| scholarly article | Q13442814 |
| review article | Q7318358 |
| P6179 | Dimensions Publication ID | 1039833483 |
| P356 | DOI | 10.1038/35096009 |
| P698 | PubMed publication ID | 11584301 |
| P50 | author | Miguel C. Seabra | Q37382816 |
| P2093 | author name string | Marks MS | |
| Seabra MC | |||
| P2860 | cites work | The beta3A subunit gene (Ap3b1) of the AP-3 adaptor complex is altered in the mouse hypopigmentation mutant pearl, a model for Hermansky-Pudlak syndrome and night blindness | Q22001500 |
| Altered trafficking of lysosomal proteins in Hermansky-Pudlak syndrome due to mutations in the beta 3A subunit of the AP-3 adaptor | Q22008778 | ||
| Transfer mechanism of melanosomes in epidermal cell culture | Q67490883 | ||
| Ultrastructural and cytochemical observations on B-16 and Harding-Passey mouse melanomas. The origin of premelanosomes and compound melanosomes | Q68578610 | ||
| Golgi-melanosome relationship in human melanoma in vitro | Q69870668 | ||
| Rab3a and SNARE proteins: potential regulators of melanosome movement | Q73443691 | ||
| The predominant defect in dilute melanocytes is in melanosome distribution and not cell shape, supporting a role for myosin V in melanosome transport | Q73830033 | ||
| Aberrant pH of melanosomes in pink-eyed dilution (p) mutant melanocytes | Q74347101 | ||
| Mouse models of Hermansky Pudlak syndrome: a review | Q74539703 | ||
| The pink-eyed dilution locus controls the biogenesis of melanosomes and levels of melanosomal proteins in the eye | Q74587768 | ||
| Ocular albinism: evidence for a defect in an intracellular signal transduction system | Q22010509 | ||
| Differential roles of syntaxin 7 and syntaxin 8 in endosomal trafficking | Q22010801 | ||
| TSG101/mammalian VPS23 and mammalian VPS28 interact directly and are recruited to VPS4-induced endosomes | Q24290676 | ||
| Rab27a: A key to melanosome transport in human melanocytes | Q24290970 | ||
| PDZ domain protein GIPC interacts with the cytoplasmic tail of melanosomal membrane protein gp75 (tyrosinase-related protein-1) | Q24291415 | ||
| AP-3 mediates tyrosinase but not TRP-1 trafficking in human melanocytes | Q24291443 | ||
| Deficient peptide loading and MHC class II endosomal sorting in a human genetic immunodeficiency disease: the Chediak-Higashi syndrome | Q24320302 | ||
| Interaction of a Golgi-associated kinesin-like protein with Rab6 | Q24322499 | ||
| A di-leucine-based motif in the cytoplasmic tail of LIMP-II and tyrosinase mediates selective binding of AP-3. | Q24533159 | ||
| Mutations in Mlph, encoding a member of the Rab effector family, cause the melanosome transport defects observed in leaden mice | Q24555217 | ||
| A millennial myosin census | Q24633678 | ||
| Distinct protein sorting and localization to premelanosomes, melanosomes, and lysosomes in pigmented melanocytic cells | Q24671475 | ||
| Defective granule exocytosis in Rab27a-deficient lymphocytes from Ashen mice | Q24671578 | ||
| Multivesicular endosomes containing internalized EGF-EGF receptor complexes mature and then fuse directly with lysosomes | Q24672025 | ||
| Rab proteins as membrane organizers | Q27860861 | ||
| Initial docking of ER-derived vesicles requires Uso1p and Ypt1p but is independent of SNARE proteins | Q27930897 | ||
| The COOH-terminal domain of Myo2p, a yeast myosin V, has a direct role in secretory vesicle targeting | Q27932330 | ||
| Sequential action of two GTPases to promote vacuole docking and fusion | Q27933688 | ||
| The exocyst is an effector for Sec4p, targeting secretory vesicles to sites of exocytosis | Q27934654 | ||
| Sec2p mediates nucleotide exchange on Sec4p and is involved in polarized delivery of post-Golgi vesicles | Q27939177 | ||
| Rab1 recruitment of p115 into a cis-SNARE complex: programming budding COPII vesicles for fusion | Q28141271 | ||
| Role of cytoplasmic dynein in melanosome transport in human melanocytes | Q28142331 | ||
| Colocalization of dynactin subunits P150Glued and P50 with melanosomes in normal human melanocytes | Q28142439 | ||
| Oligomeric complexes link Rab5 effectors with NSF and drive membrane fusion via interactions between EEA1 and syntaxin 13 | Q28142791 | ||
