Syringocystadenoma papilliferum: A study of potential tumor suppressor genes

American Journal of Dermatopathology

Volumn 23, Issue 2, 2001, Pages 87-89

  Böni, Roland ^a,b   Xin, Hong ^a,b   Hohl, Daniel ^a,b   Panizzon, Renato ^a,b   Burg, Günter ^a,b  

^a UNIVERSITY HOSPITAL ZURICH   (Switzerland)

^b LAUSANNE UNIVERSITY HOSPITAL   (Switzerland)

Author keywords

Adenocarcinoma; Basal cell carcinoma; LOH; Nevus sebaceus; p16; PTCH; Syringocystadenoma papilliferum

Indexed keywords

PROTEIN P16;

ALLELE; ARTICLE; BASAL CELL CARCINOMA; CHROMOSOME 9Q; CONTROLLED STUDY; CYSTADENOMA; FACE TUMOR; GENE DELETION; HETEROZYGOSITY LOSS; HUMAN; HUMAN CELL; HUMAN TISSUE; MALIGNANT TRANSFORMATION; METASTASIS; PAPILLARY SYRINGADENOMA; PRIORITY JOURNAL; SCALP TUMOR; SEBACEOUS NEVUS; SYRINGOMA; TUMOR SUPPRESSOR GENE;

ADENOCARCINOMA, PAPILLARY; ADENOMA, SWEAT GLAND; DISSECTION; DNA, NEOPLASM; GENES, P16; GENETIC MARKERS; HUMANS; LOSS OF HETEROZYGOSITY; MICROMANIPULATION; MICROSATELLITE REPEATS; POLYMERASE CHAIN REACTION; SWEAT GLAND NEOPLASMS;

EID: 0035058274     PISSN: 01931091     EISSN: None     Source Type: Journal    
DOI: 10.1097/00000372-200104000-00001     Document Type: Article

References (11)

1. Tumors of fibrous tissue
2. Syringadenoma papilliferum
3. Developmental defects in Gorlin syndrome related to a putative tumor suppressor gene on chromosome 9
4. Detection of loss of heterozygosity on chromosome 9q22.3 in microdissected sporadic basal cell carcinoma
5. The sebaceous nevus: A nevus with deletions of the PTCH-gene
6. Syringadenocarcinoma papilliferum
7. Trichoblastoma is the most common neoplasm developed in nevus sebaceus of Jadassohn: A clinicopathologic study of a series of 155 cases
8. Sporadic trichoepithelioma demonstrates deletions at 9q22.3
9. Ultraviolet and ionizing radiation enhance the growth of BCCs and trichoblastomas in patched heterozygous knockout mice
10. Frequency of homozygous deletion at p16/CDKN2 in primary human tumours
11. Refined mapping of genomic rearrangements involving the short arm of chromosome 9 in acute lymphoblastic leukemias and other hematologic malignancies