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Items: 3

1.
Genotype and phenotype variability in Sjögren‐Larsson syndrome
Maximilian Weustenfeld, Reiner Eidelpes, Matthias Schmuth, William B. Rizzo, Johannes Zschocke, Markus A. Keller
Hum Mutat. 2019 Feb; 40(2): 177–186. Published online 2018 Nov 26. doi: 10.1002/humu.23679
PMCID:
PMC6587760
AbstractArticlePDF–762K
2.
Activin/Smad2 and Wnt/β-catenin up-regulate HAS2 and ALDH3A2 to facilitate mesendoderm differentiation of human embryonic stem cells
Xuanhao Xu, Lu Wang, Bofeng Liu, Wei Xie, Ye-Guang Chen
J Biol Chem. 2018 Nov 30; 293(48): 18444–18453. Published online 2018 Oct 3. doi: 10.1074/jbc.RA118.003688
PMCID:
PMC6290156
AbstractArticlePDF–4.1M
3.
Genetic homogeneity in Sjögren-Larsson syndrome: linkage to chromosome 17p in families of different non-Swedish ethnic origins.
G R Rogers, W B Rizzo, A Zlotogorski, N Hashem, M Lee, J G Compton, S J Bale
Am J Hum Genet. 1995 Nov; 57(5): 1123–1129.
PMCID:
PMC1801386
SummaryPage BrowsePDF–1008K

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