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Pigment Cell & Melanoma Research|April 24, 2020
Melanocortin-1 receptor (MC1R) genotypes do not correlate with size in two cohorts of medium-to-giant congenital melanocytic neviNeus Calbet-Llopart, Mirella Pascini-Garrigos, Gemma Tell-Martí, et al.Human Mutation|March 25, 2009
Phenotypic spectrum of STRA6 mutations: from Matthew-Wood syndrome to non-lethal anophthalmiaNicolas Chassaing, Christelle Golzio, Sylvie Odent, et al.Iscience|May 8, 2026
RIPOR2 promotes multinucleation of melanoma cells downstream of the RAS/ERK oncogenic pathwayAxelle Wilmerding, Aurélie Richard, Nicolas Macagno, et al.Development (Cambridge, England)|February 10, 2025
Multi-modal refinement of the human heart atlas during the first gestational trimesterChristopher De Bono, Yichi Xu, Samina Kausar, et al.American Journal of Human Genetics|June 30, 2009
Loss-of-function mutation in the dioxygenase-encoding FTO gene causes severe growth retardation and multiple malformationsSarah Boissel, Orit Reish, Karine Proulx, et al.Human Genetics|May 11, 2005
SNPs in the neural cell adhesion molecule 1 gene (NCAM1) may be associated with human neural tube defectsKristen L Deak, Abee L Boyles, Heather C Etchevers, et al.Genome Research|February 20, 2016
Targeted resequencing identifies PTCH1 as a major contributor to ocular developmental anomalies and extends the SOX2 regulatory networkNicolas Chassaing, Erica E Davis, Kelly L McKnight, et al.Nature Communications|April 4, 2023
An epigenetic switch controls an alternative NR2F2 isoform that unleashes a metastatic program in melanomaVeronica Davalos, Claudia D Lovell, Richard Von Itter, et al.Journal of Medical Genetics|May 12, 2012
OTX2 mutations contribute to the otocephaly-dysgnathia complexNicolas Chassaing, Susanna Sorrentino, Erica E Davis, et al.Cancer Research|December 15, 2018
Macrophage-Derived IL1β and TNFα Regulate Arginine Metabolism in NeuroblastomaLivingstone Fultang, Laura D Gamble, Luciana Gneo, et al.Pageof 5