-
1
-
-
0026808763
-
Mapping the whole human genome by fingerprinting yeast artificial chromosomes
-
1. Bellannè-Chantelot, C., Lacroix, B., Ougen, P., Billault, A., Beaufils, S., Bertrand, S., Georges, I., Gilbert, F., Gros, I., Lucotte, G., Susini, L., Codani, J.-J., Gesnouin, P., Pook, S., Vaysseix, G., Lu-Kuo, J., Ried, T., Ward, D., Chumakov, I., Le Paslier, D., Barillot, E., and Cohen, D. (1992). Mapping the whole human genome by fingerprinting yeast artificial chromosomes. Cell 70: 1059-1068.
-
(1992)
Cell
, vol.70
, pp. 1059-1068
-
-
Bellannè-Chantelot, C.1
Lacroix, B.2
Ougen, P.3
Billault, A.4
Beaufils, S.5
Bertrand, S.6
Georges, I.7
Gilbert, F.8
Gros, I.9
Lucotte, G.10
Susini, L.11
Codani, J.-J.12
Gesnouin, P.13
Pook, S.14
Vaysseix, G.15
Lu-Kuo, J.16
Ried, T.17
Ward, D.18
Chumakov, I.19
Le Paslier, D.20
Barillot, E.21
Cohen, D.22
more..
-
2
-
-
0027972378
-
Two autosomal dominant neuropathies result from reciprocal DNA duplication/deletion of a region on chromosome 17
-
2. Chance, P. F., Abbas, N., Lensch, M. W., Pentao, L., Roa, B. B., Patel, P. I., and Lupski, J. R. (1994). Two autosomal dominant neuropathies result from reciprocal DNA duplication/deletion of a region on chromosome 17. Hum. Mol. Genet. 3: 223-228.
-
(1994)
Hum. Mol. Genet.
, vol.3
, pp. 223-228
-
-
Chance, P.F.1
Abbas, N.2
Lensch, M.W.3
Pentao, L.4
Roa, B.B.5
Patel, P.I.6
Lupski, J.R.7
-
3
-
-
0027509953
-
DNA deletion associated with hereditary neuropathy with liability to pressure palsies
-
3. Chance, P. F., Alderson, M. K., Leppig, K. A., Lensch, M. W., Matsunami, N., Smith, B., Swanson, P. D., Odelberg, S. J., Disteche, C. M., and Bird, T. D. (1993). DNA deletion associated with hereditary neuropathy with liability to pressure palsies. Cell 72: 143-151.
-
(1993)
Cell
, vol.72
, pp. 143-151
-
-
Chance, P.F.1
Alderson, M.K.2
Leppig, K.A.3
Lensch, M.W.4
Matsunami, N.5
Smith, B.6
Swanson, P.D.7
Odelberg, S.J.8
Disteche, C.M.9
Bird, T.D.10
-
4
-
-
0028038276
-
Isolation of a human cDNA for heme A:Farnesyltransferase by functional complementation of a yeast cox10 mutant
-
4. Glerum, D. M., and Tzagoloff, A. (1994). Isolation of a human cDNA for heme A:farnesyltransferase by functional complementation of a yeast cox10 mutant. Proc. Natl. Acad. Sci. USA 91: 8452-8456.
-
(1994)
Proc. Natl. Acad. Sci. USA
, vol.91
, pp. 8452-8456
-
-
Glerum, D.M.1
Tzagoloff, A.2
-
5
-
-
0025938038
-
Identification and characterization of the familial adenomatous polyposis coli gene
-
5. Groden, J., Thliveris, A., Samowitz, W., Carlson, M., Gelbert, L., Albertsen, H., Joslyn, G., Stevens, J., Spirio, L., Robertson, M., Sargeant, L., Krapcho, K., Wolff, E., Burt, R., Hughes, J. P., Warrington, J., McPherson, J., Wasmuth, J., Le Paslier, D., Abderrahim, H., Cohen, D., Leppert, M., and White, R. (1991). Identification and characterization of the familial adenomatous polyposis coli gene. Cell 66: 589-600.
