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Pleckstrin homology domains bind to phosphatidylinositol-4,5-bisphosphate

Nature (London), 1994-09, Vol.371 (6493), p.168-170

1994

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Structure and ligand recognition of the phosphotyrosine binding domain of Shc

Nature (London), 1995-12, Vol.378 (6557), p.584-592

1995

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X-ray and NMR structure of human Bcl-xL, an inhibitor of programmed cell death

Nature (London), 1996-05, Vol.381 (6580), p.335-341

1996

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Evidence for a requirement for both phospholipid and phosphotyrosine binding via the Shc phosphotyrosine-binding domain in vivo

Molecular and Cellular Biology, 1997-09, Vol.17 (9), p.5540-5549

1997

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NMR Structure and Mutagenesis of the N-Terminal Dbl Homology Domain of the Nucleotide Exchange Factor Trio

Cell, 1998-10, Vol.95 (2), p.269-277

1998

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Driving affinity selection by centrifugal force

Assay and drug development technologies, 2003-08, Vol.1 (4), p.507-519

2003

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Drosophila seizure disorders： genetic suppression of seizure susceptibility

Frontiers in biology, 2016-04, Vol.11 (2), p.96-108

2016

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Structural Characterization of the Interaction between a Pleckstrin Homology Domain and Phosphatidylinositol 4,5-Bisphosphate

Biochemistry (Easton), 1995-08, Vol.34 (31), p.9859-9864

1995

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The BH3 domain of Bcl-x(S) is required for inhibition of the antiapoptotic function of Bcl-x(L)

Molecular and cellular biology, 1999-10, Vol.19 (10), p.6673

1999

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Binding Affinities of Tyrosine-phosphorylated Peptides to the COOH-terminal SH2 and NH2-terminal Phosphotyrosine Binding Domains of Shc (∗)

The Journal of biological chemistry, 1995-12, Vol.270 (52), p.31119-31123

1995

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Structure of Bcl-x-Bak peptide complex: recognition between regulators of apoptosis

Science (American Association for the Advancement of Science), 1997-02, Vol.275 (5302), p.983

1997

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Calibration of Size-Exclusion Chromatography: Use of a Double Gaussian Distribution Function to Describe Pore Sizes

Analytical biochemistry, 1995-01, Vol.224 (2), p.557-563

1995

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Bad is a BH3 domain-containing protein that forms an inactivating dimer with Bcl-XL

Molecular and Cellular Biology, 1997-12, Vol.17 (12), p.7040-7046

1997

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Structure of Bcl-xL-Bak peptide complex : Recognition between regulators of apoptosis

Science (American Association for the Advancement of Science), 1997-02, Vol.275 (5302), p.983-986

1997

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Discovery of Potent Inhibitors of Dihydroneopterin Aldolase Using CrystaLEAD High-Throughput X-ray Crystallographic Screening and Structure-Directed Lead Optimization

Journal of medicinal chemistry, 2004-03, Vol.47 (7), p.1709-1718

2004

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Structure of MurF from Streptococcus pneumoniae co‐crystallized with a small molecule inhibitor exhibits interdomain closure

Protein science, 2005-12, Vol.14 (12), p.3039-3047

2005

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Azapteridine Inhibitors of Hepatitis C Virus RNA-Dependent RNA Polymerase

Letters in drug design & discovery, 2007-01, Vol.4 (1), p.1-8

2007

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NMR Studies of the Anti-Apoptotic Protein Bcl-xL in Micelles

Biochemistry (Easton), 2000-09, Vol.39 (36), p.11024-11033

2000

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Rubella susceptibility in sixth graders: effectiveness of current immunization practice

Pediatrics (Evanston), 1980-06, Vol.65 (6), p.1086-1089

1980

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A highly potent and selective farnesyltransferase inhibitor ABT-100 in preclinical studies

Anti-cancer drugs, 2005-11, Vol.16 (10), p.1059-1069

2005

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The BH3 Domain of Bcl-x sub(S) Is Required for Inhibition of the Antiapoptotic Function of Bcl-x sub(L)

Molecular and cellular biology, 1999-10, Vol.19 (10), p.6673-6681

1999

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Recreation in the context of community membership - experiences of older adults in Indiana

International Journal of Practical Approaches to Disability, 1998-01, Vol.22 (1), p.9-11

Harlan, J E

1998

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Bad is a BH3 domain-containing protein that forms an inactivating dimer with Bcl-X sub(L)

Molecular and cellular biology, 1997-12, Vol.17 (12), p.7040-7046

1997

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Rocky Mountain spotted fever. Serological evidence of previous subclinical infection in children

American journal of diseases of children (1960), 1982-01, Vol.136 (1), p.16

1982

Volltextzugriff (PDF)

The Therapeutic Value of Art for Persons with Alzheimer's Disease and Related Disorders

Loss, grief & care, 1993-05, Vol.6 (4), p.99-106

Harlan, Jane E.

1993

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Pleckstrin homology domains bind to phosphatidylinositol-4,5-bisphosphate

Structure and ligand recognition of the phosphotyrosine binding domain of Shc

X-ray and NMR structure of human Bcl-xL, an inhibitor of programmed cell death

Evidence for a requirement for both phospholipid and phosphotyrosine binding via the Shc phosphotyrosine-binding domain in vivo

NMR Structure and Mutagenesis of the N-Terminal Dbl Homology Domain of the Nucleotide Exchange Factor Trio

Driving affinity selection by centrifugal force

Drosophila seizure disorders： genetic suppression of seizure susceptibility

Structural Characterization of the Interaction between a Pleckstrin Homology Domain and Phosphatidylinositol 4,5-Bisphosphate

The BH3 domain of Bcl-x(S) is required for inhibition of the antiapoptotic function of Bcl-x(L)

Binding Affinities of Tyrosine-phosphorylated Peptides to the COOH-terminal SH2 and NH2-terminal Phosphotyrosine Binding Domains of Shc (∗)

Structure of Bcl-x-Bak peptide complex: recognition between regulators of apoptosis

Calibration of Size-Exclusion Chromatography: Use of a Double Gaussian Distribution Function to Describe Pore Sizes

Bad is a BH3 domain-containing protein that forms an inactivating dimer with Bcl-XL

Structure of Bcl-xL-Bak peptide complex : Recognition between regulators of apoptosis

Discovery of Potent Inhibitors of Dihydroneopterin Aldolase Using CrystaLEAD High-Throughput X-ray Crystallographic Screening and Structure-Directed Lead Optimization

Structure of MurF from Streptococcus pneumoniae co‐crystallized with a small molecule inhibitor exhibits interdomain closure

Azapteridine Inhibitors of Hepatitis C Virus RNA-Dependent RNA Polymerase

NMR Studies of the Anti-Apoptotic Protein Bcl-xL in Micelles

Rubella susceptibility in sixth graders: effectiveness of current immunization practice

A highly potent and selective farnesyltransferase inhibitor ABT-100 in preclinical studies

The BH3 Domain of Bcl-x sub(S) Is Required for Inhibition of the Antiapoptotic Function of Bcl-x sub(L)

Recreation in the context of community membership - experiences of older adults in Indiana

Bad is a BH3 domain-containing protein that forms an inactivating dimer with Bcl-X sub(L)

Rocky Mountain spotted fever. Serological evidence of previous subclinical infection in children

The Therapeutic Value of Art for Persons with Alzheimer's Disease and Related Disorders

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