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Regulation of Melanoblast Migration and Differentiation
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1001/archderm.135.4.478openalex-snapshot
The Pigmentary System: Physiology and Pathophysiology
inferredcites →https://doi.org/10.1001/archneurpsyc.1951.02320060135017openalex-snapshot
The Neural Crest: Its Properties and Derivatives in the Light of Experimental Research.
inferredcites →https://doi.org/10.1001/jama.1996.03540160075042openalex-snapshot
Cutaneous Medicine and Surgery: An Integrated Program in Dermatology
inferredcites →https://doi.org/10.1002/(sici)1097-0177(199812)213:4<476::aid-aja12>3.0.co;2-ropenalex-snapshot
Specification and migration of melanoblasts at the vagal level and in hyperpigmented silkie chickens
inferredcites →https://doi.org/10.1002/(sici)1097-4687(199807)237:1<53::aid-jmor5>3.0.co;2-popenalex-snapshot
Experimental analysis of character coupling across a complex life cycle: Pigment pattern metamorphosis in the tiger salamander,Ambystoma tigrinum tigrinum
inferredcites →https://doi.org/10.1002/(sici)1097-4687(199907)241:1<83::aid-jmor5>3.0.co;2-hopenalex-snapshot
Development and evolution of melanophore patterns in fishes of the genus Danio (Teleostei: Cyprinidae)
inferredcites →https://doi.org/10.1002/(sici)1520-6408(1996)18:1<64::aid-dvg7>3.0.co;2-#openalex-snapshot
Role of environmental signals and transcriptional regulators in neural crest development
inferredcites →https://doi.org/10.1002/1097-0177(20010301)220:3<212::aid-dvdy1105>3.0.co;2-9openalex-snapshot
Hyperpigmentation in the Silkie fowl correlates with abnormal migration of fate-restricted melanoblasts and loss of environmental barrier molecules
inferredcites →https://doi.org/10.1002/1521-1878(200008)22:8<708::aid-bies4>3.0.co;2-nopenalex-snapshot
Environmental signals and cell fate specification in premigratory neural crest
inferredcites →https://doi.org/10.1002/aja.1000610104openalex-snapshot
Observations upon the migration of neural crest cells, and upon the development of the spinal ganglia and vertebral arches in Amblystoma
inferredcites →https://doi.org/10.1002/aja.1001880210openalex-snapshot
Localization of pigment cells in cultured frog skin
inferredcites →https://doi.org/10.1002/aja.1001920110openalex-snapshot
Pigment cell localizations in anuran ventral skin at climactic metamorphosis
inferredcites →https://doi.org/10.1002/aja.1001950104openalex-snapshot
Segregation and early dispersal of neural crest cells in the embryonic zebrafish
inferredcites →https://doi.org/10.1002/aja.1002030111openalex-snapshot
Steel and c‐kit in the development of avian melanocytes: A study of normally pigmented birds and of the hyperpigmented mutant silky fowl
inferredcites →https://doi.org/10.1002/aja.1002030302openalex-snapshot
Stages of embryonic development of the zebrafish
inferredcites →https://doi.org/10.1002/ar.a.10078openalex-snapshot
PNA‐positive glycoconjugates are negatively correlated with the access of neural crest cells to the gut in chicken embryos
inferredcites →https://doi.org/10.1002/bdrc.20021openalex-snapshot
Developmental imaging: Insights into the avian embryo
inferredcites →https://doi.org/10.1002/bies.950150202openalex-snapshot
Steel factor and c‐Kit receptor: From mutants to a growth factor system
inferredcites →https://doi.org/10.1002/bies.950190411openalex-snapshot
Receptor tyrosine kinase‐dependent neural crest migration in response to differentially localized growth factors
inferredcites →https://doi.org/10.1002/cne.903250109openalex-snapshot
Distribution and innervation of lateral line organs in the axolotl
inferredcites →https://doi.org/10.1002/cne.903400404openalex-snapshot
Development of lateral line organs in the axolotl
inferredcites →https://doi.org/10.1002/dvdy.10334openalex-snapshot
Pigment cell organization in the hypodermis of zebrafish
inferredcites →https://doi.org/10.1002/dvdy.10465openalex-snapshot
MMP‐2 plays an essential role in producing epithelial‐mesenchymal transformations in the avian embryo
inferredcites →https://doi.org/10.1002/dvdy.10485openalex-snapshot
Comparative analysis of neural crest cell death, migration, and function during vertebrate embryogenesis
inferredcites →https://doi.org/10.1002/dvdy.10494openalex-snapshot
Skeletal and pigment cell defects in the lockjaw mutant reveal multiple roles for zebrafish tfap2a in neural crest development
inferredcites →https://doi.org/10.1002/dvdy.20341openalex-snapshot
Sox10 overexpression induces neural crest‐like cells from all dorsoventral levels of the neural tube but inhibits differentiation
inferredcites →https://doi.org/10.1002/dvg.1020010402openalex-snapshot
The developmental genetics of pigment mutants in the Mexican axolotl
inferredcites →https://doi.org/10.1002/j.1460-2075.1985.tb03793.xopenalex-snapshot
Production of plasminogen activator by migrating cephalic neural crest cells.
inferredcites →https://doi.org/10.1002/j.1460-2075.1991.tb04989.xopenalex-snapshot
Activation of the human c‐kit product by ligand‐induced dimerization mediates circular actin reorganization and chemotaxis.
inferredcites →https://doi.org/10.1002/j.1460-2075.1991.tb07744.xopenalex-snapshot
In utero manipulation of coat color formation by a monoclonal anti‐c‐kit antibody: two distinct waves of c‐kit‐dependency during melanocyte development.