-
(1991)
Cell
, vol.66
, pp. 589-600
-
-
Groden, J.1
Thliveris, A.2
Samowitz, W.3
Carlson, M.4
Gelbert, L.5
Albertsen, H.6
Joslyn, G.7
Stevens, J.8
Spirio, L.9
Robertson, M.10
Sargeant, L.11
Krapcho, K.12
Wolff, E.13
Burt, R.14
Hughes, J.P.15
Warrington, J.16
McPherson, J.17
Wasmuth, J.18
Le Paslier, D.19
Abderrahim, H.20
Cohen, D.21
Leppert, M.22
White, R.23
more..
-
6
-
-
0028201453
-
Physical mapping of chromosome 17 cosmids by fluorescence in situ hybridization and digital image analysis
-
6. Kallioniemi, O.-P., Kallioniemi, A., Mascio, L., Sudar, D., Pinkel, D., Deaven, L., and Gray, J. (1994). Physical mapping of chromosome 17 cosmids by fluorescence in situ hybridization and digital image analysis. Genomics 20: 125-128.
-
(1994)
Genomics
, vol.20
, pp. 125-128
-
-
Kallioniemi, O.-P.1
Kallioniemi, A.2
Mascio, L.3
Sudar, D.4
Pinkel, D.5
Deaven, L.6
Gray, J.7
-
7
-
-
0029999248
-
Primate origin of the CMT1A-REP repeat and analysis of a putative transposon-associated recombinational hotspot
-
7. Kiyosawa, H., and Chance, P. F. (1996). Primate origin of the CMT1A-REP repeat and analysis of a putative transposon-associated recombinational hotspot. Hum. Mol. Genet. 5: 745-753.
-
(1996)
Hum. Mol. Genet.
, vol.5
, pp. 745-753
-
-
Kiyosawa, H.1
Chance, P.F.2
-
8
-
-
0027366552
-
Inherited primary peripheral neuropathies: Molecular genetics and clinical implications of CMT1A and HNPP
-
8. Lupski, J. R., Chance, P. F., and Garcia, C. A. (1993). Inherited primary peripheral neuropathies: Molecular genetics and clinical implications of CMT1A and HNPP. J. Am. Med. Assoc. 270: 2326-2330.
-
(1993)
J. Am. Med. Assoc.
, vol.270
, pp. 2326-2330
-
-
Lupski, J.R.1
Chance, P.F.2
Garcia, C.A.3
-
9
-
-
0025868571
-
DNA duplication associated with Charcot-Marie-Tooth disease type 1A
-
9. Lupski, J. R., Montes de Oca-Luna, R., Slaugenhaupt, S., Pentao, L., Guzzetta, V., Trask, B. J., Saucedo-Cardenas, O., Barker, D. F., Killian, J. M., Garcia, C. A., Chakravarti, A., and Patel, P. I. (1991). DNA duplication associated with Charcot-Marie-Tooth disease type 1A. Cell 66: 219-232.
-
(1991)
Cell
, vol.66
, pp. 219-232
-
-
Lupski, J.R.1
Montes De Oca-Luna, R.2
Slaugenhaupt, S.3
Pentao, L.4
Guzzetta, V.5
Trask, B.J.6
Saucedo-Cardenas, O.7
Barker, D.F.8
Killian, J.M.9
Garcia, C.A.10
Chakravarti, A.11
Patel, P.I.12
-
10
-
-
0029793042
-
Reviews in molecular medicine: Charcot-Marie-Tooth disease and related inherited neuropathies
-
10. Murakami, T., Garcia, C. A., Reiter, L. T., and Lupski, J. R. (1996). Reviews in molecular medicine: Charcot-Marie-Tooth disease and related inherited neuropathies. Medicine 75: 233-250.
-
(1996)
Medicine
, vol.75
, pp. 233-250
-
-
Murakami, T.1
Garcia, C.A.2
Reiter, L.T.3
Lupski, J.R.4
-
11
-
-
0030066532
-
A 1.5-Mb cosmid contig of the CMT1A duplication /HNPP deletion critical region in 17p11.2-p12
-
11. Murakami, T., and Lupski, J. R. (1996). A 1.5-Mb cosmid contig of the CMT1A duplication /HNPP deletion critical region in 17p11.2-p12. Genomics 34: 128-133.
