Intramural Research
Online Research Resources
Human Chromosome 7
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Publications
Global Mapping and Sequencing of Human Chromosome 7
Green, E.D. and Olson, M.V.. Chromosomal region of the cystic fibrosis gene in yeast artificial chromosomes: a model for human genome mapping. Science 250: 94-98, 1990. [Entrez]
Green, E.D., Mohr, R.M., Idol, J.R., Jones, M., Buckingham, J.M., Deaven, L.L., Moyzis, R.K., and Olson, M.V.. Systematic generation of sequence-tagged sites for physical mapping of human chromosomes: application to the mapping of human chromosome 7 using yeast artificial chromosomes. Genomics 11: 548-564, 1991. [Entrez]
Green, E.D. and Green, P.. Sequence-tagged site (STS) content mapping of human chromosomes: theoretical considerations and early experiences. PCR Methods & Applications 1: 77-90, 1991. [Entrez]
Green, E.D., Idol, J.R., Mohr-Tidwell, R.M., Braden, V.V., Peluso, D.C., Fulton, R.S., Massa, H.F., Magness, C.L., Wilson, A.M., Kimura, J., Weissenbach, J., and Trask, B.J.. Integration of physical, genetic and cytogenetic maps of human chromosome 7: isolation and analysis of yeast artificial chromosome clones for 117 mapped genetic markers. Hum. Molec. Genet. 3: 489-501, 1994. [Entrez]
Green, E.D., Braden, V.V., Fulton, R.S., Lim, R., Ueltzen, M.S., Peluso, D.C., Mohr-Tidwell, R.M., Idol, J.R., Smith, L.M., Chumakov, I., Le Paslier, D., Cohen, D., Featherstone, T., and Green, P.. A human chromosome 7 yeast artificial chromosome (YAC) resource: construction, characterization, and screening. Genomics 25: 170-183, 1995. [Entrez]
Bouffard, G.G., Iyer, L.M., Idol, J.R., Braden, V.V., Cunningham, A.F., Weintraub, L.A., Mohr-Tidwell, R.M., Peluso, D.C., Fulton, R.S., Leckie, M.P., and Green, E.D.. A collection of 1814 human chromosome 7-specific STSs. Genome Research, 7:59-64, 1997.[Entrez]
Touchman, J.W., Bouffard, G.G., Weintraub, L.A., Idol, J.R., Wang, L., Robbins, C.M., Nussbaum, J.C., Lovett, M., Green, E.D.. 2, 006 expressed-sequence tags (ESTs) derived from human chromosome 7-enriched cDNA libraries. Genome Research, 7:281-292, 1997. [Entrez]
Bouffard, G.G., Idol, J.I., Braden, V.V., Iyer, L.M., Cunningham, A.F., Weintraub, L.A., Touchman, J.W., Mohr-Tidwell, R.M., Peluso, D.C., Fulton, R.S., Ueltzen, M.S., Weissenbach, J., Magness, C.L., and Green, E.D.: A physical map of human chromosome 7: an integrated YAC contig map with average STS spacing of 79 kb. Genome Research, 7:673-692, 1997.
Mapping and Sequencing of Targeted Regions of Human Chromosome 7
Umbricht, C.B., Griffen, C.A., Hawkins, A.L., Grzeschik, K.H., O'Connell, P., Leach, R., Green, E.D., and Kelly, T.J.. High-resolution genomic mapping of the three human replication protein A genes (RPA1, RPA2, RPA3). Genomics 20: 249-257, 1994. [Entrez]
Maraia, R.J., Sasaki-Tozawa, N., Driscoll, C.T., Green, E.D., and Darlington, G.J.. The human Y4 small cytoplasmic RNA gene is controlled by upstream elements and resides on chromosome 7 with all other hY scRNA genes. Nucl. Acids Res. 22: 3045-3052, 1994. [Entrez]
Lewanda, A.F., Green, E.D., Weissenbach, J., Jerald, H., Taylor, E., Summar, M.L., Phillips III, J.A., Cohen, M., Feingold, M., Mouradian, W., Clarren, S.K., and Jabs, E.W.. Evidence that the Saethre-Chotzen syndrome locus lies between D7S664 and D7S507, by genetic analysis and detection of a microdeletion in a patient. Am. J. Hum. Genet. 55: 1195-1201, 1994. [Entrez]
Wajnrajch, M.P., Chua, S.C., Green, E.D., and Leibel, R.L.. Human growth hormone-releasing hormone receptor (GHRHR) maps to a YAC at chromosome 7p15. Mammalian Genome 5: 595, 1994. [Entrez]