| Role of Rab9 GTPase in facilitating receptor recruitment by TIP47 | Q28189682 | ||
| Evolution of the Rab family of small GTP-binding proteins | Q28204091 | ||
| The mouse p (pink-eyed dilution) and human P genes, oculocutaneous albinism type 2 (OCA2), and melanosomal pH | Q28213415 | ||
| Association of the AP-3 adaptor complex with clathrin | Q28267691 | ||
| Mutation in AP-3 delta in the mocha mouse links endosomal transport to storage deficiency in platelets, melanosomes, and synaptic vesicles | Q28279070 | ||
| Cultured melanocytes from dilute mutant mice exhibit dendritic morphology and altered melanosome distribution | Q28505197 | ||
| Rab geranylgeranyl transferase alpha mutation in the gunmetal mouse reduces Rab prenylation and platelet synthesis | Q28509083 | ||
| Rab27a regulates the peripheral distribution of melanosomes in melanocytes | Q28513638 | ||
| Novel myosin heavy chain encoded by murine dilute coat colour locus | Q28590446 | ||
| Mutant myosin VIIa causes defective melanosome distribution in the RPE of shaker-1 mice | Q28591690 | ||
| The Beige/Chediak-Higashi syndrome gene encodes a widely expressed cytosolic protein | Q28592274 | ||
| A mutation in Rab27a causes the vesicle transport defects observed in ashen mice | Q28594384 | ||
| Fab1p PtdIns(3)P 5-kinase function essential for protein sorting in the multivesicular body | Q29547922 | ||
| Kinesin and dynein superfamily proteins and the mechanism of organelle transport | Q29620418 | ||
| Mutations in RAB27A cause Griscelli syndrome associated with haemophagocytic syndrome | Q29620423 | ||
| Proper folding and endoplasmic reticulum to golgi transport of tyrosinase are induced by its substrates, DOPA and tyrosine | Q31735253 | ||
| Small Gtpase rab3A is associated with melanosomes in melanoma cells | Q31816346 | ||
| Mammalian tumor susceptibility gene 101 (TSG101) and the yeast homologue, Vps23p, both function in late endosomal trafficking. | Q33285661 | ||
| Current understanding on the role of retinal pigment epithelium and its pigmentation | Q33716211 | ||
| Regulated secretion from hemopoietic cells | Q33745488 | ||
| Clinical, molecular, and cell biological aspects of Chediak-Higashi syndrome | Q33755016 | ||
| Biochemical control of melanogenesis and melanosomal organization | Q33760835 | ||
| Molecular mechanisms of pigment transport in melanophores | Q33762752 | ||
| Adaptors for clathrin-mediated traffic | Q33804351 | ||
| Membrane trafficking, organelle transport, and the cytoskeleton. | Q33840274 | ||
| Class V myosins. | Q33866590 | ||
| Two genes are responsible for Griscelli syndrome at the same 15q21 locus. | Q33892373 | ||
| Heterozygous HPS1 mutations in a case of Hermansky-Pudlak syndrome with giant melanosomes. | Q33916390 | ||
| Lysosome-related organelles | Q33956953 | ||
| Myosin VI: roles for a minus end-directed actin motor in cells | Q34038023 | ||
| Mutation of a new gene causes a unique form of Hermansky-Pudlak syndrome in a genetic isolate of central Puerto Rico | Q34084038 | ||
| Mutations in the gene encoding B, a novel transporter protein, reduce melanin content in medaka | Q34085466 | ||
| Hermansky-Pudlak syndrome and related disorders of organelle formation | Q34156519 | ||
| Ypt and Rab GTPases: insight into functions through novel interactions | Q34309095 | ||
| Griscelli disease maps to chromosome 15q21 and is associated with mutations in the myosin-Va gene | Q34431158 | ||
| The mouse SKD1, a homologue of yeast Vps4p, is required for normal endosomal trafficking and morphology in mammalian cells | Q34687885 | ||
| The tetraspanin CD63/lamp3 cycles between endocytic and secretory compartments in human endothelial cells | Q34714968 | ||
| Myosin-V stepping kinetics: a molecular model for processivity | Q35207228 | ||
| Vacuole acidification is required for trans-SNARE pairing, LMA1 release, and homotypic fusion | Q35642673 | ||
| On the possible function of coated vesicles in melanogenesis of the regenerating fowl feather | Q36192576 | ||
| Mannose 6-phosphate receptors are sorted from immature secretory granules via adaptor protein AP-1, clathrin, and syntaxin 6-positive vesicles | Q36289154 | ||
