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Publication Listing for the MeSH term heterozygosity. Found 25 abstracts

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Patel BB, Li XM, Dixon MP, Blagoi EL, Nicolas E, Seeholzer SH, Cheng D, He YA, Coudry RA, Howard SD, Riddle DM, Cooper HS, Boman BM, Conrad P, Crowell JA, Bellacosa A, Knudson A, Yeung AT, Kopelovich L. APC(+/-) alters colonic fibroblast proteome in FAP. Oncotarget. 2011 Mar;2(3):197-208.
Dong XY, Guo P, Boyd J, Sun XD, Li QN, Zhou W, Dong JT. Implication of snoRNA U50 in human breast cancer. Journal of Genetics and Genomics. 2009 Aug;36(8):447-54.   PMCID: PMCID: PMC2854654
Prowse AH, Manek S, Varma R, Liu JS, Godwin AK, Maher ER, Tomlinson IP, Kennedy SH. Molecular genetic evidence that endometriosis is a precursor of ovarian cancer. International journal of cancer. 2006 Aug;119(3):556-62.
Astrinidis A, Henske EP. Aberrant cellular differentiation and migration in renal and pulmonary tuberous sclerosis complex. Journal of Child Neurology. 2004 Sep;19(9):710-5.
Russo J, Russo IH. Genotoxicity of steroidal estrogens. Trends in Endocrinology and Metabolism. 2004 Jul;15(5):211-4.
Gutmann DH, Zhang YJ, Hasbani MJ, Goldberg MP, Plank TL, Henske EP. Expression of the tuberous sclerosis complex gene products, hamartin and tuberin, in central nervous system tissues. Acta Neuropathologica. 2000 Mar;99(3):223-30.
Crino PB, Henske EP. New developments in the neurobiology of the tuberous sclerosis complex. Neurology. 1999 Oct 22;53(7):1384-90.
Hamilton TC, Berek JS, Kaye SB. Basic research: how much do we know, and what are we likely to learn about ovarian cancer in the near future?. Annals of Oncology. 1999 Jan;10:69-73.
Plank TL, Logginidou H, Klein-Szanto A, Henske EP. The expression of hamartin, the product of the TSC1 gene, in normal human tissues and in TSC1- and TSC2-linked angiomyolipomas. Modern Pathology. 1999 May;12(5):539-45.
Zekri AR, Bahnassi AA, Bove B, Huang YJ, Russo IH, Rogatko A, Shaarawy S, Shawki OA, Hamza MR, Omer S, Khaled HM, Russo J. Allelic instability as a predictor of survival in Egyptian breast cancer patients. International Journal of Oncology. 1999 Oct;15(4):757-67.
Al-Saleem T, Wessner LL, Scheithauer BW, Patterson K, Roach ES, Dreyer SJ, Fujikawa K, Bjornsson J, Bernstein J, Henske EP. Malignant tumors of the kidney, brain, and soft tissues in children and young adults with the tuberous sclerosis complex. Cancer. 1998 Nov 15;83(10):2208-16.
Pea M, Bonetti F, Martignoni G, Henske EP, Manfrin E, Colato C, Bernstein J. Apparent renal cell carcinomas in tuberous sclerosis are heterogeneous - The identification of malignant epithelioid angiomyolipoma. American Journal of Surgical Pathology. 1998 Feb;22(2):180-7.
Plank TL, Yeung RS, Henske EP. Hamartin, the product of the tuberous sclerosis 1 (TSC1) gene, interacts with tuberin and appears to be localized to cytoplasmic vesicles. Cancer Research. 1998 Nov;58(21):4766-70.
Bell DW, Jhanwar SC, Testa JR. Multiple regions of allelic loss from chromosome arm 6q in malignant mesothelioma. Cancer Research. 1997 Sep 15;57(18):4057-62.
Henske EP, Wessner LL, Golden J, Scheithauer BW, Vortmeyer AO, Zhuang ZP, KleinSzanto AJ, Kwiatkowski DJ, Yeung RS. Loss of tuberin in both subependymal giant cell astrocytomas and angiomyolipomas supports a two-hit model for the pathogenesis of tuberous sclerosis tumors. American Journal of Pathology. 1997 Dec;151(6):1639-47.
Monaco C, Negrini M, Sozzi G, Veronese ML, Vorechovsky I, Godwin AK, Croce CM. Molecular cloning and characterization of LOH11CR2A, a new gene within a refined minimal region of LOH at 11q23. Genomics. 1997 Dec;46(2):217-22.
Pajak L, Jin F, Xiao GH, Soonpaa MH, Field LJ, Yeung RS. Sustained cardiomyocyte DNA synthesis in whole embryo cultures lacking the TSC2 gene product. American Journal of Physiology-Heart and Circulatory Physiology. 1997 Sep;42(3):H1619-H1627.
Schultz DC, Vanderveer L, Berman DB, Hamilton TC, Wong AJ, Godwin AK. Identification of two candidate tumor suppressor genes on chromosome 17p13.3. Cancer Research. 1996 May;56(9):1997-2002.
Thrashbingham CA, Salazar H, Freed JJ, Greenberg RE, Tartof KD. Genomic Alterations and Instabilities in Renal-Cell Carcinomas and Their Relationship to Tumor Pathology. Cancer Research. 1995 Dec 15;55(24):6189-95.
Bianchi AB, Hara T, Ramesh V, Gao JZ, Kleinszanto AJ, Morin F, Menon AG, Trofatter JA, Gusella JF, Seizinger BR, Kley N. Mutations in Transcript Isoforms of the Neurofibromatosis-2 Gene in Multiple Human Tumor Types. Nature genetics. 1994 Feb;6(2):185-92.
The above publications are sorted by year, faculty last name, and first author. Click on any highlighted author listed to find all publications attributed to that individual. Click on the publication title to see the abstract. First authors who are faculty are highlighted like this. Last authors who are faculty are highlighted like this. Other authors who are faculty are highlighted like this.

