메뉴 건너뛰기




Volumn , Issue , 2003, Pages 223-244

Molecular biology of Rothmund-Thomson syndrome

Author keywords

[No Author keywords available]

Indexed keywords


EID: 85056966423     PISSN: None     EISSN: None     Source Type: Book    
DOI: None     Document Type: Chapter
Times cited : (7)

References (84)
  • 1
    • 0000041048 scopus 로고
    • Uber kataract in vebindung mit einer eugntumliche haut degeneration. Cataracts in association with a peculiar degeneration of the skin
    • A Rothmund. Uber Kataract in Vebindung mit Einer Eugntumliche Haut Degeneration. Cataracts in association with a peculiar degeneration of the skin. Arch Fur Ophthalmol 4:159-182, 1887.
    • (1887) Arch Fur Ophthalmol , vol.4 , pp. 159-182
    • Rothmund, A.1
  • 2
    • 84980087875 scopus 로고
    • Poikiloderma congenitale
    • MS Thomson. Poikiloderma Congenitale. Br J Dermatol 48:221-234, 1936.
    • (1936) Br J Dermatol , vol.48 , pp. 221-234
    • Thomson, M.S.1
  • 3
    • 0008884129 scopus 로고
    • Skin diseases and cataract
    • A Carlton. Skin diseases and cataract. Br J Dermatol 55:83, 1943.
    • (1943) Br J Dermatol , vol.55 , pp. 83
    • Carlton, A.1
  • 4
    • 41049114683 scopus 로고
    • Thomson’s syndrome
    • GB Sexton. Thomson’s syndrome. Can Med Assoc J 70:662-665, 1954.
    • (1954) Can Med Assoc J , vol.70 , pp. 662-665
    • Sexton, G.B.1
  • 5
    • 0021984739 scopus 로고
    • Non-dermatological complications and genetic aspects of the rothmund-thomson syndrome
    • DG Starr, JP McClure, JM Connor. Non-dermatological complications and genetic aspects of the Rothmund-Thomson syndrome. Clin Genet 27:102-104, 1985.
    • (1985) Clin Genet , vol.27 , pp. 102-104
    • Starr, D.1    McC CONNORlure Connor, J.M.2
  • 7
    • 0026768449 scopus 로고
    • Rothmund-thomson syndrome: Review of the world literature
    • EM Vennos, M Collins, WD James. Rothmund-Thomson syndrome: review of the world literature J Am Acad Dermatol 27:750-762, 1992.
    • (1992) J am Acad Dermatol , vol.27 , pp. 750-762
    • Vennos, E.M.1    Collins, M.2    James, W.D.3
  • 8
  • 11
    • 0034737004 scopus 로고    scopus 로고
    • Rothmund-thom-son syndrome due to recql4 helicase mutations: Report and clinical and molecular comparisons with bloom syndrome and werner syndrome
    • NM Lindor, Y Furuichi, S Kitao, A Shimamoto, C Arndt, S Jalal. Rothmund-Thom-son syndrome due to RECQL4 helicase mutations: report and clinical and molecular comparisons with Bloom syndrome and Werner syndrome. Am J Med Genet 90:223-228, 2000.
    • (2000) Am J Med Genet , vol.90 , pp. 223-228
    • Lindor, N.M.Y.1    Furuichi, S.2    Kitao, A.3    Shimamoto, C.4    Arndt Jalal, S.5
  • 12
    • 0029805236 scopus 로고    scopus 로고
    • Rothmund-thomson syndrome: Two case reports show heterogeneous cutaneous abnormalities, an association with genetically programmed ageing changes, and increased chromosomal radiosensitibity
    • B Kerr, GS Ashcroft, D Scott, MA Horan, MWJ Ferguson, D Donnai. Rothmund-Thomson syndrome: two case reports show heterogeneous cutaneous abnormalities, an association with genetically programmed ageing changes, and increased chromosomal radiosensitibity. J Med Genet 33:928-934, 1996.
