The Heterochromatin Protein 1 family

por Lomberk, Gwen, Wallrath, Lori, Urrutia, Raul
Publicado 2006

Chromatin and chromosomes

por Gilbert, David M., Wallrath, Lori L.
Publicado 2011

Shining Light on the Dark Side of the Genome

por Wallrath, Lori L., Rodriguez-Tirado, Felipe, Geyer, Pamela K.
Publicado 2022

Drosophila Models Reveal Properties of Mutant Lamins That Give Rise to Distinct Diseases

por Walker, Sydney G., Langland, Christopher J., Viles, Jill, Hecker, Laura A., Wallrath, Lori L.
Publicado 2023

A Drosophila model of Epidermolysis Bullosa Simplex

por Bohnekamp, Jens, Cryderman, Diane E., Paululat, Achim, Baccam, Gabriel C., Wallrath, Lori L., Magin, Thomas M.
Publicado 2015

In Silico and In Vivo Analysis of Amino Acid Substitutions That Cause Laminopathies

por Hinz, Benjamin E., Walker, Sydney G., Xiong, Austin, Gogal, Rose A., Schnieders, Michael J., Wallrath, Lori L.
Publicado 2021

LMNA variants cause cytoplasmic distribution of nuclear pore proteins in Drosophila and human muscle

por Dialynas, George, Flannery, Kaitlin M., Zirbel, Luka N., Nagy, Peter L., Mathews, Katherine D., Moore, Steven A., Wallrath, Lori L.
Publicado 2012

Effects of mutant lamins on nucleo-cytoskeletal coupling in Drosophila models of LMNA muscular dystrophy

por Shaw, Nicholas M., Rios-Monterrosa, Jose L., Fedorchak, Gregory R., Ketterer, Margaret R., Coombs, Gary S., Lammerding, Jan, Wallrath, Lori L.
Publicado 2022

Increasing autophagy and blocking Nrf2 suppress laminopathy‐induced age‐dependent cardiac dysfunction and shortened lifespan

por Bhide, Shruti, Trujillo, Adriana S., O'Connor, Maureen T., Young, Grant H., Cryderman, Diane E., Chandran, Sahaana, Nikravesh, Mastaneh, Wallrath, Lori L., Melkani, Girish C.
Publicado 2018

Mutant lamins cause nuclear envelope rupture and DNA damage in skeletal muscle cells

por Earle, Ashley J., Kirby, Tyler J., Fedorchak, Gregory R., Isermann, Philipp, Patel, Jineet, Iruvanti, Sushruta, Moore, Steven A., Bonne, Gisèle, Wallrath, Lori L., Lammerding, Jan
Publicado 2019

Myopathic Lamin Mutations Cause Reductive Stress and Activate the Nrf2/Keap-1 Pathway

por Dialynas, George, Shrestha, Om K., Ponce, Jessica M., Zwerger, Monika, Thiemann, Dylan A., Young, Grant H., Moore, Steven A., Yu, Liping, Lammerding, Jan, Wallrath, Lori L.
Publicado 2015

Modulation of muscle redox and protein aggregation rescues lethality caused by mutant lamins

por Coombs, Gary S., Rios-Monterrosa, Jose L., Lai, Shuping, Dai, Qiang, Goll, Ashley C., Ketterer, Margaret R., Valdes, Maria F., Uche, Nnamdi, Benjamin, Ivor J., Wallrath, Lori L.
Publicado 2021

A Comparative Study of Drosophila and Human A-Type Lamins

por Schulze, Sandra R., Curio-Penny, Beatrice, Speese, Sean, Dialynas, George, Cryderman, Diane E., McDonough, Caitrin W., Nalbant, Demet, Petersen, Melissa, Budnik, Vivian, Geyer, Pamela K., Wallrath, Lori L.
Publicado 2009