-
(1996)
Genomics
, vol.34
, pp. 128-133
-
-
Murakami, T.1
Lupski, J.R.2
-
12
-
-
0031015760
-
Isolation of novel genes from the CMT1A duplication/HNPP deletion critical region in 17p11.2-p12
-
12. Murakami, T., Sun, Z. S., Lee, C. C., and Lupski, J. R. (1997). Isolation of novel genes from the CMT1A duplication/HNPP deletion critical region in 17p11.2-p12. Genomics 39: 99-103.
-
(1997)
Genomics
, vol.39
, pp. 99-103
-
-
Murakami, T.1
Sun, Z.S.2
Lee, C.C.3
Lupski, J.R.4
-
13
-
-
0025076235
-
COX10 codes for a protein homologous to the ORF1 product of Paracoccus denitrificans and is required for the synthesis of yeast cytochome oxidase
-
13. Nobrega, M. P., Nobrega, F. G., and Tzagoloff, A. (1990). COX10 codes for a protein homologous to the ORF1 product of Paracoccus denitrificans and is required for the synthesis of yeast cytochome oxidase. J. Biol. Chem. 265: 14220-14226.
-
(1990)
J. Biol. Chem.
, vol.265
, pp. 14220-14226
-
-
Nobrega, M.P.1
Nobrega, F.G.2
Tzagoloff, A.3
-
14
-
-
0028231331
-
Charcot-Marie-Tooth disease: A new paradigm for the mechanism of inherited disease
-
14. Patel, P. I., and Lupski, J. R. (1994). Charcot-Marie-Tooth disease: A new paradigm for the mechanism of inherited disease. Trends Genet. 10: 128-133.
-
(1994)
Trends Genet.
, vol.10
, pp. 128-133
-
-
Patel, P.I.1
Lupski, J.R.2
-
15
-
-
0027017033
-
Charcot-Marie-Tooth type 1A duplication appears to arise from recombination at repeat sequences flanking the 1.5Mb monomer unit
-
15. Pentao, L., Wise, C. A., Chinault, A. C., Patel, P. I., and Lupski, J. R. (1992). Charcot-Marie-Tooth type 1A duplication appears to arise from recombination at repeat sequences flanking the 1.5Mb monomer unit. Nature Genet. 2: 292-300.
-
(1992)
Nature Genet.
, vol.2
, pp. 292-300
-
-
Pentao, L.1
Wise, C.A.2
Chinault, A.C.3
Patel, P.I.4
Lupski, J.R.5
-
16
-
-
0025997898
-
Duplication in chromosome 17p11.2 in Charcot-Marie-Tooth neuropathy type 1a (CMT1a)
-
16. Raeymaekers, P., Timmerman, V., Nelis, E., De Jonghe, P., Hoogendijk, J. E., Baas, F., Barker, D. F., Martin, J. J., De Visser, M., Bolhuis, P. A., Van Broekhoven, C., and the HMSN Collaborative Research Group. (1991). Duplication in chromosome 17p11.2 in Charcot-Marie-Tooth neuropathy type 1a (CMT1a). Neuromusc. Disord. 1: 93-97.
-
(1991)
Neuromusc. Disord.
, vol.1
, pp. 93-97
-
-
Raeymaekers, P.1
Timmerman, V.2
Nelis, E.3
De Jonghe, P.4
Hoogendijk, J.E.5
Baas, F.6
Barker, D.F.7
Martin, J.J.8
De Visser, M.9
Bolhuis, P.A.10
Van Broekhoven, C.11
-
17
-
-
0029962292
-
A recombination hotspot responsible for two inherited peripheral neuropathies is located near a mariner transposon-like element
-
17. Reiter, L. T., Murakami, T., Koeuth, T., Pentao, L., Muzny, D. M., Gibbs, R. A., and Lupski, J. R. (1996). A recombination hotspot responsible for two inherited peripheral neuropathies is located near a mariner transposon-like element. Nature Genet. 12: 288-297.
-
(1996)
Nature Genet.
, vol.12
, pp. 288-297
-
-
Reiter, L.T.1
Murakami, T.2
Koeuth, T.3
Pentao, L.4
Muzny, D.M.5
Gibbs, R.A.6
Lupski, J.R.7
-
18
-
-
0011255233
-
DNA rearrangements affecting dosage sensitive genes
-
18. Reiter, L. T., Murakami, T., Warner, L. E., and Lupski, J. R. (1996). DNA rearrangements affecting dosage sensitive genes. Mental Retardat. Dev. Disabil. Res. Rev. 2: 139-146.
