Zobrazeno 1 - 9
of 9
pro vyhledávání: '"E F, Schoenmakers"'
Publikováno v:
Cancer genetics and cytogenetics. 113(2)
Deletions of the long arm of chromosome 7 constitute one of the most common clonal chromosomal changes associated with uterine leiomyoma cells. Recently, the molecular cytogenetic refinement of 7q deletions in two myoma-derived cell lines, with the u
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::83645906849aaabb9dfa4c3800731931
https://pubmed.ncbi.nlm.nih.gov/10484989
https://pubmed.ncbi.nlm.nih.gov/10484989
Publikováno v:
Cancer research. 59(1)
Recently, the high mobility group protein gene HMGIC was identified as the chromosome 12q15 target gene in a variety of benign solid tumors. Here, we report that the recombinational repair gene RAD51B on chromosome 14q23-24 is the preferential transl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1ca2ac50a4dda502c097ef0152781dd1
https://pubmed.ncbi.nlm.nih.gov/9892177
https://pubmed.ncbi.nlm.nih.gov/9892177
Publikováno v:
American journal of medical genetics. 75(2)
We report on a de novo 7q36 deletion in a 3-month-old girl with manifestations of the 7q terminal deletion syndrome. Only minimal findings of holoprosencephaly (HPE) were present since only a partial corpus callosum hypoplasia was seen on a magnetic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::124d771738baf3b11a5a60fbdac56d46
https://pubmed.ncbi.nlm.nih.gov/9450876
https://pubmed.ncbi.nlm.nih.gov/9450876
Publikováno v:
Molecular carcinogenesis. 19(2)
Human papillomavirus (HPV) DNA is integrated into the host genome in cervical cancer. The cervical carcinoma cell line SW756 has integrated HPV-18 DNA in chromosome region 12q15, in the papillomavirus-associated locus-2 (PAL2). By polymerase chain re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::eaa24108b3fab2524a20569c327f2431
https://pubmed.ncbi.nlm.nih.gov/9210958
https://pubmed.ncbi.nlm.nih.gov/9210958
Autor:
R, Vanni, S, Marras, E F, Schoenmakers, P, Dal Cin, B, Kazmierczak, G, Senger, J, Bullerdiek, W J, Van de Ven, H, Van den Berghe
Publikováno v:
Genes, chromosomescancer. 18(3)
Uterine leiomyoma cytogenetically exhibits at least six chromosomally abnormal subgroups. The largest subgroup is characterized by deletions of the long arm of chromosome 7. Few molecular and fluorescence in situ hybridization data are available that
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::414e5f13155469393dcca0b36d14abd0
https://pubmed.ncbi.nlm.nih.gov/9071567
https://pubmed.ncbi.nlm.nih.gov/9071567
Autor:
J M, Hernández, E F, Schoenmakers, P, Dal Cin, L, Michaux, W J, Van de Ven, H, Van den Berghe
Publikováno v:
Genes, chromosomescancer. 18(2)
FISH, using 16 probes, informative for more than 30 different loci, allowed us better to delineate the common deleted region in mature B-cell lymphoid malignancies with deletions of chromosome 7. The region spans about 5 cM and is located between ban
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::bfded0527da12ce72b93571325f0c5b8
https://pubmed.ncbi.nlm.nih.gov/9115965
https://pubmed.ncbi.nlm.nih.gov/9115965
Publikováno v:
Cancer research. 57(1)
The developmentally regulated HMGIC gene, which encodes an architectural transcription factor, has recently been linked to the pathogenesis of benign solid tumors with chromosome aberrations involving 12q13-15. Among these tumors are pleomorphic aden
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::fec74e13b3916f1a5cf899866b57940e
https://pubmed.ncbi.nlm.nih.gov/8988031
https://pubmed.ncbi.nlm.nih.gov/8988031
Autor:
B, Kazmierczak, S, Wanschura, J, Rosigkeit, K, Meyer-Bolte, K, Uschinsky, R, Haupt, E F, Schoenmakers, S, Bartnitzke, W J, Van de Ven, J, Bullerdiek
Publikováno v:
Cancer research. 55(12)
Chromosomal aberrations involving the chromosomal breakpoint region 12q14-15 are frequently seen in a variety of mesenchymal tumors as uterine leiomyomas, lipomas, myxoid liposarcomas, enchondromas, or hemangiopericytomas. Therefore, this breakpoint
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a78937ae644b19cce91121b0ea00e0e1
https://pubmed.ncbi.nlm.nih.gov/7780955
https://pubmed.ncbi.nlm.nih.gov/7780955
Autor:
K, Kok, A, van den Berg, P M, Veldhuis, A Y, van der Veen, M, Franke, E F, Schoenmakers, M M, Hulsbeek, A H, van der Hout, L, de Leij, W, van de Ven
Publikováno v:
Cancer research. 54(15)
All types of lung carcinoma are characterized by a high frequency of loss of sequences from the short arm of chromosome 3, the smallest region of overlap containing D3F15S2 in band p21. Here we characterize a 440-kilobase segment from this region, wh
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::cf332869857eb7571b53d9346c0e224e
https://pubmed.ncbi.nlm.nih.gov/8033151
https://pubmed.ncbi.nlm.nih.gov/8033151