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Volumn 61, Issue 3, 1997, Pages 183-206

Report on the 1996 International chromosome 9 workshop

(14)  Povey, S a   Attvvood, J a   Chadwick, B b   Frezal, J c   Haines, J L d   Knowles, M e   Kwiatkowski, D J f   Olopade, O I g   Slaugenhaupt, S d   Spurr, N K h   Smith, M i   Steel, K j   White, J A a   Pericak Vance, M A k  


Author keywords

[No Author keywords available]

Indexed keywords

ALGORITHM; ANIMAL CELL; BASAL CELL CARCINOMA; BLADDER CANCER; CANCER GENETICS; CARDIOMYOPATHY; CHROMOSOME 9; CHROMOSOME ANALYSIS; CHROMOSOME MAP; CONFERENCE PAPER; CONSENSUS SEQUENCE; DATA ANALYSIS; EHLERS DANLOS SYNDROME; FRIEDREICH ATAXIA; GENE LOCATION; GENE LOCUS; GENE MAPPING; HEARING LOSS; HUMAN; HUMAN CELL; HYPOPLASIA; LYMPHATIC LEUKEMIA; MARKER GENE; MEIOSIS; MOUSE; MUSCULAR DYSTROPHY; NEUROPATHY; NOMENCLATURE; NONHUMAN; PRIORITY JOURNAL; SEX DETERMINATION; TUBEROUS SCLEROSIS; TUMOR SUPPRESSOR GENE; WORKSHOP;

EID: 0343472016     PISSN: 00034800     EISSN: None     Source Type: Journal    
DOI: 10.1017/S0003480097006106     Document Type: Conference Paper
Times cited : (26)

