MARY DICKINSON to Female
This is a "connection" page, showing publications MARY DICKINSON has written about Female.
Connection Strength
0.229
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Three-dimensional microCT imaging of mouse development from early post-implantation to early postnatal stages. Dev Biol. 2016 11 15; 419(2):229-236.
Score: 0.021
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A specialized microvascular domain in the mouse neural stem cell niche. PLoS One. 2013; 8(1):e53546.
Score: 0.017
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In vivo imaging of the developing mouse embryonic vasculature. Methods Mol Biol. 2012; 872:205-15.
Score: 0.015
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The effects of hemodynamic force on embryonic development. Microcirculation. 2010 Apr; 17(3):164-78.
Score: 0.014
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Imaging mouse embryonic development. Methods Enzymol. 2010; 476:329-49.
Score: 0.013
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Live imaging of blood flow in mammalian embryos using Doppler swept-source optical coherence tomography. J Biomed Opt. 2008 Nov-Dec; 13(6):060506.
Score: 0.012
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Multimodal imaging of mouse development: tools for the postgenomic era. Dev Dyn. 2006 Sep; 235(9):2386-400.
Score: 0.011
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A comprehensive atlas of AAV tropism in the mouse. Mol Ther. 2025 Mar 05; 33(3):1282-1299.
Score: 0.010
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Impact of essential genes on the success of genome editing experiments generating 3313 new genetically engineered mouse lines. Sci Rep. 2024 09 30; 14(1):22626.
Score: 0.009
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Measuring hemodynamic changes during mammalian development. Am J Physiol Heart Circ Physiol. 2004 Oct; 287(4):H1561-9.
Score: 0.009
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Dynamic in vivo imaging of postimplantation mammalian embryos using whole embryo culture. Genesis. 2002 Dec; 34(4):228-35.
Score: 0.008
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Mendelian gene identification through mouse embryo viability screening. Genome Med. 2022 10 13; 14(1):119.
Score: 0.008
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COPB2 loss of function causes a coatopathy with osteoporosis and developmental delay. Am J Hum Genet. 2021 09 02; 108(9):1710-1724.
Score: 0.008
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Mouse mutant phenotyping at scale reveals novel genes controlling bone mineral density. PLoS Genet. 2020 12; 16(12):e1009190.
Score: 0.007
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Bi-allelic Variants in TONSL Cause SPONASTRIME Dysplasia and a Spectrum of Skeletal Dysplasia Phenotypes. Am J Hum Genet. 2019 03 07; 104(3):422-438.
Score: 0.006
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Generation of Cardiomyocytes From Vascular Adventitia-Resident Stem Cells. Circ Res. 2018 08 31; 123(6):686-699.
Score: 0.006
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The role of FREM2 and FRAS1 in the development of congenital diaphragmatic hernia. Hum Mol Genet. 2018 06 15; 27(12):2064-2075.
Score: 0.006
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Disease model discovery from 3,328 gene knockouts by The International Mouse Phenotyping Consortium. Nat Genet. 2017 Aug; 49(8):1231-1238.
Score: 0.006
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Prevalence of sexual dimorphism in mammalian phenotypic traits. Nat Commun. 2017 06 26; 8:15475.
Score: 0.006
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Biallelic Variants in OTUD6B Cause an Intellectual Disability Syndrome Associated with Seizures and Dysmorphic Features. Am J Hum Genet. 2017 Apr 06; 100(4):676-688.
Score: 0.006
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Multimodal embryonic imaging using optical coherence tomography, selective plane illumination microscopy, and optical projection tomography. Annu Int Conf IEEE Eng Med Biol Soc. 2016 Aug; 2016:3922-3925.
Score: 0.005
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Simultaneous in?vivo imaging of blood and lymphatic vessel growth in Prox1-GFP/Flk1::myr-mCherry mice. FEBS J. 2015 Apr; 282(8):1458-1467.
Score: 0.005
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Live confocal microscopy of the developing mouse embryonic yolk sac vasculature. Methods Mol Biol. 2015; 1214:163-72.
Score: 0.005
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Wnt-responsive cancer stem cells are located close to distorted blood vessels and not in hypoxic regions in a p53-null mouse model of human breast cancer. Stem Cells Transl Med. 2014 Jul; 3(7):857-66.
Score: 0.005
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Mouse model reveals the role of SOX7 in the development of congenital diaphragmatic hernia associated with recurrent deletions of 8p23.1. Hum Mol Genet. 2012 Sep 15; 21(18):4115-25.
Score: 0.004
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Optical coherence tomography for high-resolution imaging of mouse development in utero. J Biomed Opt. 2011 Apr; 16(4):046004.
Score: 0.004
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Live imaging of rat embryos with Doppler swept-source optical coherence tomography. J Biomed Opt. 2009 Sep-Oct; 14(5):050506.
Score: 0.003
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Molecular and phenotypic characterization of a new mouse insertional mutation that causes a defect in the distal vertebrae of the spine. Genetics. 1995 Jul; 140(3):1061-7.
Score: 0.001