-
1
-
-
0023746682
-
SEC7 encodes an unusual, high molecular weight protein required for membrane traffic from the yeast Golgi apparatus
-
Achstetter, T., Franzusoff, A., Field, C., and Schekman, R. 1988. SEC7 encodes an unusual, high molecular weight protein required for membrane traffic from the yeast Golgi apparatus. J. Biol. Chem. 263: 11711-11717.
-
(1988)
J. Biol. Chem
, vol.263
, pp. 11711-11717
-
-
Achstetter, T.1
Franzusoff, A.2
Field, C.3
Schekman, R.4
-
2
-
-
0030801002
-
Gapped BLAST and PSI-BLAST: A new generation of protein database search programs
-
Altschul, S.F., Madden, T.L., Schaffer, A.A., Zhang, J., Zhang, Z., Miller, W., and Lipman, D.J. 1997. Gapped BLAST and PSI-BLAST: A new generation of protein database search programs. Nucleic Acids Res. 25: 3389-3402.
-
(1997)
Nucleic Acids Res
, vol.25
, pp. 3389-3402
-
-
Altschul, S.F.1
Madden, T.L.2
Schaffer, A.A.3
Zhang, J.4
Zhang, Z.5
Miller, W.6
Lipman, D.J.7
-
3
-
-
0029657886
-
Localization of chl1-related helicase genes to human chromosome regions 12p11 and 12p13: Similarity between parts of these genes and conserved human telomeric-associated DNA
-
Amann, J., Valentine, M., Kidd, V.J., and Lahti, J.M. 1996. Localization of chl1-related helicase genes to human chromosome regions 12p11 and 12p13: Similarity between parts of these genes and conserved human telomeric-associated DNA. Genomics 32: 260-265.
-
(1996)
Genomics
, vol.32
, pp. 260-265
-
-
Amann, J.1
Valentine, M.2
Kidd, V.J.3
Lahti, J.M.4
-
4
-
-
0031022335
-
Characterization of putative human homologues of the yeast chromosome transmission fidelity gene, CHL1
-
Amann, J., Kidd, V.J., and Lahti, J.M. 1997. Characterization of putative human homologues of the yeast chromosome transmission fidelity gene, CHL1. J. Biol. Chem. 272: 3823-3832.
-
(1997)
J. Biol. Chem
, vol.272
, pp. 3823-3832
-
-
Amann, J.1
Kidd, V.J.2
Lahti, J.M.3
-
5
-
-
0036138187
-
Human-specific duplication and mosaic transcripts: The recent paralogous structure of chromosome 22
-
Bailey, J.A., Yavor, A.M., Viggiano, L., Misceo, D., Horvath, J.E., Archidiacono, N., Schwartz, S., Rocchi, M., and Eichler, E.E. 2002. Human-specific duplication and mosaic transcripts: The recent paralogous structure of chromosome 22. Am. J. Hum. Genet. 70: 83-100.
-
(2002)
Am. J. Hum. Genet
, vol.70
, pp. 83-100
-
-
Bailey, J.A.1
Yavor, A.M.2
Viggiano, L.3
Misceo, D.4
Horvath, J.E.5
Archidiacono, N.6
Schwartz, S.7
Rocchi, M.8
Eichler, E.E.9
-
6
-
-
0028829638
-
The mouse mutation muscle deficient (mdf) is characterized by a progressive motoneuron disease
-
Blot, S., Poirier, C., and Dreyfus, P.A. 1995. The mouse mutation muscle deficient (mdf) is characterized by a progressive motoneuron disease. J. Neuropathol. Exp. Neurol. 54: 812-825.
-
(1995)
J. Neuropathol. Exp. Neurol
, vol.54
, pp. 812-825
-
-
Blot, S.1
Poirier, C.2
Dreyfus, P.A.3
-
7
-
-
0025086570
-
Structure and polymorphism of human telomere-associated DNA
-
Brown, W.R., MacKinnon, P.J., Villasante, A., Spurr, N., Buckle, V.J., and Dobson, M.J. 1990. Structure and polymorphism of human telomere-associated DNA. Cell 63: 119-132.
