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Margot E. Bowen, Ph.D. - Publications

Affiliations: 
2014 Biology: Medical Sciences, Division of Harvard University, Cambridge, MA, United States 
Area:
Genetics, Human Development
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16 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
2019 Lanni JS, Peal D, Ekstrom L, Chen H, Stanclift C, Bowen ME, Mercado A, Gamba G, Kahle KT, Harris MP. Integrated K+ channel and K+Cl- cotransporter function are required for the coordination of size and proportion during development. Developmental Biology. PMID 31472116 DOI: 10.1016/J.Ydbio.2019.08.016  0.382
2019 Bowen ME, McClendon J, Long HK, Sorayya A, Van Nostrand JL, Wysocka J, Attardi LD. The Spatiotemporal Pattern and Intensity of p53 Activation Dictates Phenotypic Diversity in p53-Driven Developmental Syndromes. Developmental Cell. PMID 31178404 DOI: 10.1016/J.Devcel.2019.05.015  0.342
2019 Jacobs SBR, Van Nostrand JL, Bowen ME, Baker JC, Attardi LD. Siva plays a critical role in mouse embryonic development. Cell Death and Differentiation. PMID 31164717 DOI: 10.1038/S41418-019-0358-X  0.394
2019 Bowen ME, Attardi LD. The role of p53 in developmental syndromes. Journal of Molecular Cell Biology. PMID 30624728 DOI: 10.1093/Jmcb/Mjy087  0.435
2018 Durruthy-Durruthy R, Sperry ED, Bowen ME, Attardi LD, Heller S, Martin DM. Single Cell Transcriptomics Reveal Abnormalities in Neurosensory Patterning of the Mutant Mouse Ear. Frontiers in Genetics. 9: 473. PMID 30459807 DOI: 10.3389/Fgene.2018.00473  0.405
2018 Zuo C, Wang L, Kamalesh RM, Bowen ME, Moore DC, Dooner MS, Reginato AM, Wu Q, Schorl C, Song Y, Warman ML, Neel BG, Ehrlich MG, Yang W. SHP2 regulates skeletal cell fate by modifying SOX9 expression and transcriptional activity. Bone Research. 6: 12. PMID 29644115 DOI: 10.1038/S41413-018-0013-Z  0.535
2018 Calo E, Gu B, Bowen ME, Aryan F, Zalc A, Liang J, Flynn RA, Swigut T, Chang HY, Attardi LD, Wysocka J. Tissue-selective effects of nucleolar stress and rDNA damage in developmental disorders. Nature. PMID 29364875 DOI: 10.1038/Nature25449  0.396
2017 Van Nostrand JL, Bowen ME, Vogel H, Barna M, Attardi LD. The p53 family members have distinct roles during mammalian embryonic development. Cell Death and Differentiation. PMID 28211873 DOI: 10.1038/Cdd.2016.128  0.358
2014 Bowen ME, Ayturk UM, Kurek KC, Yang W, Warman ML. SHP2 regulates chondrocyte terminal differentiation, growth plate architecture and skeletal cell fates. Plos Genetics. 10: e1004364. PMID 24875294 DOI: 10.1371/Journal.Pgen.1004364  0.571
2013 Henke K, Bowen ME, Harris MP. Identification of mutations in zebrafish using next-generation sequencing. Current Protocols in Molecular Biology / Edited by Frederick M. Ausubel ... [Et Al.]. 104: Unit 7.13. PMID 24510885 DOI: 10.1002/0471142727.Mb0713S104  0.389
2013 Kedlaya R, Veera S, Horan DJ, Moss RE, Ayturk UM, Jacobsen CM, Bowen ME, Paszty C, Warman ML, Robling AG. Sclerostin inhibition reverses skeletal fragility in an Lrp5-deficient mouse model of OPPG syndrome. Science Translational Medicine. 5: 211ra158. PMID 24225945 DOI: 10.1126/Scitranslmed.3006627  0.541
2013 Henke K, Bowen ME, Harris MP. Perspectives for identification of mutations in the zebrafish: making use of next-generation sequencing technologies for forward genetic approaches. Methods (San Diego, Calif.). 62: 185-96. PMID 23748111 DOI: 10.1016/J.Ymeth.2013.05.015  0.435
2013 Adams A, McBratney-Owen B, Newby B, Bowen ME, Olsen BR, Warman ML. Presphenoidal synchondrosis fusion in DBA/2J mice. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 24: 54-62. PMID 23179633 DOI: 10.1007/S00335-012-9437-8  0.488
2012 Kurek KC, Luks VL, Ayturk UM, Alomari AI, Fishman SJ, Spencer SA, Mulliken JB, Bowen ME, Yamamoto GL, Kozakewich HP, Warman ML. Somatic mosaic activating mutations in PIK3CA cause CLOVES syndrome. American Journal of Human Genetics. 90: 1108-15. PMID 22658544 DOI: 10.1016/J.Ajhg.2012.05.006  0.58
2012 Bowen ME, Henke K, Siegfried KR, Warman ML, Harris MP. Efficient mapping and cloning of mutations in zebrafish by low-coverage whole-genome sequencing. Genetics. 190: 1017-24. PMID 22174069 DOI: 10.1534/Genetics.111.136069  0.575
2011 Bowen ME, Boyden ED, Holm IA, Campos-Xavier B, Bonafé L, Superti-Furga A, Ikegawa S, Cormier-Daire V, Bovée JV, Pansuriya TC, de Sousa SB, Savarirayan R, Andreucci E, Vikkula M, Garavelli L, et al. Loss-of-function mutations in PTPN11 cause metachondromatosis, but not Ollier disease or Maffucci syndrome. Plos Genetics. 7: e1002050. PMID 21533187 DOI: 10.1371/Journal.Pgen.1002050  0.574
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