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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1982 1
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1994 7
1995 5
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1999 12
2000 11
2001 10
2002 8
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2004 6
2005 8
2006 2
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157 results

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Quoted phrase not found in phrase index: "Loss of Chromosome 13"
Page 1
Prognostic and therapeutic significance of myeloma genetics and gene expression profiling.
Stewart AK, Fonseca R. Stewart AK, et al. J Clin Oncol. 2005 Sep 10;23(26):6339-44. doi: 10.1200/JCO.2005.05.023. J Clin Oncol. 2005. PMID: 16155017 Review.
Molecular diagnostic tools and novel therapeutics now offer the potential for accurate prognostic and personalized treatment road maps for patients with multiple myeloma (MM). We will review the evidence and provide specific recommendations for routine clinical molecular g …
Molecular diagnostic tools and novel therapeutics now offer the potential for accurate prognostic and personalized treatment road map …
Clinical and biological relevance of the transcriptomic-based prostate cancer metastasis subtypes MetA-C.
Thysell E, Köhn L, Semenas J, Järemo H, Freyhult E, Lundholm M, Thellenberg Karlsson C, Damber JE, Widmark A, Crnalic S, Josefsson A, Welén K, Nilsson RJA, Bergh A, Wikström P. Thysell E, et al. Mol Oncol. 2022 Feb;16(4):846-859. doi: 10.1002/1878-0261.13158. Epub 2021 Dec 27. Mol Oncol. 2022. PMID: 34889043 Free PMC article.
The MetB subtype demonstrated single nucleotide variants of RB transcriptional corepressor 1 (RB1) and loss of 21 genes at chromosome 13, including RB1, but provided independent prognostic value to those genetic aberrations. ...The MetA-C subtypes show diverse biolo …
The MetB subtype demonstrated single nucleotide variants of RB transcriptional corepressor 1 (RB1) and loss of 21 genes at chromosome …
Two Cases with Ring Chromosome 13 at either End of the Phenotypic Spectrum.
Çakmaklı S, Çankaya T, Gürsoy S, Koç A, Kırbıyık Ö, Kılıçarslan ÖA, Özer E, Erçal D, Bozkaya ÖG. Çakmaklı S, et al. Cytogenet Genome Res. 2017;153(4):175-180. doi: 10.1159/000486775. Epub 2018 Mar 9. Cytogenet Genome Res. 2017. PMID: 29518772 Review.
The implications of non-invasive prenatal testing failures: a review of an under-discussed phenomenon.
Yaron Y. Yaron Y. Prenat Diagn. 2016 May;36(5):391-6. doi: 10.1002/pd.4804. Epub 2016 Apr 2. Prenat Diagn. 2016. PMID: 26941176 Review.
NIPT technology that has a high failure rate may increase the false positive rates, decrease the positive predictive value, and increase the procedure-related pregnancy loss. 2016 John Wiley & Sons, Ltd....
NIPT technology that has a high failure rate may increase the false positive rates, decrease the positive predictive value, and incre …
Solitary fibrous tumors: loss of chimeric protein expression and genomic instability mark dedifferentiation.
Dagrada GP, Spagnuolo RD, Mauro V, Tamborini E, Cesana L, Gronchi A, Stacchiotti S, Pierotti MA, Negri T, Pilotti S. Dagrada GP, et al. Mod Pathol. 2015 Aug;28(8):1074-83. doi: 10.1038/modpathol.2015.70. Epub 2015 May 29. Mod Pathol. 2015. PMID: 26022454 Free article.
Solitary fibrous tumor dedifferentiation is associated with the loss of chimeric oncoprotein expression, genomic instability, and cell decommitment and reprogramming. ...
Solitary fibrous tumor dedifferentiation is associated with the loss of chimeric oncoprotein expression, genomic instability, and cel …
RB1, p16, and Human Papillomavirus in Oropharyngeal Squamous Cell Carcinoma.
Berdugo J, Rooper LM, Chiosea SI. Berdugo J, et al. Head Neck Pathol. 2021 Dec;15(4):1109-1118. doi: 10.1007/s12105-021-01317-5. Epub 2021 Apr 8. Head Neck Pathol. 2021. PMID: 33830464 Free PMC article.

