ALDH1A3-acetaldehyde metabolism potentiates transcriptional heterogeneity in melanoma
Lu, Yuting, Travnickova, Jana, Badonyi, Mihaly, Rambow, Florian, Coates, Andrea, Khan, Zaid, Marques, Jair, Murphy, Laura C., Garcia-Martinez, Pablo, Marais, Richard, Louphrasitthiphol, Pakavarin, Chan, Alex H.Y., Schofield, Christopher J., von Kriegsheim, Alex, Marsh, Joseph A., Pavet, Valeria, Sansom, Owen J., Illingworth, Robert S., Patton, E. Elizabeth
Published in Cell reports (Cambridge) (26.11.2024)
Published in Cell reports (Cambridge) (26.11.2024)
Get full text
Journal Article
USING VIDEO MODELING AND REINFORCEMENT TO TEACH PERSPECTIVE-TAKING SKILLS TO CHILDREN WITH AUTISM
LeBlanc, Linda A., Coates, Andrea M., Daneshvar, Sabrina, Charlop-Christy, Marjorie H., Morris, Caroline, Lancaster, Blake M.
Published in Journal of applied behavior analysis (2003)
Published in Journal of applied behavior analysis (2003)
Get full text
Journal Article
ALDH1A3-acetaldehyde metabolism potentiates transcriptional heterogeneity in melanoma
Lu, Yuting, Travnickova, Jana, Badonyi, Mihaly, Rambow, Florian, Coates, Andrea, Khan, Zaid, Marques, Jair, Murphy, Laura C., Garcia-Martinez, Pablo, Marais, Richard, Louphrasitthiphol, Pakavarin, Chan, Alex H.Y., Schofield, Christopher J., von Kriegsheim, Alex, Marsh, Joseph A., Pavet, Valeria, Sansom, Owen J., Illingworth, Robert S., Patton, E. Elizabeth
Published in Cell reports (Cambridge) (23.07.2024)
Published in Cell reports (Cambridge) (23.07.2024)
Get full text
Journal Article
Randomized phase 2 study to assess the safety and efficacy of CRLX101 in combination with bevacizumab in patients (pts.) with metastatic renal cell carcinoma (RCC) versus standard of care (SOC)
Voss, Martin Henner, Coates, Andrea, Garmey, Edward Graeme, Haas, Naomi B., Hutson, Thomas, Keefe, Stephen Michael, Motzer, Robert, Piscitelli, Anthony, Vogelzang, Nicholas J., Figlin, Robert A.
Published in Journal of clinical oncology (20.05.2015)
Published in Journal of clinical oncology (20.05.2015)
Get full text
Journal Article
Diagnostic whole genome sequencing and split-read mapping for nucleotide resolution breakpoint identification in CNTNAP2 deficiency syndrome
Watson, Christopher M., Crinnion, Laura A., Tzika, Antigoni, Mills, Alison, Coates, Andrea, Pendlebury, Maria, Hewitt, Sarah, Harrison, Sally M., Daly, Catherine, Roberts, Paul, Carr, Ian M., Sheridan, Eamonn G., Bonthron, David T.
Published in American journal of medical genetics. Part A (01.10.2014)
Published in American journal of medical genetics. Part A (01.10.2014)
Get full text
Journal Article