inferredcites →https://doi.org/10.1002/j.1460-2075.1991.tb07782.xopenalex-snapshot
Embryonic RNA expression patterns of the c‐kit receptor and its cognate ligand suggest multiple functional roles in mouse development.
inferredcites →https://doi.org/10.1002/j.1460-2075.1991.tb08054.xopenalex-snapshot
Pax‐3, a novel murine DNA binding protein expressed during early neurogenesis.
inferredcites →https://doi.org/10.1002/jcp.1041470206openalex-snapshot
Adhesion of mouse mast cells to fibroblasts: Adverse effects of steel (SI) mutation
inferredcites →https://doi.org/10.1002/jemt.10162openalex-snapshot
Pigment pattern formation in zebrafish: A model for developmental genetics and the evolution of form
inferredcites →https://doi.org/10.1002/jez.1400720102openalex-snapshot
An experimental study of the origin of pigment cells in Amphibia
inferredcites →https://doi.org/10.1002/jez.1400740206openalex-snapshot
Correlated genetic and embryological experiments on Triturus. I and II
inferredcites →https://doi.org/10.1002/jez.1400780407openalex-snapshot
Neural fold derivatives in the amphibia: Pigment cells, spinal ganglia and Rohon‐Beard cells
inferredcites →https://doi.org/10.1002/jez.1400800210openalex-snapshot
The production of pigment by chick neural crest in grafts to the 3‐day limb bud
inferredcites →https://doi.org/10.1002/jez.1400820203openalex-snapshot
The role of embryonic ectoderm and mesoderm in pigment production in amphibia
inferredcites →https://doi.org/10.1002/jez.1400870208openalex-snapshot
The role of the ectoderm in pigment production, studied by transplantation and hybridization
inferredcites →https://doi.org/10.1002/jez.1400950206openalex-snapshot
Chromatophore migration as a response to mutual influences of the developing pigment cells
inferredcites →https://doi.org/10.1002/jez.1401000108openalex-snapshot
The developmental analysis of specific pigment patterns
inferredcites →https://doi.org/10.1002/jez.1401080305openalex-snapshot
Causal analysis of chromatophore migration
inferredcites →https://doi.org/10.1002/jez.1401130308openalex-snapshot
The origin of epidermal melanophores during metamorphosis in Triturus torosus
inferredcites →https://doi.org/10.1002/jez.1401150109openalex-snapshot
Inhibition of chromoblast migration as a factor in the development of genetic differences in pigmentation in white and black axolotls
inferredcites →https://doi.org/10.1002/jez.1401240309openalex-snapshot
Analysis of the development of pigment patterns in larval salamanders, with special reference to the influence of epidermis and mesoderm
inferredcites →https://doi.org/10.1002/jez.1401250204openalex-snapshot
The origin and development of chromatophores of Xenopus laevis and other anurans
inferredcites →https://doi.org/10.1002/jez.1401250306openalex-snapshot
An analysis of the formation of color patterns in two fresh‐water fish
inferredcites →https://doi.org/10.1002/jez.1401350208openalex-snapshot
The developmental mechanics of pigment pattern formation in the black axolotl, Amblystoma mexicanum I. The formation of yellow and black bars in young larvae,
inferredcites →https://doi.org/10.1002/jez.1401410103openalex-snapshot
An experimental analysis of the development of a color pattern in the fish Brachydanio albolineatus Blyth
inferredcites →https://doi.org/10.1002/jez.1401660312openalex-snapshot
Temporal skin factors influencing the development of melanoblasts in piebald mice
inferredcites →https://doi.org/10.1002/jez.1401730406openalex-snapshot
Does differential adhesion govern self‐assembly processes in histogenesis? Equilibrium configurations and the emergence of a hierarchy among populations of embryonic cells
inferredcites →https://doi.org/10.1002/jez.1402050205openalex-snapshot
Dynamics of pigment pattern formation in the zebrafish, Brachydanio rerio. I. Establishment and regulation of the lateral line melanophore stripe during the first eight days of development
inferredcites →https://doi.org/10.1002/jez.1402050206openalex-snapshot
Dynamics of pigment pattern formation in the zebrafish, Brachydanio rerio. II. Lability of lateral line stripe formation and regulation of pattern defects
inferredcites →https://doi.org/10.1002/jez.1402070211openalex-snapshot
Role of neural crest in determining the numbers of pigment cells in the melanoid mutant of Ambystoma mexicanum Shaw
inferredcites →https://doi.org/10.1002/jez.1402210116openalex-snapshot
The pale mutation in Bombina orientalis: Effects on melanophores and xanthophores
inferredcites →https://doi.org/10.1002/jez.1402240219openalex-snapshot
Development of the spot pattern in the leopard frog
inferredcites →https://doi.org/10.1002/jez.1402270112openalex-snapshot
Dynamics of pigment pattern formation in the zebrafish, Brachydanio rerio. III. Effect of anteroposterior location of three‐day lateral line melanophores on colonization by the second wave of melanophores
inferredcites →https://doi.org/10.1002/jez.1402290112openalex-snapshot
Neural crest cell behavior in white and dark larvae of Ambystoma mexicanum: Differences in cell morphology, arrangement, and extracellular matrix as related to migration
inferredcites →https://doi.org/10.1002/jez.1402290113openalex-snapshot
