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Volumn 72, Issue 4, 1996, Pages 271-293

Report of the Fourth International Workshop on Human Chromosome 16 Mapping 1995

Author keywords

[No Author keywords available]

Indexed keywords

CHROMOSOME 16; CONFERENCE PAPER; GENE LOCATION; GENE MAPPING; HUMAN; PRIORITY JOURNAL; WORKSHOP;

EID: 0029990004     PISSN: 03010171     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Conference Paper
Times cited : (21)

References (45)
  • 2
    • 6844241328 scopus 로고
    • Assignment of muscle cadherin (MCAD) to human chromosome 16q24-qter and to mouse chromosome 8, and of placental cadherin (PCAD)-like sequences PCADL1 to 16q22.1 and PCADL2 to 16q24-qter
    • Becker-Follmann J, Kaupmann K, Vestweber D, Jochusch H, Starzinski-Powitz A, Scherer G: Assignment of muscle cadherin (MCAD) to human chromosome 16q24-qter and to mouse chromosome 8, and of placental cadherin (PCAD)-like sequences PCADL1 to 16q22.1 and PCADL2 to 16q24-qter. Cytogenet Cell Genet 60:168 (1992).
    • (1992) Cytogenet Cell Genet , vol.60 , pp. 168
    • Becker-Follmann, J.1    Kaupmann, K.2    Vestweber, D.3    Jochusch, H.4    Starzinski-Powitz, A.5    Scherer, G.6
  • 4
    • 0028788975 scopus 로고
    • Familial cylindromatosis (turban tumour syndrome) gene localized to chromosome 16q12-q13: Evidence for its role as a tumour supressor gene
    • Biggs PJ, Wooster R, Ford D, Chapman P, Mangion J, Quirk Y, Easton DE, Burn J, Stratton MR: Familial cylindromatosis (turban tumour syndrome) gene localized to chromosome 16q12-q13: evidence for its role as a tumour supressor gene. Nature Genetics 11:441-443 (1995).
    • (1995) Nature Genetics , vol.11 , pp. 441-443
    • Biggs, P.J.1    Wooster, R.2    Ford, D.3    Chapman, P.4    Mangion, J.5    Quirk, Y.6    Easton, D.E.7    Burn, J.8    Stratton, M.R.9
  • 5
    • 0028879076 scopus 로고
    • Epithelial sodium channel genes SCNN1B and SCNN1G are closely linked on distal mouse chromosome 7
    • Brooker DR, Kozak CA, Kleyman TR: Epithelial sodium channel genes SCNN1B and SCNN1G are closely linked on distal mouse chromosome 7. Genomics 29:784-786 (1995).
    • (1995) Genomics , vol.29 , pp. 784-786
    • Brooker, D.R.1    Kozak, C.A.2    Kleyman, T.R.3
  • 6
    • 9244252171 scopus 로고
    • Report of the committee on the genetic constituency of chromosome 16
    • Cuticchia AJ (ed): The Johns Hopkins University Press, Baltimore
    • Callen DF, Doggett NA; Report of the committee on the genetic constituency of chromosome 16, in Cuticchia AJ (ed): Human Gene Mapping 1994, A Compendium, pp 559-646 (The Johns Hopkins University Press, Baltimore 1995).
    • (1995) Human Gene Mapping 1994, A Compendium , pp. 559-646
    • Callen, D.F.1    Doggett, N.A.2
  • 11
    • 0027517493 scopus 로고
    • Smooth muscle myosin heavy chain locus (MYH11) maps to 16p13.13-p13.12 and establishes a new region of conserved synteny between human 16p and mouse 16
    • Deng ZM, Liu P, Marlton P, Claxton DF, Lane S, Callen DF, Collins FS, Siciliano MJ: Smooth muscle myosin heavy chain locus (MYH11) maps to 16p13.13-p13.12 and establishes a new region of conserved synteny between human 16p and mouse 16. Genomics 18:156-159 (1993).
    • (1993) Genomics , vol.18 , pp. 156-159
    • Deng, Z.M.1    Liu, P.2    Marlton, P.3    Claxton, D.F.4    Lane, S.5    Callen, D.F.6    Collins, F.S.7    Siciliano, M.J.8
