Search Results - "Petillo, D"

Gene and protein expression markers of response to combined antiangiogenic and epidermal growth factor targeted therapy in renal cell carcinoma by Tsavachidou-Fenner, D., Tannir, N., Tamboli, P., Liu, W., Petillo, D., Teh, B., Mills, G.B., Jonasch, E.

“…Metastatic renal cell carcinoma (mRCC) patients treated with anti-vascular endothelial growth factor (VEGF) therapies demonstrate promising outcomes but not…”
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Role of eIF3a in regulating cisplatin sensitivity and in translational control of nucleotide excision repair of nasopharyngeal carcinoma by Liu, R-Y, Dong, Z, Liu, J, Yin, J-Y, Zhou, L, Wu, X, Yang, Y, Mo, W, Huang, W, Khoo, S K, Chen, J, Petillo, D, Teh, B T, Qian, C-N, Zhang, J-T

“…Translational control at the initiation step has been recognized as a major and important regulatory mechanism of gene expression. Eukaryotic initiation…”
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HRPT2 mutations are associated with malignancy in sporadic parathyroid tumours by Howell, V M, Haven, C J, Kahnoski, K, Khoo, S K, Petillo, D, Chen, J, Fleuren, G J, Robinson, B G, Delbridge, L W, Philips, J, Nelson, A E, Krause, U, Hammje, K, Dralle, H, Hoang-Vu, C, Gimm, O, Marsh, D J, Morreau, H, Teh, B T

“…Background: Hyperparathyroidism is a common endocrinopathy characterised by the formation of parathyroid tumours. In this study, we determine the role of the…”
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Genome-wide scan identifies novel modifier loci of acromegalic phenotypes for isolated familial somatotropinoma by Khoo, S K, Pendek, R, Nickolov, R, Luccio-Camelo, D C, Newton, T L, Massie, A, Petillo, D, Menon, J, Cameron, D, Teh, B T, Chan, S-P

“…Isolated familial somatotropinoma (IFS) accounts for 18% of familial isolated pituitary adenoma (FIPA) cases. Recently, germline mutations of the aryl…”
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Germline and de novo mutations in the HRPT2 tumour suppressor gene in familial isolated hyperparathyroidism (FIHP) by Villablanca, A, Calender, A, Forsberg, L, Höög, A, Cheng, J-D, Petillo, D, Bauters, C, Kahnoski, K, Ebeling, T, Salmela, P, Richardson, A-L, Delbridge, L, Meyrier, A, Proye, C, Carpten, J D, Teh, B T, Robinson, B G, Larsson, C

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Kinetics of Antioxidant Loss in Mackerel Light and Dark Muscle by Petillo, David, Hultin, Herbert O, Krzynowek, Judith, Autio, Wesley R

“…The loss of water- and lipid-soluble antioxidants of mackerel light and dark muscle was determined as a function of time of storage on ice to provide clues as…”
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MicroRNA profiling of human kidney cancer subtypes by PETILLO, David, KORT, Eric J, ANEMA, John, FURGE, Kyle A, YANG, Ximing J, BIN TEAN TEH

“…Although the functions of most of the identified microRNAs (miRNAs) have yet to be determined, their use as potential biomarkers has been considered in several…”
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Disruption of tubular Flcn expression as a mouse model for renal tumor induction by Chen, Jindong, Huang, Dachuan, Rubera, Isabelle, Futami, Kunihiko, Wang, Pengfei, Zickert, Peter, Khoo, Sok-Kean, Dykema, Karl, Zhao, Ping, Petillo, David, Cao, Brian, Zhang, Zhongfa, Si, Shuhui, Schoen, Susan R, Yang, Ximing J, Zhou, Ming, Xiao, Guang-Qian, Wu, Guan, Nordenskjöld, Magnus, Tauc, Michel, Williams, Bart O, Furge, Kyle A, Teh, Bin Tean

“…The study of kidney cancer pathogenesis and its treatment has been limited by the scarcity of genetically defined animal models. The FLCN gene that codes for…”
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Inactivation of BHD in sporadic renal tumors by SOK KEAN KHOO, KAHNOSKI, Katherine, NORDENSKJÖLD, Magnus, BIN TEAN TEH, SUGIMURA, Jun, PETILLO, David, JINDONG CHEN, SHOCKLEY, Ken, LUDLOW, John, KNAPP, Robert, GIRAUD, Sophie, RICHARD, Stéphane