-
(1990)
Cell
, vol.63
, pp. 119-132
-
-
Brown, W.R.1
MacKinnon, P.J.2
Villasante, A.3
Spurr, N.4
Buckle, V.J.5
Dobson, M.J.6
-
8
-
-
0029844904
-
A human exchange factor for ARF contains Sec7- and pleckstrin-homology domains
-
Chardin, P., Paris, S., Antonny, B., Robineau, S., Beraud-Dufour, S., Jackson, C. L., and Chabre, M. 1996. A human exchange factor for ARF contains Sec7- and pleckstrin-homology domains. Nature 384: 481-484.
-
(1996)
Nature
, vol.384
, pp. 481-484
-
-
Chardin, P.1
Paris, S.2
Antonny, B.3
Robineau, S.4
Beraud-Dufour, S.5
Jackson C., L.6
Chabre, M.7
-
9
-
-
18544408206
-
Differentially regulated and evolved genes in the fully sequenced Xq/Yq pseudoautosomal region
-
Ciccodicola, A., D'Esposito, M., Esposito, T., Gianfrancesco, F., Migliaccio, C., Miano, M.G., Matarazzo, M.R., Vacca, M., Franze, A., Cuccurese, M., et al. 2000. Differentially regulated and evolved genes in the fully sequenced Xq/Yq pseudoautosomal region. Hum. Mol. Genet. 9: 395-401.
-
(2000)
Hum. Mol. Genet
, vol.9
, pp. 395-401
-
-
Ciccodicola, A.1
D'Esposito, M.2
Esposito, T.3
Gianfrancesco, F.4
Migliaccio, C.5
Miano, M.G.6
Matarazzo, M.R.7
Vacca, M.8
Franze, A.9
Cuccurese, M.10
-
10
-
-
0026094290
-
Nucleotide sequence and genetic analysis of a 13.1-kilobase-pair Pseudomonas denitrificans DNA fragment containing five cob genes and identification of structural genes encoding Cob(I)alamin adenosyltransferase, cobyric acid synthase, and bifunctional cobinamide kinase-cobinamide phosphate guanylyltransferase
-
Crouzet, J., Levy-Schil, S., Cameron, B., Cauchois, L., Rigault, S., Rouyez, M.C., Blanche, F., Debussche, L., and Thibaut, D. 1991. Nucleotide sequence and genetic analysis of a 13.1-kilobase-pair Pseudomonas denitrificans DNA fragment containing five cob genes and identification of structural genes encoding Cob(I)alamin adenosyltransferase, cobyric acid synthase, and bifunctional cobinamide kinase-cobinamide phosphate guanylyltransferase. J. Bacteriol. 173: 6074-6087.
-
(1991)
J. Bacteriol
, vol.173
, pp. 6074-6087
-
-
Crouzet, J.1
Levy-Schil, S.2
Cameron, B.3
Cauchois, L.4
Rigault, S.5
Rouyez, M.C.6
Blanche, F.7
Debussche, L.8
Thibaut, D.9
-
11
-
-
0024726217
-
A strategy to detect and isolate an intron-containing gene in the presence of multiple processed pseudogenes
-
Davies, B., Feo, S., Heard, E., and Fried, M. 1989. A strategy to detect and isolate an intron-containing gene in the presence of multiple processed pseudogenes. Proc. Natl. Acad. Sci. 86: 6691-6695.
-
(1989)
Proc. Natl. Acad. Sci
, vol.86
, pp. 6691-6695
-
-
Davies, B.1
Feo, S.2
Heard, E.3
Fried, M.4
-
12
-
-
0028880040
-
A novel human phosphoglucomutase (PGM5) maps to the centromeric region of chromosome 9
-
Edwards, Y.H., Putt, W., Fox, M., and Ives, J.H. 1995. A novel human phosphoglucomutase (PGM5) maps to the centromeric region of chromosome 9. Genomics 30: 350-353.
-
(1995)
Genomics
, vol.30
, pp. 350-353
-
-
Edwards, Y.H.1
Putt, W.2
Fox, M.3
Ives, J.H.4
-
13
-
-
0031439860
-
Cloning, sequencing, gene organization, and localization of the human ribosomal protein RPL23A gene
-
Fan, W., Christensen, M., Eichler, E., Zhang, X., and Lennon, G. 1997. Cloning, sequencing, gene organization, and localization of the human ribosomal protein RPL23A gene. Genomics 46: 234-239.
