Razi K, Suresh P, Mahapatra P, Al Murad M, Venkat A, Notaguchi M
Plant Direct. 2024; 8(12):e70021.
PMID: 39678018
PMC: 11646695.
DOI: 10.1002/pld3.70021.
Feliciano D
Front Neuroanat. 2020; 14:39.
PMID: 32765227
PMC: 7381175.
DOI: 10.3389/fnana.2020.00039.
Bossinger G, Spokevicius A
J Exp Bot. 2018; 69(18):4339-4348.
PMID: 29931329
PMC: 6093462.
DOI: 10.1093/jxb/ery230.
Janning W
Wilehm Roux Arch Dev Biol. 2017; 179(4):349-372.
PMID: 28304810
DOI: 10.1007/BF00848243.
Samuels M, Friedman J
Genes (Basel). 2015; 6(2):216-37.
PMID: 25898403
PMC: 4488662.
DOI: 10.3390/genes6020216.
Errors in the Elimination of X Chromosomes in SCIARA OCELLARIS.
Mori L, Perondini A
Genetics. 1980; 94(3):663-73.
PMID: 17249013
PMC: 1214166.
DOI: 10.1093/genetics/94.3.663.
Phylogenetic fate mapping.
Salipante S, Horwitz M
Proc Natl Acad Sci U S A. 2006; 103(14):5448-53.
PMID: 16569691
PMC: 1414797.
DOI: 10.1073/pnas.0601265103.
On the number of founding germ cells in humans.
Zheng C, Georg Luebeck E, Byers B, Moolgavkar S
Theor Biol Med Model. 2005; 2:32.
PMID: 16120211
PMC: 1215522.
DOI: 10.1186/1742-4682-2-32.
Immunochemical identification of intermediate-sized filaments in human neoplastic cells. A diagnostic aid for the surgical pathologist.
Gabbiani G, KAPANCI Y, Barazzone P, Franke W
Am J Pathol. 1981; 104(3):206-16.
PMID: 6170230
PMC: 1903795.
The influence of inactive chromosomes on human development. Anomalous sex chromosome complements and the phenotype.
Barlow P
Humangenetik. 1973; 17(2):105-36.
PMID: 4691146
DOI: 10.1007/BF00277906.
Evidence for a monoclonal origin of human atherosclerotic plaques.
BENDITT E, Benditt J
Proc Natl Acad Sci U S A. 1973; 70(6):1753-6.
PMID: 4515934
PMC: 433588.
DOI: 10.1073/pnas.70.6.1753.
Use of an X-linked human neutrophil marker to estimate timing of lyonization and size of the dividing stem cell pool.
Buescher E, Alling D, Gallin J
J Clin Invest. 1985; 76(4):1581-4.
PMID: 3863835
PMC: 424135.
DOI: 10.1172/JCI112140.
Fabry's disease: heterozygote detection by hair root analysis.
Grimm T, Wienker T, Ropers H
Hum Genet. 1976; 32(3):329-34.
PMID: 820627
DOI: 10.1007/BF00295824.
Stochastic models for X chromosome inactivation.
Kane V
J Math Biol. 1979; 7(3):199-218.
PMID: 469411
DOI: 10.1007/BF00275724.
Evidence for preferential X-chromosome inactivation in a family with Fabry disease.
Ropers H, Wienker T, Grimm T, Schroetter K, Bender K
Am J Hum Genet. 1977; 29(4):361-70.
PMID: 406783
PMC: 1685395.