Search Results - "Miller, Carl W."

Molecular allelokaryotyping of pediatric acute lymphoblastic leukemias by high-resolution single nucleotide polymorphism oligonucleotide genomic microarray by Kawamata, Norihiko, Ogawa, Seishi, Zimmermann, Martin, Kato, Motohiro, Sanada, Masashi, Hemminki, Kari, Yamatomo, Go, Nannya, Yasuhito, Koehler, Rolf, Flohr, Thomas, Miller, Carl W., Harbott, Jochen, Ludwig, Wolf-Dieter, Stanulla, Martin, Schrappe, Martin, Bartram, Claus R., Koeffler, H. Phillip

“…Pediatric acute lymphoblastic leukemia (ALL) is a malignant disease resulting from accumulation of genetic alterations. A robust technology, single nucleotide…”
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Epigenetic Silencing of the Candidate Tumor Suppressor Gene Per1 in Non–Small Cell Lung Cancer by GERY, Sigal, KOMATSU, Naoki, KAWAMATA, Norihiko, MILLER, Carl W, DESMOND, Julian, VIRK, Renu K, MARCHEVSKY, Alberto, MCKENNA, Robert, TAGUCHI, Hirokuni, KOEFFLER, H. Phillip

“…Purpose: Epigenetic events are a critical factor contributing to cancer development. The purpose of this study was to identify tumor suppressor genes silenced…”
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FOXA1: Growth inhibitor and a favorable prognostic factor in human breast cancer by Wolf, Ido, Bose, Shikha, Williamson, Elizabeth A., Miller, Carl W., Karlan, Beth Y., Koeffler, H. Phillip

“…The transcription factor Forkhead‐box A1 (Foxa1), a member of the FOX class of transcription factors, has been implicated in the pathogenesis of lung,…”
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ERCC5 Is a Novel Biomarker of Ovarian Cancer Prognosis by WALSH, Christine S, OGAWA, Seishi, SANADA, Masashi, NANNYA, Yasuhito, SLAMON, Dennis J, KOEFFLER, H. Phillip, KARLAN, Beth Y, KARAHASHI, Hisae, SCALES, Daniel R, PAVELKA, James C, TRAN, Hang, MILLER, Carl W, KAWAMATA, Norihiko, GINTHER, Charles, DERING, Judy

“…To identify a biomarker of ovarian cancer response to chemotherapy. PATIENTS AND METHODS Study: participants had epithelial ovarian cancer treated with surgery…”
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Cloning of genes involved in chromosomal translocations by high-resolution single nucleotide polymorphism genomic microarray by Kawamata, Norihiko, Ogawa, Seishi, Zimmermann, Martin, Niebuhr, Birte, Stocking, Carol, Sanada, Masashi, Hemminki, Kari, Yamatomo, Go, Nannya, Yasuhito, Koehler, Rolf, Flohr, Thomas, Miller, Carl W, Harbott, Jochen, Ludwig, Wolf-Dieter, Stanulla, Martin, Schrappe, Martin, Bartram, Claus R, Koeffler, H. Phillip

“…High-resolution single nucleotide polymorphism genomic microarray (SNP-chip) is a useful tool to define gene dosage levels over the whole genome, allowing…”
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Frequent genomic abnormalities in acute myeloid leukemia/myelodysplastic syndrome with normal karyotype by AKAGI, Tadayuki, OGAWA, Seishi, HAFERLACH, Torsten, HAFERLACH, Claudia, KOEFFLER, H. Phillip, DUGAS, Martin, KAWAMATA, Norihiko, YAMAMOTO, Go, NANNYA, Yasuhito, SANADA, Masashi, MILLER, Carl W, YUNG, Amanda, SCHNITTGER, Susanne

“…Acute myeloid leukemia is a clonal hematopoietic malignant disease; about 45-50% of cases do not have detectable chromosomal abnormalities. Here, we identified…”
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Association between a functional single nucleotide polymorphism in the MDM2 gene and sporadic endometrial cancer risk by Walsh, Christine S, Miller, Carl W, Karlan, Beth Y, Koeffler, H. Phillip

“…Abstract Objectives. MDM2 is an important negative regulator of the p53 tumor suppressor protein. A naturally occurring T/G single nucleotide polymorphism…”
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Genome-Wide Loss of Heterozygosity and Uniparental Disomy in BRCA1/2-Associated Ovarian Carcinomas by WALSH, Christine S, OGAWA, Seishi, SCOLES, Daniel R, MILLER, Carl W, KAWAMATA, Norihiko, NAROD, Steven A, KOEFFLER, H. Phillip, KARLAN, Beth Y

“…Purpose: The importance of the BRCA gene products in maintaining genomic stability led us to hypothesize that BRCA-associated and sporadic ovarian cancers…”
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Sociodemographic and health-related determinants of breast and cervical cancer screening behavior, 2005 by Welch, Cindy, Miller, Carl W, James, Nadine T

“…To identify sociodemographic and health-related determinants of Breast and Cervical Cancer Screening behaviors and evaluate progress toward Healthy People 2010…”
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Mutations of the CHK2 gene are found in some osteosarcomas, but are rare in breast, lung, and ovarian tumors by Miller, Carl W., Ikezoe, Takayuki, Krug, Utz, Hofmann, Wolf-K., Tavor, Sigal, Vegesna, Vijaya, Tsukasaki, Kunihiro, Takeuchi, Seisho, Koeffler, H. Phillip

