Publications By Santosh Kumar Maharana

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Skeletal progenitor LRP1 deficiency causes severe and persistent skeletal defects with Wnt pathway dysregulation., Alhashmi M, Gremida AME, Maharana SK, Antonaci M, Kerr A, Fu S, Lunn S, Turner DA, Al-Maslamani NA, Liu K, Meschis MM, Sutherland H, Wilson P, Clegg P, Wheeler GN, van 't Hof RJ, Bou-Gharios G, Yamamoto K., Bone Res. January 26, 2025; 13 (1): 17.

Molecular mechanisms of hearing loss in Nager syndrome., Maharana SK, Saint-Jeannet JP., Dev Biol. August 1, 2021; 476 200-208.

A gene regulatory network underlying the formation of pre-placodal ectoderm in Xenopus laevis., Maharana SK, Schlosser G., BMC Biol. July 16, 2018; 16 (1): 79.

Identification of novel cis-regulatory elements of Eya1 in Xenopus laevis using BAC recombineering., Maharana SK, Pollet N, Schlosser G., Sci Rep. November 3, 2017; 7 (1): 15033.

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