In the entire cohort and in p16-positive (n = 184) and p16-negative (n = 73) subgroups, AJCC 8th edition staging correlated with DFS (p < 0.01). RB1 IHC showed RB1 loss in p16-positive OSCC only (79/184, 43%). RB1 loss by IHC is associated with a better DFS, with

…
In the entire cohort and in p16-positive (n = 184) and p16-negative (n = 73) subgroups, AJCC 8th edition staging correlated with DFS (p < …
Cytogenetic analysis in the examination of solid tumors in children.
Mertens F, Mandahl N, Mitelman F, Heim S. Mertens F, et al. Pediatr Hematol Oncol. 1994 Jul-Aug;11(4):361-77. doi: 10.3109/08880019409140536. Pediatr Hematol Oncol. 1994. PMID: 7947009 Review.
The most common (80%) cytogenetic abnormality in neuroblastoma is loss of distal 1p, a chromosome segment thought to harbor at least two tumor-suppressor genes of importance in tumorigenesis. Double minute chromosomes or homogeneously staining regions are present in one-th …
The most common (80%) cytogenetic abnormality in neuroblastoma is loss of distal 1p, a chromosome segment thought to harbor at least …
Development of patients with 47,XX,+13/45,X mosaics: case report and review of the literature.
Tang HW, Liao SF, Li JS. Tang HW, et al. Eur J Pediatr. 2014 Feb;173(2):251-5. doi: 10.1007/s00431-013-2001-z. Epub 2013 May 12. Eur J Pediatr. 2014. PMID: 23666113 Review.
The child had a short neck, hypertelorism, depressed nasal ridge, epicanthal fold, mid-facial hypoplasia, thin upper lip, long philtrum, ear anomalies, postaxial polydactyly, atrial septal defect, hydronephrosis, and sensorineural hearing loss. Her weight and length were c …
The child had a short neck, hypertelorism, depressed nasal ridge, epicanthal fold, mid-facial hypoplasia, thin upper lip, long philtrum, ear …
Cytogenetic and molecular abnormalities in chronic lymphocytic leukaemia.
Oscier DG. Oscier DG. Blood Rev. 1994 Jun;8(2):88-97. doi: 10.1016/s0268-960x(05)80013-x. Blood Rev. 1994. PMID: 7950479 Review.
The genetic consequences of trisomy 12 are unknown but structural abnormalities of chromosome 13q14 frequently involve hetero or homozygous loss of a region distal to the retinoblastoma gene which may be the site of a tumour suppressor gene. Trisomy 12 or loss of on …
The genetic consequences of trisomy 12 are unknown but structural abnormalities of chromosome 13q14 frequently involve hetero or homozygous …
Loss of heterozygosity at 13q13 and 14q32 predicts BRCA2 inactivation in luminal breast carcinomas.
Pécuchet N, Popova T, Manié E, Lucchesi C, Battistella A, Vincent-Salomon A, Caux-Moncoutier V, Bollet M, Sigal-Zafrani B, Sastre-Garau X, Stoppa-Lyonnet D, Stern MH. Pécuchet N, et al. Int J Cancer. 2013 Dec 15;133(12):2834-42. doi: 10.1002/ijc.28315. Epub 2013 Jul 10. Int J Cancer. 2013. PMID: 23754601 Free article.
Independently, 7 BRCA2 and 51 control cases were used for validation. Absolute copy number and Loss of heterozygosity (LOH) profiles were obtained from SNP arrays by the genome alteration print (GAP) method. ...Estimated positive predictive value was 17.2% (confiden …
Independently, 7 BRCA2 and 51 control cases were used for validation. Absolute copy number and Loss of heterozygosity (LOH) profiles …
157 results