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Biochimica Et Biophysica Acta. Molecular Cell Research|March 29, 2025
Loss of non-muscle myosin II Zipper leads to apoptosis-induced compensatory proliferation in DrosophilaDipti Verma, Bappi Sarkar, Jyoti Singh, et al.
Biochimica Et Biophysica Acta|May 28, 2014
dLin52 is crucial for dE2F and dRBF mediated transcriptional regulation of pro-apoptotic gene hidPradeep Kumar Bhaskar, Satya Surabhi, Bipin Kumar Tripathi, et al.
Cell Death & Disease|April 7, 2021
Maheshvara regulates JAK/STAT signaling by interacting and stabilizing hopscotch transcripts which leads to apoptosis in Drosophila melanogasterBhawana Maurya, Satya Surabhi, Rituparna Das, et al.
American Journal of Medical Genetics. Part A|June 15, 2023
Identification and molecular characterization of two recurrent missense mutations in the RS1 gene in two families with X-linked retinoschisis from North IndiaSouradip Chatterjee, Shashank Gupta, Laxmi Kirola, et al.
Cellular Signalling|May 19, 2018
Deltex interacts with Eiger and consequently influences the cell death in Drosophila melanogasterDebdeep Dutta, Ankita Singh, Maimuna Sali Paul, et al.
Gene|January 6, 2022
Whole exome sequencing identifies a novel splice-site mutation in IMPG2 gene causing Stargardt-like juvenile macular dystrophy in a north Indian familySouradip Chatterjee, Shashank Gupta, Vidya Nair Chaudhry, et al.
Current Biology : CB|February 20, 2004
The spinocerebellar ataxia 8 noncoding RNA causes neurodegeneration and associates with staufen in DrosophilaMousumi Mutsuddi, Cameron M Marshall, Kellie A Benzow, et al.
G3 (Bethesda, Md.)|January 26, 2018
Pleiotropic Functions of the Chromodomain-Containing Protein Hat-trick During Oogenesis in <i>Drosophila melanogaster</i>Ankita Singh, Debdeep Dutta, Maimuna Sali Paul, et al.
Open Biology|April 29, 2025
Notch and LIM-homeodomain protein Arrowhead regulate each other in a feedback mechanism to play a role in wing and neuronal development in <i>Drosophila</i>Jyoti Singh, Dipti Verma, Bappi Sarkar, et al.
Genetics|April 2, 2005
Using Drosophila to decipher how mutations associated with human branchio-oto-renal syndrome and optical defects compromise the protein tyrosine phosphatase and transcriptional functions of eyes absentMousumi Mutsuddi, Benjamin Chaffee, Justin Cassidy, et al.
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