References (50)
  • 1
    • 0030479405 scopus 로고    scopus 로고
    • CROSSFIND: Software for detecting and displaying well-characterised meiotic breakpoints in human family data
    • ATTWOOD, J. & POVEY, S. (1996). CROSSFIND: Software for detecting and displaying well-characterised meiotic breakpoints in human family data. Ann. Hum. Genet. 60, 487-498.
    • (1996) Ann. Hum. Genet. , vol.60 , pp. 487-498
    • Attwood, J.1    Povey, S.2
  • 2
    • 0030055508 scopus 로고    scopus 로고
    • Report of a critical recombination further narrowing the TSC1 region
    • AU, K. S., MURRELL, J., BUCKLER, A., BLANTON, S. H. & NORTHRUP, H. (1996). Report of a critical recombination further narrowing the TSC1 region. J. Med. Genet. 33, 559-561.
    • (1996) J. Med. Genet. , vol.33 , pp. 559-561
    • Au, K.S.1    Murrell, J.2    Buckler, A.3    Blanton, S.H.4    Northrup, H.5
  • 3
    • 0029886028 scopus 로고    scopus 로고
    • Mutation in and lack of expression of tyrosinase related protein-1 (TRP-1) in melanocytes from an individual with brown oculocutaneous albinism: A new subtype of albinism classified as OCA3
    • BOISSY, R. E., ZHAO, H., OETTING, W. S., AUSTIN, L. M., WILDENBERG, BOISSY, Y. L., ZHAO, Y., STURM, R. A., HEARING, V. J., KING, R. A. & NORDLUND, J. J. (1996). Mutation in and lack of expression of tyrosinase related protein-1 (TRP-1) in melanocytes from an individual with brown oculocutaneous albinism: a new subtype of albinism classified as OCA3. Am. J. Hum. Genet. 58, 1145-1156
    • (1996) Am. J. Hum. Genet. , vol.58 , pp. 1145-1156
    • Boissy, R.E.1    Zhao, H.2    Oetting, W.S.3    Austin, L.M.4    Wildenberg5    Boissy, Y.L.6    Zhao, Y.7    Sturm, R.A.8    Hearing, V.J.9    King, R.A.10    Nordlund, J.J.11
  • 5
    • 0029998350 scopus 로고    scopus 로고
    • Deregulation of PAX-5 by translocation of the E-mu enhancer of the IgH locus adjacent to two alternative PAX-5 promoters in a diffuse large-cell lymphoma
    • BUSSLINGER, M., KLIX, N., PFEFFER, P., GRANINGER, P. G. & KOZMIK, Z. (1996). Deregulation of PAX-5 by translocation of the E-mu enhancer of the IgH locus adjacent to two alternative PAX-5 promoters in a diffuse large-cell lymphoma. Proc. Nat. Acad. Sci. USA 93, 6129-6134.
    • (1996) Proc. Nat. Acad. Sci. USA , vol.93 , pp. 6129-6134
    • Busslinger, M.1    Klix, N.2    Pfeffer, P.3    Graninger, P.G.4    Kozmik, Z.5
  • 9
    • 0030217921 scopus 로고    scopus 로고
    • Nuclear cap binding protein maps close to Xeroderma pigmentosum complementation group A (XPA) in man and mouse
    • CHADWICK, B., OBERMAYR, F., & FRISCHAUF, A-M. (1996). Nuclear cap binding protein maps close to Xeroderma pigmentosum complementation group A (XPA) in man and mouse. Genomics 35, 632-633.
    • (1996) Genomics , vol.35 , pp. 632-633
    • Chadwick, B.1    Obermayr, F.2    Frischauf, A.-M.3
  • 10
    • 0030033829 scopus 로고    scopus 로고
    • Fusion of the EWS gene to CHN, a member of the steroid/thyroid receptor gene superfamily, in a human myxoid chondrosarcoma
    • CLARK, J., BENJAMIN, H., GILL, S., SIDHAR, S., GOODWIN, G., CREW, J., GUSTERSON, B. A., SHIPLEY, J. & COOPER, C. S. (1996). Fusion of the EWS gene to CHN, a member of the steroid/thyroid receptor gene superfamily, in a human myxoid chondrosarcoma. Oncogene 12, 229-235.
    • (1996) Oncogene , vol.12 , pp. 229-235
    • Clark, J.1    Benjamin, H.2    Gill, S.3    Sidhar, S.4    Goodwin, G.5    Crew, J.6    Gusterson, B.A.7    Shipley, J.8    Cooper, C.S.9
  • 11
    • 0030055960 scopus 로고    scopus 로고
    • Chromosomal mapping of the human genes CKS1 to 8q21 and CKS2 to 9q22
