Normal myofibrillar development followed by progressive sarcomeric disruption with actin accumulations in a mouse Cfl2 knockout demonstrates requirement of cofilin-2 for muscle mai...

nork Agrawal, Pankaj B., Joshi, Mugdha, Savic, Talia, Chen, Zoe, Beggs, Alan H.
Argitaratua 2012

Skeletal Muscle MicroRNA and Messenger RNA Profiling in Cofilin-2 Deficient Mice Reveals Cell Cycle Dysregulation Hindering Muscle Regeneration

nork Morton, Sarah U., Joshi, Mugdha, Savic, Talia, Beggs, Alan H., Agrawal, Pankaj B.
Argitaratua izan da PLoS One (2015)

Knockin mouse model of the human CFL2 p.A35T mutation results in a unique splicing defect and severe myopathy phenotype

nork Rosen, Samantha M, Joshi, Mugdha, Hitt, Talia, Beggs, Alan H, Agrawal, Pankaj B
Argitaratua izan da Hum Mol Genet (2020)

The role of PhD faculty in advancing research in departments of surgery

nork Bell, Teresa M., Valsangkar, Nakul, Joshi, Mugdha, Mayo, John, Blanton, Casi, Zimmers, Teresa A., Torbeck, Laura, Koniaris, Leonidas G.
Argitaratua izan da Ann Surg (2017)

Development of Soft Tissue Sarcomas in Ribosomal Proteins L5 and S24 Heterozygous Mice

nork Kazerounian, Shideh, Ciarlini, Pedro D.S.C., Yuan, Daniel, Ghazvinian, Roxanne, Alberich-Jorda, Meritxell, Joshi, Mugdha, Zhang, Hong, Beggs, Alan H., Gazda, Hanna T.
Argitaratua izan da J Cancer (2016)

Whole genome sequencing identifies SCN2A mutation in monozygotic twins with Ohtahara Syndrome and unique neuropathological findings

nork Touma, Marlin, Joshi, Mugdha, Connolly, Meghan C., Grant, P. Ellen, Hansen, Anne R., Khwaja, Omar, Berry, Gerard T., Kinney, Hannah C., Poduri, Annapurna, Agrawal, Pankaj B.
Argitaratua 2013

Determining the Drivers of Academic Success in Surgery: An Analysis of 3,850 Faculty

nork Valsangkar, Nakul P., Zimmers, Teresa A., Kim, Bradford J., Blanton, Casi, Joshi, Mugdha M., Bell, Teresa M., Nakeeb, Attila, Dunnington, Gary L., Koniaris, Leonidas G.
Argitaratua izan da PLoS One (2015)

Expanding the Phenotype Associated With the NEFL Mutation Neuromuscular Disease in a Family with Overlapping Myopathic and Neurogenic Findings

nork Agrawal, Pankaj B., Joshi, Mugdha, Marinakis, Nicholas S., Schmitz-Abe, Klaus, Ciarlini, Pedro D. S. C., Sargent, Jane C., Markianos, Kyriacos, De Girolami, Umberto, Chad, David A., Beggs, Alan H.
Argitaratua izan da JAMA Neurol (2014)

Cofilin-2 Phosphorylation and Sequestration In Myocardial Aggregates: Novel Pathogenetic Mechanisms For Idiopathic Dilated Cardiomyopathy

nork Subramanian, Khaushik, Gianni, Davide, Balla, Cristina, Assenza, Gabriele Egidy, Joshi, Mugdha, Semigran, Marc J., Macgillivray, Thomas E., Van Eyk, Jennifer E., Agnetti, Giulio, Paolocci, Nazareno, Bamburg, James R., Agrawal, Pankaj B., del Monte, Federica
Argitaratua izan da J Am Coll Cardiol (2015)

Mutations in the substrate binding glycine-rich loop of the mitochondrial processing peptidase-α protein (PMPCA) cause a severe mitochondrial disease

nork Joshi, Mugdha, Anselm, Irina, Shi, Jiahai, Bale, Tejus A., Towne, Meghan, Schmitz-Abe, Klaus, Crowley, Laura, Giani, Felix C., Kazerounian, Shideh, Markianos, Kyriacos, Lidov, Hart G., Folkerth, Rebecca, Sankaran, Vijay G., Agrawal, Pankaj B.
Argitaratua izan da Cold Spring Harb Mol Case Stud (2016)

A compound heterozygous mutation in GPD1 causes hepatomegaly, steatohepatitis, and hypertriglyceridemia

nork Joshi, Mugdha, Eagan, Jacqueline, Desai, Nirav K, Newton, Stephanie A, Towne, Meghan C, Marinakis, Nicholas S, Esteves, Kristyn M, De Ferranti, Sarah, Bennett, Michael J, McIntyre, Adam, Beggs, Alan H, Berry, Gerard T, Agrawal, Pankaj B
Argitaratua 2014

SPEG Interacts with Myotubularin, and Its Deficiency Causes Centronuclear Myopathy with Dilated Cardiomyopathy

nork Agrawal, Pankaj B., Pierson, Christopher R., Joshi, Mugdha, Liu, Xiaoli, Ravenscroft, Gianina, Moghadaszadeh, Behzad, Talabere, Tiffany, Viola, Marissa, Swanson, Lindsay C., Haliloğlu, Göknur, Talim, Beril, Yau, Kyle S., Allcock, Richard J.N., Laing, Nigel G., Perrella, Mark A., Beggs, Alan H.
Argitaratua 2014