    • (1996) J Med Genet , vol.33 , pp. 928-934
    • Kerr, B.G.1    Ashcroft, D.2    Scott, M.A.3    Horan, M.4    Ferguson Donnai, D.5
  • 13
    • 41049110182 scopus 로고
    • Rothmund’s syndrome (Poikiloderma congenitale of thomson)
    • AC Curtis. Rothmund’s syndrome (Poikiloderma congenitale of Thomson). Arch Dermatol 82:116-117, 1960.
    • (1960) Arch Dermatol , vol.82 , pp. 116-117
    • Curtis, A.C.1
  • 15
    • 17344385250 scopus 로고
    • Rothmund-thomson syndrome and malignant disease (Letter)
    • MG Davies. Rothmund-Thomson syndrome and malignant disease (letter). Clin Exp Dermatol 7:455, 1982.
    • (1982) Clin Exp Dermatol , vol.7 , pp. 455
    • Davies, M.G.1
  • 16
    • 84964145707 scopus 로고
    • Congenital developmental malformation (Type described by dr. m. s. Thomson)
    • GB Dowling. Congenital developmental malformation (type described by Dr. M. S. Thomson). Proc R Soc Med 29:1633-1634, 1936.
    • (1936) Proc R Soc Med , vol.29 , pp. 1633-1634
    • Dowling, G.B.1
  • 17
    • 0018742106 scopus 로고
    • Premature multiple bowen’s disease in poikiloderma congenitale with warty hyperkeratoses
    • E Haneke, E Gutschmidt. Premature multiple Bowen’s disease in poikiloderma congenitale with warty hyperkeratoses. Dermatologica 158:384-388, 1979.
    • (1979) Dermatologica , vol.158 , pp. 384-388
    • Haneke, E.1    Gutschmidt, E.2
  • 19
    • 0023269451 scopus 로고
    • Rothmund-thomson syndrome: A case report, photo testing, and literature review
    • E Berg, T-Y Chuang, D Cripps. Rothmund-Thomson syndrome: a case report, photo testing, and literature review. J Am Acad Dermatol 17:332-338, 1987.
    • (1987) J am Acad Dermatol , vol.17 , pp. 332-338
    • Berg, E.-Y.1    Chuang Cripps, D.2
  • 20
    • 0016834543 scopus 로고
    • Hypogonadism and parathyroid adenoma in congenital poikiloderma (rothmund-thomson syndrome)
    • EA Werder, G Murset, R Illig, A Prader. Hypogonadism and parathyroid adenoma in congenital poikiloderma (Rothmund-Thomson syndrome). Clin Endocrinol 4:75-82, 1975.
    • (1975) Clin Endocrinol , vol.4 , pp. 75-82
    • Werder, E.A.G.1    Murset, R.2    Illig Prader, A.3
  • 23
    • 0015787680 scopus 로고
    • Hereditary bone dysplasia with sarcomatous degeneration
    • WH Arnold. Hereditary bone dysplasia with sarcomatous degeneration. Ann Intern Med 78:902-906, 1973.
    • (1973) Ann Intern Med , vol.78 , pp. 902-906
    • Arnold, W.H.1
  • 24
    • 0017679043 scopus 로고
    • Multiple childhood osteosarcomas in an american indian family with erithroid macrocytosis and skeltal abnormalities
    • JJ Mulvihill, HR Gralnick, J Whang-Peng. Multiple childhood osteosarcomas in an American Indian family with erithroid macrocytosis and skeltal abnormalities. Cancer 40:3115-3122, 1977.
    • (1977) Cancer , vol.40 , pp. 3115-3122
    • Mulvihill, J.1    Gralnick Whang-Peng, J.2
  • 25
    • 0016442835 scopus 로고
    • The ophthalmic manifestations of rothmund’s syndrome
    • TH Kirkham, EB Werner. The ophthalmic manifestations of Rothmund’s syndrome. Can J Ophthalmol 10:1-14, 1975.
    • (1975) Can J Ophthalmol , vol.10 , pp. 1-14
    • Kirkham, T.H.1    Werner, E.B.2
  • 26
    • 2642604278 scopus 로고
    • Congenital poikiloderma atrophicans vasculare in a mother and her son
    • N Hallman, R Patiala. Congenital poikiloderma atrophicans vasculare in a mother and her son. Acta Dermatol Venereol 1:401-406, 1951.
