244 related articles for article (PubMed ID: 33439865)
1. The MITF paralog tfec is required in neural crest development for fate specification of the iridophore lineage from a multipotent pigment cell progenitor.
Petratou K; Spencer SA; Kelsh RN; Lister JA
PLoS One; 2021; 16(1):e0244794. PubMed ID: 33439865
[TBL] [Abstract][Full Text] [Related]
2. A systems biology approach uncovers the core gene regulatory network governing iridophore fate choice from the neural crest.
Petratou K; Subkhankulova T; Lister JA; Rocco A; Schwetlick H; Kelsh RN
PLoS Genet; 2018 Oct; 14(10):e1007402. PubMed ID: 30286071
[TBL] [Abstract][Full Text] [Related]
3. Distinct interactions of Sox5 and Sox10 in fate specification of pigment cells in medaka and zebrafish.
Nagao Y; Takada H; Miyadai M; Adachi T; Seki R; Kamei Y; Hara I; Taniguchi Y; Naruse K; Hibi M; Kelsh RN; Hashimoto H
PLoS Genet; 2018 Apr; 14(4):e1007260. PubMed ID: 29621239
[TBL] [Abstract][Full Text] [Related]
4. An iterative genetic and dynamical modelling approach identifies novel features of the gene regulatory network underlying melanocyte development.
Greenhill ER; Rocco A; Vibert L; Nikaido M; Kelsh RN
PLoS Genet; 2011 Sep; 7(9):e1002265. PubMed ID: 21909283
[TBL] [Abstract][Full Text] [Related]
5. Leukocyte tyrosine kinase functions in pigment cell development.
Lopes SS; Yang X; Müller J; Carney TJ; McAdow AR; Rauch GJ; Jacoby AS; Hurst LD; Delfino-Machín M; Haffter P; Geisler R; Johnson SL; Ward A; Kelsh RN
PLoS Genet; 2008 Mar; 4(3):e1000026. PubMed ID: 18369445
[TBL] [Abstract][Full Text] [Related]
6. A gene regulatory network combining Pax3/7, Sox10 and Mitf generates diverse pigment cell types in medaka and zebrafish.
Miyadai M; Takada H; Shiraishi A; Kimura T; Watakabe I; Kobayashi H; Nagao Y; Naruse K; Higashijima SI; Shimizu T; Kelsh RN; Hibi M; Hashimoto H
Development; 2023 Oct; 150(19):. PubMed ID: 37823232
[TBL] [Abstract][Full Text] [Related]
7. Interplay between Foxd3 and Mitf regulates cell fate plasticity in the zebrafish neural crest.
Curran K; Lister JA; Kunkel GR; Prendergast A; Parichy DM; Raible DW
Dev Biol; 2010 Aug; 344(1):107-18. PubMed ID: 20460180
[TBL] [Abstract][Full Text] [Related]
8. Cyclical fate restriction: a new view of neural crest cell fate specification.
Kelsh RN; Camargo Sosa K; Farjami S; Makeev V; Dawes JHP; Rocco A
Development; 2021 Nov; 148(22):. PubMed ID: 35020872
[TBL] [Abstract][Full Text] [Related]
9. Histone variant dictates fate biasing of neural crest cells to melanocyte lineage.
Raja DA; Subramaniam Y; Aggarwal A; Gotherwal V; Babu A; Tanwar J; Motiani RK; Sivasubbu S; Gokhale RS; Natarajan VT
Development; 2020 Mar; 147(5):. PubMed ID: 32098766
[TBL] [Abstract][Full Text] [Related]
10. Mutational analysis of endothelin receptor b1 (rose) during neural crest and pigment pattern development in the zebrafish Danio rerio.
Parichy DM; Mellgren EM; Rawls JF; Lopes SS; Kelsh RN; Johnson SL
Dev Biol; 2000 Nov; 227(2):294-306. PubMed ID: 11071756
[TBL] [Abstract][Full Text] [Related]
11. Pigment Cell Progenitors in Zebrafish Remain Multipotent through Metamorphosis.
Singh AP; Dinwiddie A; Mahalwar P; Schach U; Linker C; Irion U; Nüsslein-Volhard C
Dev Cell; 2016 Aug; 38(3):316-30. PubMed ID: 27453500
[TBL] [Abstract][Full Text] [Related]
12. [Phenotypic plasticity of neural crest-derived melanocytes and Schwann cells].
Dupin E
Biol Aujourdhui; 2011; 205(1):53-61. PubMed ID: 21501576
[TBL] [Abstract][Full Text] [Related]
13. Zebrafish adult pigment stem cells are multipotent and form pigment cells by a progressive fate restriction process: Clonal analysis identifies shared origin of all pigment cell types.
Kelsh RN; Sosa KC; Owen JP; Yates CA
Bioessays; 2017 Mar; 39(3):. PubMed ID: 28009049
[TBL] [Abstract][Full Text] [Related]
14. An orthologue of the kit-related gene fms is required for development of neural crest-derived xanthophores and a subpopulation of adult melanocytes in the zebrafish, Danio rerio.
Parichy DM; Ransom DG; Paw B; Zon LI; Johnson SL
Development; 2000 Jul; 127(14):3031-44. PubMed ID: 10862741
[TBL] [Abstract][Full Text] [Related]
15. Sox5 functions as a fate switch in medaka pigment cell development.
Nagao Y; Suzuki T; Shimizu A; Kimura T; Seki R; Adachi T; Inoue C; Omae Y; Kamei Y; Hara I; Taniguchi Y; Naruse K; Wakamatsu Y; Kelsh RN; Hibi M; Hashimoto H
PLoS Genet; 2014 Apr; 10(4):e1004246. PubMed ID: 24699463
[TBL] [Abstract][Full Text] [Related]
16. Regulation of zebrafish melanocyte development by ligand-dependent BMP signaling.
Gramann AK; Venkatesan AM; Guerin M; Ceol CJ
Elife; 2019 Dec; 8():. PubMed ID: 31868592
[TBL] [Abstract][Full Text] [Related]
17. Mitf-family transcription factor function is required within cranial neural crest cells to promote choroid fissure closure.
Sinagoga KL; Larimer-Picciani AM; George SM; Spencer SA; Lister JA; Gross JM
Development; 2020 Jul; 147(21):. PubMed ID: 32541011
[TBL] [Abstract][Full Text] [Related]
18. Dicer1 is required for pigment cell and craniofacial development in zebrafish.
Weiner AMJ; Scampoli NL; Steeman TJ; Dooley CM; Busch-Nentwich EM; Kelsh RN; Calcaterra NB
Biochim Biophys Acta Gene Regul Mech; 2019 Apr; 1862(4):472-485. PubMed ID: 30840854
[TBL] [Abstract][Full Text] [Related]
19. Epigenetic dynamics shaping melanophore and iridophore cell fate in zebrafish.
Jang HS; Chen Y; Ge J; Wilkening AN; Hou Y; Lee HJ; Choi YR; Lowdon RF; Xing X; Li D; Kaufman CK; Johnson SL; Wang T
Genome Biol; 2021 Oct; 22(1):282. PubMed ID: 34607603
[TBL] [Abstract][Full Text] [Related]
20. An ongoing role for Wnt signaling in differentiating melanocytes in vivo.
Vibert L; Aquino G; Gehring I; Subkankulova T; Schilling TF; Rocco A; Kelsh RN
Pigment Cell Melanoma Res; 2017 Mar; 30(2):219-232. PubMed ID: 27977907
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