| Visualization of melanosome dynamics within wild-type and dilute melanocytes suggests a paradigm for myosin V function In vivo | Q36328552 | ||
| Intracellular sorting and targeting of melanosomal membrane proteins: identification of signals for sorting of the human brown locus protein, gp75 | Q36382701 | ||
| The mouse pale ear (ep) mutation is the homologue of human Hermansky-Pudlak syndrome | Q36560640 | ||
| Di-leucine signals mediate targeting of tyrosinase and synaptotagmin to synaptic-like microvesicles within PC12 cells. | Q36941351 | ||
| The mammalian AP-3 adaptor-like complex mediates the intracellular transport of lysosomal membrane glycoproteins. | Q38331973 | ||
| Melanosomes are specialized members of the lysosomal lineage of organelles. | Q40447735 | ||
| Actin- and microtubule-dependent organelle motors: interrelationships between the two motility systems. | Q40529200 | ||
| Weibel-Palade body membrane proteins exhibit differential trafficking after exocytosis in endothelial cells | Q40826415 | ||
| Membrane association and targeting of prenylated Ras-like GTPases | Q40857389 | ||
| Rab5 regulates motility of early endosomes on microtubules | Q40916867 | ||
| A cytoplasmic sequence in human tyrosinase defines a second class of di-leucine-based sorting signals for late endosomal and lysosomal delivery | Q40959249 | ||
| Direct interaction of microtubule- and actin-based transport motors | Q40975760 | ||
| Motors and membrane traffic. | Q41334437 | ||
| Kinesin participates in melanosomal movement along melanocyte dendrites | Q42484188 | ||
| Three modes of melanosome transfers in Caucasian facial skin: hypothesis based on an ultrastructural study. | Q42493458 | ||
| A line of non-tumorigenic mouse melanocytes, syngeneic with the B16 melanoma and requiring a tumour promoter for growth | Q42820599 | ||
| Tyrosinase stabilization by Tyrp1 (the brown locus protein). | Q42824469 | ||
| The role of intraorganellar Ca(2+) in late endosome-lysosome heterotypic fusion and in the reformation of lysosomes from hybrid organelles | Q42919564 | ||
| Rab27a is required for regulated secretion in cytotoxic T lymphocytes | Q42947316 | ||
| Intracellular distribution and late endosomal effects of the ocular albinism type 1 gene product: consequences of disease-causing mutations and implications for melanosome biogenesis | Q43549011 | ||
| Mislocalization of melanosomal proteins in melanocytes from mice with oculocutaneous albinism type 2. | Q43624874 | ||
| The Hermansky-Pudlak syndrome (HPS) protein is part of a high molecular weight complex involved in biogenesis of early melanosomes | Q47247902 | ||
| The mammalian Rab family of small GTPases: definition of family and subfamily sequence motifs suggests a mechanism for functional specificity in the Ras superfamily | Q48745906 | ||
| Two-headed binding of a processive myosin to F-actin. | Q52863984 | ||
| The pallid gene encodes a novel, syntaxin 13-interacting protein involved in platelet storage pool deficiency | Q55951827 | ||
| Secretory Lysosome Biogenesis in Cytotoxic T Lymphocytes from Normal and Chediak Higashi Syndrome Patients | Q58019241 | ||
| Chemical Composition and Terminology Of Specialized Organelles (Melanosomes and Melanin Granules) in Mammalian Melanocytes | Q59094998 | ||
| Oa1 knock-out: new insights on the pathogenesis of ocular albinism type 1. | Q61409124 | ||
| P433 | issue | 10 | |
| P921 | main subject | melanosome | Q1065756 |
| P304 | page(s) | 738-748 | |
| P577 | publication date | 2001-10-01 | |
| P1433 | published in | Nature Reviews Molecular Cell Biology | Q1573120 |
| P1476 | title | The melanosome: membrane dynamics in black and white | |
| P478 | volume | 2 |
| Q52672984 | 36H: A Novel Potent Inhibitor for Antimelanogenesis. |
| Q37024676 | A Rab3a-dependent complex essential for lysosome positioning and plasma membrane repair |
| Q39084617 | A coiled-coil domain of melanophilin is essential for Myosin Va recruitment and melanosome transport in melanocytes. |
| Q24295585 | A family of Rab27-binding proteins. Melanophilin links Rab27a and myosin Va function in melanosome transport |
| Q34390675 | A frameshift mutation in the melanophilin gene causes the dilute coat colour in rabbit (Oryctolagus cuniculus) breeds |
