165 related articles for article (PubMed ID: 33147376)
1. Periodic albinism of a widely used albino mutant of Xenopus laevis caused by deletion of two exons in the Hermansky-Pudlak syndrome type 4 gene.
Fukuzawa T
Genes Cells; 2021 Jan; 26(1):31-39. PubMed ID: 33147376
[TBL] [Abstract][Full Text] [Related]
2. no privacy, a Xenopus tropicalis mutant, is a model of human Hermansky-Pudlak Syndrome and allows visualization of internal organogenesis during tadpole development.
Nakayama T; Nakajima K; Cox A; Fisher M; Howell M; Fish MB; Yaoita Y; Grainger RM
Dev Biol; 2017 Jun; 426(2):472-486. PubMed ID: 27595926
[TBL] [Abstract][Full Text] [Related]
3. Unusual leucophore-like cells specifically appear in the lineage of melanophores in the periodic albino mutant of Xenopus laevis.
Fukuzawa T
Pigment Cell Res; 2004 Jun; 17(3):252-61. PubMed ID: 15140070
[TBL] [Abstract][Full Text] [Related]
4. A comparative ultrastructural and physiological study on melanophores of wild-type and periodic albino mutants of Xenopus laevis.
Seldenrijk R; Huijsman KG; Heussen AM; van de Veerdonk FC
Cell Tissue Res; 1982; 222(1):1-9. PubMed ID: 6800656
[TBL] [Abstract][Full Text] [Related]
5. The development of animals homozygous for a mutation causing periodic albinism (ap) in Xenopus laevis.
Hoperskaya OA
J Embryol Exp Morphol; 1975 Aug; 34(1):253-64. PubMed ID: 1185102
[TBL] [Abstract][Full Text] [Related]
6. A developmental analysis of periodic albinism in the amphibian Xenopus laevis.
Eagleson GW; van der Heijden RA; Roubos EW; Jenks BG
Gen Comp Endocrinol; 2010 Sep; 168(2):302-6. PubMed ID: 20178802
[TBL] [Abstract][Full Text] [Related]
7. A wide variety of Mitf transcript variants are expressed in the Xenopus laevis periodic albino mutant.
Fukuzawa T
Genes Cells; 2018 Jun; ():. PubMed ID: 29920861
[TBL] [Abstract][Full Text] [Related]
8. A deletion in the Hermansky-Pudlak syndrome 4 (Hps4) gene appears to be responsible for albinism in channel catfish.
Li Y; Geng X; Bao L; Elaswad A; Huggins KW; Dunham R; Liu Z
Mol Genet Genomics; 2017 Jun; 292(3):663-670. PubMed ID: 28289846
[TBL] [Abstract][Full Text] [Related]
9. Further studies on the melanophores of periodic albino mutant of Xenopus laevis.
Fukuzawa T; Ide H
J Embryol Exp Morphol; 1986 Feb; 91():65-78. PubMed ID: 3711792
[TBL] [Abstract][Full Text] [Related]
10. Ferritin H subunit gene is specifically expressed in melanophore precursor-derived white pigment cells in which reflecting platelets are formed from stage II melanosomes in the periodic albino mutant of Xenopus laevis.
Fukuzawa T
Cell Tissue Res; 2015 Sep; 361(3):733-44. PubMed ID: 25715760
[TBL] [Abstract][Full Text] [Related]
11. Experimental evidence for autonomous action of the periodic albinism (ap) gene within developing retinal pigment cells and melanophores of Xenopus laevis.
MacMillan GJ
J Embryol Exp Morphol; 1981 Aug; 64():333-41. PubMed ID: 7310308
[TBL] [Abstract][Full Text] [Related]
12. Unusual development of light-reflecting pigment cells in intact and regenerating tail in the periodic albino mutant of Xenopus laevis.
Fukuzawa T
Cell Tissue Res; 2010 Oct; 342(1):53-66. PubMed ID: 20859642
[TBL] [Abstract][Full Text] [Related]
13. An analysis of pigment cell development in the periodic albino mutant of Xenopus.
MacMillan GJ
J Embryol Exp Morphol; 1979 Aug; 52():165-70. PubMed ID: 521748
[TBL] [Abstract][Full Text] [Related]
14. Biogenesis of lysosome-related organelles complex 3 (BLOC-3): a complex containing the Hermansky-Pudlak syndrome (HPS) proteins HPS1 and HPS4.
Nazarian R; Falcón-Pérez JM; Dell'Angelica EC
Proc Natl Acad Sci U S A; 2003 Jul; 100(15):8770-5. PubMed ID: 12847290
[TBL] [Abstract][Full Text] [Related]
15. Report of Hermansky-Pudlak Syndrome in Two Families with Novel Variants in
Zaman Q; Sadeeda ; Anas M; Rehman G; Khan Q; Iftikhar A; Ahmad M; Owais M; Ahmad I; Muthaffar OY; Abdulkareem AA; Bibi F; Jelani M; Naseer MI
Genes (Basel); 2023 Jan; 14(1):. PubMed ID: 36672886
[No Abstract] [Full Text] [Related]
16. Sequence-Based Mapping and Genome Editing Reveal Mutations in Stickleback
Hart JC; Miller CT
G3 (Bethesda); 2017 Sep; 7(9):3123-3131. PubMed ID: 28739598
[TBL] [Abstract][Full Text] [Related]
17. High frequency of Hermansky-Pudlak syndrome type 1 (HPS1) among Japanese albinism patients and functional analysis of HPS1 mutant protein.
Ito S; Suzuki T; Inagaki K; Suzuki N; Takamori K; Yamada T; Nakazawa M; Hatano M; Takiwaki H; Kakuta Y; Spritz RA; Tomita Y
J Invest Dermatol; 2005 Oct; 125(4):715-20. PubMed ID: 16185271
[TBL] [Abstract][Full Text] [Related]
18. Hermansky-Pudlak syndrome is caused by mutations in HPS4, the human homolog of the mouse light-ear gene.
Suzuki T; Li W; Zhang Q; Karim A; Novak EK; Sviderskaya EV; Hill SP; Bennett DC; Levin AV; Nieuwenhuis HK; Fong CT; Castellan C; Miterski B; Swank RT; Spritz RA
Nat Genet; 2002 Mar; 30(3):321-4. PubMed ID: 11836498
[TBL] [Abstract][Full Text] [Related]
19. The BLOC-3 subunit HPS4 is required for activation of Rab32/38 GTPases in melanogenesis, but its Rab9 activity is dispensable for melanogenesis.
Ohishi Y; Kinoshita R; Marubashi S; Ishida M; Fukuda M
J Biol Chem; 2019 Apr; 294(17):6912-6922. PubMed ID: 30837268
[No Abstract] [Full Text] [Related]
20. Genetic and experimental studies on a new pigment mutant in Xenopus laevis.
Droin A
J Exp Zool; 1992 Nov; 264(2):196-205. PubMed ID: 1431781
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