Neural crest cell behavior in white and dark larvae of Ambystoma mexicanum: Time‐lapse cinemicrographic analysis of pigment cell movement in vivo and in culture
inferredcites →https://doi.org/10.1002/jez.1402300208openalex-snapshot
Quail melanoblast migration in two breeds of fowl and in their hybrids: Evidence for a dominant genic control of the mesodermal pigment cell pattern through the tissue environment
inferredcites →https://doi.org/10.1002/jez.1402510203openalex-snapshot
Plasminogen activator activity is associated with neural crest cell motility in tissue culture
inferredcites →https://doi.org/10.1002/jez.1402610410openalex-snapshot
Inhibition of neural crest cell differentiation by embryo ectodermal extract
inferredcites →https://doi.org/10.1002/jez.1402630112openalex-snapshot
Intrinsic pigment cell stimulating activity in the skin of the leopard frog, Rana pipiens
inferredcites →https://doi.org/10.1002/jez.1402640212openalex-snapshot
Genetic and experimental studies on a new pigment mutant in Xenopus laevis
inferredcites →https://doi.org/10.1002/jez.2openalex-snapshot
Homology and evolutionary novelty in the deployment of extracellular matrix molecules during pigment pattern formation in the salamanders Taricha torosa and T. rivularis (Salamandridae)
inferredcites →https://doi.org/10.1002/jmor.1050520207openalex-snapshot
The development and the regeneration of the color pattern in brachydanio rerio
inferredcites →https://doi.org/10.1002/jmor.1050690105openalex-snapshot
Growth of the adepidermal melanophore network of discoglossus pictus, studied in living tadpoles
inferredcites →https://doi.org/10.1002/jmor.1050930105openalex-snapshot
Development and migration of pigment cells in some teleost fishes
inferredcites →https://doi.org/10.1002/jmor.1051400303openalex-snapshot
Cytophysiological basis of disruptive pigmentary patterns in the leopard frog Rana pipiens. I chromatophore densities and cytophysiology
inferredcites →https://doi.org/10.1002/jmor.1051460103openalex-snapshot
Cytophysiological basis of disruptive pigmentary patterns in the leopard frog Rana pipiens. II. Wild type and mutant cell‐specific patterns,
inferredcites →https://doi.org/10.1002/jmor.1051620106openalex-snapshot
Ontogeny of melanophore patterns in haploid and diploid embryos of the frog, Bombina orientalis
inferredcites →https://doi.org/10.1002/jmor.1051790303openalex-snapshot
Pigment cell differentiation in the fire‐bellied toad, Bombina orientalis. I. Structural, chemical, and physical aspects of the adult pigment pattern
inferredcites →https://doi.org/10.1002/jmor.1052110109openalex-snapshot
Pigment pattern formation in larval ambystomatid salamanders: Ambystoma tigrinum tigrinum
inferredcites →https://doi.org/10.1002/jmor.1052150204openalex-snapshot
Pigment pattern formation in the larval salamander Ambystoma maculatum
inferredcites →https://doi.org/10.1002/jmor.1052200203openalex-snapshot
Pigment pattern formation in larval ambystomatid salamanders: Ambystoma talpoideum, Ambystoma barbouri, and Ambystoma annulatum
inferredcites →https://doi.org/10.1002/neu.480240205openalex-snapshot
Distribution of pluripotent neural crest cells in the embryo and the role of brain‐derived neurotrophic factor in the commitment to the primary sensory neuron lineage
inferredcites →https://doi.org/10.1002/neu.480241009openalex-snapshot
Pax: Gene regulators in the developing nervous system
inferredcites →https://doi.org/10.1006/dbio.1993.1122openalex-snapshot
Binding of Germ Cells to Mutant SId Sertoli Cells Is Defective and Is Rescued by Expression of the Transmembrane Form of the c-kit Ligand
inferredcites →https://doi.org/10.1006/dbio.1993.1217openalex-snapshot
Origins of Neural Crest Cell Diversity
inferredcites →https://doi.org/10.1006/dbio.1993.1218openalex-snapshot
Lineage Diversification of the Neural Crest: In Vitro Investigations
inferredcites →https://doi.org/10.1006/dbio.1993.1219openalex-snapshot
Patterning of Neural Crest Derivatives in the Avian Embryo: in Vivo and in Vitro Studies
inferredcites →https://doi.org/10.1006/dbio.1993.1221openalex-snapshot
The Role of Cell-Cell and Cell-Matrix Interactions in the Morphogenesis of the Neural Crest
inferredcites →https://doi.org/10.1006/dbio.1993.1246openalex-snapshot
Transient Steel Factor Dependence by Neural Crest-Derived Melanocyte Precursors
inferredcites →https://doi.org/10.1006/dbio.1995.1004openalex-snapshot
Genetic Control of Adult Pigment Stripe Development in Zebrafish
inferredcites →https://doi.org/10.1006/dbio.1995.1013openalex-snapshot
Evidence That MIF Plays a Role in the Development of Pigmentation Patterns in the Frog
inferredcites →https://doi.org/10.1006/dbio.1995.1021openalex-snapshot
Transcriptional Activation of the Matrix Metalloproteinase Gene stromelysin-3 Coincides with Thyroid Hormone-Induced Cell Death during Frog Metamorphosis
inferredcites →https://doi.org/10.1006/dbio.1995.1170openalex-snapshot
Steel Factor Directs Melanocyte Development in Vitro through Selective Regulation of the Number of c-kit+ Progenitors
inferredcites →https://doi.org/10.1006/dbio.1996.0114openalex-snapshot
