Author details

Full Name

Laura L Baxter

Affiliation

ORCID

Career Start Year

1999

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
37544351	Embryonic statistical analyses reveal 2 growth phenotypes in mouse models of Down syndrome.		2023
37327787	Haplotype-based analysis resolves missing heritability in oculocutaneous albinism type 1B.	Am J Hum Genet	2023
35140266	Correlation of age of onset and clinical severity in Niemann-Pick disease type C1 with lysosomal abnormalities and gene expression.	Sci Rep	2022
34407999	Improved systemic AAV gene therapy with a neurotrophic capsid in Niemann-Pick disease type C1 mice.	Life Sci Alliance	2021
34296265	Transcriptome of HPÎ²CD-treated Niemann-Pick disease type C1 cells highlights GPNMB as a biomarker for therapeutics.	Hum Mol Genet	2021
34246199	A custom capture sequence approach for oculocutaneous albinism identifies structural variant alleles at the OCA2 locus.	Hum Mutat	2021
31996359	Genetic background modifies phenotypic severity and longevity in a mouse model of Niemann-Pick disease type C1.	Dis Model Mech	2020
31399133	MEK inhibition remodels the active chromatin landscape and induces SOX10 genomic recruitment in BRAF(V600E) mutant melanoma cells.	Epigenetics Chromatin	2019
31861571	NPC1 Deficiency in Mice is Associated with Fetal Growth Restriction, Neonatal Lethality and Abnormal Lung Pathology.	J Clin Med	2019
30339321	A curated gene list for expanding the horizons of pigmentation biology.	Pigment Cell Melanoma Res	2019
29315345	Identification and functional analysis of SOX10 phosphorylation sites in melanoma.	PLoS One	2018
28168807	Hypoxia-induced HIF1Î± targets in melanocytes reveal a molecular profile associated with poor melanoma prognosis.	Pigment Cell Melanoma Res	2017
26584186	Correction: Mutation of the Diamond-Blackfan Anemia Gene Rps7 in Mouse Results in Morphological and Neuroanatomical Phenotypes.	PLoS Genet	2015
24767210	Distinct microRNA expression signatures are associated with melanoma subtypes and are regulated by HIF1A.	Pigment Cell Melanoma Res	2014
23382688	Mutation of the diamond-blackfan anemia gene Rps7 in mouse results in morphological and neuroanatomical phenotypes.	PLoS Genet	2013
23799582	The etiology and molecular genetics of human pigmentation disorders.	Wiley Interdiscip Rev Dev Biol	2013
23666527	Efficacy of N-acetylcysteine in phenotypic suppression of mouse models of Niemann-Pick disease, type C1.	Hum Mol Genet	2013
22822447	Plasma and tissue concentrations of Î±-tocopherol and Î´-tocopherol following high dose dietary supplementation in mice.	Nutrients	2012
20444197	Sox proteins in melanocyte development and melanoma.	Pigment Cell Melanoma Res	2010
20974870	A curated online resource for SOX10 and pigment cell molecular genetic pathways.	Database (Oxford)	2010
18983539	Gpnmb is a melanoblast-expressed, MITF-dependent gene.	Pigment Cell Melanoma Res	2009
19493314	Comparison of melanoblast expression patterns identifies distinct classes of genes.	Pigment Cell Melanoma Res	2009
20161540	Networks and pathways in pigmentation, health, and disease.	Wiley Interdiscip Rev Syst Biol Med	2009
18397875	A sensitized mutagenesis screen identifies Gli3 as a modifier of Sox10 neurocristopathy.	Hum Mol Genet	2008
17516927	Informatic and genomic analysis of melanocyte cDNA libraries as a resource for the study of melanocyte development and function.	Pigment Cell Res	2007
16432181	Defective cerebellar response to mitogenic Hedgehog signaling in Down [corrected] syndrome mice.	Proceedings of the National Academy of Sciences of the United States of America	2006
16412618	Genetic evidence does not support direct regulation of EDNRB by SOX10 in migratory neural crest and the melanocyte lineage.	Mech Dev	2006
16141072	The transcriptional landscape of the mammalian genome.	Science	2005
15140066	Spotlight on spotted mice: a review of white spotting mouse mutants and associated human pigmentation disorders.	Pigment Cell Res	2004
15188443	Down syndrome mouse models Ts65Dn, Ts1Cje, and Ms1Cje/Ts65Dn exhibit variable severity of cerebellar phenotypes.	Dev Dyn	2004
14643677	Pmel17 expression is Mitf-dependent and reveals cranial melanoblast migration during murine development.	Gene Expr Patterns	2003
11917121	Mutation of melanosome protein RAB38 in chocolate mice.	Proc Natl Acad Sci U S A	2002
12128226	The oculocutaneous albinism type IV gene Matp is a new marker of pigment cell precursors during mouse embryonic development.	Mech Dev	2002
11173117	Too much of a good thing: mechanisms of gene action in Down syndrome.	Trends in Genetics	2001
10706138	Parallels of craniofacial maldevelopment in Down syndrome and Ts65Dn mice.	Developmental Dynamics	2000
10607830	Discovery and genetic localization of Down syndrome cerebellar phenotypes using the Ts65Dn mouse.	Human Molecular Genetics	2000
10395793	Integration of cytogenetic with recombinational and physical maps of mouse chromosome 16.	Genomics	1999