324
Xenopus
Vijay, K., 2018. Toll-like receptors in immunity and inf ammatory
diseases: Past, present, and future. Int. Immunopharmacol.
59, 391–412. doi:10.1016/j.intimp.2018.03.002
Visser, G.H.A., Bilardo, C.M., Lees, C., 2014. Fetal growth restriction at the limits of viability. Fetal Diagn. Ther. 36, 162–165.
doi:10.1159/000358058
Voelkl, B., Altman, N.S., Forsman, A., Forstmeier, W., Gurevitch,
J., Jaric, I., Karp, N.A., Kas, M.J., Schielzeth, H., Van de
Casteele, T., Würbel, H., 2020. Reproducibility of animal
research in light of biological variation. Nat. Rev. Neurosci.
21, 384–393. doi:10.1038/s41583-020-0313-3
Watanabe, M., Yasuoka, Y., Mawaribuchi, S., Kuretani, A., Ito,
M., Kondo, M., Ochi, H., Ogino, H., Fukui, A., Taira, M.,
Kinoshita, T., 2017. Conservatism and variability of gene
expression profles among homeologous transcription factors
in Xenopus laevis. Dev. Biol. 426, 301–324. doi:10.1016/j.
ydbio.2016.09.017
White, D., Rabago-Smith, M., 2011. Genotype-phenotype associations and human eye color. J. Hum. Genet. 56, 5–7.
doi:10.1038/jhg.2010.126
Wong, K.H.Y., Ma, W., Wei, C.-Y., Yeh, E.-C., Lin, W.-J., Wang,
E.H.F., Su, J.-P., Hsieh, F.-J., Kao, H.-J., Chen, H.-H., Chow,
S.K., Young, E., Chu, C., Poon, A., Yang, C.-F., Lin, D.-S.,
Hu, Y.-F., Wu, J.-Y., Lee, N.-C., Hwu, W.-L., Kwok, P.-Y.,
2020. Towards a reference genome that captures global
genetic diversity. Nat. Commun. 11, 5482. doi:10.1038/
s41467-020-19311-w
Wu, H., Yang, L., 2015. Arg753Gln polymorphisms in toll-like
receptor 2 gene are associated with tuberculosis risk: A metaanalysis. Med. Sci. Monit. 21, 2196–2202. doi:10.12659/
MSM.893214
Zarrei, M., MacDonald, J.R., Merico, D., Scherer, S.W., 2015. A
copy number variation map of the human genome. Nat. Rev.
Genet. 16, 172–183. doi:10.1038/nrg3871
Zeng, S.L., Sudlow, L.C., Berezin, M.Y., 2020. Using Xenopus
oocytes in neurological disease drug discovery. Expert
Opin. Drug Discov. 15, 39–52. doi:10.1080/17460441.20
20.1682993
Zerbino, D.R., Frankish, A., Flicek, P., 2020. Progress, challenges, and surprises in annotating the human genome.
Annu. Rev. Genomics Hum. Genet. 21, 55–79. doi:10.1146/
annurev-genom-121119-083418
Zhang, B.N., Wong, T.C.B., Yip, Y.W.Y., Liu, Z., Wang, C., Wong,
J.S.C., He, J.N., Chan, T.C.Y., Jhanji, V., Pang, C.P., Zhao,
H., Chu, W.K., 2019. A sclerocornea-associated RAD21
variant induces corneal stroma disorganization. Exp. Eye
Res. 185, 107687. doi:10.1016/j.exer.2019.06.001
Zhou, S.-F., Liu, J.-P., Chowbay, B., 2009. Polymorphism of human
cytochrome P450 enzymes and its clinical impact. Drug
Metab. Rev. 41, 89–295. doi:10.1080/03602530902843483
Zhou, Y., Ingelman-Sundberg, M., Lauschke, V.M., 2017.
Worldwide distribution of cytochrome P450 alleles: A metaanalysis of population-scale sequencing projects. Clin.