| Q30499499 | A general role for Rab27a in secretory cells |
| Q35594079 | A lumenal domain-dependent pathway for sorting to intralumenal vesicles of multivesicular endosomes involved in organelle morphogenesis |
| Q37357717 | A mutation within the transmembrane domain of melanosomal protein Silver (Pmel17) changes lumenal fragment interactions |
| Q30008817 | A novel P53/POMC/Gαs/SASH1 autoregulatory feedback loop activates mutated SASH1 to cause pathologic hyperpigmentation |
| Q37476322 | A novel splice variant of Pmel17 expressed by human melanocytes and melanoma cells lacking some of the internal repeats. |
| Q33492479 | A potent activator of melanogenesis identified from small-molecule screening |
| Q36288889 | A role for the inositol kinase Ipk1 in ciliary beating and length maintenance |
| Q24624821 | A unique region of RILP distinguishes it from its related proteins in its regulation of lysosomal morphology and interaction with Rab7 and Rab34 |
| Q39510173 | AAV-mediated tyrosinase gene transfer restores melanogenesis and retinal function in a model of oculo-cutaneous albinism type I (OCA1). |
| Q35125908 | Amyloid as a natural product |
| Q24653554 | Amyloids: friend or foe? |
| Q24318501 | An unconventional dileucine-based motif and a novel cytosolic motif are required for the lysosomal and melanosomal targeting of OA1 |
| Q52680468 | Anorectal mucosal melanoma. |
| Q39171077 | Autophagy has a significant role in determining skin color by regulating melanosome degradation in keratinocytes |
| Q64102849 | Autophagy: a new mechanism for regulating VEGF and PEDF expression in retinal pigment epithelium cells |
| Q24337651 | BLOC-1 is required for cargo-specific sorting from vacuolar early endosomes toward lysosome-related organelles |
| Q24297788 | BLOC-1, a novel complex containing the pallidin and muted proteins involved in the biogenesis of melanosomes and platelet-dense granules |
| Q24315003 | BLOC-2, AP-3, and AP-1 proteins function in concert with Rab38 and Rab32 proteins to mediate protein trafficking to lysosome-related organelles |
| Q24302143 | BLOC-3, a protein complex containing the Hermansky-Pudlak syndrome gene products HPS1 and HPS4 |
| Q24300539 | Bardet-Biedl syndrome genes are important in retrograde intracellular trafficking and Kupffer's vesicle cilia function |
| Q28209818 | Biochemical and molecular characterization of diseases linked to motor proteins |
| Q58450115 | Biogenesis of Melanosomes |
| Q24678933 | Biogenesis of lysosome-related organelles complex 3 (BLOC-3): a complex containing the Hermansky-Pudlak syndrome (HPS) proteins HPS1 and HPS4 |
| Q36889096 | Biology and pathogenesis of Fonsecaea pedrosoi, the major etiologic agent of chromoblastomycosis |
| Q36996595 | Biology of epidermal and hair pigmentation in cattle: a mini-review |
| Q47390380 | Brain size and the expression of pheomelanin-based colour in birds |
| Q33613085 | Cell-specific ATP7A transport sustains copper-dependent tyrosinase activity in melanosomes |
| Q34171093 | Characterization of the molecular defects in Rab27a, caused by RAB27A missense mutations found in patients with Griscelli syndrome |
| Q34722897 | Chediak-Higashi Syndrome: a rare disorder of lysosomes and lysosome related organelles |
| Q33305811 | Chemical genetic screening identifies tricyclic compounds that decrease cellular melanin content |
| Q50952385 | Classical autophagy proteins LC3B and ATG4B facilitate melanosome movement on cytoskeletal tracks. |
| Q30786606 | Cortactin promotes exosome secretion by controlling branched actin dynamics |
| Q92930286 | Cultured Epidermal Melanocyte Transplantation in Vitiligo: A Review Article |
| Q89273060 | Depigmenting effect of argan press-cake extract through the down-regulation of Mitf and melanogenic enzymes expression in B16 murine melanoma cells |
| Q36161681 | Differential recognition of a dileucine-based sorting signal by AP-1 and AP-3 reveals a requirement for both BLOC-1 and AP-3 in delivery of OCA2 to melanosomes |
| Q37187795 | Disorders of lysosome-related organelle biogenesis: clinical and molecular genetics |
| Q24804161 | Dorsoventral patterning of the mouse coat by Tbx15 |