Pigment Patterns of Larval Salamanders (Ambystomatidae, Salamandridae): The Role of the Lateral Line Sensory System and the Evolution of Pattern-Forming Mechanisms
inferredcites →https://doi.org/10.1006/dbio.1996.0115openalex-snapshot
When Neural Crest and Placodes Collide: Interactions between Melanophores and the Lateral Lines That Generate Stripes in the SalamanderAmbystoma tigrinum tigrinum(Ambystomatidae)
inferredcites →https://doi.org/10.1006/dbio.1996.0178openalex-snapshot
Ectopic c-kit Expression Affects the Fate of Melanocyte Precursors in Patch Mutant Embryos
inferredcites →https://doi.org/10.1006/dbio.1996.0269openalex-snapshot
Distinct and Overlapping Expression Patterns of Ligands for Eph-Related Receptor Tyrosine Kinases during Mouse Embryogenesis
inferredcites →https://doi.org/10.1006/dbio.1997.8800openalex-snapshot
Role of Mitf in Differentiation and Transdifferentiation of Chicken Pigmented Epithelial Cell
inferredcites →https://doi.org/10.1006/dbio.1998.8910openalex-snapshot
Survival of patchwork Melanoblasts Is Dependent upon Their Number in the Hair Follicle at the End of Embryogenesis
inferredcites →https://doi.org/10.1006/dbio.1998.8963openalex-snapshot
The Delayed Entry of Thoracic Neural Crest Cells into the Dorsolateral Path Is a Consequence of the Late Emigration of Melanogenic Neural Crest Cells from the Neural Tube
inferredcites →https://doi.org/10.1006/dbio.2000.9840openalex-snapshot
Genetic Analysis of Melanophore Development in Zebrafish Embryos
inferredcites →https://doi.org/10.1006/dbio.2000.9856openalex-snapshot
MGF (KIT Ligand) Is a Chemokinetic Factor for Melanoblast Migration into Hair Follicles
inferredcites →https://doi.org/10.1006/dbio.2000.9899openalex-snapshot
Mutational Analysis of Endothelin Receptor b1 (rose) during Neural Crest and Pigment Pattern Development in the Zebrafish Danio rerio
inferredcites →https://doi.org/10.1006/dbio.2001.0167openalex-snapshot
Analysis of Melanocyte Precursors in Nf1 Mutants Reveals That MGF/KIT Signaling Promotes Directed Cell Migration Independent of Its Function in Cell Survival
inferredcites →https://doi.org/10.1006/dbio.2001.0222openalex-snapshot
Wnt and BMP Signaling Govern Lineage Segregation of Melanocytes in the Avian Embryo
inferredcites →https://doi.org/10.1006/dbio.2001.0372openalex-snapshot
Analysis of SOX10 Function in Neural Crest-Derived Melanocyte Development: SOX10-Dependent Transcriptional Control of Dopachrome Tautomerase
inferredcites →https://doi.org/10.1006/dbio.2001.0418openalex-snapshot
How the Zebrafish Gets Its Stripes
inferredcites →https://doi.org/10.1007/978-3-642-75056-4openalex-snapshot
The Development of the Larval Pigment Patterns in Triturus alpestris and Ambystoma mexicanum
inferredcites →https://doi.org/10.1007/bf00215855openalex-snapshot
Expression of the HNK-1/NC-1 epitope in early vertebrate neurogenesis
inferredcites →https://doi.org/10.1007/bf00363214openalex-snapshot
Neurulation in the anterior trunk region of the zebrafish Brachydanio rerio
inferredcites →https://doi.org/10.1007/bf00573467openalex-snapshot
Zur Entwicklung der Ganglienleiste y. �ber die Differenzierung des Rumpfganglienleistenmaterials
inferredcites →https://doi.org/10.1007/bf00573807openalex-snapshot
The production of pigment in vitro by chick neural crest
inferredcites →https://doi.org/10.1007/bf00576356openalex-snapshot
Zur entwicklung der Ganglienleiste. I. Die Kinematik der Ganglienleistenentwicklung bei den Urodelen
inferredcites →https://doi.org/10.1007/bf00848226openalex-snapshot
Xanthophores in chromatophore groups of the premigratory neural crest initiate the pigment pattern of the axolotl larva
inferredcites →https://doi.org/10.1007/bf00848526openalex-snapshot
Untersuchungen �ber das Farbmuster der ZebrabarbeBrachydanio rerio (Cyprinidae, Teleostei)
inferredcites →https://doi.org/10.1007/bf01826278openalex-snapshot
Über die Entwicklung des Haut- und Haarpigmentes beim menschlichen Embryo und über das Erlöschen der Pigmentbildung im ergrauenden Haar (Ursache der Canities)
inferredcites →https://doi.org/10.1007/bf01827851openalex-snapshot
Das Problem der Pigmentbildung in der Haut
inferredcites →https://doi.org/10.1007/bf02616114openalex-snapshot
Contact inhibition in tissue culture
inferredcites →https://doi.org/10.1007/bf02620988openalex-snapshot
The effects of various nutritional supplements on the growth, migration and differentiation ofxenopus laevis neural crest cells in vitro
inferredcites →https://doi.org/10.1007/bf02630960openalex-snapshot
Effects of fetal bovine serum and serum-free conditions on white and dark axolotl neural crest explants
inferredcites →https://doi.org/10.1007/s004270050051openalex-snapshot
Mutations affecting pigmentation and shape of the adult zebrafish
inferredcites →https://doi.org/10.1007/s004270100155openalex-snapshot
Zebrafish hybrids suggest genetic mechanisms for pigment pattern diversification in Danio
inferredcites →https://doi.org/10.1007/s004390000328openalex-snapshot
Transcription factor hierarchy in Waardenburg syndrome: regulation of MITF expression by SOX10 and PAX3
inferredcites →https://doi.org/10.1007/s004410050927openalex-snapshot
Ephrins and their receptors: a repulsive topic?
