Compound heterozygous loss of function variants in MYL9 in a child with megacystis–microcolon–intestinal hypoperistalsis syndrome

por Kandler, Justin L., Sklirou, Evgenia, Woerner, Audrey, Walsh, Leslie, Cox, Eleina, Xue, Yuan
Publicado 2020

Identification of Two Homozygous Variants in MYBPC3 and SMYD1 Genes Associated with Severe Infantile Cardiomyopathy

por Szulik, Marta W., Reyes-Múgica, Miguel, Marker, Daniel F., Gomez, Ana M., Zinn, Matthew D., Walsh, Leslie K., Ochoa, Juan Pablo, Franklin, Sarah, Ghaloul-Gonzalez, Lina
Publicado 2023

Comparison of pharmacological inhibitors of lysine-specific demethylase 1 in glioblastoma stem cells reveals inhibitor-specific efficacy profiles

por Stitzlein, Lea M., Gangadharan, Achintyan, Walsh, Leslie M., Nam, Deokhwa, Espejo, Alexsandra B., Singh, Melissa M., Patel, Kareena H., Lu, Yue, Su, Xiaoping, Ezhilarasan, Ravesanker, Gumin, Joy, Singh, Sanjay, Sulman, Erik, Lang, Frederick F., Chandra, Joya
Publicado 2023

Seventy-One Important Questions for the Conservation of Marine Biodiversity

por PARSONS, E C M, FAVARO, BRETT, AGUIRRE, A ALONSO, BAUER, AMY L, BLIGHT, LOUISE K, CIGLIANO, JOHN A, COLEMAN, MELINDA A, CÔTÉ, ISABELLE M, DRAHEIM, MEGAN, FLETCHER, STEPHEN, FOLEY, MELISSA M, JEFFERSON, REBECCA, JONES, MIRANDA C, KELAHER, BRENDAN P, LUNDQUIST, CAROLYN J, MCCARTHY, JULIE-BETH, NELSON, ANNE, PATTERSON, KATHERYN, WALSH, LESLIE, WRIGHT, ANDREW J, SUTHERLAND, WILLIAM J
Publicado 2014