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Tyrosine Phosphorylation of CD2AP Affects Stability of the Slit Diaphragm Complex

Journal of the American Society of Nephrology, 2019-07, Vol.30 (7), p.1220-1237

2019

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CD2AP/CIN85 Balance Determines Receptor Tyrosine Kinase Signaling Response in Podocytes

The Journal of biological chemistry, 2007-03, Vol.282 (10), p.7457-7464

2007

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Physiological signals and oncogenesis mediated through Crk family adapter proteins

Journal of cellular physiology, 1998-12, Vol.177 (4), p.535-552

1998

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Tyrosine phosphatase SHP-2 is a regulator of p27Kip1 tyrosine phosphorylation

Cell cycle (Georgetown, Tex.), 2008-12, Vol.7 (24), p.3858-3868

2008

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Tyrosine phosphorylation modulates binding preference to cyclin-dependent kinases and subcellular localization of p27Kip1 in the acute promyelocytic leukemia cell line NB4

Blood, 2006-02, Vol.107 (3), p.1133-1140

2006

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SHP-1 Acts as a Key Regulator of Alloresponses by Modulating LFA-1-Mediated Adhesion in Primary Murine T Cells

Molecular and cellular biology, 2016-12, Vol.36 (24), p.3113-3127

2016

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Tyrosine Phosphatase SHP-1 Acts As a Key Regulator Of Alloresponses In Primary Murine T Cells

Blood, 2013-11, Vol.122 (21), p.3489-3489

2013

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Cell‐penetrating SH3 domain blocker peptides inhibit proliferation of primary blast cells from CML patients

The FASEB journal, 2000-08, Vol.14 (11), p.1529-1538

2000

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Herpesvirus Ateles Gene Product Tio Interacts with Nonreceptor Protein Tyrosine Kinases

Journal of Virology, 1999-06, Vol.73 (6), p.4631-4639

1999

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Rac1 and PAK1 are upstream of IKK-ε and TBK-1 in the viral activation of interferon regulatory factor-3

FEBS letters, 2004-06, Vol.567 (2), p.230-238

2004

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An ataxia-telangiectasia-mutated (ATM) kinase mediated response to DNA damage down-regulates the mRNA-binding potential of THOC5

RNA (Cambridge), 2011-11, Vol.17 (11), p.1957-1966

2011

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Tyrosine phosphatase SHP-2 is a regulator of p27(Kip1) tyrosine phosphorylation

Cell cycle (Georgetown, Tex.), 2008-12, Vol.7 (24), p.3858-3868

2008

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Structural Investigation of the Binding of a Herpesviral Protein to the SH3 Domain of Tyrosine Kinase Lck

Biochemistry (Easton), 2002-04, Vol.41 (16), p.5120-5130

2002

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Chronic myelogenous leukemia blast cell proliferation is inhibited by peptides that disrupt Grb2-SoS complexes

Blood, 2001-09, Vol.98 (6), p.1773-1781

2001

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Tyrosine phosphatase SHP-2 is a regulator of p27 Kip1 tyrosine phosphorylation

Cell cycle (Georgetown, Tex.), 2008-12, Vol.7 (24), p.3858-3868

2008

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The C-terminal SH3 domain of the adapter protein Grb2 binds with high affinity to sequences in Gab1 and SLP-76 which lack the SH3-typical P-x-x-P core motif

Oncogene, 2001-03, Vol.20 (9), p.1052-1062

2001

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The leukaemic oncoproteins Bcr-Abl and Tel-Abl (ETV6/Abl) have altered substrate preferences and activate similar intracellular signalling pathways

Oncogene, 2000-03, Vol.19 (13), p.1684-1690

2000

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Development of highly selective SH3 binding peptides for Crk and CRKL which disrupt Crk-complexes with DOCK180, SoS and C3G

Oncogene, 1998-04, Vol.16 (15), p.1903-1912

1998

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Rac1 and PAK1 are upstream of IKK- and TBK-1 in the viral activation of interferon regulatory factor-3

FEBS letters, 2004-06, Vol.567 (2-3), p.230-238

2004

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Targeting Molecular Recognition: Exploring the Dual Role of Functional Pseudoprolines in the Design of SH3 Ligands