| Q34886367 | Dual loss of ER export and endocytic signals with altered melanosome morphology in the silver mutation of Pmel17 |
| Q38715541 | E-cadherin mediates ultraviolet radiation- and calcium-induced melanin transfer in human skin cells |
| Q52715407 | Essential Role of the a3 Isoform of V-ATPase in Secretory Lysosome Trafficking via Rab7 Recruitment. |
| Q28728912 | Essential role of RAB27A in determining constitutive human skin color |
| Q36106321 | Estradiol differently affects melanin synthesis of malignant and normal melanocytes: a relationship with clock and clock-controlled genes. |
| Q27341766 | Extracellular vesicles are transferred from melanocytes to keratinocytes after UVA irradiation |
| Q35819839 | Eye development: a view from the retina pigmented epithelium |
| Q51887075 | FGF/MAPK/Ets signaling renders pigment cell precursors competent to respond to Wnt signal by directly controlling Ci-Tcf transcription. |
| Q92072033 | Flow Cytometry Contributions for the Diagnosis and Immunopathological Characterization of Primary Immunodeficiency Diseases With Immune Dysregulation |
| Q21092782 | Functional amyloid formation within mammalian tissue |
| Q34718121 | Functional analysis of BBS3 A89V that results in non-syndromic retinal degeneration |
| Q38315957 | Functional analysis of slac2-a/melanophilin as a linker protein between Rab27A and myosin Va in melanosome transport. |
| Q24552904 | Functional redundancy of Rab27 proteins and the pathogenesis of Griscelli syndrome |
| Q51847405 | General strategy to analyse coat colour phenotypes in mice. |
| Q33877064 | Genetic analysis of lysosomal trafficking in Caenorhabditis elegans |
| Q33979104 | Genetic interaction between Bardet-Biedl syndrome genes and implications for limb patterning |
| Q37548448 | Genome-wide linkage, exome sequencing and functional analyses identify ABCB6 as the pathogenic gene of dyschromatosis universalis hereditaria. |
| Q39997440 | Glycolipid-dependent sorting of melanosomal from lysosomal membrane proteins by lumenal determinants |
| Q42820740 | Griscelli syndrome types 1 and 2. |
| Q36011857 | Hair follicle pigmentation |
| Q34485728 | Hermansky-Pudlak syndrome: a disease of protein trafficking and organelle function |
| Q35009608 | Hermansky-Pudlak syndrome: vesicle formation from yeast to man. |
| Q91173488 | Homogentisic acid-derived pigment as a biocompatible label for optoacoustic imaging of macrophages |
| Q38106424 | Hypopigmentation in Hermansky-Pudlak syndrome |
| Q27347938 | Identification and functional analysis of the vision-specific BBS3 (ARL6) long isoform |
| Q28259174 | Identification of EPI64 as a GTPase-activating protein specific for Rab27A |
| Q35057299 | Identification of novel rab27a/melanophilin blockers by pharmacophore-based virtual screening |
| Q24337584 | Identification of snapin and three novel proteins (BLOS1, BLOS2, and BLOS3/reduced pigmentation) as subunits of biogenesis of lysosome-related organelles complex-1 (BLOC-1) |
| Q35134926 | Interferon-γ induces senescence in normal human melanocytes |
| Q24541556 | Interorganellar regulation of lysosome positioning by the Golgi apparatus through Rab34 interaction with Rab-interacting lysosomal protein |
| Q34874686 | Introduction: lysosome-related organelles |
| Q46182217 | Inulavosin, a melanogenesis inhibitor, leads to mistargeting of tyrosinase to lysosomes and accelerates its degradation |
| Q46924618 | Investigation of Known Genetic Mutations of Arabian Horses in Egyptian Arabian Foals with Juvenile Idiopathic Epilepsy |
| Q35826372 | Involvement of vps33a in the fusion of uroplakin-degrading multivesicular bodies with lysosomes |
| Q38230708 | Ion transport in pigmentation |
| Q42594298 | It takes two to tango to the melanosome. |
| Q92015292 | Knockdown of microRNA‑143‑5p by STTM technology affects eumelanin and pheomelanin production in melanocytes |
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| Q43924342 | Loci associated with skin pigmentation identified in African populations. |
| Q24540828 | Loss-of-function mutations in the keratin 5 gene lead to Dowling-Degos disease |
| Q36880252 | Lysosome-related organelles: driving post-Golgi compartments into specialisation |
