1 | AP3D1, HPS10 |
Mutations in AP3D1 associated with immunodeficiency and seizures define a new type of Hermansky-Pudlak syndrome. | |
Ammann S, Schulz A, Krägeloh-Mann I, Dieckmann NM, Niethammer K, Fuchs S, Eckl KM, Plank R, Werner R, Altmüller J, Thiele H, Nürnberg P, Bank J, Strauss A, von Bernuth H, Zur Stadt U, Grieve S, Griffiths GM, Lehmberg K, Hennies HC, Ehl S. | |
Blood 127(8):997-1006. doi: 10.1182/blood-2015-09-671636. 2016 | |
2 | AP3D1, HPS10 |
A new type of syndromic albinism associated with mutations in AP3D1. | |
Montoliu L, Marks MS. | |
Pigment Cell Melanoma Res igment Cell Melanoma Res. 2016 Oct 19. doi: 10.1111/pcmr.12543. [Epub ahead of print] No abstract available. 2016 | |
3 | AP3D1 |
The HIV-1 matrix protein does not interact directly with the protein interactive domain of AP-3δ. | |
Kyere SK, Mercredi PY, Dong X, Spearman P, Summers MF. | |
Virus Res 169(2):411-4. doi: 10.1016/j.virusres.2012.06.007. 2012 | |
4 | AP3D1 |
Altered retinal cell differentiation in the AP-3 delta mutant (Mocha) mouse. | |
Baguma-Nibasheka M, Kablar B. | |
Int J Dev Neurosci 27(7):701-8. doi: 10.1016/j.ijdevneu.2009.07.005. 2009 | |
5 | AP3D1 |
HIV-1 replication in dendritic cells occurs through a tetraspanin-containing compartment enriched in AP-3. | |
Garcia E, Nikolic DS, Piguet V. | |
Traffic 9(2):200-14. Epub 2007 Nov 22. 2008 | |
6 | AP3D1 |
Mapping of the spontaneous deletion in the Ap3d1 gene of mocha mice: fast and reliable genotyping. | |
Drasbek KR, Holm MM, Delenclos M, Jensen K. | |
BMC Res Notes 1:119. doi: 10.1186/1756-0500-1-119. 2008 | |
7 | ABL2, AKAP8, ANKRD13D, AP3D1, ARFGAP3, ARMCX6, ASUN, BAT2L, BCl2L13, BNIP3L, BPTF, BRD7, BZW1, BZW2, C12orf43, C19orf26, C1orf105, C2orf49, C6orf81, CA10, CAD, CARHSP1, CBX4, CCDC55, CCDC61, CCNK, CDC42BPB, CDC42EP3, CDC42EP4, CDS2, CENPN, CLK1, COPA, CSDA, CTPS2, DBN1, DCP1A, DECR2, DPF2, DPM1, EIF2AK1, EPB41L4A, EPN1, FAM91A1, FOSL2, FOXK1, GDF5OS, GFOD2, GIGYF2, GPATCH8, GTPBP1, HES7, HNRNPUL1, KIF1C, LPIN2, LRCH4, MAN2C1, MAST1, MED13, MED24, MED26, MINK1, MISP, MYO10, NKTR, OSBP, PAM, PCDH7, PEX14, PHF16, PHRF1, PLCB4, PLXNC1, POM121, POM121L2, PPHLN1, PRICKLE3, PRX, PUM2, RABGGTB, RBEL1, RIMS1, RIMS2, RPL14, RRP1B, RRP8, SAFB, SCAMP3, SCMH1, SCYL1, SENP6, SERBP1, SFRS13A, SFRS17A, SIPA1L1, SLC26A6, SLIRP, SLMAP, SNTA1, SORBS3, SPICE1, SSFA2, STAM, SUB1, TFIP11, TLN2, TMC6, TMEM104, TMEM106B, TMEM22, TOM1, UHRF1, UTP14A, WDR43, ZNF324, ZNF648 |
Global, in vivo, and site-specific phosphorylation dynamics in signaling networks. | |
Olsen JV, Blagoev B, Gnad F, Macek B, Kumar C, Mortensen P, Mann M. | |
Cell. 127(3):635-48. 2006 | |
8 | AP3S1, AP3D1 |
Characterization of the adaptor-related protein complex, AP-3. | |
Simpson F, Peden AA, Christopoulou L, Robinson MS. | |
J Cell Biol 137(4):835-45. 1997 | |
9 | AP3D1 |
Altered expression of a novel adaptin leads to defective pigment granule biogenesis in the Drosophila eye color mutant garnet. | |
Ooi CE, Moreira JE, Dell'Angelica EC, Poy G, Wassarman DA, Bonifacino JS. | |
EMBO J 16(15):4508-18. 1997 | |