Angewandte Chemie (International ed.), 2001-08, Vol.40 (15), p.2844-2848

2001

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The germinal center kinase (GCK)-related protein kinases HPK1 and KHS are candidates for highly selective signal transducers of Crk family adapter proteins

Oncogene, 1998-10, Vol.17 (15), p.1893-1901

1998

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Preparation of Disulfide-Bonded Polypeptide Heterodimers by Titration of Thio-Activated Peptides with Thiol-Containing Peptides

Tetrahedron, 2000-06, Vol.56 (24), p.3889-3891

2000

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Cell-penetrating SH3 domain blocker peptides inhibit proliferation of primary blast cells from CML patients

The FASEB journal, 2000-08, Vol.14 (11), p.1529-1538

KARDINAL, C.

2000

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Rational Development of Cell-Penetrating High Affinity SH3 Domain Binding Peptides That Selectively Disrupt the Signal Transduction of Crk Family Adapters

Annals of the New York Academy of Sciences, 1999-12, Vol.886 (1), p.289-292

1999

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Der molekularen Erkennung auf der Spur: die duale Funktion von Pseudoprolinen für das Design von SH3-Liganden

Angewandte Chemie, 2001-08, Vol.113 (15), p.2930-2934

2001

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Tyrosine Phosphorylation of CD2AP Affects Stability of the Slit Diaphragm Complex

CD2AP/CIN85 Balance Determines Receptor Tyrosine Kinase Signaling Response in Podocytes

Physiological signals and oncogenesis mediated through Crk family adapter proteins

Tyrosine phosphatase SHP-2 is a regulator of p27Kip1 tyrosine phosphorylation

Tyrosine phosphorylation modulates binding preference to cyclin-dependent kinases and subcellular localization of p27Kip1 in the acute promyelocytic leukemia cell line NB4

SHP-1 Acts as a Key Regulator of Alloresponses by Modulating LFA-1-Mediated Adhesion in Primary Murine T Cells

Tyrosine Phosphatase SHP-1 Acts As a Key Regulator Of Alloresponses In Primary Murine T Cells

Cell‐penetrating SH3 domain blocker peptides inhibit proliferation of primary blast cells from CML patients

Herpesvirus Ateles Gene Product Tio Interacts with Nonreceptor Protein Tyrosine Kinases

Rac1 and PAK1 are upstream of IKK-ε and TBK-1 in the viral activation of interferon regulatory factor-3

An ataxia-telangiectasia-mutated (ATM) kinase mediated response to DNA damage down-regulates the mRNA-binding potential of THOC5

Tyrosine phosphatase SHP-2 is a regulator of p27(Kip1) tyrosine phosphorylation

Structural Investigation of the Binding of a Herpesviral Protein to the SH3 Domain of Tyrosine Kinase Lck

Chronic myelogenous leukemia blast cell proliferation is inhibited by peptides that disrupt Grb2-SoS complexes

Tyrosine phosphatase SHP-2 is a regulator of p27 Kip1 tyrosine phosphorylation

The C-terminal SH3 domain of the adapter protein Grb2 binds with high affinity to sequences in Gab1 and SLP-76 which lack the SH3-typical P-x-x-P core motif

The leukaemic oncoproteins Bcr-Abl and Tel-Abl (ETV6/Abl) have altered substrate preferences and activate similar intracellular signalling pathways

Development of highly selective SH3 binding peptides for Crk and CRKL which disrupt Crk-complexes with DOCK180, SoS and C3G

Rac1 and PAK1 are upstream of IKK- and TBK-1 in the viral activation of interferon regulatory factor-3

Targeting Molecular Recognition: Exploring the Dual Role of Functional Pseudoprolines in the Design of SH3 Ligands

The germinal center kinase (GCK)-related protein kinases HPK1 and KHS are candidates for highly selective signal transducers of Crk family adapter proteins

Preparation of Disulfide-Bonded Polypeptide Heterodimers by Titration of Thio-Activated Peptides with Thiol-Containing Peptides

Cell-penetrating SH3 domain blocker peptides inhibit proliferation of primary blast cells from CML patients

Rational Development of Cell-Penetrating High Affinity SH3 Domain Binding Peptides That Selectively Disrupt the Signal Transduction of Crk Family Adapters

Der molekularen Erkennung auf der Spur: die duale Funktion von Pseudoprolinen für das Design von SH3-Liganden

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