    • DEMETRICK, D., ZHANG, H. & BEACH, D. (1996). Chromosomal mapping of the human genes CKS1 to 8q21 and CKS2 to 9q22. Cytogenet Cell Genet. 73, 250-254.
    • (1996) Cytogenet Cell Genet. , vol.73 , pp. 250-254
    • Demetrick, D.1    Zhang, H.2    Beach, D.3
  • 12
    • 0030020856 scopus 로고    scopus 로고
    • High frequency of chromosome 9 deletion in ovarian cancer: Evidence for three tumour-suppressor loci
    • DEVLIN, J., ELDER, P., GABRA, H., STEEL, C. & KNOWLES, M. (1996). High frequency of chromosome 9 deletion in ovarian cancer: evidence for three tumour-suppressor loci. British Journal of Cancer 73, 420-423.
    • (1996) British Journal of Cancer , vol.73 , pp. 420-423
    • Devlin, J.1    Elder, P.2    Gabra, H.3    Steel, C.4    Knowles, M.5
  • 14
    • 0342350481 scopus 로고    scopus 로고
    • DOCUMENTATION, CODE AND DATA AVAILABLE FROM ANONYMOUS FTP SERVERS AT LIRMM.LIRMM.FR, CELE.MRC-LMB.CAM.AC.UK AND NCBI.NLM.NIH.GOV
    • DOCUMENTATION, CODE AND DATA AVAILABLE FROM ANONYMOUS FTP SERVERS AT LIRMM.LIRMM.FR, CELE.MRC-LMB.CAM.AC.UK AND NCBI.NLM.NIH.GOV.
  • 19
    • 0023222358 scopus 로고
    • Nevoid basal cell carcinoma syndrome
    • GORLIN, R. (1987). Nevoid basal cell carcinoma syndrome. Medicine 66, 98-113.
    • (1987) Medicine , vol.66 , pp. 98-113
    • Gorlin, R.1
  • 20
    • 0030041515 scopus 로고    scopus 로고
    • Clonality of tuberous sclerosis hamartomas shown by non-random X-chromosome inactivation
    • GREEN, A. J., SEPP, T. & YATES, J. R. W. (1996). Clonality of tuberous sclerosis hamartomas shown by non-random X-chromosome inactivation. Hum. Genet. 97: 240-243.
    • (1996) Hum. Genet. , vol.97 , pp. 240-243
    • Green, A.J.1    Sepp, T.2    Yates, J.R.W.3
  • 23
    • 0030015888 scopus 로고    scopus 로고
    • Differential allele loss on chromosome 9q22.3 in human non-melanoma skin cancer
    • HOLMBERG, E., ROZELL, B., & TOFTGARD, R. (1996). Differential allele loss on chromosome 9q22.3 in human non-melanoma skin cancer. British Journal of Cancer 74, 246-250.
    • (1996) British Journal of Cancer , vol.74 , pp. 246-250
    • Holmberg, E.1    Rozell, B.2    Toftgard, R.3
  • 24
    • 0026041203 scopus 로고
    • Coronin, an actin binding protein of Dictyotelium discoideum localized to cell surface projections, has sequence similarities to G protein beta subunits
    • HOSTOS, E., BRADTKE, B., LOTTSPEICH, F., GEGGENHEIM, R. & GERISCH. (1991). Coronin, an actin binding protein of Dictyotelium discoideum localized to cell surface projections, has sequence similarities to G protein beta subunits. EMBO 10, 4097-4104.
    • (1991) EMBO , vol.10 , pp. 4097-4104
    • Hostos, E.1    Bradtke, B.2    Lottspeich, F.3    Geggenheim, R.4    Gerisch5
  • 25
    • 0028837681 scopus 로고
    • A human recessiveneurosensory nonsyndromic hearing impairment locus is potential homologue of murine deafness (dn) locus
    • JAIN, P. ET AL (1995). A human recessiveneurosensory nonsyndromic hearing impairment locus is potential homologue of murine deafness (dn) locus. Hum. Mol. Genet. 4, 2391-2394.
    • (1995) Hum. Mol. Genet. , vol.4 , pp. 2391-2394
    • Jain, P.1
  • 28
    • 0029945346 scopus 로고    scopus 로고
    • Investigation of chromosome 9q22.3-q31 DNA marker loss in odontogenic keratocysts
    • LENCH, N., HIGH, A., MARKHAM, A., HUME, W., & ROBINSON, P. (1996). Investigation of chromosome 9q22.3-q31 DNA marker loss in odontogenic keratocysts. Oral Oncol., Eur. J. Cancer 32B, 3, 202-206.
    • (1996) Oral Oncol., Eur. J. Cancer , vol.32 B , Issue.3 , pp. 202-206
