HANUMANTHA PULIVARTHI to Karyotyping
This is a "connection" page, showing publications HANUMANTHA PULIVARTHI has written about Karyotyping.
Connection Strength
1.015
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Spectral karyotyping analysis of head and neck squamous cell carcinoma. Laryngoscope. 2001 Sep; 111(9):1545-50.
Score: 0.088
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Multicolor spectral karyotyping identifies novel translocations in childhood acute lymphoblastic leukemia. Leukemia. 2001 Mar; 15(3):468-72.
Score: 0.085
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Multicolor spectral karyotyping identifies new recurring breakpoints and translocations in multiple myeloma. Blood. 1998 Sep 01; 92(5):1743-8.
Score: 0.072
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Novel t(1;3)(q21,p21) translocation in a basal cell adenocarcinoma of the parotid gland: potential association with tumorigenesis. Hum Pathol. 2016 08; 54:189-92.
Score: 0.061
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Translocation t(7;12) as the sole chromosomal abnormality resulting in ACTB-GLI1 fusion in pediatric gastric pericytoma. Hum Pathol. 2016 07; 53:137-41.
Score: 0.060
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Coamplification of Myc/Pvt1 and homozygous deletion of Nlrp1 locus are frequent genetics changes in mouse osteosarcoma. Genes Chromosomes Cancer. 2015 Dec; 54(12):796-808.
Score: 0.058
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Molecular cytogenetic characterization of mammary neuroendocrine carcinoma. Hum Pathol. 2014 Sep; 45(9):1951-6.
Score: 0.054
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Telomere stability correlates with longevity of human beings exposed to ionizing radiations. Oncol Rep. 2003 Nov-Dec; 10(6):1733-6.
Score: 0.051
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De novo B lymphoblastic leukemia/lymphoma in an adult with t(14;18)(q32;q21) and c-MYC gene rearrangement involving 10p13. Leuk Lymphoma. 2011 Nov; 52(11):2195-9.
Score: 0.044
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Molecular characterization of permanent cell lines from primary, metastatic and recurrent malignant peripheral nerve sheath tumors (MPNST) with underlying neurofibromatosis-1. Anticancer Res. 2009 Apr; 29(4):1255-62.
Score: 0.037
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Establishment and genomic characterization of primary salivary duct carcinoma cell line. Oral Oncol. 2017 06; 69:108-114.
Score: 0.033
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Molecular cytogenetic analysis of follicular lymphoma (FL) provides detailed characterization of chromosomal instability associated with the t(14;18)(q32;q21) positive and negative subsets and histologic progression. Cytogenet Genome Res. 2007; 118(2-4):337-44.
Score: 0.032
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i(5p) and del(6q) are nonrandom abnormalities in carcinoma cervix uteri. Cytogenetics of two newly developed cell lines. Cancer Genet Cytogenet. 1994 Aug; 76(1):56-8.
Score: 0.027
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Development and characterization of salivary adenoid cystic carcinoma cell line. Oral Oncol. 2014 Oct; 50(10):991-9.
Score: 0.027
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Comprehensive molecular cytogenetic characterization of cervical cancer cell lines. Genes Chromosomes Cancer. 2003 Mar; 36(3):233-41.
Score: 0.024
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Coexistence of independent myelodysplastic and Philadelphia chromosome positive clones in a patient treated with hydroxyurea. Leuk Res. 2002 Apr; 26(4):417-20.
Score: 0.023
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Spectral karyotyping identifies new rearrangements, translocations, and clinical associations in diffuse large B-cell lymphoma. Blood. 2002 Apr 01; 99(7):2554-61.
Score: 0.023
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Multicolor spectral karyotyping of serous ovarian adenocarcinoma. Genes Chromosomes Cancer. 2002 Feb; 33(2):123-32.
Score: 0.023
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Molecular cytogenetic characterization of head and neck squamous cell carcinoma and refinement of 3q amplification. Cancer Res. 2001 Jun 01; 61(11):4506-13.
Score: 0.022
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Trisomy 1q, 2, and 20 in a case of hepatoblastoma: possible significance of 2q35-q37 and 1q12-q21 rearrangements. Cancer Genet Cytogenet. 2000 Dec; 123(2):140-3.
Score: 0.021
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Improving degenerate oligonucleotide primed PCR-comparative genomic hybridization for analysis of DNA copy number changes in tumors. Genes Chromosomes Cancer. 2000 Aug; 28(4):395-403.
Score: 0.020
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Comparative genomic hybridization study of de novo myeloid neoplasia. Acta Haematol. 2000; 104(1):25-30.
Score: 0.020
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Clinical utility of array comparative genomic hybridization for detection of chromosomal abnormalities in pediatric acute lymphoblastic leukemia. Pediatr Blood Cancer. 2008 Aug; 51(2):171-7.
Score: 0.018
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Cytogenetics of gastric and esophageal adenocarcinomas. 3q deletion as a possible primary chromosomal change. Cancer Genet Cytogenet. 1995 Jun; 81(2):139-43.
Score: 0.014
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Consistent chromosomal losses in head and neck squamous cell carcinoma cell lines. Genes Chromosomes Cancer. 1994 Sep; 11(1):29-39.
Score: 0.014
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Frequent amplification and rearrangement of chromosomal bands 6p12-p21 and 17p11.2 in osteosarcoma. Genes Chromosomes Cancer. 2004 Jan; 39(1):11-21.
Score: 0.013
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Cytogenetic analysis of a juvenile granulosa cell tumor. Cancer Genet Cytogenet. 1992 Jul 15; 61(2):207-9.
Score: 0.012
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Transformation of human kidney proximal tubule cells by a src-containing retrovirus. Oncogene. 1991 Nov; 6(11):2105-11.
Score: 0.011
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11p13-15 is a specific region of chromosomal rearrangement in gastric and esophageal adenocarcinomas. Cancer Res. 1990 Oct 01; 50(19):6410-6.
Score: 0.010
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Deregulation of BCL6 in non-Hodgkin lymphoma by insertion of IGH sequences in complex translocations involving band 3q27. Genes Chromosomes Cancer. 1998 Dec; 23(4):328-36.
Score: 0.009
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Chromosomal amplification is associated with cisplatin resistance of human male germ cell tumors. Cancer Res. 1998 Oct 01; 58(19):4260-3.
Score: 0.009