Publications by authors named "Nitin Sabherwal"

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Inhibiting ERK5 overcomes breast cancer resistance to anti-HER2 therapy by targeting the G1/S cell cycle transition.
Jingwei Zhang, Adam J Pearson, Nitin Sabherwal, Brian A Telfer, Nisha Ali

Cancer Res Commun· March 2022

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Differential phase register of Hes1 oscillations with mitoses underlies cell-cycle heterogeneity in ER breast cancer cells.
Nitin Sabherwal, Andrew Rowntree, Elli Marinopoulou, Tom Pettini, Sean Hourihane

Proc Natl Acad Sci U S A· November 2021

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HES1 protein oscillations are necessary for neural stem cells to exit from quiescence.
Elli Marinopoulou, Veronica Biga, Nitin Sabherwal, Anzy Miller, Jayni Desai

iScience· October 2021

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aPKC phosphorylates p27Xic1, providing a mechanistic link between apicobasal polarity and cell-cycle control.
Nitin Sabherwal, Raphael Thuret, Robert Lea, Peter Stanley, Nancy Papalopulu

Dev Cell· December 2014

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Atypical protein kinase C couples cell sorting with primitive endoderm maturation in the mouse blastocyst.
Néstor Saiz, Joanna B Grabarek, Nitin Sabherwal, Nancy Papalopulu, Berenika Plusa

Development· November 2013

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Apicobasal polarity and cell proliferation during development.
Nitin Sabherwal, Nancy Papalopulu

Essays Biochem· December 2012

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pTransgenesis: a cross-species, modular transgenesis resource.
Nick R Love, Raphael Thuret, Yaoyao Chen, Shoko Ishibashi, Nitin Sabherwal

Development· December 2011

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The apicobasal polarity kinase aPKC functions as a nuclear determinant and regulates cell proliferation and fate during Xenopus primary neurogenesis.
Nitin Sabherwal, Akiko Tsutsui, Sarah Hodge, Jun Wei, Andrew D Chalmers

Development· August 2009

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Long-range conserved non-coding SHOX sequences regulate expression in developing chicken limb and are associated with short stature phenotypes in human patients.
Nitin Sabherwal, Fiona Bangs, Ralph Röth, Birgit Weiss, Karin Jantz

Hum Mol Genet· January 2007

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Identification of a major recombination hotspot in patients with short stature and SHOX deficiency.
Katja U Schneider, Nitin Sabherwal, Karin Jantz, Ralph Röth, Nadja Muncke

Am J Hum Genet· July 2005

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Alteration of DNA binding, dimerization, and nuclear translocation of SHOX homeodomain mutations identified in idiopathic short stature and Leri-Weill dyschondrosteosis.
Katja U Schneider, Antonio Marchini, Nitin Sabherwal, Ralph Röth, Beate Niesler

Hum Mutat· July 2005

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Impairment of SHOX nuclear localization as a cause for Léri-Weill syndrome.
Nitin Sabherwal, Katja U Schneider, Rüdiger J Blaschke, Antonio Marchini, Gudrun Rappold

J Cell Sci· June 2004

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