    • Lench, N.1    High, A.2    Markham, A.3    Hume, W.4    Robinson, P.5
  • 29
    • 0029948270 scopus 로고    scopus 로고
    • Biochemical evidence that Patched is the Hedgehog receptor
    • MARIGO, V., DAVEY, R. A., ZUO, Y., CUNNINGHAM, J. M., & TABIN, C. J. (1996). Biochemical evidence that Patched is the Hedgehog receptor. Nature 384, 176-179.
    • (1996) Nature , vol.384 , pp. 176-179
    • Marigo, V.1    Davey, R.A.2    Zuo, Y.3    Cunningham, J.M.4    Tabin, C.J.5
  • 30
    • 0029871143 scopus 로고    scopus 로고
    • Detailed deletion mapping in squamous cell carcinomas of the esophagus narrows a region containing a putative tumor suppressor gene to about 200 kilobases on distal chromosome 9q
    • MIURA, K., SUZUKI, K., TOKINO, T., ISOMURA, M., INZAWA, J., MATSUNO, S., & NAKAMURA, Y. (1996). Detailed deletion mapping in squamous cell carcinomas of the esophagus narrows a region containing a putative tumor suppressor gene to about 200 kilobases on distal chromosome 9q. Cancer Research 56, 1629-1634.
    • (1996) Cancer Research , vol.56 , pp. 1629-1634
    • Miura, K.1    Suzuki, K.2    Tokino, T.3    Isomura, M.4    Inzawa, J.5    Matsuno, S.6    Nakamura, Y.7
  • 32
    • 0028049612 scopus 로고
    • A YAC contig spanning the nevoid basal cell carcinoma syndrome, Fanconi anaemia group C, and xeroderma pigmentosum group A loci on chromosome 9q
    • MORRIS, D. J. & REIS, A. (1994). A YAC contig spanning the nevoid basal cell carcinoma syndrome, Fanconi anaemia group C, and xeroderma pigmentosum group A loci on chromosome 9q. Genomics 23, 23-29.
    • (1994) Genomics , vol.23 , pp. 23-29
    • Morris, D.J.1    Reis, A.2
  • 34
    • 0030586946 scopus 로고    scopus 로고
    • Assignment of two human autoantigen genes-isoleucyl-tRNA synthetase locates to 9q21 and lysyl-tRNA synthetase locates to 16q23-q24
    • NICHOLS, R., BLINDER, J., PAI, S., GE, Q., TARGOFF, I., PLOTZ, P. & LIU, P. (1996). Assignment of two human autoantigen genes-isoleucyl-tRNA synthetase locates to 9q21 and lysyl-tRNA synthetase locates to 16q23-q24. Genomics 36, 210-213.
    • (1996) Genomics , vol.36 , pp. 210-213
    • Nichols, R.1    Blinder, J.2    Pai, S.3    Ge, Q.4    Targoff, I.5    Plotz, P.6    Liu, P.7
  • 35
    • 0027585031 scopus 로고
    • Targets of cyclin-dependent protein kinases
    • NIGG, E. (1993). Targets of cyclin-dependent protein kinases. Curr. Opin. Cell Biol. 5, 187-193.
    • (1993) Curr. Opin. Cell Biol. , vol.5 , pp. 187-193
    • Nigg, E.1
  • 37
    • 0025688120 scopus 로고
    • A nuclear cap binding protein from HeLa cells
    • OHNO, M., KATAOKA, N., & SHIMURA, Y. (1990). A nuclear cap binding protein from HeLa cells. Nucleic Acids Research 18, 6989-6995.
    • (1990) Nucleic Acids Research , vol.18 , pp. 6989-6995
    • Ohno, M.1    Kataoka, N.2    Shimura, Y.3
  • 38
    • 0028878820 scopus 로고
    • Report on the fourth international workshop on chromosome 9
    • PERICAK-VANCE ET AL. (1995). Report on the fourth international workshop on chromosome 9, Ann. Hum. Genet. 59, 347-365.
    • (1995) Ann. Hum. Genet. , vol.59 , pp. 347-365
    • Pericak-Vance1
  • 39
    • 0343219982 scopus 로고    scopus 로고
    • High resolution genetic linkage analysis of mouse chromosome 2 in the region of homology with human chromosome 9
    • PILZ, A, POVEY, S & ABBOTT, C. (1996). High resolution genetic linkage analysis of mouse chromosome 2 in the region of homology with human chromosome 9. Mouse Genome 94, 877-9.
    • (1996) Mouse Genome , vol.94 , pp. 877-879
    • Pilz, A.1    Povey, S.2    Abbott, C.3
  • 40
    • 0028966156 scopus 로고