inferredcites →https://doi.org/10.1007/s004410051365openalex-snapshot
Genesis, a Winged Helix transcriptional repressor, has embryonic expression limited to the neural crest, and stimulates proliferation in vitro in a neural development model
inferredcites →https://doi.org/10.1016/0012-1606(62)90014-3openalex-snapshot
Effects of different doses and combinations of spotting genes in the leopard frog, Rana pipiens
inferredcites →https://doi.org/10.1016/0012-1606(65)90042-4openalex-snapshot
The development of piebald spotting in mice
inferredcites →https://doi.org/10.1016/0012-1606(67)90051-6openalex-snapshot
Pigment cell migration in piebald mice
inferredcites →https://doi.org/10.1016/0012-1606(68)90023-7openalex-snapshot
An experimental analysis of the pigment defect caused by mutations at the W and Sl loci in mice
inferredcites →https://doi.org/10.1016/0012-1606(70)90100-4openalex-snapshot
A comparison of pigment cell development in albino, steel, and dominant-spotting mutant mouse embryos
inferredcites →https://doi.org/10.1016/0012-1606(73)90337-0openalex-snapshot
The migratory pathway of neural crest cells into the skin of mouse embryos
inferredcites →https://doi.org/10.1016/0012-1606(74)90176-6openalex-snapshot
Morphogenesis of the dorsal pigmentary pattern in wild-type and mutant Rana pipiens
inferredcites →https://doi.org/10.1016/0012-1606(74)90187-0openalex-snapshot
Ultrastructural investigation of autophagocytosis of melanosomes and programmed death of melanocytes in White Leghorn feathers: a study of morphogenetic events leading to hypomelanosis
inferredcites →https://doi.org/10.1016/0012-1606(74)90291-7openalex-snapshot
Experimental analysis of the migration and differentiation of neuroblasts of the autonomic nervous system and of neurectodermal mesenchymal derivatives, using a biological cell marking technique
inferredcites →https://doi.org/10.1016/0012-1606(77)90259-7openalex-snapshot
Dosage effects of the white (d) and melanoid (m) genes on pigment pattern in the Mexican axolotl, Ambystoma mexicanum, Shaw
inferredcites →https://doi.org/10.1016/0012-1606(77)90268-8openalex-snapshot
Enhancement of melanocyte development from piebald neural crest by a favorable tissue environment
inferredcites →https://doi.org/10.1016/0012-1606(78)90219-1openalex-snapshot
The early migration of neural crest cells in the trunk region of the avian embryo: An electron microscopic study
inferredcites →https://doi.org/10.1016/0012-1606(80)90151-7openalex-snapshot
Neural crest cell migration in relation to extracellular matrix organization in the embryonic axolotl trunk
inferredcites →https://doi.org/10.1016/0012-1606(80)90462-5openalex-snapshot
Analysis of migratory behavior of neural crest and fibroblastic cells in embryonic tissues
inferredcites →https://doi.org/10.1016/0012-1606(80)90481-9openalex-snapshot
Restrictions of developmental capabilities in neural crest cell derivatives as tested by in vivo transplantation experiments
inferredcites →https://doi.org/10.1016/0012-1606(80)90501-1openalex-snapshot
Clonal analysis of quail neural crest cells
inferredcites →https://doi.org/10.1016/0012-1606(82)90058-6openalex-snapshot
Formation of pigment cell patterns in Triturus alpestris embryos
inferredcites →https://doi.org/10.1016/0012-1606(82)90306-2openalex-snapshot
Neural crest cell behavior in white and dark embryos of Ambystoma mexicanum: Epidermal inhibition of pigment cell migration in the white axolotl
inferredcites →https://doi.org/10.1016/0012-1606(82)90349-9openalex-snapshot
The early development of cranial sensory ganglia and the potentialities of their component cells studied in quail-chick chimeras
inferredcites →https://doi.org/10.1016/0012-1606(83)90192-6openalex-snapshot
Negative chemotaxis does not control quail neural crest cell dispersion
inferredcites →https://doi.org/10.1016/0012-1606(84)90286-0openalex-snapshot
Cell division in the ciliary ganglion of quail embryos in situ and after back-transplantation into the neural crest migration pathways of chick embryos
inferredcites →https://doi.org/10.1016/0012-1606(85)90326-4openalex-snapshot
Stimulation of initial neural crest cell migration in the axolotl embryo by tissue grafts and extracellular matrix transplanted on microcarriers
inferredcites →https://doi.org/10.1016/0012-1606(85)90442-7openalex-snapshot
Control of neural crest cell dispersion in the trunk of the avian embryo
inferredcites →https://doi.org/10.1016/0012-1606(86)90094-1openalex-snapshot
Pigment cell pattern formation in Taricha torosa: The role of the extracellular matrix in controlling pigment cell migration and differentiation
inferredcites →https://doi.org/10.1016/0012-1606(86)90168-5openalex-snapshot
Promotion of chromatophore differentiation in isolated premigratory neural crest cells by extracellular material explanted on microcarriers
inferredcites →https://doi.org/10.1016/0012-1606(86)90226-5openalex-snapshot
Analysis of the early stages of trunk neural crest migration in avian embryos using monoclonal antibody HNK-1
inferredcites →https://doi.org/10.1016/0012-1606(87)90101-1openalex-snapshot
Behavior of neural crest cells on embryonic basal laminae