-
(1996)
Mental Retardat. Dev. Disabil. Res. Rev.
, vol.2
, pp. 139-146
-
-
Reiter, L.T.1
Murakami, T.2
Warner, L.E.3
Lupski, J.R.4
-
19
-
-
0027086985
-
Heme O biosynthesis in Escherichia coli: The CyoE gene in the cytochrome bo operon encodes a protoheme IX farnesyltransferase
-
19. Saiki, K., Mogi, T., and Anraku, Y. (1992). Heme O biosynthesis in Escherichia coli: The CyoE gene in the cytochrome bo operon encodes a protoheme IX farnesyltransferase. Biochem. Biophys. Res. Commun. 189: 1491-1497.
-
(1992)
Biochem. Biophys. Res. Commun.
, vol.189
, pp. 1491-1497
-
-
Saiki, K.1
Mogi, T.2
Anraku, Y.3
-
20
-
-
0027442655
-
In vitro heme O synthesis by the cyoE gene product from Escherichia coli
-
20. Saiki, K., Mogi, T., Ogura, K., and Anraku, Y. (1993). In vitro heme O synthesis by the cyoE gene product from Escherichia coli. J. Biol. Chem. 268: 26041-26044.
-
(1993)
J. Biol. Chem.
, vol.268
, pp. 26041-26044
-
-
Saiki, K.1
Mogi, T.2
Ogura, K.3
Anraku, Y.4
-
21
-
-
0023651307
-
RNA splice junctions of different classes of eukaryotes: Sequence statistics and functional implications in gene expression
-
21. Shapiro, M. B., and Senapathy, P. (1987). RNA splice junctions of different classes of eukaryotes: Sequence statistics and functional implications in gene expression. Nucleic Acids Res. 15: 7155-7174.
-
(1987)
Nucleic Acids Res.
, vol.15
, pp. 7155-7174
-
-
Shapiro, M.B.1
Senapathy, P.2
-
22
-
-
0030013766
-
BCM Search Launcher - An integrated interface to molecular biology database search and analysis services available on the World Wide Web
-
22. Smith, R. F., Wiese, B. A., Wojzynski, M. K., Davison, D. B., and Worley, K. C. (1996). BCM Search Launcher - An integrated interface to molecular biology database search and analysis services available on the World Wide Web. Genome Res. 6: 454-462.
-
(1996)
Genome Res.
, vol.6
, pp. 454-462
-
-
Smith, R.F.1
Wiese, B.A.2
Wojzynski, M.K.3
Davison, D.B.4
Worley, K.C.5
-
23
-
-
0017767139
-
Is recombination confined to structural genes on the eukaryotic genome?
-
23. Thuriaux, P. (1977). Is recombination confined to structural genes on the eukaryotic genome? Nature 268: 460-462.
-
(1977)
Nature
, vol.268
, pp. 460-462
-
-
Thuriaux, P.1
-
24
-
-
0027134002
-
On the functions of the yeast COX10 and COX11 gene products
-
24. Tzagoloff, A., Nobrega, M., Gorman, N., and Sinclair, P. (1993). On the functions of the yeast COX10 and COX11 gene products. Biochem. Mol. Biol. Int. 31: 593-598.
-
(1993)
Biochem. Mol. Biol. Int.
, vol.31
, pp. 593-598
-
-
Tzagoloff, A.1
Nobrega, M.2
Gorman, N.3
Sinclair, P.4
-
25
-
-
0030428795
-
Molecular mechanisms for Charcot-Marie-Tooth disease and related demyelinating peripheral neuropathies
-
25. Warner, L. E., Reiter, L. T., Murakmai, T., and Lupski, J. R. (1997). Molecular mechanisms for Charcot-Marie-Tooth disease and related demyelinating peripheral neuropathies. Cold Spring Harbor Symp. Quant. Biol. 61: 659-671.
-
(1997)
Cold Spring Harbor Symp. Quant. Biol.
, vol.61
, pp. 659-671
-
-
Warner, L.E.1
Reiter, L.T.2
Murakmai, T.3
Lupski, J.R.4
|