Skip to Content

Publications

A B C D E F G H I J K L M N O P Q R S T U V W X Y Z 
B
Estrogen Receptor-Positive Breast Cancer Cells Drive CAFs to Secrete Leptin and Support Tumor Invasiveness, Barone, Ines, Catalano Stefania, Gelsomino Luca, Panza Salvatore, Marsico Stefania, Giordano Cinzia, Bonofiglio Daniela, Casaburi Ivan, Covington Kyle R., Fuqua Suzanne, et al. , The FASEB Journal, Volume 26, p.142–7, (2012)
Phosphorylation of the mutant K303R estrogen receptor alpha at serine 305 affects aromatase inhibitor sensitivity., Barone, I., Iacopetta D., Covington K. R., Cui Y., Tsimelzon A., Beyer A., Andò S., and Fuqua S. A. W. , Oncogene, 2010 Apr 22, Volume 29, Issue 16, p.2404-14, (2010) Abstract
Loss of Rho GDIα and resistance to tamoxifen via effects on estrogen receptor α., Barone, Ines, Brusco Lauren, Gu Guowei, Selever Jennifer, Beyer Amanda, Covington Kyle R., Tsimelzon Anna, Wang Tao, Hilsenbeck Susan G., Chamness Gary C., et al. , Journal of the National Cancer Institute, 2011 Apr 6, Volume 103, Issue 7, p.538-52, (2011) Abstract
No evidence for genome-wide interactions on plasma fibrinogen by smoking, alcohol consumption and body mass index: results from meta-analyses of 80,607 subjects., Baumert, Jens, Huang Jie, McKnight Barbara, Sabater-Lleal Maria, Steri Maristella, Chu Audrey Y., Trompet Stella, Lopez Lorna M., Fornage Myriam, Teumer Alexander, et al. , PloS one, 2014, Volume 9, Issue 12, p.e111156, (2014) Abstract
Whole exome sequencing identifies three novel mutations in ANTXR1 in families with GAPO syndrome., Bayram, Yavuz, Pehlivan Davut, Karaca Ender, Gambin Tomasz, Jhangiani Shalini N., Erdin Serkan, Gonzaga-Jauregui Claudia, Wiszniewski Wojciech, Muzny Donna, Elcioglu Nursel H., et al. , American journal of medical genetics. Part A, 2014 Sep, Volume 164A, Issue 9, p.2328-34, (2014) Abstract
Exome sequencing identifies a homozygous C5orf42 variant in a Turkish kindred with oral-facial-digital syndrome type VI., Bayram, Yavuz, Aydin Hatip, Gambin Tomasz, Akdemir Zeynep Coban, Atik Mehmed M., Karaca Ender, Karaman Ali, Pehlivan Davut, Jhangiani Shalini N., Gibbs Richard A., et al. , American journal of medical genetics. Part A, 2015 Apr 6, (2015) Abstract
Homozygous loss-of-function mutations in SOHLH1 in patients with non-syndromic hypergonadotropic hypogonadism., Bayram, Yavuz, Gulsuner Suleyman, Guran Tulay, Abaci Ayhan, Yesil Gozde, Gulsuner Hilal Unal, Atay Zeynep, Pierce Sarah B., Gambin Tomasz, Lee Ming, et al. , The Journal of clinical endocrinology and metabolism, 2015 Mar 16, p.jc20151150, (2015) Abstract
Comparative genomic study of arachnid immune systems indicates loss of βGRPs and the IMD pathway., Bechsgaard, Jesper, Vanthournout Bram, Funch Peter, Vestbo Stine, Gibbs Richard A., Richards Stephen, Sanggaard Kristian W., Enghild Jan J., and Bilde Trine , Journal of evolutionary biology, 2015 Nov 3, (2015) Abstract
FBN1 contributing to familial congenital diaphragmatic hernia., Beck, Tyler F., Campeau Philippe M., Jhangiani Shalini N., Gambin Tomasz, Li Alexander H., Abo-Zahrah Reem, Jordan Valerie K., Hernandez-Garcia Andres, Wiszniewski Wojciech K., Muzny Donna, et al. , American journal of medical genetics. Part A, 2015 Apr, Volume 167, Issue 4, p.831-6, (2015) Abstract
Glucocorticosteroid suppression of alpha1-fetoprotein synthesis in developing rat liver. Evidence for selective gene repression at the transcriptional level., Bélanger, L., Frain M., Baril P., Gingras M. C., Bartkowiak J., and Sala-Trepat J. M. , Biochemistry, 1981 Nov 10, Volume 20, Issue 23, p.6665-72, (1981)
Oncodevelopmental and hormonal regulation of alpha 1-fetoprotein gene expression., Belanger, L., Baril P., Guertin M., Gingras M. C., Gourdeau H., Anderson A., Hamel D., and Boucher J. M. , Advances in enzyme regulation, 1983, Volume 21, p.73-99, (1983) Abstract
High-resolution identity by descent mapping uncovers the genetic basis for blood pressure differences between spontaneously hypertensive rat lines., Bell, Rebecca, Herring Stacy M., Gokul Nisha, Monita Monique, Grove Megan L., Boerwinkle Eric, and Doris Peter A. , Circulation. Cardiovascular genetics, 2011 Jun, Volume 4, Issue 3, p.223-31, (2011) Abstract