inferredcites →https://doi.org/10.1016/0012-1606(87)90154-0openalex-snapshot
Neural crest cell migratory pathways in the trunk of the chick embryo
inferredcites →https://doi.org/10.1016/0012-1606(87)90463-5openalex-snapshot
Neural crest development in the Xenopus laevis embryo, studied by interspecific transplantation and scanning electron microscopy
inferredcites →https://doi.org/10.1016/0012-1606(88)90158-3openalex-snapshot
A ventrally localized inhibitor of melanization in Xenopus laevis skin
inferredcites →https://doi.org/10.1016/0012-1606(88)90194-7openalex-snapshot
Mapping of neural crest pathways in Xenopus laevis using inter- and intra-specific cell markers
inferredcites →https://doi.org/10.1016/0012-1606(88)90420-4openalex-snapshot
Changes in the migratory properties of neural crest and early crest-derived cells in vivo following treatment with a phorbol ester drug
inferredcites →https://doi.org/10.1016/0012-1606(89)90295-9openalex-snapshot
Neural fold formation at newly created boundaries between neural plate and epidermis in the axolotl
inferredcites →https://doi.org/10.1016/0012-1606(90)90002-zopenalex-snapshot
Inhibition of neural crest cell migration by aggregating chondroitin sulfate proteoglycans is mediated by their hyaluronan-binding region
inferredcites →https://doi.org/10.1016/0012-1606(90)90380-2openalex-snapshot
The origins of neural crest cells in the axolotl
inferredcites →https://doi.org/10.1016/0012-1606(91)90224-qopenalex-snapshot
Terminal migration and early differentiation of melanocytes in embryonic chick skin
inferredcites →https://doi.org/10.1016/0012-1606(91)90233-sopenalex-snapshot
Expression of c-kit encoded at the W locus of mice in developing embryonic germ cells and presumptive melanoblasts
inferredcites →https://doi.org/10.1016/0012-1606(92)90124-yopenalex-snapshot
Steel factor is required for maintenance, but not differentiation, of melanocyte precursors in the neural crest
inferredcites →https://doi.org/10.1016/0012-1606(92)90231-5openalex-snapshot
Descriptive and experimental analysis of the dispersion of neural crest cells along the dorsolateral path and their entry into ectoderm in the chick embryo
inferredcites →https://doi.org/10.1016/0016-6480(91)90113-kopenalex-snapshot
Effect of background color and low temperature on skin color and circulating α-MSH in two species of leopard frog
inferredcites →https://doi.org/10.1016/0040-8166(92)90074-hopenalex-snapshot
Role of the dermal tracts in the pigment pattern of the frog
inferredcites →https://doi.org/10.1016/0045-6039(86)90092-8openalex-snapshot
Pigment cell differentiation: the relationship between pterin content, allopurinol treatment, and the melanoid gene in axolotls
inferredcites →https://doi.org/10.1016/0092-8674(88)90020-7openalex-snapshot
The dominant-white spotting (W) locus of the mouse encodes the c-kit proto-oncogene
inferredcites →https://doi.org/10.1016/0092-8674(90)90297-ropenalex-snapshot
Identification of a ligand for the c-kit proto-oncogene
inferredcites →https://doi.org/10.1016/0092-8674(90)90299-topenalex-snapshot
The kit ligand: A cell surface molecule altered in steel mutant fibroblasts
inferredcites →https://doi.org/10.1016/0092-8674(90)90300-4openalex-snapshot
Identification, purification, and biological characterization of hematopoietic stem cell factor from buffalo rat liver-conditioned medium
inferredcites →https://doi.org/10.1016/0092-8674(90)90301-topenalex-snapshot
Primary structure and functional expression of rat and human stem cell factor DNAs
inferredcites →https://doi.org/10.1016/0092-8674(90)90302-uopenalex-snapshot
Stem cell factor is encoded at the SI locus of the mouse and is the ligand for the c-kit tyrosine kinase receptor
inferredcites →https://doi.org/10.1016/0092-8674(90)90303-vopenalex-snapshot
The hematopoietic growth factor KL is encoded by the SI locus and is the ligand of the c-kit receptor, the gene product of the W locus
inferredcites →https://doi.org/10.1016/0092-8674(90)90304-wopenalex-snapshot
Molecular cloning of mast cell growth factor, a hematopoietin that is active in both membrane bound and soluble forms
inferredcites →https://doi.org/10.1016/0092-8674(91)90326-topenalex-snapshot
Transmembrane form of the kit ligand growth factor is determined by alternative splicing and is missing in the SId mutant
inferredcites →https://doi.org/10.1016/0092-8674(93)90429-topenalex-snapshot
Mutations at the mouse microphthalmia locus are associated with defects in a gene encoding a novel basic-helix-loop-helix-zipper protein
inferredcites →https://doi.org/10.1016/0092-8674(94)90017-5openalex-snapshot
Targeted and natural (piebald-lethal) mutations of endothelin-B receptor gene produce megacolon associated with spotted coat color in mice
inferredcites →https://doi.org/10.1016/0092-8674(94)90018-3openalex-snapshot
Interaction of endothelin-3 with endothelin-B receptor is essential for development of epidermal melanocytes and enteric neurons
inferredcites →https://doi.org/10.1016/0168-9525(93)90015-aopenalex-snapshot
From white spots to stem cells: the role of the Kit receptor in mammalian development
inferredcites →https://doi.org/10.1016/0925-4773(94)00331-gopenalex-snapshot