-
(1997)
Genomics
, vol.46
, pp. 234-239
-
-
Fan, W.1
Christensen, M.2
Eichler, E.3
Zhang, X.4
Lennon, G.5
-
14
-
-
0036851314
-
Genomic Structure and Evolution of the Ancestral Chromosome Fusion Site in 2q13-2q14.1 and Paralogous Regions on Other Human Chromosomes
-
(this issue)
-
Fan, Y., Linardopoulou, E., Friedman, C., Williams, E., and Trask, B.J. 2002. Genomic Structure and Evolution of the Ancestral Chromosome Fusion Site in 2q13-2q14.1 and Paralogous Regions on Other Human Chromosomes. Genome Res. (this issue).
-
(2002)
Genome Res
-
-
Fan, Y.1
Linardopoulou, E.2
Friedman, C.3
Williams, E.4
Trask, B.J.5
-
15
-
-
0033646615
-
Mutations in FOXC2 (MFH-1), a forkhead family transcription factor, are responsible for the hereditary lymphedema-distichiasis syndrome
-
Fang, J., Dagenais, S.L., Erickson, R.P., Arlt, M.F., Glynn, M.W., Gorski, J.L., Seaver, L.H., and Glover, T.W. 2000. Mutations in FOXC2 (MFH-1), a forkhead family transcription factor, are responsible for the hereditary lymphedema-distichiasis syndrome. Am. J. Hum. Genet. 67: 1382-1388.
-
(2000)
Am. J. Hum. Genet
, vol.67
, pp. 1382-1388
-
-
Fang, J.1
Dagenais, S.L.2
Erickson, R.P.3
Arlt, M.F.4
Glynn, M.W.5
Gorski, J.L.6
Seaver, L.H.7
Glover, T.W.8
-
16
-
-
0025597055
-
The CHL 1 (CTF 1) gene product of Saccharomyces cerevisiae is important for chromosome transmission and normal cell cycle progression in G2/M
-
Gerring, S.L., Spencer, F., and Hieter, P. 1990. The CHL 1 (CTF 1) gene product of Saccharomyces cerevisiae is important for chromosome transmission and normal cell cycle progression in G2/M. EMBO J. 9: 4347-4358.
-
(1990)
EMBO J
, vol.9
, pp. 4347-4358
-
-
Gerring, S.L.1
Spencer, F.2
Hieter, P.3
-
17
-
-
0028920914
-
A human 12p-derived cosmid hybridizing to subsets of human and chimpanzee telomeres
-
Hoglund, M., Mitelman, F., and Mandahl, N. 1995. A human 12p-derived cosmid hybridizing to subsets of human and chimpanzee telomeres. Cytogenet. Cell Genet. 70: 88-91.
-
(1995)
Cytogenet. Cell Genet
, vol.70
, pp. 88-91
-
-
Hoglund, M.1
Mitelman, F.2
Mandahl, N.3
-
18
-
-
0026040880
-
Origin of human chromosome 2: An ancestral telomere-telomere fusion
-
Ijdo, J., Baldini, A., Ward, D.C., Reeders, S.T., and Wells, R.A. 1991. Origin of human chromosome 2: An ancestral telomere-telomere fusion. Proc. Natl. Acad. Sci. 88: 9051-9055.
-
(1991)
Proc. Natl. Acad. Sci
, vol.88
, pp. 9051-9055
-
-
Ijdo, J.1
Baldini, A.2
Ward, D.C.3
Reeders, S.T.4
Wells, R.A.5
-
19
-
-
0034028921
-
Structure of chromosomal duplicons and their role in mediating human genomic disorders
-
Ji, Y., Eichler, E.E., Schwartz, S., and Nicholls, R.D. 2000. Structure of chromosomal duplicons and their role in mediating human genomic disorders. Genome Res. 10: 597-610.
-
(2000)
Genome Res
, vol.10
, pp. 597-610
-
-
Ji, Y.1
Eichler, E.E.2
Schwartz, S.3
Nicholls, R.D.4
-
20
-
-
0029562220
-
The mouse fkh-2 gene. Implications for notochord, foregut, and midbrain regionalization
-
Kaestner, K.H., Monaghan, A.P., Kern, H., Ang, S.L., Weitz, S., Lichter, P., and Schutz, G. 1995. The mouse fkh-2 gene. Implications for notochord, foregut, and midbrain regionalization. J. Biol. Chem. 270: 30029-30035.
