Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Kirk Vandezande"'
Autor:
Usha Kini, Cesare Danesino, Arupa Ganguly, Andreas Lux, Barbara A. Bernhardt, Douglas A. Marchuk, Reed E. Pyeritz, Johannes K Ploos van Amstel, Marie E. Faughnan, Kirk Vandezande, J. Deane Waldman, Sara Mazzucco, Carol L. Clericuzio, Nadia L. Prigoda-Lee, Arthur S. Aylsworth, Carol J. Gallione, Carla Olivieri, Zheng Fan, Jill Beis, Katharine J. Henderson, Joanne M. Drautz, Charles A. Williams, John Garvie, Robert I. White, Mark Ludman, Willie Reardon, Melissa K. Maisenbacher, Jeffrey Fahl, Tracey P. Leedom, Robin D. Clark, Terri Berk
Publikováno v:
American Journal of Medical Genetics Part A. :333-339
Juvenile polyposis (JP) and hereditary hemorrhagic telangiectasia (HHT) are clinically distinct diseases caused by mutations in SMAD4 and BMPR1A (for JP) and endoglin and ALK1 (for HHT). Recently, a combined syndrome of JP-HHT was described that is a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c8715243860145d186aa91e6681359c9
https://doi.org/10.1002/ajmg.a.33206
https://doi.org/10.1002/ajmg.a.33206
Autor:
N L Prigoda, E Zhang, Hilmi Ozcelik, Kirk Vandezande, Sevtap Savas, Beata Piovesan, S A Abdalla, Diane Rushlow, Michelle Letarte, Brenda L. Gallie
Publikováno v:
Journal of Medical Genetics. 43:722-728
Background: Hereditary haemorrhagic telangiectasia (HHT) is a genetic disorder present in 1 in 8000 people and associated with arteriovenous malformations. Genetic testing can identify individuals at risk of developing the disease and is a useful dia
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fe5cdce1214f818a84ee8a5b72484833
https://doi.org/10.1136/jmg.2006.042606
https://doi.org/10.1136/jmg.2006.042606
Autor:
Maria Zielenska, Gloria Lim, Kirk Vandezande, Yves Fradet, Michael A.S. Jewett, Jeremy A. Squire, Andrew Evans, John Underwood, Paula Marrano, Gregory R. Pond, Brenda L. Gallie
Publikováno v:
The American Journal of Pathology. 164:285-293
Metaphase-based comparative genomic hybridization (CGH) has identified recurrent regions of gain on different chromosomes in bladder cancer, including 6p22. These regions may contain activated oncogenes important in disease progression. Using quantit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2b404fda48c4903666e85b342b3be7fc
https://doi.org/10.1016/s0002-9440(10)63118-5
https://doi.org/10.1016/s0002-9440(10)63118-5
Autor:
George Blazenko, Kirk Vandezande
Publikováno v:
Journal of Economics and Business. 55:255-266
This paper investigates the effects of stock out avoidance and market competition on corporate holding of finished goods inventories. We consider two adverse consequences of stock outs: immediate forgone profit and long-run loss of revenue from the s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8ec836b82af497efa51cc3f98bd50495
https://doi.org/10.1016/s0148-6195(03)00023-7
https://doi.org/10.1016/s0148-6195(03)00023-7
Autor:
George Blazenko, Kirk Vandezande
Publikováno v:
Managerial and Decision Economics. 24:457-469
The product differentiation hypothesis for trade credit says that business managers use trade credit like advertising to differentiate their products. Prior studies of this hypothesis conclude that higher profit margins induce firms to increase trade
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::242f72ee643cc3809c6418b8b45dba0a
https://doi.org/10.1002/mde.1113
https://doi.org/10.1002/mde.1113
Publikováno v:
Pediatric bloodcancer. 49
The RB1 gene is important in all human cancers. Studies of human retinoblastoma point to a rare retinal cell with extreme dependency on RB1 for initiation but not progression to full malignancy. In developed countries, genetic testing within affected
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f6580c46875a15b2112156bbaa0139fa
https://pubmed.ncbi.nlm.nih.gov/17943957
https://pubmed.ncbi.nlm.nih.gov/17943957
Autor:
Kirk Vandezande, Joanne Sutherland, Julie Anderson, Rachel L. Panton, Ning Chen, Li-Ping Han, Suzanne Richter, Katherine Zhang, Brenda L. Gallie, Patricia Branco
Publikováno v:
The American Journal of Human Genetics. (2):253-269
Timely molecular diagnosis of RB1 mutations enables earlier treatment, lower risk, and better health outcomes for patients with retinoblastoma; empowers families to make informed family-planning decisions; and costs less than conventional surveillanc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0ea550bc09f0580b57aa90a88002b10c