MeSH cloud from publications including the MeSH term heterozygosity

heterozygosity identification carcinomas carcinoma protein tuberin chromosome 9q34 expression angiomyolipoma growth suppressor breast-cancer lesions tumor-suppressor gene tumors region target rap1 lymphangiomyomatosis tuberous sclerosis complex rna suppressor tuberous sclerosis allelotype microsatellite instability eker allelic loss frequent loss tumor suppressor gene kidney brain renal cell carcinoma tuberous-sclerosis-2 tsc2 gene tsc2 breast cancer candidate APC dominantly inherited cancer deletions long arm growth malignant transformation hamartin chromosome 13q12-q13 colon fibroblasts chromosome 16p133 human ovarian-cancer families papillary tuberous-sclerosis cancer endometriosis molecular markers loci mismatch repair deficiency frequency cortical tubers tumor suppressors BRCA1 deletion lung-cancer p53 gene mutation oxidative cardiac regeneration antioncogenes cancer patients Oncology Eker rat product 6q allele loss model clear cell ovarian cancer lung poor-prognosis ROSE allelic receptor-alpha neurons beta ovarian tumours loss eker rat neurobiology Adenomatous polyposis glioblastoma artificial chromosome contig prognostic factors nervous-system lesions telangiectasia prostate-cancer rat model rsu-1 tuberous sclerosis gene U50 glia kinase activation cancer-cells epithelial-cells loss of heterozygosity division unit abnormalities experimental mod somatic mutations astrocytomas spontaneous transformation genetic-map induced apoptosis ataxia- mutational analysis immunohistochemistry pten p53 brca2 in-situ surface epithelial-cells hamartomas breast epithelial-cells allelic imbalance genetic-linkage proteomics familial adenomatous polyposis distinct precursor lesions astrocytes proximal 6q chromosome-22 endometrioid ovarian cancers tsc1 chromosome-3 drosophila renal-cell carcinoma tumor suppressor origin rat tumors distal antibody hmb-45 HMB45 melanocytic tumors giant-cell astrocytoma ras suppressor cardiac tumor dj-1 sugar map suppression drosophila-melanogaster involvement er-alpha polyposis
Last updated on Friday, December 06, 2019