Articles with public access mandates - Deepak Srivastava - US National Institutes of HealthLearn more
NoteFor this mandate, articles should be available from specific locations.
OverallNIHMRCAHAHHMIWellcomeNIHRNSFCIHRState of CalifoniaSNSFBBSRCAlzheimers's UKDamon Runyon Cancer Research FoundationRoyal Society UKICARNational Centre for the Replacement, Refinement and Reduction of Animals in Research, UKDFGEuropean CommissionAutism Speaks Inc, USADoDLeducq Foundation, USADOEHSFNSFCDSTDoris Duke Charitable FoundationARCNHMRCINSERMOTKACSIRFormasSwedish Research CouncilA*StarBMBFNKFIGovernment of ItalyUK Research & Innovation
Not available based on mandate: 33
Thymosin beta-4 denotes new directions towards developing prosperous anti-aging regenerative therapies
I Bock-Marquette, K Maar, S Maar, B Lippai, G Faskerti, F Gallyas Jr, ...
International Immunopharmacology 116, 109741, 2023
Single Cell Epigenetics Reveal Cell-Cell Communication Networks in Normal and Abnormal Cardiac Morphogenesis
SS Ranade, S Whalen, I Zlatanova, T Nishino, B van Soldt, L Ye, ...
bioRxiv, 2022.07. 25.501458, 2022
Cellular cross-talk in heart repair
D Srivastava
Science 376 (6599), 1271-1272, 2022
An oligogenic inheritance test detects risk genes and their interactions in congenital heart defects and developmental comorbidities
M Pittman, K Lee, D Srivastava, KS Pollard
bioRxiv, 2022.04. 08.487704, 2022
The maternal X chromosome impairs cognition and accelerates brain aging through epigenetic modulation in female mice
S Abdulai-Saiku, S Gupta, D Wang, AJ Moreno, Y Huang, D Srivastava, ...
bioRxiv, 2022.03. 09.483691, 2022
Ebstein’s anomaly: review of arrhythmia types and morphogenesis of the anomaly
BJ He, AF Merriman, I Cakulev, BS Stambler, D Srivastava, ...
Clinical Electrophysiology 7 (9), 1198-1206, 2021
Integration of protein interactome networks with congenital heart disease variants reveals candidate disease genes
B Gonzalez-Teran, M Pittman, F Felix, D Richmond-Buccola, R Thomas, ...
bioRxiv, 2021.01. 05.423837, 2021
Transient Cell Cycle Induction in Cardiomyocytes to Treat Ischemic Heart Failure
R Abouleisa, Q Ou, XL Tang, M Solanki, Y Guo, Y Nong, L Mcnally, ...
CSDE1 is a post-transcriptional regulator of the LDL receptor
GA Smith, A Padmanabhan, BH Lau, A Pampana, L Li, Y Clara Lee, ...
bioRxiv, 2020.08. 03.235028, 2020
A transcriptional switch governing fibroblast plasticity underlies reversibility of chronic heart disease
M Alexanian, PF Przytycki, R Micheletti, A Padmanabhan, L Ye, ...
BioRxiv, 2020.07. 21.214874, 2020
Brain‐synthesized oestrogens regulate cortical migration in a sexually divergent manner
KJ Sellers, MCS Denley, A Saito, EM Foster, I Salgarella, A Delogu, ...
European Journal of Neuroscience 52 (1), 2646-2663, 2020
Schizophrenia risk from locus-specific human endogenous retroviruses
RRR Duarte, ML Bendall, M de Mulder, CE Ormsby, GA Beckerle, ...
bioRxiv, 798017, 2019
Early post-zygotic mutations contribute to congenital heart disease
A Hsieh, SU Morton, JAL Willcox, JM Gorham, AC Tai, H Qi, S DePalma, ...
BioRxiv, 733105, 2019
Unique Transcription Factor Functions Regulate Epigenetic and Transcriptional Dynamics During Cardiac Reprogramming
NR Stone, CA Gifford, R Thomas, KJB Pratt, K Samse-Knapp, ...
bioRxiv, 642900, 2019
Comparative analysis of diverse cell states establishes an epigenetic basis for inferring regulatory genes governing cell identity
WJ Shim, E Sinniah, J Xu, B Vitrinel, M Alexanian, G Andreoletti, S Shen, ...
bioRxiv, 635516, 2019
EPAC2 is required for corticotropin-releasing hormone-mediated spine loss
Z Xie, P Penzes, DP Srivastava
bioRxiv, 607598, 2019
Loss of EPAC2 results in altered synaptic composition of dendritic spines and excitatory and inhibitory balance
KA Jones, M Sumiya, KM Woolfrey, DP Srivastava, P Penzes
bioRxiv, 526772, 2019
Psychiatric risk gene NT5C2 regulates protein translation in human neural progenitor cells
RRR Duarte, ND Bachtel, MC Côtel, SH Lee, S Selvackadunco, ...
bioRxiv, 468546, 2018
Single-cell transcriptome analysis during cardiogenesis reveals basis for organ level developmental anomalies
TY de Soysa, SS Ranade, S Okawa, S Ravichandran, Y Huang, ...
bioRxiv, 365734, 2018
Oligogenic inheritance of congenital heart disease involving a NKX2-5 modifier
CA Gifford, SS Ranade, R Samarakoon, HT Salunga, TY de Soysa, ...
bioRxiv, 266726, 2018
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