Reddy JK, Le Beau MM.

Cytogenet Cell Genet. 1992;61(2):121-2.

PMID:
1395718
24.

Chromosome microdissection and cloning in human genome and genetic disease analysis.

Kao FT, Yu JW.

Proc Natl Acad Sci U S A. 1991 Mar 1;88(5):1844-8.

25.

The gene for the alpha 2 chain of the human fibrillar collagen type XI (COL11A2) assigned to the short arm of chromosome 6.

Law ML, Chan SD, Berger R, Jones C, Kao FT, Solomon E, Cheah KS.

Ann Hum Genet. 1990 Jan;54(1):23-9.

PMID:
2321911
26.

Microdissection and microcloning of human chromosome 21.

Kao FT.

Prog Clin Biol Res. 1990;360:89-104.

PMID:
2247512
27.

Isolation and chromosomal localization of the human En-2 gene.

Poole SJ, Law ML, Kao FT, Lau YF.

Genomics. 1989 Apr;4(3):225-31.

PMID:
2565873
28.

Chromosomal localization of the human gene for brain Ca2+/calmodulin-dependent protein kinase type IV.

Sikela JM, Law ML, Kao FT, Hartz JA, Wei Q, Hahn WE.

Genomics. 1989 Jan;4(1):21-7.

PMID:
2536634
29.

Localization of human ERBA2 to the 3p22----3p24.1 region of chromosome 3 and variable deletion in small cell lung cancer.

Drabkin H, Kao FT, Hartz J, Hart I, Gazdar A, Weinberger C, Evans R, Gerber M.

Proc Natl Acad Sci U S A. 1988 Dec;85(23):9258-62.

30.

Mapping of the gene encoding the beta-amyloid precursor protein and its relationship to the Down syndrome region of chromosome 21.

Patterson D, Gardiner K, Kao FT, Tanzi R, Watkins P, Gusella JF.

Proc Natl Acad Sci U S A. 1988 Nov;85(21):8266-70.

31.

Assignment of human gene encoding testis-specific lactate dehydrogenase C to chromosome 11, region p14.3-p15.5.

Kao FT, Wu KC, Law ML, Hartz JA, Lau YF.

Somat Cell Mol Genet. 1988 Sep;14(5):515-8.

PMID:
3175768
32.

The GLI-Kruppel family of human genes.

Ruppert JM, Kinzler KW, Wong AJ, Bigner SH, Kao FT, Law ML, Seuanez HN, O'Brien SJ, Vogelstein B.

Mol Cell Biol. 1988 Aug;8(8):3104-13.

33.

Regional assignment of human tissue factor gene (F3) to chromosome 1p21-p22.

Kao FT, Hartz J, Horton R, Nemerson Y, Carson SD.

Somat Cell Mol Genet. 1988 Jul;14(4):407-10.

PMID:
3399965
34.

The hemopexin gene maps to the same location as the beta-globin gene cluster on human chromosome 11.

Law ML, Cai GY, Hartz JA, Jones C, Kao FT.

Genomics. 1988 Jul;3(1):48-52.

PMID:
3220477
35.

Isolation and analysis of DNA markers specific to human chromosome 15.

Tasset DM, Hartz JA, Kao FT.

Am J Hum Genet. 1988 Jun;42(6):854-66.

36.

Regional localization of the gene coding for sphingolipid activator protein SAP-1 on human chromosome 10.

Kao FT, Law ML, Hartz J, Jones C, Zhang XL, Dewji N, O'Brien JS, Wenger DA.

Somat Cell Mol Genet. 1987 Nov;13(6):685-8.

PMID:
3478817
37.

Human placental Na+,K+-ATPase alpha subunit: cDNA cloning, tissue expression, DNA polymorphism, and chromosomal localization.

Chehab FF, Kan YW, Law ML, Hartz J, Kao FT, Blostein R.

Proc Natl Acad Sci U S A. 1987 Nov;84(22):7901-5.

38.

Confirmation of assignment of the human alpha 1-crystallin gene (CRYA1) to chromosome 21 with regional localization to q22.3.

Hawkins JW, Van Keuren ML, Piatigorsky J, Law ML, Patterson D, Kao FT.

Hum Genet. 1987 Aug;76(4):375-80.

PMID:
3610158
39.

Chromosome microdissection and microcloning in human molecular genetics.

Kao FT.

Somat Cell Mol Genet. 1987 Jul;13(4):375-80. Review. No abstract available.

PMID:
3331830
41.

The progesterone receptor gene maps to human chromosome band 11q13, the site of the mammary oncogene int-2.

Law ML, Kao FT, Wei Q, Hartz JA, Greene GL, Zarucki-Schulz T, Conneely OM, Jones C, Puck TT, O'Malley BW, et al.

Proc Natl Acad Sci U S A. 1987 May;84(9):2877-81. Erratum in: Proc Natl Acad Sci U S A 1988 Dec;85(24):9688.

42.

Chromosomal location of human genes encoding major heat-shock protein HSP70.

Harrison GS, Drabkin HA, Kao FT, Hartz J, Hart IM, Chu EH, Wu BJ, Morimoto RI.

Somat Cell Mol Genet. 1987 Mar;13(2):119-30.

43.

A somatic cell hybrid with a single human chromosome 22 corrects the defect in the CHO mutant (Ade-I) lacking adenylosuccinase activity.

Van Keuren ML, Hart IM, Kao FT, Neve RL, Bruns GA, Kurnit DM, Patterson D.

Cytogenet Cell Genet. 1987;44(2-3):142-7.

PMID:
3568763
44.

Chromosomal assignment of the human erythropoietin gene and its DNA polymorphism.

Law ML, Cai GY, Lin FK, Wei Q, Huang SZ, Hartz JH, Morse H, Lin CH, Jones C, Kao FT.

Proc Natl Acad Sci U S A. 1986 Sep;83(18):6920-4.

45.

Ribosomal protein gene sequences map to human chromosomes 5, 8, and 17.

Nakamichi NN, Kao FT, Wasmuth J, Roufa DJ.

Somat Cell Mol Genet. 1986 May;12(3):225-36.

PMID:
3459254
46.

Identification of 200,000-dalton human cell surface protein encoded by gene mapped to long arm of chromosome 11.

Imada M, Kao FT, Law ML, Jones C.

Somat Cell Mol Genet. 1986 Mar;12(2):197-201.

PMID:
3457478
47.

Assignment of the human tyrosine aminotransferase gene to chromosome 16.

Natt E, Kao FT, Rettenmeier R, Scherer G.

Hum Genet. 1986 Mar;72(3):225-8.

PMID:
2870018
48.

Localization of a beta-crystallin gene, Hu beta A3/A1 (gene symbol: CRYB1), to the long arm of human chromosome 17.

Law ML, Cai GY, Hartz J, Kao FT, Hogg D, Breitman ML, Tsui LC.

Cytogenet Cell Genet. 1986;42(4):202-7.

PMID:
3757553
49.

Genetic mapping of apolipoprotein genes in the human genome by somatic cell hybrids.

Kao FT, Chan L.

Methods Enzymol. 1986;128:851-63. No abstract available.

PMID:
3724531
50.

Regional mapping of the phenylalanine hydroxylase gene and the phenylketonuria locus in the human genome.

Lidsky AS, Law ML, Morse HG, Kao FT, Rabin M, Ruddle FH, Woo SL.

Proc Natl Acad Sci U S A. 1985 Sep;82(18):6221-5.

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