-
(1995)
J. Biol. Chem
, vol.270
, pp. 30029-30035
-
-
Kaestner, K.H.1
Monaghan, A.P.2
Kern, H.3
Ang, S.L.4
Weitz, S.5
Lichter, P.6
Schutz, G.7
-
21
-
-
0342614209
-
Unified nomenclature for the winged helix/forkhead transcription factors
-
Kaestner, K.H., Knochel, W., and Martinez, D.E. 2000. Unified nomenclature for the winged helix/forkhead transcription factors. Genes Dev. 14: 142-146.
-
(2000)
Genes Dev
, vol.14
, pp. 142-146
-
-
Kaestner, K.H.1
Knochel, W.2
Martinez, D.E.3
-
22
-
-
17344379513
-
Five years on the wings of fork head
-
Kaufmann, E. and Knochel, W. 1996. Five years on the wings of fork head. Mech. Dev. 57: 3-20.
-
(1996)
Mech. Dev
, vol.57
, pp. 3-20
-
-
Kaufmann, E.1
Knochel, W.2
-
23
-
-
0027441203
-
Alternative splicing of Pax-8 gene transcripts is developmentally regulated and generates isoforms with different transactivation properties
-
Kozmik, Z., Kurzbauer, R., Dorfler, P., and Busslinger, M. 1993. Alternative splicing of Pax-8 gene transcripts is developmentally regulated and generates isoforms with different transactivation properties. Mol. Cell. Biol. 13: 6024-6035.
-
(1993)
Mol. Cell. Biol
, vol.13
, pp. 6024-6035
-
-
Kozmik, Z.1
Kurzbauer, R.2
Dorfler, P.3
Busslinger, M.4
-
24
-
-
0030832612
-
Alternatively spliced insertions in the paired domain restrict the DNA sequence specificity of Pax6 and Pax8
-
Kozmik, Z., Czerny, T., and Busslinger, M. 1997. Alternatively spliced insertions in the paired domain restrict the DNA sequence specificity of Pax6 and Pax8. EMBO J. 16: 6793-6803.
-
(1997)
EMBO J
, vol.16
, pp. 6793-6803
-
-
Kozmik, Z.1
Czerny, T.2
Busslinger, M.3
-
25
-
-
0035807360
-
A forkhead-domain gene is mutated in a severe speech and language disorder
-
Lai, C.S., Fisher, S.E., Hurst, J.A., Vargha-Khadem, F., and Monaco, A.P. 2001. A forkhead-domain gene is mutated in a severe speech and language disorder. Nature 413: 519-523.
-
(2001)
Nature
, vol.413
, pp. 519-523
-
-
Lai, C.S.1
Fisher, S.E.2
Hurst, J.A.3
Vargha-Khadem, F.4
Monaco, A.P.5
-
26
-
-
0026083212
-
Hepatocyte nuclear factor 3 alpha belongs to a gene family in mammals that is homologous to the Drosophila homeotic gene fork head
-
Lai, E., Prezioso, V.R., Tao, W.F., Chen, W.S., and Darnell Jr., J.E. 1991. Hepatocyte nuclear factor 3 alpha belongs to a gene family in mammals that is homologous to the Drosophila homeotic gene fork head. Genes Dev. 5: 416-427.
-
(1991)
Genes Dev
, vol.5
, pp. 416-427
-
-
Lai, E.1
Prezioso, V.R.2
Tao, W.F.3
Chen, W.S.4
Darnell J.E., Jr.5
-
27
-
-
0029572447
-
Chromosomal localization of six human forkhead genes, freac-1 (FKHL5), - 3 (FKHL7), -4 (FKHL8), -5 (FKHL9), -6 (FKHL10), and -8 (FKHLI2)
-
Larsson, C., Hellqvist, M., Pierrou, S., White, I., Enerback, S., and Carlsson, P. 1995. Chromosomal localization of six human forkhead genes, freac-1 (FKHL5), - 3 (FKHL7), -4 (FKHL8), -5 (FKHL9), -6 (FKHL10), and -8 (FKHLI2). Genomics 30: 464-469.
-
(1995)
Genomics
, vol.30
, pp. 464-469
-
-
Larsson, C.1
Hellqvist, M.2
Pierrou, S.3
White, I.4
Enerback, S.5
Carlsson, P.6
-
28
-
-
0027173427
-
The retroviral oncogene qin belongs to the transcription factor family that includes the homeotic gene fork head
-
Li, J. and Vogt, P.K. 1993. The retroviral oncogene qin belongs to the transcription factor family that includes the homeotic gene fork head. Proc. Natl. Acad. Sci. 90: 4490-4494.
