Biotinylation by antibody recognition—a method for proximity labeling von Bar, Daniel Z, Atkatsh, Kathleen, Tavarez, Urraca, Erdos, Michael R, Gruenbaum, Yosef, Collins, Francis S

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SARS-CoV-2 infection induces beta cell transdifferentiation von Tang, Xuming, Uhl, Skyler, Zhang, Tuo, Xue, Dongxiang, Li, Bo, Vandana, J. Jeya, Acklin, Joshua A., Bonnycastle, Lori L., Narisu, Narisu, Erdos, Michael R., Bram, Yaron, Chandar, Vasuretha, Chong, Angie Chi Nok, Lacko, Lauretta A., Min, Zaw, Lim, Jean K., Borczuk, Alain C., Xiang, Jenny, Naji, Ali, Collins, Francis S., Evans, Todd, Liu, Chengyang, tenOever, Benjamin R., Schwartz, Robert E., Chen, Shuibing

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A targeted antisense therapeutic approach for Hutchinson–Gilford progeria syndrome von Erdos, Michael R., Cabral, Wayne A., Tavarez, Urraca L., Cao, Kan, Gvozdenovic-Jeremic, Jelena, Narisu, Narisu, Zerfas, Patricia M., Crumley, Stacy, Boku, Yoseph, Hanson, Gunnar, Mourich, Dan V., Kole, Ryszard, Eckhaus, Michael A., Gordon, Leslie B., Collins, Francis S.

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Integrative analysis of gene expression, DNA methylation, physiological traits, and genetic variation in human skeletal muscle von Taylor, D. Leland, Jackson, Anne U., Narisu, Narisu, Hemani, Gibran, Erdos, Michael R., Chines, Peter S., Swift, Amy, Idol, Jackie, Didion, John P., Welch, Ryan P., Kinnunen, Leena, Saramies, Jouko, Lakka, Timo A., Laakso, Markku, Tuomilehto, Jaakko, Parker, Stephen C. J., Koistinen, Heikki A., Smith, George Davey, Boehnke, Michael, Scott, Laura J., Birney, Ewan, Collins, Francis S.

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Single-cell ATAC-Seq in human pancreatic islets and deep learning upscaling of rare cells reveals cell-specific type 2 diabetes regulatory signatures von Rai, Vivek, Quang, Daniel X., Erdos, Michael R., Cusanovich, Darren A., Daza, Riza M., Narisu, Narisu, Zou, Luli S., Didion, John P., Guan, Yuanfang, Shendure, Jay, Parker, Stephen C.J., Collins, Francis S.

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Recurrent de novo point mutations in lamin A cause Hutchinson-Gilford progeria syndrome von Collins, Francis S, Eriksson, Maria, Brown, W. Ted, Gordon, Leslie B, Glynn, Michael W, Singer, Joel, Scott, Laura, Erdos, Michael R, Robbins, Christiane M, Moses, Tracy Y, Berglund, Peter, Dutra, Amalia, Pak, Evgenia, Durkin, Sandra, Csoka, Antonei B, Boehnke, Michael, Glover, Thomas W

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Mutant Nuclear Lamin a Leads to Progressive Alterations of Epigenetic Control in Premature Aging von Shumaker, Dale K., Dechat, Thomas, Kohlmaier, Alexander, Adam, Stephen A., Bozovsky, Matthew R., Erdos, Michael R., Eriksson, Maria, Goldman, Anne E., Khuon, Satya, Collins, Francis S., Jenuwein, Thomas, Goldman, Robert D.

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The role of lamin B1 for the maintenance of nuclear structure and function von Camps, Jordi, Erdos, Michael R, Ried, Thomas

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Heritable Individual-Specific and Allele-Specific Chromatin Signatures in Humans von McDaniell, Ryan, Lee, Bum-Kyu, Song, Lingyun, Liu, Zheng, Boyle, Alan P., Erdos, Michael R., Scott, Laura J., Morken, Mario A., Kucera, Katerina S., Battenhouse, Anna, Keefe, Damian, Collins, Francis S., Willard, Huntington F., Lieb, Jason D., Furey, Terrence S., Crawford, Gregory E., lyer, Vishwanath R., Birney, Ewan

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Accumulation of Mutant Lamin A Causes Progressive Changes in Nuclear Architecture in Hutchinson-Gilford Progeria Syndrome von 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.

