RecQ Helicase Somatic Alterations in Cancer

por Thakkar, Megha K., Lee, Jamie, Meyer, Stefan, Chang, Vivian Y.
Publicado 2022

Identification of somatic and germline mutations using whole exome sequencing of congenital acute lymphoblastic leukemia

por Chang, Vivian Y, Basso, Giuseppe, Sakamoto, Kathleen M, Nelson, Stanley F
Publicado 2013

Bloom syndrome patients and mice display accelerated epigenetic aging

por Lee, Jamie, Zhang, Joshua, Flanagan, Maeve, Martinez, Julian A., Cunniff, Christopher, Kucine, Nicole, Lu, Ake T., Haghani, Amin, Gordevičius, Juozas, Horvath, Steve, Chang, Vivian Y.
Publicado 2023

High-Dose Chemotherapy with Autologous Hematopoietic Stem-Cell Rescue for Pediatric Brain Tumor Patients: A Single Institution Experience from UCLA

por Panosyan, Eduard H., Ikeda, Alan K., Chang, Vivian Y., Laks, Dan R., Reeb, Charles L., Bowles, La Vette, Lasky, Joseph L., Moore, Theodore B.
Publicado 2011

Evaluation of clonal hematopoiesis in pediatric ADA-SCID gene therapy participants

por White, Shanna L., Lee, Thomas D., Toy, Traci, Carroll, Judith E., Polsky, Lilian, Campo Fernandez, Beatriz, Davila, Alejandra, Kohn, Donald B., Chang, Vivian Y.
Publicado 2022

Is polycystic kidney disease associated with malignancy in children?

por Friend, Brian D., Wolfe Schneider, Kami, Garrington, Timothy, Truscott, Laurel, Martinez‐Agosto, Julian A., Venick, Robert S., Tsai Chambers, Eileen, Weng, Patricia, Farmer, Douglas G., Chang, Vivian Y., Federman, Noah
Publicado 2019

LGG-10. AN UNUSUAL PRESENTATION OF BILATERAL OPTIC NERVE GLIOMA IN CROUZON SYNDROME

por Na, Brian, Wang, Anthony C, Watterson, Christopher Travis, Martinez-Agosto, Julian A, Saitta, Sulagna, Dutra-Clarke, Marina, Hinkamp, Franceska, Pineles, Stacy L, de Blank, Peter, Chang, Vivian Y, Moore, Theodore
Publicado 2021

Neuropilin 1 regulates bone marrow vascular regeneration and hematopoietic reconstitution

por Termini, Christina M., Pang, Amara, Fang, Tiancheng, Roos, Martina, Chang, Vivian Y., Zhang, Yurun, Setiawan, Nicollette J., Signaevskaia, Lia, Li, Michelle, Kim, Mindy M., Tabibi, Orel, Lin, Paulina K., Sasine, Joshua P., Chatterjee, Avradip, Murali, Ramachandran, Himburg, Heather A., Chute, John P.
Publicado 2021

CTCF variants in 39 individuals with a variable neurodevelopmental disorder broaden the mutational and clinical spectrum

por Konrad, Enrico D. H., Nardini, Niels, Caliebe, Almuth, Nagel, Inga, Young, Dana, Horvath, Gabriella, Santoro, Stephanie L., Shuss, Christine, Ziegler, Alban, Bonneau, Dominique, Kempers, Marlies, Pfundt, Rolph, Legius, Eric, Bouman, Arjan, Stuurman, Kyra E., Õunap, Katrin, Pajusalu, Sander, Wojcik, Monica H., Vasileiou, Georgia, Le Guyader, Gwenaël, Schnelle, Hege M., Berland, Siren, Zonneveld-Huijssoon, Evelien, Kersten, Simone, Gupta, Aditi, Blackburn, Patrick R., Ellingson, Marissa S., Ferber, Matthew J., Dhamija, Radhika, Klee, Eric W., McEntagart, Meriel, Lichtenbelt, Klaske D., Kenney, Amy, Vergano, Samantha A., Abou Jamra, Rami, Platzer, Konrad, Ella Pierpont, Mary, Khattar, Divya, Hopkin, Robert J., Martin, Richard J., Jongmans, Marjolijn C. J., Chang, Vivian Y., Martinez-Agosto, Julian A., Kuismin, Outi, Kurki, Mitja I., Pietiläinen, Olli, Palotie, Aarno, Maarup, Timothy J., Johnson, Diana S., Venborg Pedersen, Katja, Laulund, Lone W., Lynch, Sally A., Blyth, Moira, Prescott, Katrina, Canham, Natalie, Ibitoye, Rita, Brilstra, Eva H., Shinawi, Marwan, Fassi, Emily, Sticht, Heinrich, Gregor, Anne, Van Esch, Hilde, Zweier, Christiane
Publicado 2019