Keen, T.J., Inglehearn,C.F., Patel, R.J., Green, E.D., Peluso, D.C., and Bhattacharya, S.S.. Localization of the Aquaporin 1 (AQP1) gene within a YAC contig containing the polymorphic markers D7S632 and D7S526. Genomics 25: 599-600, 1995. [Entrez]
Curran, M.E., Splawski, I., Timothy, K.W., Vincent, G.M., Green, E.D., and Keating, M.T.. A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome. Cell 80: 795-803, 1995. [Entrez]
Lee, S., Zambas, E., Green, E.D., and Redman, C.. Organization of the gene encoding the human Kell blood group protein. Blood 85: 1364-1370, 1995. [Entrez]
Green, E.D., Maffei, M., Braden, V.V., Proenca, R., DeSilva, U., Zhang, Y., Chua Jr., S.C., Leibel, R.L., Weissenbach, J., and Friedman, J.M.. The human Obese (OB) gene: RNA expression pattern and mapping on the physical, cytogenetic, and genetic maps of chromosome 7. Genome Research 5: 5-12, 1995. [Entrez]
Keen, T.J., Inglehearn, C.F., Green, E.D., Cunningham, A.F., Patel, R.J., Peacock, R.E., Gerken, S., White, R., Weissenbach, J., and Bhattacharya, S.S.. A YAC contig spanning the dominant retinitis pigmentosa locus (RP9) on chromosome 7p. Genomics 28: 383-388, 1995. [Entrez]
Torigoe, K., Sato, S., Kusaba, H., Kohno, K., Kuwano, M., Okumura, K., Green, E.D., Tsui, L.-C., Scherer, S.W., Schlessinger, D., and Wada, M. A.. YAC-based contig of 1.5 Mb spanning the human multidrug resistance gene region and delineating the amplification unit in three human multidrug-resistant cell lines. Genome Research 5: 233-244, 1995. [Entrez]
Kusaba, H., Kohno, K., Asakuno, K., Kuwano, M., Okumura, K., Green, E.D., Schlessinger, D., and Wada, M.. Functional expression of yeast artificial chromosome-human multidrug resistance genes in mouse cells. Genome Research 5: 245-258, 1995.[Entrez]
Johnson, E.W., Iyer, L.M., Rich, S.S., Orr, H.T., Gil-Nagel, A., Kurth, J.H., Zabramski, J.M., Marchuk, D.A., Weissenbach, J., Clericuzio, C.L., Davis, L.E., Hart, B.L., Gusella, J.F., Kosofsky, B.E., Louis, D.N., Morrison, L.A., Green, E.D., and Weber, J.L.. Refined localization of the cerebral cavernous malformation gene (CCM1) to a 4-cM interval of chromosome 7q contained in a well-defined YAC contig. Genome Research 5: 368-380, 1995. [Entrez]
Hoglund, P., Haila, S., Scherer, S.W., Tsui, L.-C., Green, E.D., Weissenbach, J., Holmberg, C., de la Chapelle, A., and Kere, J.. Positional candidate genes for congenital chloride diarrhea suggested by high-resolution physical mapping in chromosome region 7q31. Genome Research 6: 202-120, 1996. [Entrez]
McGuire, R.E., Jordan, S.A., Braden, V.V., Bouffard, G.G., Humphries, P., Green, E.D., and Daiger, S.P.. Mapping the RP10 locus for autosomal dominant retinitis pigmentosa on 7q: refined genetic positioning and localization within a well-defined YAC contig. Genome Research 6: 255-266, 1996. [Entrez]
Reed, D.R., Ding,Y., Xu, W., Cather, C., Green, E.D., and Price, R.A. Extreme obesity may be linked to markers flanking the human OB gene. Diabetes 45: 691-694, 1996. [Entrez]
Frangiskakis, J.M., Ewart, A.K., Morris, C.A., Mervis, C.B., Bertrand, J., Robinson, B.F., Klein, B.P., Ensing, G.J., Everett, L.A., Green, E.D., Proschel, C., Gutowski, N.J., Noble, M., Atkinson, D.L., Odelberg, S.J., and Keating, M.T.: LIM-kinase1 hemizygosity implicated in impaired visuospatial constructive cognition. Cell 86: 59-69, 1996. [Entrez]
Clendenning, J.B., Humbert, R., Green, E.D., Wood, C., Traver, D., Furlong, C.E. Structural organization of the human PON1 gene. Genomics 35: 586-589, 1996. [Entrez]
Le Beau, M.M., Espinosa III,., Larson, R.A., and Green, E.D. Cytogenetic and molecular delineation of the region of chromosont myeloid diseases. Blood 88: 1930-1935, 1996. [Entrez]
