SwePub
Sök i LIBRIS databas

  Utökad sökning

WFRF:(Williams Cecilia)
 

Sökning: WFRF:(Williams Cecilia) > Genetic instability...

LIBRIS Formathandbok  (Information om MARC21)
FältnamnIndikatorerMetadata
00003144naa a2200397 4500
001oai:DiVA.org:kth-197609
003SwePub
008161205s1998 | |||||||||||000 ||eng|
024a https://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-1976092 URI
024a https://doi.org/10.1038/sj.onc.12020802 DOI
040 a (SwePub)kth
041 a engb eng
042 9 SwePub
072 7a ref2 swepub-contenttype
072 7a art2 swepub-publicationtype
100a Ahmadian, Afshinu KTH,Genteknologi4 aut0 (Swepub:kth)u1kjb6gb
2451 0a Genetic instability in the 9q22.3 region is a late event in the development of squamous cell carcinoma.
264 c 1998-10-09
264 1b Springer Science and Business Media LLC,c 1998
338 a print2 rdacarrier
500 a QCR 20161207
520 a Squamous cell carcinoma (SCC) of the skin represents a group of neoplasms which is associated with exposure to UV light. Recently, we obtained data suggesting that invasive skin cancer and its precursors derive from one original neoplastic clone. Here, the analysis were extended by loss of heterozygosity (LOH) analysis in the chromosome 9q22.3 region. A total of 85 samples, taken from twenty-two sections of sun-exposed sites, corresponding to normal epidermis, morphological normal cells with positive immuno-staining for the p53 protein (p53 patches), dysplasias, cancer in situ (CIS) and squamous cell carcinomas (SCC) of the skin were analysed. Overall, about 70% of p53 patches had mutations in the p53 gene but not LOH in the p53 gene or 9q22.3 region. Approximately 70% of the dysplasias showed p53 mutations of which about 40% had LOH in the p53 region but not in the 9q22.3 region. In contrast, about 65% of SCC and CIS displayed LOH in the 9q22.3 region, as well as frequent (80%) mutations and/or LOH in the p53 gene. These findings strongly suggest that alterations in the p53 gene is an early event in the progression towards SCC, whereas malignant development involves LOH and alterations in at least one (or several) tumor suppressor genes located in chromosome 9q22.3.
650 7a MEDICIN OCH HÄLSOVETENSKAPx Medicinska och farmaceutiska grundvetenskaperx Cell- och molekylärbiologi0 (SwePub)301082 hsv//swe
650 7a MEDICAL AND HEALTH SCIENCESx Basic Medicinex Cell and Molecular Biology0 (SwePub)301082 hsv//eng
700a Ren, Z P4 aut
700a Williams, Cecilia,d 1969-u KTH,Proteomik och nanobioteknologi4 aut0 (Swepub:kth)u1ygqmuy
700a Pontén, F4 aut
700a Odeberg, Jacobu KTH,Proteomik och nanobioteknologi4 aut0 (Swepub:kth)u1e4yljo
700a Pontén, J4 aut
700a Uhlén, Mathiasu KTH,Proteomik och nanobioteknologi4 aut0 (Swepub:kth)u1dulvmw
700a Lundeberg, Joakimu KTH,Genteknologi4 aut0 (Swepub:kth)u1qkn9kw
710a KTHb Genteknologi4 org
773t Oncogened : Springer Science and Business Media LLCg 17:14q 17:14x 0950-9232x 1476-5594
856u https://www.nature.com/articles/1202080.pdf
8564 8u https://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-197609
8564 8u https://doi.org/10.1038/sj.onc.1202080

Hitta via bibliotek

  • Oncogene (Sök värdpublikationen i LIBRIS)

Till lärosätets databas

Sök utanför SwePub

Kungliga biblioteket hanterar dina personuppgifter i enlighet med EU:s dataskyddsförordning (2018), GDPR. Läs mer om hur det funkar här.
Så här hanterar KB dina uppgifter vid användning av denna tjänst.

 
pil uppåt Stäng

Kopiera och spara länken för att återkomma till aktuell vy