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Lalit Kaurani
Lalit Kaurani
German Center for Neurodegenerative Diseases (DZNE)
Geverifieerd e-mailadres voor gwdg.de
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Innate immune memory in the brain shapes neurological disease hallmarks
AC Wendeln, K Degenhardt, L Kaurani, M Gertig, T Ulas, G Jain, ...
Nature 556 (7701), 332-338, 2018
7352018
Childhood trauma in schizophrenia: current findings and research perspectives
D Popovic, A Schmitt, L Kaurani, F Senner, S Papiol, B Malchow, ...
Frontiers in neuroscience 13, 422393, 2019
2022019
HDAC1 links early life stress to schizophrenia-like phenotypes
S Bahari-Javan, H Varbanov, R Halder, E Benito, L Kaurani, S Burkhardt, ...
Proceedings of the National Academy of Sciences 114 (23), E4686-E4694, 2017
1002017
KMT2A and KMT2B mediate memory function by affecting distinct genomic regions
C Kerimoglu, MS Sakib, G Jain, E Benito, S Burkhardt, V Capece, ...
Cell reports 20 (3), 538-548, 2017
932017
A combined miRNA–piRNA signature to detect Alzheimer’s disease
G Jain, A Stuendl, P Rao, T Berulava, T Pena Centeno, L Kaurani, ...
Translational psychiatry 9 (1), 250, 2019
902019
The diphenylpyrazole compound anle138b blocks Aβ channels and rescues disease phenotypes in a mouse model for amyloid pathology
A Martinez Hernandez, H Urbanke, AL Gillman, J Lee, S Ryazanov, ...
EMBO molecular medicine 10 (1), 32-47, 2018
792018
A microRNA signature that correlates with cognition and is a target against cognitive decline
MR Islam, L Kaurani, T Berulava, U Heilbronner, M Budde, TP Centeno, ...
EMBO molecular medicine 13 (11), e13659, 2021
352021
Conserved reduction of m6A RNA modifications during aging and neurodegeneration is linked to changes in synaptic transcripts
R Castro-Hernández, T Berulava, M Metelova, R Epple, T Peña Centeno, ...
Proceedings of the National Academy of Sciences 120 (9), e2204933120, 2023
242023
Genetic association and stress mediated down-regulation in trabecular meshwork implicates MPP7 as a novel candidate gene in primary open angle glaucoma
M Vishal, A Sharma, L Kaurani, G Alfano, S Mookherjee, K Narta, ...
BMC medical genomics 9, 1-10, 2016
192016
Engineered skeletal muscle recapitulates human muscle development, regeneration and dystrophy
M Shahriyari, MR Islam, SM Sakib, M Rinn, A Rika, D Krüger, L Kaurani, ...
Journal of Cachexia, Sarcopenia and Muscle 13 (6), 3106-3121, 2022
172022
Neuronal extracellular vesicles and associated microRNAs induce circuit connectivity downstream BDNF
A Antoniou, L Auderset, L Kaurani, E Sebastian, Y Zeng, M Allahham, ...
Cell reports 42 (2), 2023
162023
Interferon-driven brain phenotype in a mouse model of RNaseT2 deficient leukoencephalopathy
M Kettwig, K Ternka, K Wendland, DM Krüger, S Zampar, C Schob, ...
Nature Communications 12 (1), 6530, 2021
152021
H3 acetylation selectively promotes basal progenitor proliferation and neocortex expansion
C Kerimoglu, L Pham, AB Tonchev, MS Sakib, Y Xie, G Sokpor, PA Ulmke, ...
Science advances 7 (38), eabc6792, 2021
152021
TBK1 duplication is found in normal tension and not in high tension glaucoma patients of Indian origin
L Kaurani, M Vishal, J Ray, A Sen, K Ray, A Mukhopadhyay
Journal of genetics 95, 459-461, 2016
152016
Evaluation of genetic association of the INK4 locus with primary open angle glaucoma in East Indian population
M Vishal, A Sharma, L Kaurani, S Chakraborty, J Ray, A Sen, ...
Scientific Reports 4 (1), 5115, 2014
132014
Integrated multi-omics analysis reveals common and distinct dysregulated pathways for genetic subtypes of Frontotemporal Dementia
K Menden, M Francescatto, T Nyima, C Blauwendraat, A Dhingra, ...
bioRxiv, 2020.12. 01.405894, 2020
122020
Fusion transcripts in normal human cortex increase with age and show distinct genomic features for single cells and tissues
B Mehani, K Narta, D Paul, A Raj, D Kumar, A Sharma, L Kaurani, ...
Scientific Reports 10 (1), 1368, 2020
112020
Gene-rich large deletions are overrepresented in POAG patients of Indian and Caucasian origins
L Kaurani, M Vishal, D Kumar, A Sharma, B Mehani, C Sharma, ...
Investigative ophthalmology & visual science 55 (5), 3258-3264, 2014
102014
Postnatal expression of the lysine methyltransferase SETD1B is essential for learning and the regulation of neuron‐enriched genes
A Michurina, MS Sakib, C Kerimoglu, DM Krüger, L Kaurani, MR Islam, ...
The EMBO journal 41 (1), e106459, 2022
92022
Human engineered skeletal muscle of hypaxial origin from pluripotent stem cells with advanced function and regenerative capacity
M Shahriyari, MR Islam, MS Sakib, A Rika, D Krüger, L Kaurani, ...
bioRxiv, 2021.07. 12.452030, 2021
32021
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Artikelen 1–20