Showing results (11-20 of 64) with videos related to

Sort By:
Pageof 7
Plos Genetics|October 2, 2010
Identification of early requirements for preplacodal ectoderm and sensory organ developmentHye-Joo Kwon, Neha Bhat, Elly M Sweet, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|November 14, 2008
A double TRPtych: six views of transient receptor potential channels in disease and healthRobert A Cornell, Michelle Aarts, Diana Bautista, et al.
Development (Cambridge, England)|January 14, 2012
Novel Tfap2-mediated control of soxE expression facilitated the evolutionary emergence of the neural crestEric Van Otterloo, Wei Li, Aaron Garnett, et al.
The Journal of Investigative Dermatology|February 10, 2007
Cell death of melanophores in zebrafish trpm7 mutant embryos depends on melanin synthesisMatthew S McNeill, Jennifer Paulsen, Gregory Bonde, et al.
Epilepsia Open|October 19, 2021
The opioid antagonist naltrexone decreases seizure-like activity in genetic and chemically induced epilepsy modelsMorgan L Sturgeon, Rachel Langton, Shaunik Sharma, et al.
The Journal of Investigative Dermatology|November 28, 2025
Phenotype switching in melanoma cells: MITF regulates the expression of CDH1 through E-boxes in an intronic regionEvangeline Breeta Raja David Isac, Sara Sigurbjörnsdóttir, Ramile Dilshat, et al.
Developmental Dynamics : an Official Publication of the American Association of Anatomists|June 22, 2005
The fate of human malignant melanoma cells transplanted into zebrafish embryos: assessment of migration and cell division in the absence of tumor formationLisa M J Lee, Elisabeth A Seftor, Gregory Bonde, et al.
Plos Genetics|September 24, 2010
Differentiation of zebrafish melanophores depends on transcription factors AP2 alpha and AP2 epsilonEric Van Otterloo, Wei Li, Gregory Bonde, et al.
Mechanisms of Development|September 30, 2004
Touchtone promotes survival of embryonic melanophores in zebrafishRobert A Cornell, Elizabeth Yemm, Gregory Bonde, et al.
Frontiers in Genetics|June 26, 2020
Functional Characterization of a Novel IRF6 Frameshift Mutation From a Van Der Woude Syndrome FamilyMengqi Zhang, Jieni Zhang, Huaxiang Zhao, et al.
Pageof 7