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Molecular and Cellular Biology|August 5, 2003
Pex13 inactivation in the mouse disrupts peroxisome biogenesis and leads to a Zellweger syndrome phenotypeMegan Maxwell, Jonas Bjorkman, Tam Nguyen, et al.Nature Structural & Molecular Biology|July 27, 2010
The A-repeat links ASF/SF2-dependent Xist RNA processing with random choice during X inactivationMorgan E Royce-Tolland, Angela A Andersen, Hannah R Koyfman, et al.Molecular and Cellular Biology|April 3, 2004
Conditional inactivation of the MEN1 gene leads to pancreatic and pituitary tumorigenesis but does not affect normal development of these tissuesChristine A Biondi, Michael G Gartside, Paul Waring, et al.Nature|May 23, 1991
Conservation of position and exclusive expression of mouse Xist from the inactive X chromosomeN Brockdorff, A Ashworth, G F Kay, et al.Cancer Research|December 1, 1992
Loss of heterozygosity involves multiple tumor suppressor genes in human esophageal cancersY Huang, R F Boynton, P L Blount, et al.International Journal of Cancer|October 18, 2006
Broad tumor spectrum in a mouse model of multiple endocrine neoplasia type 1Kelly A Loffler, Christine A Biondi, Michael Gartside, et al.Blood|August 9, 2001
Loss of heterozygosity in childhood de novo acute myelogenous leukemiaD A Sweetser, C S Chen, A A Blomberg, et al.Pigment Cell Research|July 21, 2005
Melanocytes in conditional Rb-/- mice are normal in vivo but exhibit proliferation and pigmentation defects in vitroIan D Tonks, Elke Hacker, Nicole Irwin, et al.Journal of Orthopaedic Trauma|October 24, 2013
The effects of American Society of Anesthesiologists physical status on length of stay and inpatient cost in the surgical treatment of isolated orthopaedic fracturesHarrison F Kay, Vasanth Sathiyakumar, Zachary T Yoneda, et al.Proceedings of the National Academy of Sciences of the United States of America|April 15, 1992
Loss of heterozygosity involving the APC and MCC genetic loci occurs in the majority of human esophageal cancersR F Boynton, P L Blount, J Yin, et al.Pageof 38