    • Comparative mapping of 50 human chromosome 9 loci in the laboratory mouse
    • PILZ, A., WOODWARD, K., POVEY, S. & ABBOTT, C. (1995) Comparative mapping of 50 human chromosome 9 loci in the laboratory mouse. Genomics 25, 139-149.
    • (1995) Genomics , vol.25 , pp. 139-149
    • Pilz, A.1    Woodward, K.2    Povey, S.3    Abbott, C.4
  • 41
    • 0028476207 scopus 로고
    • Report on the third international workshop on chromosome 9
    • POVEY ET AL. (1994). Report on the third international workshop on chromosome 9. Ann. Hum. Genet. 58, 177-250.
    • (1994) Ann. Hum. Genet. , vol.58 , pp. 177-250
    • Povey1
  • 43
    • 0029811339 scopus 로고    scopus 로고
    • An autosomal recessive non-syndromic hearing loss locus identified by DNA pooling using two inbred bedouin kindreds
    • SCOTT, D., CARMI, R., ELBEDOUR, K., YOSEFSBERG, S., STONE, E., & SHEFFIELD, V. (1996). An autosomal recessive non-syndromic hearing loss locus identified by DNA pooling using two inbred bedouin kindreds. Am. J. Hum. Genet. 59, 385-391.
    • (1996) Am. J. Hum. Genet. , vol.59 , pp. 385-391
    • Scott, D.1    Carmi, R.2    Elbedour, K.3    Yosefsberg, S.4    Stone, E.5    Sheffield, V.6
  • 44
    • 10244230901 scopus 로고    scopus 로고
    • A Gene Map of the Human Genome
    • SCHULER, G. D., M. S. BOGUSKI & 102 OTHERS (1996). A Gene Map of the Human Genome. Science 274, 540-545.
    • (1996) Science , vol.274 , pp. 540-545
    • Schuler, G.D.1    Boguski, M.S.2
  • 46
    • 0028114849 scopus 로고
    • Refined mapping of a gene responsible for Fukuyama-type congenital muscular dystrophy: Evidence for strong linkage disequilibrium
    • TODA ET AL. (1994). Refined mapping of a gene responsible for Fukuyama-type congenital muscular dystrophy: Evidence for strong linkage disequilibrium. Am. J. Hum. Genet. 55, 946-950.
    • (1994) Am. J. Hum. Genet. , vol.55 , pp. 946-950
    • Toda1
  • 48
    • 0029160025 scopus 로고
    • Receptor tyrosine kinase specific for skeletal muscle lineage: Expression in embryonic muscle at the neuromuscular junction, and after injury
    • VALENZUELA, D. M. STITT, T. N. DISTEFANO, P. S., ROJAS, E., MATTSON, K., COMPTON, D. L. & NUNEZ, L. (1995). Receptor tyrosine kinase specific for skeletal muscle lineage: expression in embryonic muscle at the neuromuscular junction, and after injury. Neuron 15, 573-584.
    • (1995) Neuron , vol.15 , pp. 573-584
    • Valenzuela, D.M.1    Stitt, T.N.2    Distefano, P.S.3    Rojas, E.4    Mattson, K.5    Compton, D.L.6    Nunez, L.7
  • 49
    • 0028099996 scopus 로고
    • Tropomodulin caps the pointed ends of actin filaments
    • WEBER, A., PENNISE, C., BABCOCK, G. & FOWLER, V. (1994). Tropomodulin caps the pointed ends of actin filaments. J. Cell Biol. 127, 1627-1635.
    • (1994) J. Cell Biol. , vol.127 , pp. 1627-1635
    • Weber, A.1    Pennise, C.2    Babcock, G.3    Fowler, V.4
  • 50
    • 0029806968 scopus 로고    scopus 로고
    • A splice junction mutation in the region of COL5A1 that codes for the carboxy propeptide alpha1(v) chains results in the gravis form of Ehlers-Danlos syndrome (type 1)
    • WENSTRUP, R. R., LANGLAND, G. T., WILLING, M. C., V. N. D'SOUZA & COLE, W. G. (1996). A splice junction mutation in the region of COL5A1 that codes for the carboxy propeptide alpha1(v) chains results in the gravis form of Ehlers-Danlos syndrome (type 1). Hum. Mol. Genet. 5, 1733-1736.
    • (1996) Hum. Mol. Genet. , vol.5 , pp. 1733-1736
    • Wenstrup, R.R.1    Langland, G.T.2    Willing, M.C.3    D'Souza, V.N.4    Cole, W.G.5


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