☰

Soma Dash - Publications

Affiliations: 
2013-2018 Stowers Instistute for Medical Research 
Tree Info Similar researchers PubMed Report error

14 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2023 Dash S, Lamb MC, Lange JJ, McKinney MC, Tsuchiya D, Guo F, Zhao X, Corbin TJ, Kirkman M, Delventhal K, Moore EL, McKinney S, Shiang R, Trainor PA. rRNA transcription is integral to phase separation and maintenance of nucleolar structure. Plos Genetics. 19: e1010854. PMID 37639467 DOI: 10.1371/journal.pgen.1010854  0.44
2022 Falcon KT, Watt KEN, Dash S, Zhao R, Sakai D, Moore EL, Fitriasari S, Childers M, Sardiu ME, Swanson S, Tsuchiya D, Unruh J, Bugarinovic G, Li L, Shiang R, et al. Dynamic regulation and requirement for ribosomal RNA transcription during mammalian development. Proceedings of the National Academy of Sciences of the United States of America. 119: e2116974119. PMID 35881792 DOI: 10.1073/pnas.2116974119  0.492
2022 Dash S, Trainor PA. Nucleolin loss of function leads to aberrant Fibroblast Growth Factor signaling and craniofacial anomalies. Development (Cambridge, England). 149. PMID 35762670 DOI: 10.1242/dev.200349  0.424
2020 Dash S, Bhatt S, Sandell LL, Seidel CW, Ahn Y, Krumlauf RE, Trainor PA. The Mediator Subunit, Med23 Is Required for Embryonic Survival and Regulation of Canonical WNT Signaling During Cranial Ganglia Development. Frontiers in Physiology. 11: 531933. PMID 33192541 DOI: 10.3389/fphys.2020.531933  0.35
2020 Dash S, Bhatt S, Falcon KT, Sandell LL, Trainor PA. Med23 Regulates Sox9 Expression during Craniofacial Development. Journal of Dental Research. 22034520969109. PMID 33155500 DOI: 10.1177/0022034520969109  0.444
2020 Barnum CE, Al Saai S, Patel SD, Cheng C, Anand D, Xu X, Dash S, Siddam AD, Glazewski L, Paglione E, Polson SW, Chuma S, Mason RW, Wei S, Batish M, et al. The Tudor-domain protein TDRD7, mutated in congenital cataract, controls the heat shock protein HSPB1 (HSP27) and lens fiber cell morphology. Human Molecular Genetics. PMID 32420594 DOI: 10.1093/Hmg/Ddaa096  0.633
2019 Dash S, Brastrom LK, Patel SD, Scott CA, Slusarski DC, Lachke SA. The master transcription factor SOX2, mutated in anophthalmia/microphthalmia, is post-transcriptionally regulated by the conserved RNA-binding protein RBM24 in vertebrate eye development. Human Molecular Genetics. PMID 31814023 DOI: 10.1093/Hmg/Ddz278  0.776
2018 Budak G, Dash S, Srivastava R, Lachke SA, Janga SC. Express: A database of transcriptome profiles encompassing known and novel transcripts across multiple development stages in eye tissues. Experimental Eye Research. PMID 29337142 DOI: 10.1016/J.Exer.2018.01.009  0.766
2017 Srivastava R, Budak G, Dash S, Lachke SA, Janga SC. Transcriptome analysis of developing lens reveals abundance of novel transcripts and extensive splicing alterations. Scientific Reports. 7: 11572. PMID 28912564 DOI: 10.1038/S41598-017-10615-4  0.762
2016 Dash S, Siddam AD, Barnum CE, Janga SC, Lachke SA. RNA-binding proteins in eye development and disease: implication of conserved RNA granule components. Wiley Interdisciplinary Reviews. Rna. PMID 27133484 DOI: 10.1002/Wrna.1355  0.637
2015 Dash S, Dang CA, Beebe DC, Lachke SA. Deficiency of the RNA binding protein caprin2 causes lens defects and features of peters anomaly. Developmental Dynamics : An Official Publication of the American Association of Anatomists. 244: 1313-27. PMID 26177727 DOI: 10.1002/Dvdy.24303  0.784
2015 Agrawal SA, Anand D, Siddam AD, Kakrana A, Dash S, Scheiblin DA, Dang CA, Terrell AM, Waters SM, Singh A, Motohashi H, Yamamoto M, Lachke SA. Compound mouse mutants of bZIP transcription factors Mafg and Mafk reveal a regulatory network of non-crystallin genes associated with cataract. Human Genetics. 134: 717-35. PMID 25896808 DOI: 10.1007/S00439-015-1554-5  0.683
2015 Dash S, Dang CA, Beebe DC, Lachke SA. Deficiency of the RNA binding protein caprin2 causes lens defects and features of peters anomaly Developmental Dynamics. DOI: 10.1002/dvdy.24303  0.683
2014 Modelski MJ, Menlah G, Wang Y, Dash S, Wu K, Galileo DS, Martin-DeLeon PA. Hyaluronidase 2: a novel germ cell hyaluronidase with epididymal expression and functional roles in mammalian sperm. Biology of Reproduction. 91: 109. PMID 25232017 DOI: 10.1095/Biolreprod.113.115857  0.321
Show low-probability matches.