Maraia, R., Sakulich, A.L., Brinkmann, E., and Green, E.D. Gene for human Ro-associated autoantigen Y5 RNA. Nucl. Acids Res. 24: 3552-3559, 1996. [Entrez]
Tazawa, R., Green, E.D., Ohashi, K., Wu, K.K., Wang, L.H. Characterization of the complete genomic structure of human thromboxane synthase gene and functional analysis of its promoter. Arch. Biochem. Biophys. 334: 349-359, 1996. [Entrez]
Zhan, S., Vazquez, N., Zhan, S., Wientjes, F.B., Budarf, M.L., Schrock, E., Ried, T., Green, E.D., and Chanock, S.J.: Genomic structure, chromosomal localization, start of transcription, and tissue expression of the human p40-phox, a new component of the nicotinamide adenine dinucleotide phosphate-oxidase complex. Blood, 88:2714-2721, 1996. [Entrez]
Reynolds, P.A., Powlesland, R.M., Keen, T.J., Inglehearn, C.F., Cunningham, A.F., Green, E.D., and Brown, K.W.: Localization of a novel t(1;7) translocation associated with Wilmsí tumor predisposition and skeletal abnormalities. Genes Chromosomes Cancer, 17:151-155, 1996. [Entrez]
DeSilva, U., D'Arcangelo, G., Braden, V.V., Chen, J., Miao, G.G., Curran, T., and Green, E.D. The human reelin gene: isolation, sequencing, and mapping on chromosome 7. Genome Research, 7:157-164, 1997. [Entrez]
McGuire, R.E., Daiger, S.P., and Green, E.D.: Localization and characterization of the human ADP-ribosylation factor 5 (ARF5) gene, Genomics, 41:481-484, 1997 [Entrez].
Howard, T.D., Paznekas, W.A., Green, E.D., Chiang, L.C., Ma, N., De Luna, R.I.O., Delgado, C.G., Gonzalez-Ramos, M., Kline, A.D., and Jabs, E.W.: Mutations in TWIST, a basic helix-loop-helix transcription factor, in Saethre-Chotzen syndrome. Nature Genetics, 15:36-41, 1997. [Entrez]
Van Laer, L., Van Camp, G., Green, E.D., Huizing, E.H., and Willems, P.J.: Physical mapping of the HOXA1 gene and the hnRPA2B1 gene in a YAC contig from human chromosome 7p14-p15. Human Genetics, 99:831-833, 1997. [Entrez]
Kang, S., Allen, J., Graham, Jr., J.M., Grebe, T., Clericuzio, C., Patronas, N., Ondrey, F., Green, E., Schaffer, A., Abbott, M, and Biesecker, L.G.: Linkage mapping and phenotypic analysis of autosomal dominant Pallister-Hall syndrome. J. Med. Genet., 34:441-446, 1997. [Entrez]
Behrens, F., Claussen, U., Iyer, L.M., Green, E.D., Horsthemke, B., Williamson, R., Huxley, C., and Coutelle, C.: Isolation of DNA from the centromere of human chromosome 7 by microdissection. Chromosome Research, 5:215-220, 1997. [Entrez]
Gorlach, A., Lee, P.L., Roesler, J., Hopkins, P.J., Christensen, B., Green, E.D., Chanock, S.J., and Curnutte, J.T.: A p47-phox pseudogene carries the most common mutation causing p47-phox-deficient chronic granulomatous disease. J. Clin. Invest., 100:1907-1918, 1997. [Entrez]
Everett, L.A., Glaser, B., Beck, J.C., Idol, J.R., Buchs, A., Heyman, M., Adawi, F., Hazani, E., Nassir, E., Baxevanis, A., Sheffield, V.C., and Green, E.D.: Pendred syndrome is caused by mutations in a putative sulphate transporter gene (PDS). Nature Genetics, 17:411-422, 1997. [Entrez]
Van Laer, L., Van Camp, G., van Zuijlen, D., Green, E.D., Verstreken, M., Schatteman, I., Van de Heyning, P., Balesmans, W., Coucke, P., Greinwald, J.H., Smith, R.J.H., Huizing, E., and Willems, P.: Refined mapping of a gene for autosomal dominant progressive sensorineural hearing loss (DFNA5) to a 2-cM region, and exclusion of a candidate gene that is expressed in the cochlea. Eur. J. Hum. Genet. 5:397-405, 1997. [Entrez]
Liang, H., Fairman, J., Claxton, D.F., Nowell, P.C., Green, E.D., and Nagarajan, L.: Molecular anatomy of chromosome 7q deletions in myeloid neoplasms: evidence for multiple critical loci. Proc. Natl. Acad. Sci. USA, 95:3781-3785, 1998. [Entrez]
