다음과 같은 기능을 한번의 로그인으로 사용 할 수 있습니다.
NTIS 바로가기
Journal of Korean medical science : JKMS, v.20 no.2 = no.102, 2005년, pp.340 - 343
Ha, Tae-Won (Department of Plastic and Reconstructive Surgery, Keimyung University School of Medicine, Daegu, Korea.) , Han, Ki-Hwan (Department of Plastic and Reconstructive Surgery, Keimyung University School of Medicine, Daegu, Korea.) , Son, Dae-Gu (Department of Plastic and Reconstructive Surgery, Keimyung University School of Medicine, Daegu, Korea.) , Kim, Sang-Pyo (Department of Pathology, Keimyung University School of Medicine, Daegu, Korea.) , Kim, Dae-Kwang (Department of Anatomy, Institute for Medical Genetics, Keimyung University School of Medicine, Daegu, Korea.)
AI-Helper
Loss of heterozygosity (LOH) has been established as an important genetic mechanism giving rise to malignant neoplasia. The mechanism of LOH has been shown to cause basal cell carcinoma and malignant melanoma as well as other types of skin cancer. A few studies on LOH in sporadic keratoacanthomas ha...
1 Kern WH McCray MK The histopathologic differentiation of keratoacanthoma and squamous cell carcinoma of the skin J Cutan Pathol 1980 7 318 325 7430483
2 Schwartz RA Keratoacanthoma J Am Acad Dermatol 1994 30 1 19 8277007
3 Sanders GH Miller TA Are kearatoacanthomas really squamous cell carcinomas? Ann Plast Surg 1982 9 306 309 7149561
4 Requena L Romero E Sanchez M Ambrojo P Sanchez Yus E Aggressive keratoacanthoma of the eyelid: "malignant" keratoacanthoma or squamous cell carcinoma? J Dermatol Surg Oncol 1990 16 564 568 2355136
5 Hodak E Jones RE Ackerman AB Solitary keratoacanthoma is a squamous cell carcinoma: three examples with metastases Am J Dermatopathol 1993 15 332 342 8214391
6 Fearon ER Human cancer syndromes: clues to the origin nature of cancer Science 1997 278 1043 1050 9353177
7 Mao LI Fan YH Lotan R Hong WK Frequent abnormalities of FHIT, a candidate tumor suppressor gene, in head and neck cancer cell lines Cancer Res 1996 56 5128 5131 8912845
8 Fearon ER Vogelstein B A genetic model for colorectal tumorigenesis Cell 1990 61 759 767 2188735
9 Califano J van der Riet P Westra W Nawroz H Clayman G Piantadosi S Corio R Lee D Greenberg B Koch W Sidransky D Genetic progression model for head and neck cancer: implications for field cancerization Cancer Res 1996 56 2488 2492 8653682
10 Peris K Magrini F Keller G Manente L D'Alessandro E Onorati MT Hofler H Chimenti S Analysis of microsatellite instability and loss of heterozygosity in keratoacanthoma Arch Dermatol Res 1997 289 185 188 9143733
11 Langenbach N Kroiss MM Rüschoff J Schlegel J Landthaler M Stolz W Assessment of microsatellite instability and loss of heterozygosity in sporadic keratoacanthomas Arch Dermatol Res 1999 291 1 5 10025721
12 Waring AJ Takata M Rehman I Rees JL Loss of heterozygosity analysis of keratoacanthoma reveals multiple differences from cutaneous squamous cell carcinoma Br J Cancer 1996 73 649 653 8605102
13 Kim DK Kim JY Kim HT Han KH Shon DG A specific chromosome aberration in a keratoacanthoma Cancer Genet Cytogenet 2003 142 70 72 12660037
14 Akalu A Reichardt JK A reliable PCR amplification method for microdissected tumor cells obtained from paraffin-embedded tissue Genet Anal 1999 15 229 233 10609759
15 Sepp T Yates JR Green AJ Loss of heterozygosity in tuberous sclerosis hamartomas J Med Genet 1996 33 962 964 8950679
16 Matt D Xin H Vortmeyer AO Zhuang Z Burg G Böni R Sporadic trichoepithelioma demonstrates deletions at 9q22.3 Arch Dermatol 2000 136 657 660 10815860
17 Verhoef S Schrander-Stumpel CT Vuzevski VD Tempelaars A Jansen LA Malfeyt GA Ceelen TL Lindhout D Halley DJ van den Ouweland AM Familial cylindromatosis mimicking tuberous sclerosis complex and confirmation of the cylindromatosis locus, CYLD1, in a large family J Med Genet 1998 35 841 845 9783709
18 Böni R Zhuang Z Albuquerque A Vortmeyer A Duray P Loss of heterozygosity detected on 1p and 9q in microdissected atypical nevi Arch Dermatol 1998 134 882 883 9681364
19 Pack S Turner ML Zhuang Z Vortmeyer AO Böni R Skarulis M Marx SJ Darling TN Cutaneous tumors in patients with multiple endocrine neoplasia type 1 show allelic deletion of the MEN1 gene J Invest Dermatol 1998 110 438 440 9540988
20 Colman SD Williams CA Wallace MR Benign neurofibromas in type1 neurofibromatosis (NF1) show somatic deletions of the NF1 gene Nat Genet 1995 11 90 92 7550323
21 Mertens F Heim S Mandahl N Johansson B Rydholm A Biorklund A Wennerberg J Jonsson N Mitelman F Clonal chromosome aberrations in a keratoacanthoma and a basal cell papilloma Cancer Genet Cytogenet 1989 39 227 232 2752375
22 Schwartz RA Torre DP The Muir-Torre syndrome: a 25-year retrospect J Am Acad Dermatol 1995 33 90 104 7601953
23 Rehman I Quinn AG Healy E Rees JL High frequency of loss of heterozygosity in actinic keratoses, a usually benign disease Lancet 1994 344 788 789 7916075
24 Borkowski A Bennett WP Jones RT Borkowski P Harris CC Ferreira LR Kao GF Trump BF Quantitative image analysis of p53 protein accumulation in keratoacanthomas Am J Dermatopathol 1995 17 335 338 8600795
25 Perez MI Robins P Biria S Roco J Siegel E Pellicer A P53 oncoprotein expression and gene mutations in some keratoacanthomas Arch Dermatol 1997 133 189 193 9041832
26 Clausen OP Beigi M Bolund L Kølvraa S Gjersvik PJ Mork G de Angelis PM Keratoacanthomas frequently show chromosomal aberrations as assessed by comparative genomic hybridization J Invest Dermatol 2002 119 1367 1372 12485441
Copyright KISTI. All Rights Reserved.
※ AI-Helper는 부적절한 답변을 할 수 있습니다.