-
(1993)
Proc. Natl. Acad. Sci
, vol.90
, pp. 4490-4494
-
-
Li, J.1
Vogt, P.K.2
-
29
-
-
0027403961
-
Unbiased estimation of the rates of synonymous and nonsynonymous substitution
-
Li, W.H. 1993. Unbiased estimation of the rates of synonymous and nonsynonymous substitution. J. Mol. Evol. 36: 96-99.
-
(1993)
J. Mol. Evol
, vol.36
, pp. 96-99
-
-
Li, W.H.1
-
30
-
-
0022005270
-
A new method for estimating synonymous and nonsynonymous rates of nucleotide substitution considering the relative likelihood of nucleotide and codon changes
-
Li, W.H., Wu, C.I., and Luo, C.C. 1985. A new method for estimating synonymous and nonsynonymous rates of nucleotide substitution considering the relative likelihood of nucleotide and codon changes. Mol. Biol. Evol. 2: 150-174.
-
(1985)
Mol. Biol. Evol
, vol.2
, pp. 150-174
-
-
Li, W.H.1
Wu, C.I.2
Luo, C.C.3
-
31
-
-
0035504778
-
Transcriptional activity of multiple copies of a subtelomerically located olfactory receptor gene that is polymorphic in number and location
-
Linardopoulou, E., Mefford, H.C., Nguyen, O.T., Friedman, C., van den Engh, G., Farwell, D.G., Coltrera, M., and Trask, B.J. 2001. Transcriptional activity of multiple copies of a subtelomerically located olfactory receptor gene that is polymorphic in number and location. Hum. Mol. Genet. 10: 2373-2383.
-
(2001)
Hum. Mol. Genet
, vol.10
, pp. 2373-2383
-
-
Linardopoulou, E.1
Mefford, H.C.2
Nguyen, O.T.3
Friedman, C.4
van den Engh, G.5
Farwell, D.G.6
Coltrera, M.7
Trask, B.J.8
-
32
-
-
0034634395
-
The evolutionary fate and consequences of duplicate genes
-
Lynch, M. and Conery, J.S. 2000. The evolutionary fate and consequences of duplicate genes. Science 290: 1151-1155.
-
(2000)
Science
, vol.290
, pp. 1151-1155
-
-
Lynch, M.1
Conery, J.S.2
-
33
-
-
17344374131
-
PAX8 mutations associated with congenital hypothyroidism caused by thyroid dysgenesis
-
Macchia, P.E., Lapi, P., Krude, H., Pirro, M.T., Missero, C., Chiovato, L., Souabni, A., Baserga, M., Tassi, V., Pinchera, A., et al. 1998. PAX8 mutations associated with congenital hypothyroidism caused by thyroid dysgenesis. Nat. Genet. 19: 83-86.
-
(1998)
Nat. Genet
, vol.19
, pp. 83-86
-
-
Macchia, P.E.1
Lapi, P.2
Krude, H.3
Pirro, M.T.4
Missero, C.5
Chiovato, L.6
Souabni, A.7
Baserga, M.8
Tassi, V.9
Pinchera, A.10
-
34
-
-
0035977491
-
Identification of a novel retina-specific gene located in a subtelomeric region with polymorphic distribution among multiple human chromosomes
-
1522
-
Mah, N., Stoehr, H., Schulz, H.L., White, K., and Weber, B.H. 2001. Identification of a novel retina-specific gene located in a subtelomeric region with polymorphic distribution among multiple human chromosomes. Biochim. Biophys. Acta 1522: 167-174.
-
(2001)
Biochim. Biophys. Acta
, pp. 167-174
-
-
Mah, N.1
Stoehr, H.2
Schulz, H.L.3
White, K.4
Weber, B.H.5
-
35
-
-
0036206759
-
The evolutionary origin of human subtelomeric homologies - Or where the ends begin
-
Martin, C.L., Wong, A., Gross, A., Chung, J., Fantes, J.A., and Ledbetter, D.H. 2002. The evolutionary origin of human subtelomeric homologies-or where the ends begin. Am. J. Hum. Genet. 70: 972-984.
