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 |
0.493 |
|
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 |
0.445 |
|
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 |
0.634 |
|
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 |
0.777 |
|
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 |
0.767 |
|
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 |
0.763 |
|
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 |
0.638 |
|
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 |
0.785 |
|
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 |
0.685 |
|
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 |
|
Low-probability matches (unlikely to be authored by this person) |
2015 |
Smith MA, Michael R, Aravindan RG, Dash S, Shah SI, Galileo DS, Martin-DeLeon PA. Anatase titanium dioxide nanoparticles in mice: evidence for induced structural and functional sperm defects after short-, but not long-, term exposure. Asian Journal of Andrology. 17: 261-8. PMID 25370207 DOI: 10.4103/1008-682X.143247 |
0.264 |
|
2020 |
Dash S, Trainor PA. The development, patterning and evolution of neural crest cell differentiation into cartilage and bone. Bone. 137: 115409. PMID 32417535 DOI: 10.1016/J.Bone.2020.115409 |
0.202 |
|
2023 |
Dash S, Trainor PA. Correction: Nucleolin loss of function leads to aberrant Fibroblast Growth Factor signaling and craniofacial anomalies. Development (Cambridge, England). 150. PMID 36971306 DOI: 10.1242/dev.201584 |
0.125 |
|
Hide low-probability matches. |