    • (1951) Acta Dermatol Venereol , vol.1 , pp. 401-406
    • Hallman, N.1    Patiala, R.2
  • 27
    • 0024802636 scopus 로고
    • The poikiloderma of rothmund-thomson syndrome: Changes in langerhans cell morphology and distribution
    • JH Sillevis-Smitt, MH Gons, JW Oorthuys, SR Kreig, JD Bos. The poikiloderma of Rothmund-Thomson syndrome: changes in Langerhans cell morphology and distribution. Dermatologica 179:187-190, 1989.
    • (1989) Dermatologica , vol.179 , pp. 187-190
    • Sillevis-Smitt, J.1    Gons, J.W.2    Oorthuys, S.R.3    Kreig Bos, J.D.4
  • 28
    • 0019252743 scopus 로고
    • Rothmund-thomson syndrome (poikiloderma congenitale) associated with hydrocephalus
    • EA Mitchell, LM Cairns, JL Hodge. Rothmund-Thomson syndrome (poikiloderma congenitale) associated with hydrocephalus. Aust Paediatr J 16:290-291, 1980.
    • (1980) Aust Paediatr J , vol.16 , pp. 290-291
    • Mitchell, E.1    Cairns Hodge, J.L.2
  • 29
    • 0016757132 scopus 로고
    • Endocrine aspects of the rothmund-thomson syndrome (abst)
    • H Guyda, P Macleod, E Colle. Endocrine aspects of the Rothmund-Thomson syndrome (abst). Pediatr Res 9:689, 1975.
    • (1975) Pediatr Res , vol.9 , pp. 689
    • Guyda, H.P.1    Macleod Colle, E.2
  • 31
    • 0030888233 scopus 로고    scopus 로고
    • Recq dna helicase is a suppressor of illegitimate recombination in escherichia coli
    • K Hanada, T Ukita, Y Kohno, K Saito, J Kato, H Ikeda. RecQ DNA helicase is a suppressor of illegitimate recombination in Escherichia coli. Proc Natl Acad Sci USA 94:3860-3865, 1997.
    • (1997) Proc Natl Acad Sci USA , vol.94 , pp. 3860-3865
    • Hanada, K.T.1    Ukita, Y.2    Kohno, K.3    Saito, J.4    Kato Ikeda, H.5
  • 36
    • 0028033989 scopus 로고
    • The yeast type i topoi-somerase top3 interacts with sgs1, a dna helicase homolog: A potential eukaryotic reverse gyrase
    • S Gangloff, JP McDonald, C Bendixen, L Arthur, R Rothstein. The yeast type I topoi-somerase Top3 interacts with Sgs1, a DNA helicase homolog: a potential eukaryotic reverse gyrase. Mol Cell Biol 14:8391-8398, 1994.
    • (1994) Mol Cell Biol , vol.14 , pp. 8391-8398
    • Gangloff, S.J.1    McDonald, C.2    Bendixen, L.3    Arthur Rothstein, R.4
  • 37
    • 0029002965 scopus 로고
    • Sgs1: A eukaryotic homolog of e. Coli recq that interacts with topoisomerase ii in vivo and required for faithful chromosome segregation
    • PM Watt, EJ Louis, RH Borts, ID Hickson. Sgs1: a eukaryotic homolog of E. Coli RecQ that interacts with topoisomerase II in vivo and required for faithful chromosome segregation. Cell 81:253-260, 1995.
    • (1995) Cell , vol.81 , pp. 253-260
    • Watt, P.1    Louis, R.H.2    Borts Hickson, I.D.3
  • 38
    • 0030994386 scopus 로고    scopus 로고
    • Rqhl+, a fission yeast gene related to the bloom’s and werner’s syndrome genes, is required for reversible s phase arrest
    • +, a fission yeast gene related to the Bloom’s and Werner’s syndrome genes, is required for reversible S phase arrest. EMBO J 16:2682-2692, 1997.
