Anne L. Calof

University of California, Irvine, Irvine, CA 
Neuroscience Biology
"Anne Calof"
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Newkirk DA, Chen YY, Chien R, et al. (2017) The effect of Nipped-B-like (Nipbl) haploinsufficiency on genome-wide cohesin binding and target gene expression: modeling Cornelia de Lange syndrome. Clinical Epigenetics. 9: 89
Santos R, Kawauchi S, Jacobs RE, et al. (2016) Conditional Creation and Rescue of Nipbl-Deficiency in Mice Reveals Multiple Determinants of Risk for Congenital Heart Defects. Plos Biology. 14: e2000197
Lopez-Burks ME, Santos R, Kawauchi S, et al. (2016) Genetic enhancement of limb defects in a mouse model of Cornelia de Lange syndrome. American Journal of Medical Genetics. Part C, Seminars in Medical Genetics
Kawauchi S, Santos R, Muto A, et al. (2016) Using mouse and zebrafish models to understand the etiology of developmental defects in Cornelia de Lange Syndrome. American Journal of Medical Genetics. Part C, Seminars in Medical Genetics
Kunche S, Yan H, Calof AL, et al. (2016) Feedback, Lineages and Self-Organizing Morphogenesis. Plos Computational Biology. 12: e1004814
Chiang M, Hallman S, Cinquin A, et al. (2015) Analysis of in vivo single cell behavior by high throughput, human-in-the-loop segmentation of three-dimensional images. Bmc Bioinformatics. 16: 397
Kline AD, Calof AL, Lander AD, et al. (2015) Clinical, developmental and molecular update on Cornelia de Lange syndrome and the cohesin complex: Abstracts from the 2014 Scientific and Educational Symposium. American Journal of Medical Genetics. Part A. 167: 1179-92
Muto A, Ikeda S, Lopez-Burks ME, et al. (2014) Nipbl and mediator cooperatively regulate gene expression to control limb development. Plos Genetics. 10: e1004671
Kline AD, Calof AL, Schaaf CA, et al. (2014) Cornelia de Lange syndrome: further delineation of phenotype, cohesin biology and educational focus, 5th Biennial Scientific and Educational Symposium abstracts. American Journal of Medical Genetics. Part A. 164: 1384-93
Visnes T, Giordano F, Kuznetsova A, et al. (2014) Localisation of the SMC loading complex Nipbl/Mau2 during mammalian meiotic prophase I. Chromosoma. 123: 239-52
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