The role of lamin B1 for the maintenance of nuclear structure and function

door Camps, Jordi, Erdos, Michael R, Ried, Thomas
Gepubliceerd in Nucleus (2015)

A lamin A protein isoform overexpressed in Hutchinson–Gilford progeria syndrome interferes with mitosis in progeria and normal cells

door Cao, Kan, Capell, Brian C., Erdos, Michael R., Djabali, Karima, Collins, Francis S.
Gepubliceerd in 2007

Motif signatures in stretch enhancers are enriched for disease-associated genetic variants

door Quang, Daniel X, Erdos, Michael R, Parker, Stephen C J, Collins, Francis S
Gepubliceerd in Epigenetics Chromatin (2015)

Biotinylation by antibody recognition - A method for proximity labeling

door Bar, Daniel Z, Atkatsh, Kathleen, Tavarez, Urraca, Erdos, Michael R, Gruenbaum, Yosef, Collins, Francis S
Gepubliceerd in Nat Methods (2017)

Human BRCA1 inhibits growth in yeast: Potential use in diagnostic testing

door Humphrey, Jeffrey S., Salim, Ali, Erdos, Michael R., Collins, Francis S., Brody, Lawrence C., Klausner, Richard D.
Gepubliceerd in 1997

Loss of lamin B1 results in prolongation of S phase and decondensation of chromosome territories

door Camps, Jordi, Wangsa, Darawalee, Falke, Martin, Brown, Markus, Case, Chanelle M., Erdos, Michael R., Ried, Thomas
Gepubliceerd in 2014

Global genome splicing analysis reveals an increased number of alternatively spliced genes with aging

door Rodríguez, Sofía A., Grochová, Diana, McKenna, Tomás, Borate, Bhavesh, Trivedi, Niraj S., Erdos, Michael R., Eriksson, Maria
Gepubliceerd in Aging Cell (2015)

Everolimus rescues multiple cellular defects in laminopathy-patient fibroblasts

door DuBose, Amanda J., Lichtenstein, Stephen T., Petrash, Noreen M., Erdos, Michael R., Gordon, Leslie B., Collins, Francis S.
Gepubliceerd in Proc Natl Acad Sci U S A (2018)

Analysis of somatic mutations identifies signs of selection during in vitro aging of primary dermal fibroblasts

door Narisu, Narisu, Rothwell, Rebecca, Vrtačnik, Peter, Rodríguez, Sofía, Didion, John, Zöllner, Sebastian, Erdos, Michael R., Collins, Francis S., Eriksson, Maria
Gepubliceerd in Aging Cell (2019)

Addressing Bias in Small RNA Library Preparation for Sequencing: A New Protocol Recovers MicroRNAs that Evade Capture by Current Methods

door Baran-Gale, Jeanette, Kurtz, C. Lisa, Erdos, Michael R., Sison, Christina, Young, Alice, Fannin, Emily E., Chines, Peter S., Sethupathy, Praveen
Gepubliceerd in Front Genet (2015)

Progerin and telomere dysfunction collaborate to trigger cellular senescence in normal human fibroblasts

door Cao, Kan, Blair, Cecilia D., Faddah, Dina A., Kieckhaefer, Julia E., Olive, Michelle, Erdos, Michael R., Nabel, Elizabeth G., Collins, Francis S.
Gepubliceerd in 2011

BoostMe accurately predicts DNA methylation values in whole-genome bisulfite sequencing of multiple human tissues

door Zou, Luli S., Erdos, Michael R., Taylor, D. Leland, Chines, Peter S., Varshney, Arushi, Parker, Stephen C. J., Collins, Francis S., Didion, John P.
Gepubliceerd in BMC Genomics (2018)

Single-cell transcriptomics from human pancreatic islets: sample preparation matters

door Bonnycastle, Lori L, Gildea, Derek E, Yan, Tingfen, Narisu, Narisu, Swift, Amy J, Wolfsberg, Tyra G, Erdos, Michael R, Collins, Francis S
Gepubliceerd in Biol Methods Protoc (2019)

Correlated alterations in genome organization, histone methylation, and DNA–lamin A/C interactions in Hutchinson-Gilford progeria syndrome

door McCord, Rachel Patton, Nazario-Toole, Ashley, Zhang, Haoyue, Chines, Peter S., Zhan, Ye, Erdos, Michael R., Collins, Francis S., Dekker, Job, Cao, Kan
Gepubliceerd in 2013

High-throughput screening for evidence of association by using mass spectrometry genotyping on DNA pools

door Mohlke, Karen L., Erdos, Michael R., Scott, Laura J., Fingerlin, Tasha E., Jackson, Anne U., Silander, Kaisa, Hollstein, Pablo, Boehnke, Michael, Collins, Francis S.
Gepubliceerd in 2002

DNase-chip: a high-resolution method to identify DNase I hypersensitive sites using tiled microarrays

door Crawford, Gregory E, Davis, Sean, Scacheri, Peter C, Renaud, Gabriel, Halawi, Mohamad J, Erdos, Michael R, Green, Roland, Meltzer, Paul S, Wolfsberg, Tyra G, Collins, Francis S
Gepubliceerd in 2006

Accumulation of mutant lamin A causes progressive changes in nuclear architecture in Hutchinson–Gilford progeria syndrome

door Goldman, Robert D., Shumaker, Dale K., Erdos, Michael R., Eriksson, Maria, Goldman, Anne E., Gordon, Leslie B., Gruenbaum, Yosef, Khuon, Satya, Mendez, Melissa, Varga, Renée, Collins, Francis S.
Gepubliceerd in 2004

Multiple Loci Associated with Renal Function in African Americans

door Shriner, Daniel, Herbert, Alan, Doumatey, Ayo P., Zhou, Jie, Huang, Hanxia, Erdos, Michael R., Chen, Guanjie, Gerry, Norman P., Christman, Michael F., Adeyemo, Adebowale, Rotimi, Charles N.
Gepubliceerd in 2012

Inhibiting farnesylation of progerin prevents the characteristic nuclear blebbing of Hutchinson-Gilford progeria syndrome

door Capell, Brian C., Erdos, Michael R., Madigan, James P., Fiordalisi, James J., Varga, Renee, Conneely, Karen N., Gordon, Leslie B., Der, Channing J., Cox, Adrienne D., Collins, Francis S.
Gepubliceerd in 2005

A progeria mutation reveals functions for lamin A in nuclear assembly, architecture, and chromosome organization

door Taimen, Pekka, Pfleghaar, Katrin, Shimi, Takeshi, Möller, Dorothee, Ben-Harush, Kfir, Erdos, Michael R., Adam, Stephen A., Herrmann, Harald, Medalia, Ohad, Collins, Francis S., Goldman, Anne E., Goldman, Robert D.
Gepubliceerd in 2009