    • (1997) EMBO J , vol.16 , pp. 2682-2692
    • Stewart, E.C.1    Chapman, F.2    Al-Khodairy Carr, A.M.3    Enoch, T.4
  • 39
    • 0030699088 scopus 로고    scopus 로고
    • Role of schizosaccharomyces pombe recq homolog, recombination, and checkpoint genes in uv damage tolerance
    • JM Murray, HD Lindsay, CA Munday, AM Carr. Role of Schizosaccharomyces pombe RecQ homolog, recombination, and checkpoint genes in UV damage tolerance. Mol Cell Biol 17:6868-6875, 1997.
    • (1997) Mol Cell Biol , vol.17 , pp. 6868-6875
    • Murray, J.1    Lindsay, C.A.2    Munday Carr, A.M.3
  • 40
    • 0033046015 scopus 로고    scopus 로고
    • Evolution of the recq family of helicases: A drosophila homolog, dmblm, is similar to the human bloom syndrome gene
    • K Kusano, ME Berres, RE Engels. Evolution of the RECQ family of helicases: a Drosophila homolog, Dmblm, is similar to the human Bloom syndrome gene. Genetics 151:1027-1039, 1999.
    • (1999) Genetics , vol.151 , pp. 1027-1039
    • Kusano, K.M.1    Berres Engels, R.E.2
  • 41
    • 0034708480 scopus 로고    scopus 로고
    • The genome sequence of drosophila melanogaster (Review)
    • MD Adams, SE Celniker, RA Holt, CA Evans, JD Gocayne, et al. The genome sequence of Drosophila melanogaster (review). Science 287, 2185-2195, 2000.
    • (2000) Science , vol.287 , pp. 2185-2195
    • Adams, M.1    Celniker, R.A.2    Holt, C.A.3    Evans Gocayne, J.D.4
  • 42
    • 0034164070 scopus 로고    scopus 로고
    • Human recq5, a large isomer of recq5 dna helicase, localizes in the nucleoplasm and interacts with topoisomerase 3 and 3
    • A Shimamoto, K Nishikawa, S Kitao, Y Furuichi. Human RecQ5, a large isomer of RecQ5 DNA helicase, localizes in the nucleoplasm and interacts with topoisomerase 3 and 3. Nucleic Acid Res 7:1647-1655, 2000.
    • (2000) Nucleic Acid Res , vol.7 , pp. 1647-1655
    • Shimamoto, A.K.1    Nishikawa, S.2    Kitao Furuichi, Y.3
  • 43
    • 0033820714 scopus 로고    scopus 로고
    • Analysis of genomic instability using multiple assays in a patient with rothmund-thomson syndrome
    • SG Grant, SL Wenger, JJ Latimer, D Thull, LW Burke. Analysis of genomic instability using multiple assays in a patient with Rothmund-Thomson syndrome. Clin Genet 58:209-215, 2000.
    • (2000) Clin Genet , vol.58 , pp. 209-215
    • Grant, S.1    Wenger, J.J.2    Latimer, D.3    Thull Burke, L.W.4
  • 44
    • 0025215315 scopus 로고
    • Rothmund-thomson syndrome associated with trisomy 8 mosaicism
    • KL Ying, J Oizumi, CJR Curry. Rothmund-Thomson syndrome associated with trisomy 8 mosaicism. J Med Genet 27:258-260, 1990.
    • (1990) J Med Genet , vol.27 , pp. 258-260
    • Ying, K.L.J.1    Oizumi Curry, C.2
  • 48
    • 84981986800 scopus 로고
    • Rothmund-thompson syndrome: Two case reports
    • S Alexander. Rothmund-Thompson syndrome: two case reports. Br J Dermatol 91(suppl):62-64, 1974.
    • (1974) Br J Dermatol , vol.91 , pp. 62-64
    • Alexander, S.1
  • 49
    • 0023259214 scopus 로고
    • Epidermal dysplasia and skeletal deformity in congenital poikiloderma
    • D Shuttleworth, R Marks. Epidermal dysplasia and skeletal deformity in congenital poikiloderma. Br J Dermatol 117:377-384, 1987.