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lamin A protein isoform overexpressed in Hutchinson-Gilford progeria syndrome interferes with mitosis in progeria and normal cells von Cao, Kan, Capell, Brian C, Erdos, Michael R, Djabali, Karima, Collins, Francis S

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A Type 2 Diabetes-Associated Functional Regulatory Variant in a Pancreatic Islet Enhancer at the ADCY5 Locus von Roman, Tamara S, Cannon, Maren E, Vadlamudi, Swarooparani, Buchkovich, Martin L, Wolford, Brooke N, Welch, Ryan P, Morken, Mario A, Kwon, Grace J, Varshney, Arushi, Kursawe, Romy, Wu, Ying, Jackson, Anne U, Erdos, Michael R, Kuusisto, Johanna, Laakso, Markku, Scott, Laura J, Boehnke, Michael, Collins, Francis S, Parker, Stephen C J, Stitzel, Michael L, Mohlke, Karen L

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

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BoostMe accurately predicts DNA methylation values in whole-genome bisulfite sequencing of multiple human tissues von Zou, Luli S, Erdos, Michael R, Taylor, D Leland, Chines, Peter S, Varshney, Arushi, Parker, Stephen C J, Collins, Francis S, Didion, John P

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Characterization of the craniofacial abnormalities of the homozygous G608G progeria mouse model von Beeram, Indeevar, Cubria, Maria Belen, Kamalapathy, Pramod, Yeritsyan, Diana, Dubose, Amanda J., Razavi, Ahmad Hedayatzadeh, Nafisi, Nazanin, Erdos, Michael R., Snyder, Brian D., Cabral, Wayne A., Collins, Francis S., Nazarian, Ara

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Inhibiting Farnesylation of Progerin Prevents the Characteristic Nuclear Blebbing of Hutchinson-Gilford Progeria Syndrome von 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.

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farnesyltransferase inhibitor prevents both the onset and late progression of cardiovascular disease in a progeria mouse model von Capell, Brian C, Olive, Michelle, Erdos, Michael R, Cao, Kan, Faddah, Dina A, Tavarez, Urraca L, Conneely, Karen N, Qu, Xuan, San, Hong, Ganesh, Santhi K, Chen, Xiaoyan, Avallone, Hedwig, Kolodgie, Frank D, Virmani, Renu, Nabel, Elizabeth G, Collins, Francis S

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Progressive Vascular Smooth Muscle Cell Defects in a Mouse Model of Hutchinson-Gilford Progeria Syndrome von Varga, Renee, Eriksson, Maria, Erdos, Michael R., Olive, Michelle, Harten, Ingrid, Kolodgie, Frank, Capell, Brian C., Cheng, Jun, Faddah, Dina, Perkins, Stacie, Avallone, Hedwig, San, Hong, Qu, Xuan, Ganesh, Santhi, Gordon, Leslie B., Virmani, Renu, Wight, Thomas N., Nabel, Elizabeth G., Collins, Francis S.

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

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Association of Transcription Factor 7-Like 2 (TCF7L2) Variants With Type 2 Diabetes in a Finnish Sample von SCOTT, Laura J, BONNYCASTLE, Lori L, VALLE, Timo T, TUOMILEHTO, Jaakko, BERGMAN, Richard N, MOHLKE, Karen L, COLLINS, Francis S, BOEHNKE, Michael, WILLER, Cristen J, SPRAU, Andrew G, JACKSON, Anne U, NARISU, Narisu, DUREN, William L, CHINES, Peter S, STRINGHAM, Heather M, ERDOS, Michael R

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