Jaiprakash Sharma

发表

Co-chaperone CHIP Stabilizes Aggregate-prone Malin, a Ubiquitin Ligase Mutated in Lafora Disease*

N. Jana, Sudheendra N. R. Rao, Ranjan Maity, 2009, The Journal of Biological Chemistry.

NADPH oxidase promotes Parkinsonian phenotypes by impairing autophagic flux in an mTORC1-independent fashion in a cellular model of Parkinson’s disease

J. Neilson, M. Sardiello, M. Palmieri, 2016, Scientific Reports.

Malin Regulates Wnt Signaling Pathway through Degradation of Dishevelled2*

N. Jana, Diptendu Mukherjee, Shalaka Mulherkar, 2012, The Journal of Biological Chemistry.

Capsaicin induces apoptosis through ubiquitin–proteasome system dysfunction

N. Jana, Ranjan Maity, Jaiprakash Sharma, 2010, Journal of cellular biochemistry.

Sequestration of chaperones and proteasome into Lafora bodies and proteasomal dysfunction induced by Lafora disease-associated mutations of malin.

S. Shankar, P. Satishchandra, N. Jana, 2010, Human molecular genetics.

Identification of a Peptide Inhibitor of the RPM-1 (cid:2) FSN-1 Ubiquitin Ligase Complex *

A. Gurney, Scott T. Baker, Jaiprakash Sharma, 2014 .

Neuronatin-mediated Aberrant Calcium Signaling and Endoplasmic Reticulum Stress Underlie Neuropathology in Lafora Disease*

S. Shankar, P. Satishchandra, N. Jana, 2013, The Journal of Biological Chemistry.

Disease Stress Underlie Neuropathology in Lafora Signaling and Endoplasmic Reticulum Neuronatin-mediated Aberrant Calcium Neurobiology :

S. Shankar, N. Jana, Sudheendra N. R. Rao, 2013 .

Lysosome biogenesis in health and disease

M. Sardiello, P. Lotfi, A. Ronza, 2018, Journal of neurochemistry.

E6-AP Promotes Misfolded Polyglutamine Proteins for Proteasomal Degradation and Suppresses Polyglutamine Protein Aggregation and Toxicity*

Amit Mishra, Nobuyuki Nukina, N. Nukina, 2008, Journal of Biological Chemistry.

Identification of a Peptide Inhibitor of the RPM-1·FSN-1 Ubiquitin Ligase Complex*

A. Gurney, Scott T. Baker, Jaiprakash Sharma, 2014, The Journal of Biological Chemistry.

A CLN6-CLN8 complex recruits lysosomal enzymes at the ER for Golgi transfer

R. Schekman, S. Jung, Rui Chen, 2019, bioRxiv.

CLN8 is an ER cargo receptor that regulates lysosome biogenesis

F. Santorelli, Laura Segatori, M. Sardiello, 2018, Nature Cell Biology.

Lafora disease ubiquitin ligase malin promotes proteasomal degradation of neuronatin and regulates glycogen synthesis

S. Shankar, P. Satishchandra, N. Jana, 2011, Neurobiology of Disease.

Lysosomes and Brain Health.

M. Sardiello, Alberto di Ronza, P. Lotfi, 2018, Annual review of neuroscience.

CLN8 is an ER cargo receptor that regulates lysosome biogenesis

Carolyn J. Adamski, F. Santorelli, Laura Segatori, 2018, Nature Cell Biology.

The ubiquitin ligase E6‐AP promotes degradation of α‐synuclein

N. Jana, Shalaka Mulherkar, Jaiprakash Sharma, 2009, Journal of neurochemistry.

Title: Bowel dysmotility and enteric neuron degeneration in lysosomal storage disease mice is prevented by gene therapy Short title: Treatment of enteric disease by gene therapy

J. Cooper, R. Heuckeroth, M. Sardiello, 2023 .

Calpain activity is negatively regulated by a KCTD7–Cullin-3 complex via non-degradative ubiquitination

Y. Goo, K. Tolias, M. Sardiello, 2023, Cell Discovery.