-
(2002)
Am. J. Hum. Genet
, vol.70
, pp. 972-984
-
-
Martin, C.L.1
Wong, A.2
Gross, A.3
Chung, J.4
Fantes, J.A.5
Ledbetter, D.H.6
-
36
-
-
0028886716
-
Molecular analysis of a novel subtelomeric repeat with polymorphic chromosomal distribution
-
Martin-Gallardo, A., Lamerdin, J., Sopapan, P., Friedman, C., Fertitta, A,L., Garcia, E., Carrano, A., Negorev, D., Macina, R.A., Trask, B.J., et al. 1995. Molecular analysis of a novel subtelomeric repeat with polymorphic chromosomal distribution. Cytogenet. Cell Genet. 71: 289-295.
-
(1995)
Cytogenet. Cell Genet
, vol.71
, pp. 289-295
-
-
Martin-Gallardo, A.1
Lamerdin, J.2
Sopapan, P.3
Friedman, C.4
Fertitta, A.L.5
Garcia, E.6
Carrano, A.7
Negorev, D.8
Macina, R.A.9
Trask, B.J.10
-
37
-
-
0035942221
-
Controlling small guanine-nucleotide-exchange factor function through cytoplasmic RNA intramers
-
Mayer, G., Blind, M., Nagel, W., Bohm, T., Knorr, T., Jackson, C.L., Kolanus, W., and Famulok, M. 2001. Controlling small guanine-nucleotide-exchange factor function through cytoplasmic RNA intramers. Proc. Natl. Acad. Sci. 98: 4961-4965.
-
(2001)
Proc. Natl. Acad. Sci
, vol.98
, pp. 4961-4965
-
-
Mayer, G.1
Blind, M.2
Nagel, W.3
Bohm, T.4
Knorr, T.5
Jackson, C.L.6
Kolanus, W.7
Famulok, M.8
-
38
-
-
0035504448
-
Comparative sequencing of a multicopy subtelomeric region containing olfactory receptor genes reveals multiple interactions between non-homologous chromosomes
-
Mefford, H.C., Linardopoulou, E., Coil, D., van den Engh, G., and Trask, B.J. 2001. Comparative sequencing of a multicopy subtelomeric region containing olfactory receptor genes reveals multiple interactions between non-homologous chromosomes. Hum. Mol. Genet. 10: 2363-2372.
-
(2001)
Hum. Mol. Genet
, vol.10
, pp. 2363-2372
-
-
Mefford, H.C.1
Linardopoulou, E.2
Coil, D.3
van den Engh, G.4
Trask, B.J.5
-
39
-
-
0030021413
-
A novel dystrophin/utrophin-associated protein is an enzymatically inactive member of the phosphoglucomutase superfamily
-
Moiseeva, E.P., Belkin, A.M., Spurr, N.K., Koteliansky, V.E., and Critchley, D.R. 1996. A novel dystrophin/utrophin-associated protein is an enzymatically inactive member of the phosphoglucomutase superfamily. Eur. J. Biochem. 235: 103-113.
-
(1996)
Eur. J. Biochem
, vol.235
, pp. 103-113
-
-
Moiseeva, E.P.1
Belkin, A.M.2
Spurr, N.K.3
Koteliansky, V.E.4
Critchley, D.R.5
-
40
-
-
0030791307
-
Evolution by the birth-and-death process in multigene families of the vertebrate immune system
-
Nei, M., Gu, X., and Sitnikova, T. 1997. Evolution by the birth-and-death process in multigene families of the vertebrate immune system. Proc. Natl. Acad. Sci. 94: 7799-7806.
-
(1997)
Proc. Natl. Acad. Sci
, vol.94
, pp. 7799-7806
-
-
Nei, M.1
Gu, X.2
Sitnikova, T.3
-
41
-
-
0029965984
-
Isolation of the human chromosome 22q telomere and its application to detection of cryptic chromosomal abnormalities
-
Ning, Y., Rosenberg, M., Biesecker, L.G., and Ledbetter, D.H. 1996. Isolation of the human chromosome 22q telomere and its application to detection of cryptic chromosomal abnormalities. Hum. Genet. 97: 765-769.
