Pages that link to "Q34304686"
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The following pages link to Loss of heterozygosity on chromosome 1q in human breast cancer (Q34304686):
Displaying 43 items.
- Identification of BTG2, an antiproliferative p53-dependent component of the DNA damage cellular response pathway (Q24324455) (← links)
- Down-regulation of a member of the S100 gene family in mammary carcinoma cells and reexpression by azadeoxycytidine treatment (Q24562633) (← links)
- (C-A)n microsatellite repeat D7S522 is the most commonly deleted region in human primary breast cancer (Q24564525) (← links)
- A novel zinc finger gene on human chromosome 1qter that is alternatively spliced in human tissues and cell lines (Q28116018) (← links)
- Molecular mechanisms of cancer (Q30498610) (← links)
- A systematic search for downstream mediators of tumor suppressor function of p53 reveals a major role of BTG2 in suppression of Ras-induced transformation (Q33231831) (← links)
- Genetic analysis of breast cancer progression (Q33962744) (← links)
- Neoplastic transformation of human breast epithelial cells by estrogens and chemical carcinogens (Q34580748) (← links)
- Genetic regulation of mammary carcinogenesis in the rat by susceptibility and suppressor genes (Q35034169) (← links)
- Identification of a cell-surface glycoprotein associated with normal mammary and extramammary epithelial cells (Q35978337) (← links)
- Sequential alteration of peanut agglutinin binding-glycoprotein expression during progression of murine mammary neoplasia (Q35993010) (← links)
- Loss of heterozygosity at chromosome 11 in breast cancer: association of prognostic factors with genetic alterations (Q36081181) (← links)
- A gene involved in control of human cellular senescence on human chromosome 1q (Q36649408) (← links)
- Molecular and cellular lesions associated with breast cancer progression (Q37253425) (← links)
- Chromosomal abnormalities in human breast cancer (Q37956450) (← links)
- 1p13 is the most frequently involved band in structural chromosomal rearrangements in human breast cancer (Q38017676) (← links)
- A-to-I RNA Editing Up-regulates Human Dihydrofolate Reductase in Breast Cancer (Q38289096) (← links)
- The 2-5A system: modulation of viral and cellular processes through acceleration of RNA degradation (Q38336728) (← links)
- Estradiol downregulation of the tumor suppressor gene BTG2 requires estrogen receptor-alpha and the REA corepressor (Q39899859) (← links)
- Frequent loss of chromosome arm 1p DNA in parathyroid adenomas (Q40402300) (← links)
- Familial breast cancer and genes involved in breast carcinogenesis (Q40466587) (← links)
- Tumor suppressor genes and their roles in breast cancer (Q40568049) (← links)
- Identification of a </= 600-kb region on human chromosome 1q42.3 inducing cellular senescence (Q40677588) (← links)
- 17Beta-estradiol is carcinogenic in human breast epithelial cells (Q40744274) (← links)
- Molecular genetic changes in human breast cancer (Q40832210) (← links)
- Interphase cytogenetic analysis of solid tumors by non-isotopic DNA in situ hybridization (Q41236837) (← links)
- Subchromosomal mapping of a putative transformation suppressor gene on human chromosome 1. (Q41347781) (← links)
- Amplification of Chromosome 1q Genes Encoding the Phosphoinositide Signalling Enzymes PI4KB, AKT3, PIP5K1A and PI3KC2B in Breast Cancer (Q42971476) (← links)
- Loss of heterozygosity of the L-myc oncogene in human breast tumors (Q44117539) (← links)
- Identification of high-risk breast cancer patients from genetic changes of their tumors (Q44311705) (← links)
- Chromosome 1 alterations in breast cancer: allelic loss on 1p and 1q is related to lymphogenic metastases and poor prognosis (Q46404137) (← links)
- Expression of the NF-kappaB-responsive gene BTG2 is aberrantly regulated in breast cancer (Q50792279) (← links)
- Chromosome 1q25.3 copy number alterations in primary breast cancers detected by multiplex ligation-dependent probe amplification and allelic imbalance assays and its comparison with fluorescent in situ hybridization assays. (Q54279108) (← links)
- Allelotype of uterine cancer by analysis of RFLP and microsatellite polymorphisms: frequent loss of heterozygosity on chromosome arms 3p, 9q, 10q, and 17p. (Q54642275) (← links)
- Functional characterization of novel presenilin-2 variants identified in human breast cancers (Q57419070) (← links)
- Allelic imbalance on chromosome I in human breast cancer. II. Microsatellite repeat analysis (Q59289363) (← links)
- Genetic alterations of the tumour suppressor gene regions 3p, 11p, 13q, 17p, and 17q in human breast carcinomas (Q67534085) (← links)
- Allelic imbalance study of 16q in human primary breast carcinomas using microsatellite markers (Q70970955) (← links)
- Allelic imbalance on chromosome 1 in human breast cancer. I. Minisatellite and RFLP analysis (Q71680202) (← links)
- Frequent loss of heterozygosity at the deleted in colorectal carcinoma gene locus and its association with histologic phenotypes in breast carcinoma (Q71953906) (← links)
- Aberrations of the APC gene in primary breast carcinoma (Q72352366) (← links)
- Allelotype analysis of the myelodysplastic syndrome (Q73769148) (← links)
- Identification of a novel amplicon at 1q31 in pancreatic cancer cell lines (Q78255014) (← links)