    • (1987) Br J Dermatol , vol.117 , pp. 377-384
    • Shuttleworth, D.1    Marks, R.2
  • 52
    • 0020060968 scopus 로고
    • Rothmund-thomson syndrome and osteogenic sarcoma
    • DC Dick, WN Morley, JT Watson. Rothmund-Thomson syndrome and osteogenic sarcoma. Clin Exp Dermatol 7:119-123, 1982.
    • (1982) Clin Exp Dermatol , vol.7 , pp. 119-123
    • Dick, D.1    Morley Watson, J.T.2
  • 53
    • 85056943371 scopus 로고
    • Rothmund’s syndrome-thomson’s syndrome
    • WB Taylor. Rothmund’s syndrome-Thomson’s syndrome. Arch Dermatol 75:236244, 1957.
    • (1957) Arch Dermatol , pp. 75
    • Taylor, W.B.1
  • 54
    • 0009561442 scopus 로고
    • Rothmund-thomson syndrome
    • Y Fujiwara. Rothmund-Thomson syndrome. Pediatr Int 21:126-128, 1989.
    • (1989) Pediatr Int , vol.21 , pp. 126-128
    • Fujiwara, Y.1
  • 55
    • 0014760913 scopus 로고
    • Dna damage and repair in light sensitive human skin disease
    • JE Cleaver. DNA damage and repair in light sensitive human skin disease. J Invest Dermatol 54:181-195, 1970.
    • (1970) J Invest Dermatol , vol.54 , pp. 181-195
    • Cleaver, J.E.1
  • 57
    • 0026021469 scopus 로고
    • Rothmund-thomson syndrome (Letter; comment)
    • NP Walker, CM Fidley. Rothmund-Thomson syndrome (letter; comment). Br J Dermatol 124:300, 1991.
    • (1991) Br J Dermatol , vol.124 , pp. 300
    • Walker, N.P.1    Fidley, C.M.2
  • 60
    • 0020066137 scopus 로고
    • Enhanced radiosensitivity and defective dna repair in cultured fibroblasts derived from rothmund-thomson syndrome patients
    • PV Smith, MC Paterson. Enhanced radiosensitivity and defective DNA repair in cultured fibroblasts derived from Rothmund-Thomson syndrome patients. Mutat Res 94:213-228, 1982.
    • (1982) Mutat Res , vol.94 , pp. 213-228
    • Smith, P.V.1    Paterson, M.C.2
  • 62
    • 0014728555 scopus 로고
    • Investigations on dark repair in various light sensitive inherited disorders
    • EG Jung. Investigations on dark repair in various light sensitive inherited disorders. Hum Genet 9:191-192, 1970.
    • (1970) Hum Genet , vol.9 , pp. 191-192
    • Jung, E.G.1
  • 63
    • 0025107378 scopus 로고
    • Rf mueller. “isolated” radial ray defect may be due to rothmund-thomson syndrome
    • C Moss, CJ Bacon, RF Mueller. “Isolated” radial ray defect may be due to Rothmund-Thomson syndrome. Clin Genet 38:318-319, 1990.
    • (1990) Clin Genet , vol.38 , pp. 318-319
    • Moss, C.1    Bacon, C.J.2
  • 65
    • 0035034884 scopus 로고    scopus 로고
    • Premature aging and predisposition to cancers caused by mutations in recq family helicases
    • SC Park, ES Hwang, H-S Kim, W-Y Park, eds., New York: New York Academy of Sciences
    • Y Furuichi. Premature aging and predisposition to cancers caused by mutations in RecQ family helicases. In: SC Park, ES Hwang, H-S Kim, W-Y Park, eds. Healthy Aging for Functional Longevity: Molecular and Cellular Interactions in Senescence. New York: New York Academy of Sciences, 2001, pp 121-131.