-
(1996)
Hum. Genet
, vol.97
, pp. 765-769
-
-
Ning, Y.1
Rosenberg, M.2
Biesecker, L.G.3
Ledbetter, D.H.4
-
42
-
-
17344368672
-
The forkhead transcription factor gene FKHL7 is responsible for glaucoma phenotypes which map to 6p25
-
Nishimura, D.Y., Swiderski, R.E., Alward, W.L., Searby, C.C., Patil, S.R., Bennet, S.R., Kanis, A.B., Gastier, J.M., Stone, E.M., and Sheffield, V.C. 1998. The forkhead transcription factor gene FKHL7 is responsible for glaucoma phenotypes which map to 6p25. Nat. Genet. 19: 140-147.
-
(1998)
Nat. Genet
, vol.19
, pp. 140-147
-
-
Nishimura, D.Y.1
Swiderski, R.E.2
Alward, W.L.3
Searby, C.C.4
Patil, S.R.5
Bennet, S.R.6
Kanis, A.B.7
Gastier, J.M.8
Stone, E.M.9
Sheffield, V.C.10
-
43
-
-
0034705848
-
Newly identified repeat sequences, derived from human chromosome 21qter, are also localized in the subtelomeric region of particular chromosomes and 2q13, and are conserved in the chimpanzee genome
-
Park, H.S., Nogami, M., Okumura, K., Hattori, M., Sakakia, Y., and Fujiyama, A. 2000. Newly identified repeat sequences, derived from human chromosome 21qter, are also localized in the subtelomeric region of particular chromosomes and 2q13, and are conserved in the chimpanzee genome. FEBS Lett. 475: 167-169.
-
(2000)
FEBS Lett
, vol.475
, pp. 167-169
-
-
Park, H.S.1
Nogami, M.2
Okumura, K.3
Hattori, M.4
Sakakia, Y.5
Fujiyama, A.6
-
44
-
-
0028046675
-
Cloning and characterization of seven human forkhead proteins: Binding site specificity and DNA bending
-
Pierrou, S., Hellqvist, M., Samuelsson, L., Enerback, S., and Carlsson, P. 1994. Cloning and characterization of seven human forkhead proteins: Binding site specificity and DNA bending. EMBO J. 13: 5002-5012.
-
(1994)
EMBO J
, vol.13
, pp. 5002-5012
-
-
Pierrou, S.1
Hellqvist, M.2
Samuelsson, L.3
Enerback, S.4
Carlsson, P.5
-
45
-
-
0031834147
-
A high-resolution genetic map of mouse chromosome 19 encompassing the muscle-deficient osteochondrodystrophy (mdf-ocd) region
-
Poirier, C., Blot, S., Fernandes, M., Carle, G.F., Stanescu, V., Stanescu, R., and Guenet, J.L. 1998. A high-resolution genetic map of mouse chromosome 19 encompassing the muscle-deficient osteochondrodystrophy (mdf-ocd) region. Mamm. Genome 9: 390-391.
-
(1998)
Mamm. Genome
, vol.9
, pp. 390-391
-
-
Poirier, C.1
Blot, S.2
Fernandes, M.3
Carle, G.F.4
Stanescu, V.5
Stanescu, R.6
Guenet, J.L.7
-
46
-
-
0027295651
-
Ectopic neural expression of a floor plate marker in frog embryos injected with the midline transcription factor Pintallavis
-
Ruiz i Altaba, A., Cox, C., Jessell, T.M., and Klar, A. 1993. Ectopic neural expression of a floor plate marker in frog embryos injected with the midline transcription factor Pintallavis. Proc. Natl. Acad. Sci. 90: 8268-8272.
-
(1993)
Proc. Natl. Acad. Sci
, vol.90
, pp. 8268-8272
-
-
Ruiz i Altaba, A.1
Cox, C.2
Jessell, T.M.3
Klar, A.4
-
47
-
-
0036245495
-
Segmental duplications and the evolution of the primate genome
-
Samonte, R.V. and Eichler, E.E. 2002. Segmental duplications and the evolution of the primate genome. Nat. Rev. Genet. 3: 65-72.
-
(2002)
Nat. Rev. Genet
, vol.3
, pp. 65-72
-
-
Samonte, R.V.1
Eichler, E.E.2
-
48
-
-
0035839244
-
Identification of dopamine responsive mRNAs in glial cells by suppression subtractive hybridization
-
Shi, J., Cai, W., Chen, X., Ying, K., Zhang, K., and Xie, Y. 2001. Identification of dopamine responsive mRNAs in glial cells by suppression subtractive hybridization. Brain Res. 910: 29-37.