  • 12
    • 0028915805 scopus 로고
    • Report of the third international workshop on human chromosome 16 mapping 1994
    • Doggett NA, Callen DF: Report of the third international workshop on human chromosome 16 mapping 1994. Cytogenet Cell Genet 68:165-184 (1995).
    • (1995) Cytogenet Cell Genet , vol.68 , pp. 165-184
    • Doggett, N.A.1    Callen, D.F.2
  • 15
    • 0027167456 scopus 로고
    • Cloning and characterization of a mouse 3-methyladenine/7-methylguanine/3-methylguanine DNA glycosylase cDNA whose gene maps to chromosome 11
    • Engelward BP, Boosalis MS, Chen BJ, Deng ZM, Siciliano MJ, Samson L: Cloning and characterization of a mouse 3-methyladenine/7-methylguanine/3-methylguanine DNA glycosylase cDNA whose gene maps to chromosome 11. Carcinogenesis 14:175-181 (1993).
    • (1993) Carcinogenesis , vol.14 , pp. 175-181
    • Engelward, B.P.1    Boosalis, M.S.2    Chen, B.J.3    Deng, Z.M.4    Siciliano, M.J.5    Samson, L.6
  • 16
    • 0028091349 scopus 로고
    • Mapping of the gene encoding the melanocortin-1 (alpha-melanocyte stimulating hormone) receptor (MC1R) to human chromosome 16q24.3 by fluorescence in situ hybridization
    • Gantz I, Yamada T, Tashiro T, Konda Y, Shimoto Y, Miwa H, Trent JM: Mapping of the gene encoding the melanocortin-1 (alpha-melanocyte stimulating hormone) receptor (MC1R) to human chromosome 16q24.3 by fluorescence in situ hybridization. Genomics 19:394-5 (1994).
    • (1994) Genomics , vol.19 , pp. 394-395
    • Gantz, I.1    Yamada, T.2    Tashiro, T.3    Konda, Y.4    Shimoto, Y.5    Miwa, H.6    Trent, J.M.7
  • 18
    • 0029004047 scopus 로고
    • Structure of the leukemia-associated human CBFB gene
    • Hajra A, Collins FS: Structure of the leukemia-associated human CBFB gene. Genomics 26:571-579 (1995).
    • (1995) Genomics , vol.26 , pp. 571-579
    • Hajra, A.1    Collins, F.S.2
  • 21
    • 0028049934 scopus 로고
    • Mapping the gene that encodes phosphatidylinositol-specific phospholipase C-gamma 2 in the human and the mouse
    • Hernandez D, Egan SE, Yulug IG, Fisher EMC: Mapping the gene that encodes phosphatidylinositol-specific phospholipase C-gamma 2 in the human and the mouse. Genomics 23:504-7 (1994).
    • (1994) Genomics , vol.23 , pp. 504-507
    • Hernandez, D.1    Egan, S.E.2    Yulug, I.G.3    Fisher, E.M.C.4
  • 26
    • 0028830856 scopus 로고
    • A germline insertion in the tuberous sclerosis (TSC2) gene gives rise to the Eker rat model of dominantly inherited cancer
    • Kobayashi T, Hirayama Y, Kobayashi E, Kubo Y, Hino O: A germline insertion in the tuberous sclerosis (TSC2) gene gives rise to the Eker rat model of dominantly inherited cancer. Nature Genetics 9:70-74 (1995).
    • (1995) Nature Genetics , vol.9 , pp. 70-74
    • Kobayashi, T.1    Hirayama, Y.2    Kobayashi, E.3    Kubo, Y.4    Hino, O.5
  • 27
  • 29
    • 0029240217 scopus 로고
    • Mouse cyclin F maps to a conserved linkage group on mouse chromosome 17
    • Obermayr F, Sutherland HF, Kraus B, Frischauf AM: Mouse cyclin F maps to a conserved linkage group on mouse chromosome 17 Mammal Genome 6:149-150 (1995).
    • (1995) Mammal Genome , vol.6 , pp. 149-150
    • Obermayr, F.1    Sutherland, H.F.2    Kraus, B.3    Frischauf, A.M.4
  • 30
    • 0028939384 scopus 로고
    • The mouse homologue of the tuberin gene (TSC2) maps to a conserved synteny group between mouse chromosome 17 and human 16p13.3