Mammalian Y chromosomes retain widely expressed dosage-sensitive regulators, Bellott, Daniel W., Hughes Jennifer F., Skaletsky Helen, Brown Laura G., Pyntikova Tatyana, Cho Ting-Jan, Koutseva Natalia, Zaghlul Sara, Graves Tina, Rock Susie, et al. , Nature, 4/2014, Volume 508, Issue 7497, p.494 - 499, (2014)
Genome-wide linkage disequilibrium and haplotype maps., Belmont, John W., and Gibbs Richard A. , American journal of pharmacogenomics : genomics-related research in drug development and clinical practice, 2004, Volume 4, Issue 4, p.253-62, (2004) Abstract
Unique features of a global human ectoparasite identified through sequencing of the bed bug genome., Benoit, Joshua B., Adelman Zach N., Reinhardt Klaus, Dolan Amanda, Poelchau Monica, Jennings Emily C., Szuter Elise M., Hagan Richard W., Gujar Hemant, Shukla Jayendra Nath, et al. , Nature communications, 2016, Volume 7, p.10165, (2016) Abstract
Quantitative trait loci for peripheral blood cell counts: a study in baboons., Bertin, Angéline, Mahaney Michael C., Cox Laura A., Rogers Jeffrey, VandeBerg John L., Brugnara Carlo, and Platt Orah S. , Mammalian genome : official journal of the International Mammalian Genome Society, 2007 May, Volume 18, Issue 5, p.361-72, (2007) Abstract
The GABA Transaminase, ABAT, Is Essential for Mitochondrial Nucleoside Metabolism., Besse, Arnaud, Wu Ping, Bruni Francesco, Donti Taraka, Graham Brett H., Craigen William J., McFarland Robert, Moretti Paolo, Lalani Seema, Scott Kenneth L., et al. , Cell metabolism, 2015 Mar 3, Volume 21, Issue 3, p.417-27, (2015) Abstract
Pancreatic cancer genomes reveal aberrations in axon guidance pathway genes., Biankin, Andrew V., Waddell Nicola, Kassahn Karin S., Gingras Marie-Claude, Muthuswamy Lakshmi B., Johns Amber L., Miller David K., Wilson Peter J., Patch Ann-Marie, Wu Jianmin, et al. , Nature, 2012 Nov 15, Volume 491, Issue 7424, p.399-405, (2012) Abstract
Somatic sequence variation at the Friedreich ataxia locus includes complete contraction of the expanded GAA triplet repeat, significant length variation in serially passaged lymphoblasts and enhanced mutagenesis in the flanking sequence., Bidichandani, S. I., Purandare S. M., Taylor E. E., Gumin G., Machkhas H., Harati Y., Gibbs R. A., Ashizawa T., and Patel P. I. , Human molecular genetics, 1999 Dec, Volume 8, Issue 13, p.2425-36, (1999) Abstract
Graded phenotypic response to partial and complete deficiency of a brain-specific transcript variant of the winged helix transcription factor RFX4., Blackshear, Perry J., Graves Joan P., Stumpo Deborah J., Cobos Inma, Rubenstein John L. R., and Zeldin Darryl C. , Development (Cambridge, England), 2003 Oct, Volume 130, Issue 19, p.4539-52, (2003) Abstract
Investigation of the conformation of lactate dehydrogenase and of its catalytic activity., Bolotina, I. A., Markovich D. S., Volkenstein M. V., and Zavodzky P. , Biochimica et biophysica acta, 1967 Mar 15, Volume 132, Issue 2, p.271-81, (1967)
Evaluating potential for whole-genome studies in Kosrae, an isolated population in Micronesia., Bonnen, Penelope E., Pe'er Itsik, Plenge Robert M., Salit Jackie, Lowe Jennifer K., Shapero Michael H., Lifton Richard P., Breslow Jan L., Daly Mark J., Reich David E., et al. , Nature genetics, 2006 Feb, Volume 38, Issue 2, p.214-7, (2006) Abstract
Haplotype and linkage disequilibrium architecture for human cancer-associated genes., Bonnen, Penelope E., Wang Peggy J., Kimmel Marek, Chakraborty Ranajit, and Nelson David L. , Genome research, 2002 Dec, Volume 12, Issue 12, p.1846-53, (2002) Abstract
European admixture on the Micronesian island of Kosrae: lessons from complete genetic information., Bonnen, Penelope E., Lowe Jennifer K., Altshuler David M., Breslow Jan L., Stoffel Markus, Friedman Jeffrey M., and Pe'er Itsik , European journal of human genetics : EJHG, 2010 Mar, Volume 18, Issue 3, p.309-16, (2010) Abstract
Haplotypes at ATM identify coding-sequence variation and indicate a region of extensive linkage disequilibrium., Bonnen, P. E., Story M. D., Ashorn C. L., Buchholz T. A., Weil M. M., and Nelson D. L. , American journal of human genetics, 2000 Dec, Volume 67, Issue 6, p.1437-51, (2000) Abstract


about seo