Pharmacol. Ther. 102, 688–700. doi:10.1002/cpt.690
Xenopus
Vijay, K., 2018. Toll-like receptors in immunity and inf ammatory
diseases: Past, present, and future. Int. Immunopharmacol.
59, 391–412. doi:10.1016/j.intimp.2018.03.002
Visser, G.H.A., Bilardo, C.M., Lees, C., 2014. Fetal growth restriction at the limits of viability. Fetal Diagn. Ther. 36, 162–165.
doi:10.1159/000358058
Voelkl, B., Altman, N.S., Forsman, A., Forstmeier, W., Gurevitch,
J., Jaric, I., Karp, N.A., Kas, M.J., Schielzeth, H., Van de
Casteele, T., Würbel, H., 2020. Reproducibility of animal
research in light of biological variation. Nat. Rev. Neurosci.
21, 384–393. doi:10.1038/s41583-020-0313-3
Watanabe, M., Yasuoka, Y., Mawaribuchi, S., Kuretani, A., Ito,
M., Kondo, M., Ochi, H., Ogino, H., Fukui, A., Taira, M.,
Kinoshita, T., 2017. Conservatism and variability of gene
expression profles among homeologous transcription factors
in Xenopus laevis. Dev. Biol. 426, 301–324. doi:10.1016/j.
ydbio.2016.09.017
White, D., Rabago-Smith, M., 2011. Genotype-phenotype associations and human eye color. J. Hum. Genet. 56, 5–7.
doi:10.1038/jhg.2010.126
Wong, K.H.Y., Ma, W., Wei, C.-Y., Yeh, E.-C., Lin, W.-J., Wang,
E.H.F., Su, J.-P., Hsieh, F.-J., Kao, H.-J., Chen, H.-H., Chow,
S.K., Young, E., Chu, C., Poon, A., Yang, C.-F., Lin, D.-S.,
Hu, Y.-F., Wu, J.-Y., Lee, N.-C., Hwu, W.-L., Kwok, P.-Y.,
2020. Towards a reference genome that captures global
genetic diversity. Nat. Commun. 11, 5482. doi:10.1038/
s41467-020-19311-w
Wu, H., Yang, L., 2015. Arg753Gln polymorphisms in toll-like
receptor 2 gene are associated with tuberculosis risk: A metaanalysis. Med. Sci. Monit. 21, 2196–2202. doi:10.12659/
MSM.893214
Zarrei, M., MacDonald, J.R., Merico, D., Scherer, S.W., 2015. A
copy number variation map of the human genome. Nat. Rev.
Genet. 16, 172–183. doi:10.1038/nrg3871
Zeng, S.L., Sudlow, L.C., Berezin, M.Y., 2020. Using Xenopus
oocytes in neurological disease drug discovery. Expert
Opin. Drug Discov. 15, 39–52. doi:10.1080/17460441.20
20.1682993
Zerbino, D.R., Frankish, A., Flicek, P., 2020. Progress, challenges, and surprises in annotating the human genome.
Annu. Rev. Genomics Hum. Genet. 21, 55–79. doi:10.1146/
annurev-genom-121119-083418
Zhang, B.N., Wong, T.C.B., Yip, Y.W.Y., Liu, Z., Wang, C., Wong,
J.S.C., He, J.N., Chan, T.C.Y., Jhanji, V., Pang, C.P., Zhao,
H., Chu, W.K., 2019. A sclerocornea-associated RAD21
variant induces corneal stroma disorganization. Exp. Eye
Res. 185, 107687. doi:10.1016/j.exer.2019.06.001
Zhou, S.-F., Liu, J.-P., Chowbay, B., 2009. Polymorphism of human
cytochrome P450 enzymes and its clinical impact. Drug
Metab. Rev. 41, 89–295. doi:10.1080/03602530902843483
Zhou, Y., Ingelman-Sundberg, M., Lauschke, V.M., 2017.
Worldwide distribution of cytochrome P450 alleles: A metaanalysis of population-scale sequencing projects. Clin.
Pharmacol. Ther. 102, 688–700. doi:10.1002/cpt.690