    • Olsson PG, Sutherland HF, Nowicka U, Kom B, Poustka A, Frischauf AM: The mouse homologue of the tuberin gene (TSC2) maps to a conserved synteny group between mouse chromosome 17 and human 16p13.3. Genomics 25:339-340 (1995).
    • (1995) Genomics , vol.25 , pp. 339-340
    • Olsson, P.G.1    Sutherland, H.F.2    Nowicka, U.3    Kom, B.4    Poustka, A.5    Frischauf, A.M.6
  • 32
    • 0026708517 scopus 로고
    • Mapping of the human GSPT1 gene, a human homolog of the yeast GST1 gene, to chromosomal band 16p13.1 Somat Cell molec
    • Ozawa K, Murakami Y, Eki T, Yokoyama K, Soeda E, Hoshino S, Ui M, Hanaoka F: Mapping of the human GSPT1 gene, a human homolog of the yeast GST1 gene, to chromosomal band 16p13.1 Somat Cell molec Genet 18:189-194 (1992).
    • (1992) Genet , vol.18 , pp. 189-194
    • Ozawa, K.1    Murakami, Y.2    Eki, T.3    Yokoyama, K.4    Soeda, E.5    Hoshino, S.6    Ui, M.7    Hanaoka, F.8
  • 35
    • 0028969225 scopus 로고
    • The mouse homologue of the human tuberous sclerosis 2 (TSC2) gene maps to chromosome 17, but does not fall within the t(w18) or t(h20) deletions
    • Pilz A, Glenister P, Povey S, Lyon M, Abbott C: The mouse homologue of the human tuberous sclerosis 2 (TSC2) gene maps to chromosome 17, but does not fall within the t(w18) or t(h20) deletions. Genomics 26:420-21 (1995).
    • (1995) Genomics , vol.26 , pp. 420-421
    • Pilz, A.1    Glenister, P.2    Povey, S.3    Lyon, M.4    Abbott, C.5
  • 36
    • 0004402555 scopus 로고
    • A paracentric inversion of 16q in a patient with anus, hand, and ear anomalies: Further evidence for a Townes-Brocks syndrome gene at 16q12.1
    • Powell CM, Reitnauer PJ, Kaiser-Rogers KA, Rao KW: A paracentric inversion of 16q in a patient with anus, hand, and ear anomalies: further evidence for a Townes-Brocks syndrome gene at 16q12.1. Am J hum Genet 57:suppl:A100 (1995).
    • (1995) Am J Hum Genet , vol.57 , Issue.SUPPL.
    • Powell, C.M.1    Reitnauer, P.J.2    Kaiser-Rogers, K.A.3    Rao, K.W.4
  • 38
    • 0025990209 scopus 로고
    • Cloning and characterization of a 3-melhyladenine DNA glycosylase cDNA from human cells whose gene maps to chromosome 16
    • Samson L, Derfler B, Boosalis M, Call K: Cloning and characterization of a 3-melhyladenine DNA glycosylase cDNA from human cells whose gene maps to chromosome 16. Prot natl Acad Sci, USA 88:9127-9131 (1991).
    • (1991) Prot Natl Acad Sci, USA , vol.88 , pp. 9127-9131
    • Samson, L.1    Derfler, B.2    Boosalis, M.3    Call, K.4
  • 40
    • 84951605684 scopus 로고
    • Genomic rearrangement of the alpha-globin gene complex during mamalian evolution
    • Tan H, Whitney JB: Genomic rearrangement of the alpha-globin gene complex during mamalian evolution. Biochem Genet 31:473-84 (1993).
    • (1993) Biochem Genet , vol.31 , pp. 473-484
    • Tan, H.1    Whitney, J.B.2
  • 43
    • 0028786945 scopus 로고
    • Variants of the melanocyte-stimulating hormone receptor gene are associated with red hair and fair skin in humans
    • Valverde P, Healy E, Jackson I, Rees JL, Thody AJ: Variants of the melanocyte-stimulating hormone receptor gene are associated with red hair and fair skin in humans. Nature Genetics 11:328-330 (1995).
    • (1995) Nature Genetics , vol.11 , pp. 328-330
    • Valverde, P.1    Healy, E.2    Jackson, I.3    Rees, J.L.4    Thody, A.J.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.