    • (2001) Healthy Aging for Functional Longevity: Molecular and Cellular Interactions in Senescence , pp. 121-131
    • Furuichi, Y.1
  • 66
    • 0032589644 scopus 로고    scopus 로고
    • Incorrect use of “immortalization” for b-lym-phoblastoid cell lines transformed by epstein-barr virus
    • M Sugimoto, T Ide, M Goto, Y Furuichi. Incorrect use of “Immortalization” for B-lym-phoblastoid cell lines transformed by Epstein-Barr virus. J Virol 73:9690-9691, 1999.
    • (1999) J Virol , vol.73 , pp. 9690-9691
    • Sugimoto, M.T.1    Ide, M.2    Goto Furuichi, Y.3
  • 69
    • 0029330286 scopus 로고
    • When cells stop making sense: Effects of nonsense codons on rna metabolism in vertebrate cells
    • LE Maquat. When cells stop making sense: effects of nonsense codons on RNA metabolism in vertebrate cells. RNA 1:453-465, 1995.
    • (1995) RNA , vol.1 , pp. 453-465
    • Maquat, L.E.1
  • 70
    • 0029835707 scopus 로고    scopus 로고
    • Defects in rna splicing and the consequence of shortened translational reading frames
    • LE Maquat. Defects in RNA splicing and the consequence of shortened translational reading frames. Am J Hum Genet 59:279-286, 1996.
    • (1996) Am J Hum Genet , vol.59 , pp. 279-286
    • Maquat, L.E.1
  • 71
    • 0031204917 scopus 로고    scopus 로고
    • Impaired nuclear localization of defective dna helicases in werner’s syndrome
    • T Matsumoto, A Shimamoto, M Goto, Y Furuichi. Impaired nuclear localization of defective DNA helicases in Werner’s syndrome. Nat Genet 16:335-336, 1997.
    • (1997) Nat Genet , vol.16 , pp. 335-336
    • Matsumoto, T.A.1    Shimamoto, M.2    Goto Furuichi, Y.3
  • 72
    • 0031598783 scopus 로고    scopus 로고
    • Characterization of the nuclear localization signal in the dna helicase involved in werner’s syndrome
    • T Matsumoto, O Imamura, M Goto, Y Furuichi. Characterization of the nuclear localization signal in the DNA helicase involved in Werner’s syndrome. Int J Mol Med 1:71-76, 1998.
    • (1998) Int J Mol Med , vol.1 , pp. 71-76
    • Matsumoto, T.O.1    Imamura, M.2    Goto Furuichi, Y.3
  • 74
    • 0032555220 scopus 로고    scopus 로고
    • Bloom’s and werner’s syndrome genes suppress hyperrecombination in yeast sgs1 mutant: Implication for genomic instability in human diseases
    • K Yamagata, J Kato, A Shimamoto, M Goto, Y Furuichi, H Ikeda. Bloom’s and Werner’s syndrome genes suppress hyperrecombination in yeast sgs1 mutant: implication for genomic instability in human diseases. Proc Natl Acad Sci USA 95: 8733-8738, 1998.
    • (1998) Proc Natl Acad Sci USA , vol.95 , pp. 8733-8738
    • Yamagata, K.J.1    Kato, A.2    Shimamoto, M.3    Goto, Y.4    Furuichi Ikeda, H.5
  • 75
    • 0032736140 scopus 로고    scopus 로고
    • Rothmund-thomson syndrome responsible gene, recql4: Genomic structure and products
    • S Kitao, NM Lindor, M Shiratori, Y Furuichi, A Shimamoto. Rothmund-Thomson syndrome responsible gene, RECQL4: genomic structure and products. Genomics 61:268-276, 1999.
    • (1999) Genomics , vol.61 , pp. 268-276
    • Kitao, S.N.1    Lindor, M.2    Shiratori, Y.3    Furuichi Shimamoto, A.4
  • 76
    • 0034739792 scopus 로고    scopus 로고
    • Cloning, genomic structure and chromosomal localization of the gene encoding mouse dna helicase recq helicase protein-like 4
    • T Ohhata, R Araki, R Fukumura, A Kuroiwa, Y Matsuda, K Tatsumi, M Abe. Cloning, genomic structure and chromosomal localization of the gene encoding mouse DNA helicase RecQ helicase protein-like 4.Gene 261:251-258, 2000.