-
(2001)
Brain Res
, vol.910
, pp. 29-37
-
-
Shi, J.1
Cai, W.2
Chen, X.3
Ying, K.4
Zhang, K.5
Xie, Y.6
-
49
-
-
0024599315
-
Molecular cloning of the cDNA for the human U2 snRNA-specific A' protein
-
Sillekens, P.T., Beijer, R.P., Habets, W.J., and van Verooij, W.J. 1989. Molecular cloning of the cDNA for the human U2 snRNA-specific A' protein. Nucleic Acids Res. 17: 1893-1906.
-
(1989)
Nucleic Acids Res
, vol.17
, pp. 1893-1906
-
-
Sillekens, P.T.1
Beijer, R.P.2
Habets, W.J.3
van Verooij, W.J.4
-
50
-
-
0036468807
-
Genome architecture, rearrangements and genomic disorders
-
Stankiewicz, P. and Lupski, J.R. 2002. Genome architecture, rearrangements and genomic disorders. Trends Genet. 18: 74-82.
-
(2002)
Trends Genet
, vol.18
, pp. 74-82
-
-
Stankiewicz, P.1
Lupski, J.R.2
-
51
-
-
0031931669
-
What PAX genes do in the kidney
-
Torban, E. and Goodyer, P. 1998. What PAX genes do in the kidney. Exp. Nephrol. 6: 7-11.
-
(1998)
Exp. Nephrol
, vol.6
, pp. 7-11
-
-
Torban, E.1
Goodyer, P.2
-
52
-
-
0027516045
-
Fluorescence in situ hybridization mapping of human chromosome 19: Cytogenetic band location of 540 cosmids and 70 genes or DNA markers
-
Trask, B., Fertitta, A., Christensen, M., Youngblom, J., Bergmann, A., Copeland, A., de Jong, P., Mohrenweiser, H., Olsen, A., Carrano, A., et al. 1993. Fluorescence in situ hybridization mapping of human chromosome 19: Cytogenetic band location of 540 cosmids and 70 genes or DNA markers. Genomics 15: 133-145.
-
(1993)
Genomics
, vol.15
, pp. 133-145
-
-
Trask, B.1
Fertitta, A.2
Christensen, M.3
Youngblom, J.4
Bergmann, A.5
Copeland, A.6
de Jong, P.7
Mohrenweiser, H.8
Olsen, A.9
Carrano, A.10
-
53
-
-
6844242311
-
Members of the olfactory receptor gene family are contained in large blocks of DNA duplicated polymorphically near the ends of human chromosomes
-
Trask, B.J., Friedman, C., Martin-Gallardo, A., Rowen, L., Akinbami, C., Blankenship, J., Collins, C., Giorgi, D., Iadonato, S., Johnson, F., et al. 1998. Members of the olfactory receptor gene family are contained in large blocks of DNA duplicated polymorphically near the ends of human chromosomes. Hum. Mol. Genet. 7: 13-26.
-
(1998)
Hum. Mol. Genet
, vol.7
, pp. 13-26
-
-
Trask, B.J.1
Friedman, C.2
Martin-Gallardo, A.3
Rowen, L.4
Akinbami, C.5
Blankenship, J.6
Collins, C.7
Giorgi, D.8
Iadonato, S.9
Johnson, F.10
-
54
-
-
0033180514
-
Two novel human RAB genes with near identical sequence each map to a telomere-associated region: The subtelomeric region of 22q13.3 and the ancestral telomere band 2q13
-
Wong, A.C., Shkolny, D., Dorman, A., Willingham, D., Roe, B.A., and McDermid, H.E. 1999. Two novel human RAB genes with near identical sequence each map to a telomere-associated region: The subtelomeric region of 22q13.3 and the ancestral telomere band 2q13. Genomics 59: 326-334.
-
(1999)
Genomics
, vol.59
, pp. 326-334
-
-
Wong, A.C.1
Shkolny, D.2
Dorman, A.3
Willingham, D.4
Roe, B.A.5
McDermid, H.E.6
-
55
-
-
0020027910
-
The origin of man: A chromosomal pictorial legacy
-
Yunis, J.J. and Prakash, O. 1982. The origin of man: A chromosomal pictorial legacy. Science 215: 1525-1530.
-
(1982)
Science
, vol.215
, pp. 1525-1530
-
-
Yunis, J.J.1
Prakash, O.2
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