| Q34766328 | Lysosomes and the plasma membrane: trypanosomes reveal a secret relationship |
| Q37367668 | Many variations on a few themes: a broader look at development of iridescent scales (and feathers). |
| Q35936316 | Mechanisms of protein delivery to melanosomes in pigment cells. |
| Q39308499 | Melanin and lipofuscin as hallmarks of skin aging |
| Q34285375 | Melanin from Fonsecaea pedrosoi induces production of human antifungal antibodies and enhances the antimicrobial efficacy of phagocytes. |
| Q38869790 | Melanin: the biophysiology of oral melanocytes and physiological oral pigmentation |
| Q35129447 | Melanocytes derived from patients with Hermansky-Pudlak Syndrome types 1, 2, and 3 have distinct defects in cargo trafficking |
| Q34718290 | Melanocytic galectin-3 is associated with tyrosinase-related protein-1 and pigment biosynthesis. |
| Q40279232 | Melanogenesis and evidence for melanosome transport to the plasma membrane in a CD83 teleost leukocyte cell line |
| Q34133114 | Melanophilin directly links Rab27a and myosin Va through its distinct coiled-coil regions |
| Q40004019 | Melanosomal damage in normal human melanocytes induced by UVB and metal uptake--a basis for the pro-oxidant state of melanoma |
| Q27322910 | Melanosomal dynamics assessed with a live-cell fluorescent melanosomal marker |
| Q28301085 | Melanosome uptake is associated with the proliferation and differentiation of keratinocytes |
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| Q35176389 | Melanosomes and MHC class II antigen-processing compartments: a tinted view of intracellular trafficking and immunity |
| Q36864980 | Melanosomes in pigmented epithelia maintain eye lens transparency during zebrafish embryonic development. |
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| Q28658197 | Melanosomes or microbes: testing an alternative hypothesis for the origin of microbodies in fossil feathers |
| Q24647195 | Melanosomes--dark organelles enlighten endosomal membrane transport |
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| Q35153478 | Membrane targeting of Rab GTPases is influenced by the prenylation motif |
| Q93221684 | Membrane transport proteins in melanosomes: Regulation of ions for pigmentation |
| Q40993191 | Mimicking Melanosomes: Polydopamine Nanoparticles as Artificial Microparasols |
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| Q56622749 | Molecular and microstructural inventory of an isolated fossil bird feather from the Eocene Fur Formation of Denmark |
| Q37226089 | More than just a cargo adapter, melanophilin prolongs and slows processive runs of myosin Va |
| Q21092441 | Mutation in archain 1, a subunit of COPI coatomer complex, causes diluted coat color and Purkinje cell degeneration |
| Q28511673 | Mutation of FIG4 causes neurodegeneration in the pale tremor mouse and patients with CMT4J |
| Q34048569 | Mutation of melanosome protein RAB38 in chocolate mice |
| Q24294793 | MyRIP, a novel Rab effector, enables myosin VIIa recruitment to retinal melanosomes |
| Q36828209 | Myosins in melanocytes: to move or not to move? |
| Q56520846 | Non-integumentary melanosomes can bias reconstructions of the colours of fossil vertebrates |
| Q28187080 | OTX2 activates the molecular network underlying retina pigment epithelium differentiation |
| Q40757472 | P-selectin targeting to secretory lysosomes of Rbl-2H3 cells. |
| Q30577235 | PKA-dependent dynein switching from lysosomes to adenovirus: a novel form of host-virus competition |
| Q35564835 | Pigment Cells: A Model for the Study of Organelle Transport |
| Q88674269 | Pigmentation and vision: Is GPR143 in control? |
| Q37808732 | Pleiotropic effects of pigmentation genes in horses |
| Q36965785 | Preferential gene expression in the limbus of the vervet monkey |
| Q36726485 | Premelanosome amyloid-like fibrils are composed of only golgi-processed forms of Pmel17 that have been proteolytically processed in endosomes |
| Q36015036 | Primary hemophagocytic syndromes point to a direct link between lymphocyte cytotoxicity and homeostasis |
| Q36323476 | Proprotein convertase cleavage liberates a fibrillogenic fragment of a resident glycoprotein to initiate melanosome biogenesis |