Mutations at the W locus affect survival of neural crest-derived melanocytes in the mouse
inferredcites →https://doi.org/10.1016/0925-4773(94)00338-nopenalex-snapshot
A Xenopus c-kit-related receptor tyrosine kinase expressed in migrating stem cells of the lateral line system
inferredcites →https://doi.org/10.1016/b978-1-4832-2888-4.50006-1openalex-snapshot
Extrinsic and Intrinsic Factors Influencing Amphibian Pigment Pattern Formation
inferredcites →https://doi.org/10.1016/b978-1-4832-2888-4.50015-2openalex-snapshot
Precursors of Epidermal Melanocytes in the Negro Fetus
inferredcites →https://doi.org/10.1016/j.cub.2003.11.038openalex-snapshot
Pigment patterns: fish in stripes and spots
inferredcites →https://doi.org/10.1016/j.cub.2005.02.030openalex-snapshot
erbb3 and erbb2 Are Essential for Schwann Cell Migration and Myelination in Zebrafish
inferredcites →https://doi.org/10.1016/j.cub.2005.02.050openalex-snapshot
Defective Skeletogenesis with Kidney Stone Formation in Dwarf Zebrafish Mutant for trpm7
inferredcites →https://doi.org/10.1016/j.devcel.2004.12.010openalex-snapshot
The Transcriptional Control of Trunk Neural Crest Induction, Survival, and Delamination
inferredcites →https://doi.org/10.1016/j.mod.2004.01.004openalex-snapshot
The Tomita collection of medaka pigmentation mutants as a resource for understanding neural crest cell development
inferredcites →https://doi.org/10.1016/j.mod.2004.03.011openalex-snapshot
Medaka as a research organism: past, present and future
inferredcites →https://doi.org/10.1016/j.mod.2004.03.012openalex-snapshot
Stages of normal development in the medaka Oryzias latipes
inferredcites →https://doi.org/10.1016/j.mod.2004.04.022openalex-snapshot
Strategies of vertebrate neurulation and a re-evaluation of teleost neural tube formation
inferredcites →https://doi.org/10.1016/j.mod.2004.06.005openalex-snapshot
Touchtone promotes survival of embryonic melanophores in zebrafish
inferredcites →https://doi.org/10.1016/j.mod.2004.06.006openalex-snapshot
Melanophore sublineage-specific requirement for zebrafish touchtone during neural crest development
inferredcites →https://doi.org/10.1016/j.modgep.2003.07.002openalex-snapshot
Pmel17 expression is Mitf-dependent and reveals cranial melanoblast migration during murine development
inferredcites →https://doi.org/10.1016/j.ydbio.2003.09.029openalex-snapshot
Transcription factor Ap-2α is necessary for development of embryonic melanophores, autonomic neurons and pharyngeal skeleton in zebrafish
inferredcites →https://doi.org/10.1016/j.ydbio.2004.01.020openalex-snapshot
Chemokine signaling regulates sensory cell migration in zebrafish
inferredcites →https://doi.org/10.1016/j.ydbio.2004.09.029openalex-snapshot
Esrom, an ortholog of PAM (protein associated with c-myc), regulates pteridine synthesis in the zebrafish
inferredcites →https://doi.org/10.1016/j.ydbio.2005.03.021openalex-snapshot
Slit/Robo signaling is necessary to confine early neural crest cells to the ventral migratory pathway in the trunk
inferredcites →https://doi.org/10.1016/j.ydbio.2005.06.001openalex-snapshot
A mutation in the silver gene leads to defects in melanosome biogenesis and alterations in the visual system in the zebrafish mutant fading vision
inferredcites →https://doi.org/10.1016/s0002-9440(10)63657-7openalex-snapshot
MLANA/MART1 and SILV/PMEL17/GP100 Are Transcriptionally Regulated by MITF in Melanocytes and Melanoma
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What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.4767229openalex-extracted
Transcriptome and Metabolome Provide Insight into the Formation Mechanism of Skin Pigmentation Diversity in Chinese Soft-Shelled Turtle (Pelodiscus Sinensis)
inferred← citeshttps://doi.org/10.1002/dvdy.22440openalex-snapshot
Origin of adult‐type pigment cells forming the asymmetric pigment pattern, in Japanese flounder (Paralichthys olivaceus)
inferred← citeshttps://doi.org/10.1002/jez.b.21141openalex-snapshot
Homology and the evolution of novelty duringDanioadult pigment pattern development
inferred← citeshttps://doi.org/10.1006/dbio.2000.9899openalex-snapshot
Mutational Analysis of Endothelin Receptor b1 (rose) during Neural Crest and Pigment Pattern Development in the Zebrafish Danio rerio
inferred← citeshttps://doi.org/10.1007/978-981-16-1490-3_10openalex-snapshot
Evolution of Pigment Pattern Formation in Teleosts
inferred← citeshttps://doi.org/10.1016/j.semcdb.2008.11.012openalex-snapshot
Not just black and white: Pigment pattern development and evolution in vertebrates
inferred← citeshttps://doi.org/10.1016/j.ydbio.2021.04.007openalex-snapshot
Immunoglobulin superfamily receptor Junctional adhesion molecule 3 (Jam3) requirement for melanophore survival and patterning during formation of zebrafish stripes
inferred← citeshttps://doi.org/10.1016/s0925-4773(00)00308-7openalex-snapshot
Keratinocyte expression of transgenic hepatocyte growth factor affects melanocyte development, leading to dermal melanocytosis
inferred← citeshttps://doi.org/10.1016/s1567-133x(02)00072-8openalex-snapshot
