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Pin-Xian Xu

Showing results (41-50 of 47) with videos related to

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Developmental Cell|December 3, 2014
Eya1 interacts with Six2 and Myc to regulate expansion of the nephron progenitor pool during nephrogenesisJinshu Xu, Elaine Y M Wong, Chunming Cheng, et al.
Annals of Translational Medicine|July 19, 2021
SIX1/EYA1 are novel liver damage biomarkers in chronic hepatitis B and other liver diseasesBaoyan Xu, Qiao Yang, Yingzi Tang, et al.
Molecular and Cellular Biology|July 1, 2004
Six1 and Eya1 expression can reprogram adult muscle from the slow-twitch phenotype into the fast-twitch phenotypeRaphaelle Grifone, Christine Laclef, François Spitz, et al.
Developmental Cell|March 31, 2015
The Eya1 phosphatase promotes Shh signaling during hindbrain development and oncogenesisAdriana Eisner, Maria F Pazyra-Murphy, Ershela Durresi, et al.
American Journal of Human Genetics|March 16, 2007
Transcription factor SIX5 is mutated in patients with branchio-oto-renal syndromeBethan E Hoskins, Carl H Cramer, Derek Silvius, et al.
Developmental Neuroscience|January 20, 2021
The Eya1 Phosphatase Mediates Shh-Driven Symmetric Cell Division of Cerebellar Granule Cell PrecursorsDaniel J Merk, Pengcheng Zhou, Samuel M Cohen, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 14, 2004
SIX1 mutations cause branchio-oto-renal syndrome by disruption of EYA1-SIX1-DNA complexesRainer G Ruf, Pin-Xian Xu, Derek Silvius, et al.
Pageof 5

Showing results (41-50 of 47) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 47 results.
Developmental Cell|December 3, 2014
Eya1 interacts with Six2 and Myc to regulate expansion of the nephron progenitor pool during nephrogenesisJinshu Xu, Elaine Y M Wong, Chunming Cheng, et al.
Annals of Translational Medicine|July 19, 2021
SIX1/EYA1 are novel liver damage biomarkers in chronic hepatitis B and other liver diseasesBaoyan Xu, Qiao Yang, Yingzi Tang, et al.
Molecular and Cellular Biology|July 1, 2004
Six1 and Eya1 expression can reprogram adult muscle from the slow-twitch phenotype into the fast-twitch phenotypeRaphaelle Grifone, Christine Laclef, François Spitz, et al.
Developmental Cell|March 31, 2015
The Eya1 phosphatase promotes Shh signaling during hindbrain development and oncogenesisAdriana Eisner, Maria F Pazyra-Murphy, Ershela Durresi, et al.
American Journal of Human Genetics|March 16, 2007
Transcription factor SIX5 is mutated in patients with branchio-oto-renal syndromeBethan E Hoskins, Carl H Cramer, Derek Silvius, et al.
Developmental Neuroscience|January 20, 2021
The Eya1 Phosphatase Mediates Shh-Driven Symmetric Cell Division of Cerebellar Granule Cell PrecursorsDaniel J Merk, Pengcheng Zhou, Samuel M Cohen, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 14, 2004
SIX1 mutations cause branchio-oto-renal syndrome by disruption of EYA1-SIX1-DNA complexesRainer G Ruf, Pin-Xian Xu, Derek Silvius, et al.
Pageof 5