| Q34317344 | Rab GTPases and myosin motors in organelle motility |
| Q34109808 | Rab GTPases, intracellular traffic and disease. |
| Q45258553 | Rab11b mediates melanin transfer between donor melanocytes and acceptor keratinocytes via coupled exo/endocytosis |
| Q40492183 | Rab27A-binding protein Slp2-a is required for peripheral melanosome distribution and elongated cell shape in melanocytes. |
| Q45376056 | Rab36 regulates the spatial distribution of late endosomes and lysosomes through a similar mechanism to Rab34. |
| Q36119125 | Rab38 and Rab32 control post-Golgi trafficking of melanogenic enzymes |
| Q42175722 | Rab40C is a novel Varp-binding protein that promotes proteasomal degradation of Varp in melanocytes |
| Q90185908 | Recent advances in amniote palaeocolour reconstruction and a framework for future research |
| Q41818361 | Regulation of melanosome number, shape and movement in the zebrafish retinal pigment epithelium by OA1 and PMEL. |
| Q34249792 | Regulation of tyrosinase trafficking and processing by presenilins: partial loss of function by familial Alzheimer's disease mutation |
| Q54356402 | Release of TNF-α from macrophages is mediated by small GTPase Rab37. |
| Q58450118 | Reply to Valencia et al |
| Q30494855 | Retinal pigment epithelium defects in humans and mice with mutations in MYO7A: imaging melanosome-specific autofluorescence. |
| Q44445179 | Screening of human primary melanocytes of defined melanocortin-1 receptor genotype: pigmentation marker, ultrastructural and UV-survival studies. |
| Q34522863 | Secretory lysosomes |
| Q35690713 | Semi-automated analysis of organelle movement and membrane content: understanding rab-motor complex transport function |
| Q41383927 | Sequence-Based Mapping and Genome Editing Reveal Mutations in Stickleback Hps5 Cause Oculocutaneous Albinism and the casper Phenotype |
| Q91825626 | Shedding light on melanins within in situ human eye melanocytes using 2-photon microscopy profiling techniques |
| Q26739678 | Signaling Pathways in Melanogenesis |
| Q33913618 | Signaling pathways in melanosome biogenesis and pathology |
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| Q36791981 | Structural and regulatory functions of keratins. |
| Q34606390 | Structure-function analysis of VPS9-ankyrin-repeat protein (Varp) in the trafficking of tyrosinase-related protein 1 in melanocytes. |
| Q37174502 | Sublethal photic stress and the motility of RPE phagosomes and melanosomes |
| Q24299097 | Synaptotagmin-like protein 5: a novel Rab27A effector with C-terminal tandem C2 domains |
| Q64106298 | Synthesis and physiological implications of melanic pigments |
| Q93151010 | Terahertz spectroscopy of human skin tissue models with different melanin content |
| Q28510459 | The BLOS1-interacting protein KXD1 is involved in the biogenesis of lysosome-related organelles |
| Q44420447 | The Inhibition of Early N-Glycan Processing Targets TRP-2 to Degradation in B16 Melanoma Cells |
| Q30499095 | The N-terminal region of centrosomal protein 290 (CEP290) restores vision in a zebrafish model of human blindness. |
| Q36257261 | The Silver locus product Pmel17/gp100/Silv/ME20: controversial in name and in function |
| Q28214394 | The Slp homology domain of synaptotagmin-like proteins 1-4 and Slac2 functions as a novel Rab27A binding domain |
| Q39791257 | The actin-binding domain of Slac2-a/melanophilin is required for melanosome distribution in melanocytes |
| Q38266405 | The ascidian pigmented sensory organs: structures and developmental programs |
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| Q24657251 | The colour of fossil feathers |
| Q35098810 | The contribution of melanin to microbial pathogenesis |
| Q34585581 | The dark side of lysosome-related organelles: specialization of the endocytic pathway for melanosome biogenesis |
| Q38965381 | The feelgood mutation in zebrafish dysregulates COPII-dependent secretion of select extracellular matrix proteins in skeletal morphogenesis |
| Q90589889 | The function and clinical application of extracellular vesicles in innate immune regulation |
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