Protein phosphatase 1 is essential for Greatwall inactivation at mitotic exit

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Location: Deutsche Nationalbibliothek Frankfurt am Main

Extent: Online-Ressource

Language: Englisch

Bibliographic citation: In: EMBO Reports ; 16 (2015), 11. - S. 1501-1510. - ISSN 1469-221X. - eISSN 1469-3178

Classification: Biowissenschaften, Biologie

Event: Veröffentlichung

(where): Konstanz

(who): Bibliothek der Universität Konstanz

(when): 2015

Creator: Heim, Andreas
Konietzny, Anja
Mayer, Thomas U.

URN: urn:nbn:de:bsz:352-0-309257

Rights: Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 25.03.2025, 1:53 PM CET

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Associated

Heim, Andreas
Konietzny, Anja
Mayer, Thomas U.
Bibliothek der Universität Konstanz

Time of origin

2015

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Inactivation of the tyrosine phosphatase SHP-2 drives vascular dysfunction in sepsis

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The novel proteasomal substrate Far10 contributes to control of mitotic exit in yeast

Phosphatase of regenerating liver (PRL)-3 disrupts epithelial architecture by altering the post-mitotic midbody position

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An essential developmental function for murine phosphoglycolate phosphatase in safeguarding cell proliferation

Blocking mitotic exit of ovarian cancer cells by pharmaceutical inhibition of the anaphase-promoting complex reduces chromosomal instability

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Mitotic Stages in Animal Cells

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Inactivation of the tyrosine phosphatase SHP-2 drives vascular dysfunction in sepsis

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The novel proteasomal substrate Far10 contributes to control of mitotic exit in yeast

Phosphatase of regenerating liver (PRL)-3 disrupts epithelial architecture by altering the post-mitotic midbody position

Pptc7 is an essential phosphatase for promoting mammalian mitochondrial metabolism and biogenesis

An essential developmental function for murine phosphoglycolate phosphatase in safeguarding cell proliferation

Blocking mitotic exit of ovarian cancer cells by pharmaceutical inhibition of the anaphase-promoting complex reduces chromosomal instability

zweidimensionales bewegtes Bild

Mitotic Stages in Animal Cells

A Non-Motor Microtubule Binding Site Is Essential for the High Processivity and Mitotic Function of Kinesin-8 Kif18A

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Protein phosphatase 1 is essential for Greatwall inactivation at mitotic exit

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Other Objects (12)

Inactivation of the tyrosine phosphatase SHP-2 drives vascular dysfunction in sepsis

The novel proteasomal substrate Far10 contributes to control of mitotic exit in yeast

Phosphatase of regenerating liver (PRL)-3 disrupts epithelial architecture by altering the post-mitotic midbody position

Pptc7 is an essential phosphatase for promoting mammalian mitochondrial metabolism and biogenesis

An essential developmental function for murine phosphoglycolate phosphatase in safeguarding cell proliferation

Blocking mitotic exit of ovarian cancer cells by pharmaceutical inhibition of the anaphase-promoting complex reduces chromosomal instability

Mitotic Stages in Animal Cells

A Non-Motor Microtubule Binding Site Is Essential for the High Processivity and Mitotic Function of Kinesin-8 Kif18A

EXIT

Exit

EXIt

Exit

Inactivation of the tyrosine phosphatase SHP-2 drives vascular dysfunction in sepsis

The novel proteasomal substrate Far10 contributes to control of mitotic exit in yeast

Phosphatase of regenerating liver (PRL)-3 disrupts epithelial architecture by altering the post-mitotic midbody position

Pptc7 is an essential phosphatase for promoting mammalian mitochondrial metabolism and biogenesis

An essential developmental function for murine phosphoglycolate phosphatase in safeguarding cell proliferation

Blocking mitotic exit of ovarian cancer cells by pharmaceutical inhibition of the anaphase-promoting complex reduces chromosomal instability

Mitotic Stages in Animal Cells

A Non-Motor Microtubule Binding Site Is Essential for the High Processivity and Mitotic Function of Kinesin-8 Kif18A

EXIT

Exit

EXIt

Exit

Inactivation of the tyrosine phosphatase SHP-2 drives vascular dysfunction in sepsis

The novel proteasomal substrate Far10 contributes to control of mitotic exit in yeast

Phosphatase of regenerating liver (PRL)-3 disrupts epithelial architecture by altering the post-mitotic midbody position

Pptc7 is an essential phosphatase for promoting mammalian mitochondrial metabolism and biogenesis

An essential developmental function for murine phosphoglycolate phosphatase in safeguarding cell proliferation

Blocking mitotic exit of ovarian cancer cells by pharmaceutical inhibition of the anaphase-promoting complex reduces chromosomal instability

Mitotic Stages in Animal Cells

A Non-Motor Microtubule Binding Site Is Essential for the High Processivity and Mitotic Function of Kinesin-8 Kif18A

EXIT

Exit

EXIt

Exit

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