about
Isolation, characterization, and precise physical localization of human CDX1, a caudal-type homeobox geneNiemann-Pick C1 disease gene: homology to mediators of cholesterol homeostasisGpnmb is a melanoblast-expressed, MITF-dependent geneA polymorphism in IRF4 affects human pigmentation through a tyrosinase-dependent MITF/TFAP2A pathwayA Sox10 expression screen identifies an amino acid essential for Erbb3 function.A sensitized mutagenesis screen identifies Gli3 as a modifier of Sox10 neurocristopathyCloning of the human heparan sulfate-N-deacetylase/N-sulfotransferase gene from the Treacher Collins syndrome candidate region at 5q32-q33.1Identification of neural crest and glial enhancers at the mouse Sox10 locus through transgenesis in zebrafish.Networks and pathways in pigmentation, health, and disease.Oligodendroglial and pan-neural crest expression of Cre recombinase directed by Sox10 enhancer.SOX10 directly modulates ERBB3 transcription via an intronic neural crest enhancer.Sox proteins in melanocyte development and melanoma.Mutation of melanosome protein RAB38 in chocolate mice.Distinct microRNA expression signatures are associated with melanoma subtypes and are regulated by HIF1A.Genetic evidence does not support direct regulation of EDNRB by SOX10 in migratory neural crest and the melanocyte lineageComparison of melanoblast expression patterns identifies distinct classes of genesThe pleiotropic mouse phenotype extra-toes spotting is caused by translation initiation factor Eif3c mutations and is associated with disrupted sonic hedgehog signaling.Spotlight on spotted mice: a review of white spotting mouse mutants and associated human pigmentation disorders.Genomic analysis reveals distinct mechanisms and functional classes of SOX10-regulated genes in melanocytes.TFAP2 paralogs regulate melanocyte differentiation in parallel with MITF.Integration of ChIP-seq and machine learning reveals enhancers and a predictive regulatory sequence vocabulary in melanocytes.Substantial narrowing of the Niemann-Pick C candidate interval by yeast artificial chromosome complementation.SOX10 ablation arrests cell cycle, induces senescence, and suppresses melanomagenesisFrequent mutations in the MITF pathway in melanomaA combined genetic and radiation hybrid map surrounding the Treacher Collins syndrome locus on chromosome 5q.Generation of RCAS vectors useful for functional genomic analyses.Loci associated with skin pigmentation identified in African populations.Identification and functional analysis of SOX10 phosphorylation sites in melanoma.Hypoxia-induced HIF1α targets in melanocytes reveal a molecular profile associated with poor melanoma prognosis.The next generation of melanocyte data: Genetic, epigenetic, and transcriptional resource datasets and analysis tools.Complementation of melanocyte development in SOX10 mutant neural crest using lineage-directed gene transfer.A defect in a novel ADAMTS family member is the cause of the belted white-spotting mutation.Meeting report: 16th International Mouse Genome Conference.Genomic Organization of the Human Heparan Sulfate-N-Deacetylase/N-Sulfotransferase Gene: Exclusion from a Causative Role in the Pathogenesis of Treacher Collins Syndrome
P50
Q24311801-26D19971-2AE9-4382-89D9-0C8C2E18D255Q24315133-445CA917-52E3-4422-80A1-E1A5D551B49CQ24646177-332DBCE0-D5D5-4440-B7D2-36D73C197B0EQ28302540-F095A0FD-51B7-4622-8F91-5DFA23714528Q28473562-0061482B-043E-4754-BCE9-ECB419436F7EQ28590547-59471E91-01C6-4112-B42B-204015DE582BQ28609282-C1F843B8-5B96-4E94-86E0-7FC65E3B654FQ33367100-3288E015-DE3E-443C-8C6B-18AAB19503B8Q33584524-E8355F64-5857-475E-9A8A-593022E49401Q33714632-2D377CD5-5470-46FB-928D-36F327BF29C7Q33932242-6C9DDB57-564C-4360-A882-810BB05F0D60Q34005547-F9E655F3-ADD4-49A8-98FF-F71BEE6FF194Q34048569-4BFBD011-4E0B-4440-BCDF-85BFB538AAA5Q34115628-2CEA558D-5D57-4B20-8D16-C3CBB7047DCFQ34374616-8FBFC524-D91B-49A6-8AEE-DD141247925FQ34428830-76075A37-210E-47E1-8641-680E42C09765Q34813367-901D8E81-FD25-46DD-BD96-77AE88C07721Q35771686-0FC7DA77-D3B3-4AE3-8389-39EFED6BE21EQ36065451-E1C4425A-F0C5-4D24-8AE0-39677A19E63DQ36294018-A587C5DA-323E-49D5-B6BF-44622E3C2A8AQ36354909-B44314A6-215E-4CCA-AB2A-49E531E4D8A6Q36656106-36F24563-90FA-4EA5-AE36-EEC9EC2D957AQ37243181-BDE7B3F9-86E1-4A10-8BD2-9D5175E52988Q37309027-DE4CC5D3-4EF2-4985-B76D-1520C9CFB285Q41516132-1030BBB0-9A1C-425E-9A30-F6048E928208Q43826373-D481E241-FDA8-4F5B-BE1F-4BFB4BF2E9D4Q43924342-EE4272AF-95F4-4E51-B7AB-D32937F10BFDQ47190315-CF2CD4EF-607C-4936-A0C5-E34294AECC0FQ47980225-C518EB0D-3AAA-4039-9A11-3AFFED3D1DDEQ48236454-53BFD430-AD11-472B-814B-C8636B88001EQ52095660-31E35C91-E033-4028-A9D4-107E3AEE9F58Q52101514-C9684352-83E3-4798-9DDA-1642A64C1D70Q53295901-8E021502-D373-46BC-9BDA-D2989802467CQ62782906-991C1BAC-2FC2-4DC1-A743-70ACE3D452E9
P50
description
onderzoeker
@nl
researcher, ORCID id # 0000-0002-1958-4689
@en
name
Stacie K Loftus
@ast
Stacie K Loftus
@en
Stacie K Loftus
@es
Stacie K Loftus
@nl
type
label
Stacie K Loftus
@ast
Stacie K Loftus
@en
Stacie K Loftus
@es
Stacie K Loftus
@nl
prefLabel
Stacie K Loftus
@ast
Stacie K Loftus
@en
Stacie K Loftus
@es
Stacie K Loftus
@nl
P106
P1153
7004762782
P31
P496
0000-0002-1958-4689