“…Checkpoint genes, activated in response to DNA damage and other stresses, are frequently targeted for alteration in cancer. Checkpoint kinase 2 (CHK2, CDS1,…”
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Functional analysis of a novel DNA polymorphism of a tandem repeated sequence in the asparagine synthetase gene in acute lymphoblastic leukemia cells by Akagi, Tadayuki, Yin, Dong, Kawamata, Norihiko, Bartram, Claus R, Hofmann, Wolf-K, Song, Jee Hoon, Miller, Carl W, den Boer, Monique L, Koeffler, H. Phillip

“…Abstract Asparagine synthetase (ASNS) is an enzyme expressed ubiquitously in mammalian cells. Here, we discovered two 14-bp tandem repeat (2R, wild-type)…”
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Cyr61 Suppresses Growth of Human Endometrial Cancer Cells by Chien, Wenwen, Kumagai, Takashi, Miller, Carl W., Desmond, Julian C., Frank, Jonathan M., Said, Jonathan W., Koeffler, H. Phillip

“…Cyr61 (CCN1) is a member of the CCN protein family; these secreted proteins are involved in diverse biological processes such as cell adhesion, angiogenesis,…”
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Xeroderma pigmentosum complementation group C single‐nucleotide polymorphisms in the nucleotide excision repair pathway correlate with prolonged progression‐free survival in advanced ovarian cancer by Fleming, Nicole D., Agadjanian, Hasmik, Nassanian, Hoorig, Miller, Carl W., Orsulic, Sandra, Karlan, Beth Y., Walsh, Christine S.

“…BACKGROUND: The nucleotide excision repair (NER) pathway is the principal DNA repair pathway for removing bulky platinum DNA adducts. Suboptimal DNA repair may…”
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Health status, physical disability, and obesity among adult Mississippians with chronic joint symptoms or doctor-diagnosed arthritis: findings from the Behavioral Risk Factor Surveillance System, 2003 by James, Nadine T, Miller, Carl W, Fos, Peter J, Zhang, Lei, Wall, Peggy, Welch, Cindy

“…The purpose of this study was to analyze 2003 Mississippi Behavioral Risk Factor Surveillance System (BRFSS) data to describe the health of Mississippians with…”
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Mutation analysis of the DNA-damage checkpoint gene CHK2 in myelodysplastic syndromes and acute myeloid leukemias by Hofmann, Wolf-K., Miller, Carl W., Tsukasaki, Kunihiro, Tavor, Sigal, Ikezoe, Takayuki, Hoelzer, Dieter, Takeuchi, Seisho, Koeffler, H.Phillip

“…Checkpoint genes code for a family of proteins which sense DNA damage in eukaryotic cells. They play an important role in the control of the cell cycle. The…”
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Hidden abnormalities and novel classification of t(15;17) acute promyelocytic leukemia (APL) based on genomic alterations by Akagi, Tadayuki, Shih, Lee-Yung, Kato, Motohiro, Kawamata, Norihiko, Yamamoto, Go, Sanada, Masashi, Okamoto, Ryoko, Miller, Carl W., Liang, Der-Cherng, Ogawa, Seishi, Koeffler, H. Phillip

“…Acute promyelocytic leukemia (APL) is a hematopoietic malignant disease characterized by the chromosomal translocation t(15;17), resulting in the formation of…”
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Chromosomal abnormalities and novel disease‐related regions in progression from Barrett's esophagus to esophageal adenocarcinoma by Akagi, Tadayuki, Ito, Tetsuo, Kato, Motohiro, Jin, Zhe, Cheng, Yulan, Kan, Takatsugu, Yamamoto, Go, Olaru, Alexandru, Kawamata, Norihiko, Boult, Jessica, Soukiasian, Harmik J., Miller, Carl W., Ogawa, Seishi, Meltzer, Stephen J., Koeffler, H. Phillip

“…Barrett's esophagus (BE) is a metaplastic condition caused by chronic gastroesophageal reflux which represents an early step in the development of esophageal…”
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Mutations in the gene encoding the transcription factor CCAAT/enhancer binding protein α in myelodysplastic syndromes and acute myeloid leukemias by Gombart, Adrian F., Hofmann, Wolf-K., Kawano, Seiji, Takeuchi, Seisho, Krug, Utz, Kwok, Scott H., Larsen, Renee J., Asou, Hiroya, Miller, Carl W., Hoelzer, Dieter, Koeffler, H. Phillip

“…The CCAAT/enhancer binding protein α (C/EBPα) protein is essential for proper lung and liver function and granulocytic and adipose tissue differentation. It…”
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Absence of R24C mutation of the CDK4 gene in leukemias and solid tumors by MORI, Naoki, RONG YANG, KAWAMATA, Norihiko, MILLER, Carl W, MIZOGUCHI, Hideaki, KOEFFLER, H. Phillip

“…A mutation of the p16(INK4a)-binding domain of the cyclin dependent kinase 4 (CDK4) gene, R24C, has been reported in some cases of melanoma. This mutation…”
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Genetic profiling of myeloproliferative disorders by single-nucleotide polymorphism oligonucleotide microarray by Kawamata, Norihiko, Ogawa, Seishi, Yamamoto, Go, Lehmann, Soren, Levine, Ross L, Pikman, Yana, Nannya, Yasuhito, Sanada, Masashi, Miller, Carl W, Gilliland, D. Gary, Koeffler, H. Phillip

“…Objective Myeloproliferative disorders (MPD) are clonal hematopoietic diseases that include polycythemia vera (PV), essential thrombocytosis (ET), and primary…”
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