List of works - Laura L Baxter

A curated gene list for expanding the horizons of pigmentation biology

A curated online resource for SOX10 and pigment cell molecular genetic pathways

scientific article

A sensitized mutagenesis screen identifies Gli3 as a modifier of Sox10 neurocristopathy

scientific journal article

Comparison of melanoblast expression patterns identifies distinct classes of genes

scientific article

Correction: Mutation of the Diamond-Blackfan Anemia Gene Rps7 in Mouse Results in Morphological and Neuroanatomical Phenotypes

scientific article published on 19 November 2015

Defective cerebellar response to mitogenic Hedgehog signaling in Down [corrected] syndrome mice

scholarly article

Distinct microRNA expression signatures are associated with melanoma subtypes and are regulated by HIF1A.

scientific article

Down syndrome mouse models Ts65Dn, Ts1Cje, and Ms1Cje/Ts65Dn exhibit variable severity of cerebellar phenotypes.

scientific article published in July 2004

Efficacy of N-acetylcysteine in phenotypic suppression of mouse models of Niemann-Pick disease, type C1.

scientific article published on 10 May 2013

Genetic evidence does not support direct regulation of EDNRB by SOX10 in migratory neural crest and the melanocyte lineage

scientific article

Gpnmb is a melanoblast-expressed, MITF-dependent gene

scientific article

Hypoxia-induced HIF1α targets in melanocytes reveal a molecular profile associated with poor melanoma prognosis

scientific article published on 6 February 2017

Identification and functional analysis of SOX10 phosphorylation sites in melanoma

scientific article published on 9 January 2018

Informatic and genomic analysis of melanocyte cDNA libraries as a resource for the study of melanocyte development and function

scientific article

Integration of Cytogenetic with Recombinational and Physical Maps of Mouse Chromosome 16

scientific article published on 01 July 1999

Mutation of melanosome protein RAB38 in chocolate mice

scientific article

Mutation of the diamond-blackfan anemia gene Rps7 in mouse results in morphological and neuroanatomical phenotypes

scientific article (publication date: 2013)

Networks and pathways in pigmentation, health, and disease

scientific article

Parallels of craniofacial maldevelopment in Down syndrome and Ts65Dn mice

scientific article published in February 2000

Plasma and tissue concentrations of α-tocopherol and δ-tocopherol following high dose dietary supplementation in mice

scientific article

Pmel17 expression is Mitf-dependent and reveals cranial melanoblast migration during murine development

scientific article

Sox proteins in melanocyte development and melanoma

scientific article

Spotlight on spotted mice: a review of white spotting mouse mutants and associated human pigmentation disorders

scientific article published on June 2004

The etiology and molecular genetics of human pigmentation disorders ⬇️

scientific article published on May 17, 2012

The oculocutaneous albinism type IV gene Matp is a new marker of pigment cell precursors during mouse embryonic development

scientific article

The transcriptional landscape of the mammalian genome

scientific article

Too much of a good thing: mechanisms of gene action in Down syndrome.

scientific article

List of works by Laura L Baxter

A curated gene list for expanding the horizons of pigmentation biology

A curated online resource for SOX10 and pigment cell molecular genetic pathways

A sensitized mutagenesis screen identifies Gli3 as a modifier of Sox10 neurocristopathy

Comparison of melanoblast expression patterns identifies distinct classes of genes

Correction: Mutation of the Diamond-Blackfan Anemia Gene Rps7 in Mouse Results in Morphological and Neuroanatomical Phenotypes

Defective cerebellar response to mitogenic Hedgehog signaling in Down [corrected] syndrome mice

Distinct microRNA expression signatures are associated with melanoma subtypes and are regulated by HIF1A.

Down syndrome mouse models Ts65Dn, Ts1Cje, and Ms1Cje/Ts65Dn exhibit variable severity of cerebellar phenotypes.

Efficacy of N-acetylcysteine in phenotypic suppression of mouse models of Niemann-Pick disease, type C1.

Genetic evidence does not support direct regulation of EDNRB by SOX10 in migratory neural crest and the melanocyte lineage

Gpnmb is a melanoblast-expressed, MITF-dependent gene

Hypoxia-induced HIF1α targets in melanocytes reveal a molecular profile associated with poor melanoma prognosis

Identification and functional analysis of SOX10 phosphorylation sites in melanoma

Informatic and genomic analysis of melanocyte cDNA libraries as a resource for the study of melanocyte development and function

Integration of Cytogenetic with Recombinational and Physical Maps of Mouse Chromosome 16

Mutation of melanosome protein RAB38 in chocolate mice

Mutation of the diamond-blackfan anemia gene Rps7 in mouse results in morphological and neuroanatomical phenotypes

Networks and pathways in pigmentation, health, and disease

Parallels of craniofacial maldevelopment in Down syndrome and Ts65Dn mice

Plasma and tissue concentrations of α-tocopherol and δ-tocopherol following high dose dietary supplementation in mice

Pmel17 expression is Mitf-dependent and reveals cranial melanoblast migration during murine development

Sox proteins in melanocyte development and melanoma

Spotlight on spotted mice: a review of white spotting mouse mutants and associated human pigmentation disorders

The etiology and molecular genetics of human pigmentation disorders ⬇️

The oculocutaneous albinism type IV gene Matp is a new marker of pigment cell precursors during mouse embryonic development

The transcriptional landscape of the mammalian genome

Too much of a good thing: mechanisms of gene action in Down syndrome.