Kusaba, H., Nakayama, M., Harada, T., Torigoe, K., Green, E.D., Scherer, S., Kohno, K., Kuwano, M, and Wada, M.: Maintenance of hypomethylation status and preferential expression of exogenous human MDR1/PGY1 gene in mouse L cells by YAC mediated transfer. Somat. Cell Molec. Genetics 23:259-274, 1998. [Entrez]
Torigoe, K., Harada, T., Kusaba, H., Uchiumi, T., Kohno, K., Green, E.D., Scherer, S.W., Tsui, L.-C., Schlessinger, D., Kuwano, M., and Wada, M.: Localization of 67 exons on a YAC contig spanning 1.5 Mb around the multidrug resistance gene region of human chromosome 7q21.1. Genomics 49:14-22, 1998. [Entrez]
Knutsen, T., Mickley, L.A., Ried, T., Green, E.D., du Manoir, S., Schrock, E., Macville, M., Ning, Y., Robey, R., Polymeropoulos, M., Torres, R., and Fojo, T.: Cytogenetic and molecular characterization of random chromosomal rearrangements activating the drug resistance gene, MDR1/P-Glycoprotein, in drug-selected cell lines and patients with drug refractory ALL. Genes Chromosom. Cancer 23:44-54, 1998. [Entrez]
Meng, X., Lu, X., Li, Z., Green, E.D., Massa, H., Trask, B.J., Morris, C.A., and Keating, M.T.: Complete physical map of the common deletion region in Williams syndrome and identification and characterization of three novel genes. Hum. Genet., 103:590-599, 1998. [Entrez]
Jin, D.-Y., Kozak, C.A., Pangilinan, F., Spencer, F., Green, E.D., and Jeang, K.-T.: Mitotic checkpoint locus MAD1L1 maps to human chromosome 7q22 and mouse chromosome 5. Genomics, 55:563-564, 1999. [Entrez]
Zenklusen, J.C., Weintraub, L.A., and Green, E.D.: Construction of a high-resolution physical map of the ~1-Mb region of human chromosome 7q31.1-q31.2 harboring a putative tumor suppressor gene. Neoplasia, 1:16-22, 1999.
DeSilva, U., Massa, H., Trask, B.J., and Green, E.D.: Comparative mapping of the region of human chromosome 7 deleted in Williams syndrome. Genome Research, 9:428-436, 1999. [Entrez]
Ellsworth, R.E., Ionasescu, V., Searby, C., Sheffield, V.C., Braden, V.V., Kucaba, T.A., McPherson, J.D., Marra, M.A., and Green, E.D.: The CMT2D locus: refined genetic position and construction of a bacterial clone-based physical map. Genome Research, 9:568-574, 1999. [Entrez]
Thomas, J.W., Lee-Lin, S.-Q., and Green, E.D.: Human-mouse comparative mapping of the genomic region containing CDK6: localization of an evolutionary breakpoint. Mammalian Genome, 10:764-767, 1999. [Entrez]
Sahoo, T., Johnson, E.W., Thomas, J.W., Kuehl, P.M., Jones, T.L., Dokken, C.G., Touchman, J.W., Gallione, C.J., Lee-Lin, S.-Q., Kosofsky, B., Kurth, J.H., Louis, D.N., Mettler, G., Morrison, L., Gil-Nagel, A., Rich, S.S., Zabramski, J.M., Boguski, M.S., Green, E.D., and Marchuk, D.A.: Mutations in the gene encoding KRIT1, a Krev-1/rap1a binding protein, cause cerebral cavernous malformations (CCM1). Hum. Molec. Genet., 8:2325-2333, 1999. [Entrez]
Ellsworth, R.E., Jamison, D.C., Touchman, J.W., Chissoe, S.L., Braden Maduro, V.V., Bouffard, G.G., Dietrich, N.L., Beckstrom-Sternberg, S.M., Iyer, L.M., Weintraub, L.A., Cotton, M., Courtney, L., Edwards, J., Maupin, R., Ozersky, P., Rohlfing, T., Wohldmann, P., Miner, T., Kemp, K., Kramer, J., Korf, I., Pepin, K., Antonacci-Fulton, L., Fulton, R.S., Minx, P., Hillier, L.W., Wilson, R.K., Waterston, R.H., Miller, W., and Green, E.D.: Comparative genomic sequence analysis of the human and mouse cystic fibrosis transmembrane conductance regulator genes. Proc. Natl. Acad. Sci. USA, 97:1172-1177, 2000. [Entrez]
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