نتائج البحث - C. Anthony Scott
- يعرض 1 - 5 نتائج من 5
-
1
The master transcription factor SOX2, mutated in anophthalmia/microphthalmia, is post-transcriptionally regulated by the conserved RNA-binding protein RBM24 in vertebrate eye devel... حسب Soma Dash, Lindy K. Brastrom, Shaili Patel, C. Anthony Scott, Diane C. Slusarski, Salil A. Lachke
منشور في 2019Artigo -
2
-
3
Systemic interindividual epigenetic variation in humans is associated with transposable elements and under strong genetic control حسب Chathura Gunasekara, Harry A. Mackay, C. Anthony Scott, Shaobo Li, Eleonora Laritsky, Maria S. Baker, Sandra L. Grimm, Goo Jun, Yumei Li, Rui Chen, Joseph L. Wiemels, Cristian Coarfa, Robert A. Waterland
منشور في 2023Artigo -
4
Hypomorphic mutations in<i>TRNT1</i>cause retinitis pigmentosa with erythrocytic microcytosis حسب Adam P. DeLuca, S. Scott Whitmore, Jenna Barnes, Tasneem Putliwala Sharma, Trudi A. Westfall, C. Anthony Scott, Matthew C. Weed, Jill S. Wiley, Luke A. Wiley, Rebecca M. Johnston, Michael J. Schnieders, Steven R. Lentz, Budd A. Tucker, Robert F. Mullins, Todd E. Scheetz, Edwin M. Stone, Diane C. Slusarski
منشور في 2015Artigo -
5
A genomic atlas of systemic interindividual epigenetic variation in humans حسب Chathura Gunasekara, C. Anthony Scott, Eleonora Laritsky, Maria S. Baker, Harry A. Mackay, Jack Duryea, Noah J. Kessler, Garrett Hellenthal, Alexis C. Wood, Kelly R. Hodges, Manisha Gandhi, Amy B. Hair, Matt J. Silver, Sophie E. Moore, Andrew M. Prentice, Yumei Li, Rui Chen, Cristian Coarfa, Robert A. Waterland
منشور في 2019Artigo
أدوات البحث:
موضوعات ذات صلة
Biology
Gene
Genetics
CpG site
DNA methylation
Epigenetics
Epigenomics
Gene expression
Phenotype
Retinal degeneration
Retinitis pigmentosa
Anemia
Anophthalmia
Bardet–Biedl syndrome
Ciliopathy
Copy-number variation
Demography
Dystrophy
Epigenome
Eye development
Genetic variation
Genome
Genome-wide association study
Genotype
Haploinsufficiency
Human genetics
Human genome
Internal medicine
Iron deficiency
Linguistics