    • (2000) Gene , vol.261 , pp. 251-258
    • Ohhata, T.R.1    Araki, R.2    Fukumura, A.3    Kuroiwa, Y.4    Matsuda Tatsumi, K.5    Abe, M.6
  • 77
    • 0031792774 scopus 로고    scopus 로고
    • Furuichi. Spl-mediated transcription of the werner helicase gene is modulated by rb and p53
    • Y Yamabe, A Shimamoto, M Goto, J Yokota, M Sugawara, Y Furuichi. Spl-mediated transcription of the Werner helicase gene is modulated by Rb and p53. Mol Cell Biol 18:6191-6200, 1998.
    • (1998) Mol Cell Biol , vol.18 , pp. 6191-6200
    • Yamabe, Y.A.1    Shimamoto, M.2    Goto, J.3    Yokota M, Y.4
  • 78
    • 0032146147 scopus 로고    scopus 로고
    • Werner helicase is localized to transcriptionally active nucleoli of cycling cells
    • MD Gray, L Wang, H Youssoufian, GM Martin, J Oshima. Werner helicase is localized to transcriptionally active nucleoli of cycling cells. Exp Cell Res 242:487-494, 1998.
    • (1998) Exp Cell Res , vol.242 , pp. 487-494
    • Gray, M.D.L.1    Wang, H.2    Youssoufian, G.M.3    Martin Oshima, J.4
  • 79
    • 0032499703 scopus 로고    scopus 로고
    • Nucleolar localization of the werner syndrome protein in human cells
    • RA Marciniak, DB Lombard, FB Johnson, L Guarente. Nucleolar localization of the Werner syndrome protein in human cells. Proc Natl Acad Sci USA 95:6887-6892, 1998.
    • (1998) Proc Natl Acad Sci USA , vol.95 , pp. 6887-6892
    • Marciniak, R.1    Lombard, F.B.2    Johnson Guarente, L.3
  • 80
    • 0033545238 scopus 로고    scopus 로고
    • Detection by epitope-defined monoclonal antibodies of werner dna helicases in the nucleoplasm and their upregulation by cell transformation and immortalization
    • M Shiratori, S Sakamoto, N Suzuki, Y Tokutake, Y Kawabe, T Enomoto, M Sugi-moto, M Goto, T Matsumoto, Y Furuichi. Detection by epitope-defined monoclonal antibodies of Werner DNA helicases in the nucleoplasm and their upregulation by cell transformation and immortalization. J Cell Biol 144:1-9, 1999.
    • (1999) J Cell Biol , vol.144 , pp. 1-9
    • Shiratori, M.S.1    Sakamoto, N.2    Suzuki, Y.3    Tokutake, Y.4    Kawabe, T.5    Enomoto, M.6    Sugi-Moto, M.7    Goto, T.8    Matsumoto Furuichi, Y.9
  • 82
    • 0034489683 scopus 로고    scopus 로고
    • Blm, the bloom’s syndrome protein, varies during the cell cycle in its amount, distribution, and colocalization with other nuclear proteins
    • MM Sanz, M Proytcheva, NA Ellis, WK Holloman, J German. BLM, the Bloom’s syndrome protein, varies during the cell cycle in its amount, distribution, and colocalization with other nuclear proteins. Cytogenet Cell Genet 91:217-223, 2000.
    • (2000) Cytogenet Cell Genet , vol.91 , pp. 217-223
    • Sanz, M.M.M.1    Proytcheva, N.A.2    Ellis, W.K.3    Holloman German, J.4
  • 83
    • 0032573157 scopus 로고    scopus 로고
    • A deletion within the murine werner syndrome helicase induces sensitivity to inhibitors of topoisomerase and loss of cellular proliferative capacity
    • M Lebel, P Leder. A deletion within the murine Werner syndrome helicase induces sensitivity to inhibitors of topoisomerase and loss of cellular proliferative capacity. Proc Natl Acad Sci USA 95:13097-13102, 1998.
    • (1998) Proc Natl Acad Sci USA , vol.95 , pp. 13097-13102
    • Lebel, M.1    Leder, P.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.