The expression patterns of c-kit and Sl in chicken embryos suggest unexpected roles for these genes in somite and limb development
inferred← citeshttps://doi.org/10.1038/s41598-017-12352-0openalex-snapshot
Melanoblast development coincides with the late emerging cells from the dorsal neural tube in turtle Trachemys scripta
inferred← citeshttps://doi.org/10.1038/sj.hdy.6800867openalex-snapshot
Evolution of danio pigment pattern development
inferred← citeshttps://doi.org/10.1046/j.1523-1747.2000.00836.xopenalex-snapshot
The Cytotoxicity and Apoptosis Induced by 4-Tertiary Butylphenol in Human Melanocytes are Independent of Tyrosinase Activity
inferred← citeshttps://doi.org/10.1046/j.1523-1747.2003.12562.xopenalex-snapshot
Human Melanoblasts in Culture: Expression of BRN2 and Synergistic Regulation by Fibroblast Growth Factor-2, Stem Cell Factor, and Endothelin-3
inferred← citeshttps://doi.org/10.1056/nejm199904293401707openalex-snapshot
The Pathogenesis of Melanoma Induced by Ultraviolet Radiation
inferred← citeshttps://doi.org/10.1093/jhered/esq044openalex-snapshot
Quantitative Genetics of Pigmentation Development in 2 Populations of the Common Garter Snake, Thamnophis sirtalis
inferred← citeshttps://doi.org/10.1111/bjd.12652openalex-snapshot
Classification of segmental vitiligo on the trunk
inferred← citeshttps://doi.org/10.1111/ede.12272openalex-snapshot
Experimental evidence of the role of heterochrony in evolution of the Mesoamerican cichlids pigment patterns
inferred← citeshttps://doi.org/10.1111/j.1365-4632.2010.04641.xopenalex-snapshot
Aplasia cutis congenita with hair collar sign and dermal melanocytosis
inferred← citeshttps://doi.org/10.1111/j.1467-2494.2004.00254_12.xopenalex-snapshot
Role and modulation of tyrosinase/tyrosinase related protein‐1 complex and PKC beta‐I in melanogenesis
inferred← citeshttps://doi.org/10.1111/pcmr.12332openalex-snapshot
Origins of adult pigmentation: diversity in pigment stem cell lineages and implications for pattern evolution
inferred← citeshttps://doi.org/10.1134/s0032945216020120openalex-snapshot
Effects of hyperthyroidism on the Labeobarbus (= Barbus) intermedius (Cyprinidae) early larval melanophores development
inferred← citeshttps://doi.org/10.1134/s1022795419030098openalex-snapshot
Structure and Variability of 5'UTR, Exon 1 and Fragment of Intron 1 of the Pax3 Gene in American Mink (Neovison vison)
inferred← citeshttps://doi.org/10.1134/s1022795419060073openalex-snapshot
Structure and Variability of the Pax3 and EDNRB Genes in American Mink (Neovison vison)
inferred← citeshttps://doi.org/10.1146/annurev.ecolsys.38.091206.095537openalex-snapshot
Developmental Genetics of Adaptation in Fishes: The Case for Novelty
inferred← citeshttps://doi.org/10.11606/t.5.2013.tde-05022014-110422openalex-snapshot
Melanoma primário da mucosa oral: estudo dos aspectos clínico-patológicos e da expressão das imunoglobulinas e integrinas em 35 casos
inferred← citeshttps://doi.org/10.11606/t.5.2023.tde-25082023-145122openalex-snapshot
Melanoma em crianças, adolescentes e adultos jovens: epidemiologia, correlação clínico-patológica e estudo genético
inferred← citeshttps://doi.org/10.11606/t.60.2016.tde-08072016-080653openalex-snapshot
Estudo sistemático da ação melanogênica do ext rato de Brosimum gaudichaudii Trécul
inferred← citeshttps://doi.org/10.1186/1471-2164-14-171openalex-snapshot
Transcriptomics of morphological color change in polychromatic Midas cichlids
inferred← citeshttps://doi.org/10.1186/s12862-020-01604-9openalex-snapshot
Distinct patterns of pigment development underlie convergent hyperpigmentation between nocturnal and diurnal geckos (Squamata: Gekkota)
inferred← citeshttps://doi.org/10.1242/dev.02799openalex-snapshot
Deconstructing evolution of adult phenotypes: genetic analyses ofkitreveal homology and evolutionary novelty during adult pigment pattern development ofDaniofishes
inferred← citeshttps://doi.org/10.1371/journal.pbio.1001966openalex-snapshot
Melanoma Cells Break Down LPA to Establish Local Gradients That Drive Chemotactic Dispersal
inferred← citeshttps://doi.org/10.1371/journal.pgen.1000744openalex-snapshot
Basonuclin-2 Requirements for Zebrafish Adult Pigment Pattern Development and Female Fertility
inferred← citeshttps://doi.org/10.1371/journal.pgen.1002899openalex-snapshot
Melanophore Migration and Survival during Zebrafish Adult Pigment Stripe Development Require the Immunoglobulin Superfamily Adhesion Molecule Igsf11
inferred← citeshttps://doi.org/10.1371/journal.pgen.1003561openalex-snapshot
Interactions with Iridophores and the Tissue Environment Required for Patterning Melanophores and Xanthophores during Zebrafish Adult Pigment Stripe Formation
inferred← citeshttps://doi.org/10.3410/f.726938986.793537855openalex-snapshot
Faculty Opinions recommendation of Inference of the drivers of collective movement in two cell types: Dictyostelium and melanoma.
inferred← citeshttps://doi.org/10.5194/aab-61-173-2018openalex-snapshot
Genetic background of coat colour in sheep
inferred← citeshttps://doi.org/10.5772/67647openalex-snapshot
An Update On Natural Compounds and Their Modern Formulations for the Management of Malignant Melanoma
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