“…Studies of families with Birt-Hogg-Dubé syndrome (BHD) have recently revealed protein-truncating mutations in the BHD gene, leading to tumorigenesis of the…”
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The t(1;3) breakpoint-spanning involved in clear cell renal cell genes LSAMP and NORE1 are carcinomas by Chen, JD, Lui, WO, Vos, MD, Clark, GJ, Takahashi, M, Schoumans, J, Khoo, SK, Petillo, D, Lavery, T, Sugimura, J

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Birt-Hogg-Dubé renal tumors are genetically distinct from other renal neoplasias and are associated with up-regulation of mitochondrial gene expression by Klomp, Jeff A, Petillo, David, Niemi, Natalie M, Dykema, Karl J, Chen, Jindong, Yang, Ximing J, Sääf, Annika, Zickert, Peter, Aly, Markus, Bergerheim, Ulf, Nordenskjöld, Magnus, Gad, Sophie, Giraud, Sophie, Denoux, Yves, Yonneau, Laurent, Méjean, Arnaud, Vasiliu, Viorel, Richard, Stéphane, MacKeigan, Jeffrey P, Teh, Bin T, Furge, Kyle A

“…Germline mutations in the folliculin (FLCN) gene are associated with the development of Birt-Hogg-Dubé syndrome (BHDS), a disease characterized by papular skin…”
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The t(1;3) breakpoint-spanning genes LSAMP and NORE1 are involved in clear cell renal cell carcinomas by Chen, Jindong, Lui, Weng-Onn, Vos, Michele D., Clark, Geoffrey J., Takahashi, Masayuki, Schoumans, Jacqueline, Khoo, Sok Kean, Petillo, David, Lavery, Todd, Sugimura, Jun, Astuti, Dewi, Zhang, Chun, Kagawa, Susumu, Maher, Eamonn R., Larsson, Catharina, Alberts, Arthur S., Kanayama, Hiro-omi, Teh, Bin Tean

“…By positional cloning, we identified two breakpoint-spanning genes in a familial clear cell renal cell carcinoma (CCRCC)-associated t(1;3)(q32.1;q13.3): LSAMP…”
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The mechanism of action and resistance of sunitinib in RCC by Teh, B. T., Huang, D., Ding, Y., Zhou, M., Rini, B. I., Petillo, D., Qian, C., Kahnoski, R. J., Futreal, P., Furge, K. A.

“…Abstract only…”
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Detection of submicroscopic constitutional chromosome aberrations in clinical diagnostics: a validation of the practical performance of different array platforms by ZHANG, Zhong-Fa, RUIVENKAMP, Claudia, STAAF, Johan, HONGBO ZHU, BARBARO, Michela, PETILLO, David, SOK KEAN KHOO, BORG, Ake, FAN, Yao-Shan, SCHOUMANS, Jacqueline

“…For several decades etiological diagnosis of patients with idiopathic mental retardation (MR) and multiple congenital anomalies (MCA) has relied on chromosome…”
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Indigenous Pop: Native American Music from Jazz to Hip Hop ed. by Jeff Berglund, Jan Johnson, and Kimberli Lee (review) by Petillo, April D. J

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A bean as a nucleus in a vesical calculus by PETILLO, D

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A screwless filiform follower by PETILLO, D

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Transillumination of the bladder; a preliminary note by PETILLO, D

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A comparison study reveals important features of agreement and disagreement between summarized DNA and RNA data obtained from renal cell carcinoma by ZHANG, Zhong-Fa, MATSUDA, Daisuke, SOK KEAN KHOO, BUZZITTA, Kristin, BLOCK, Elizabeth, PETILLO, David, RICHARD, Stéphane, ANEMA, John, FURGE, Kyle A, TEH, Bin T

“…Cytogenetic abnormalities, such as DNA amplifications and deletions, often lead to significant changes in gene expression levels within a chromosomal region…”
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Germline and de novo mutations in the HRPT2 tumour suppressor gene in familial isolated hyperparathyroidism (FIHP) -: art. no. e32 by Villablanca, A, Calender, A, Forsberg, L, Höög, A, Cheng, JD, Petillo, D, Bauters, C, Kahnoski, K, Ebeling, T, Salmela, P

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