Lista de obras - Meytal Landau - Dominio Público Uruguay

A 13-bp deletion in alpha(IIb) gene is a founder mutation that predominates in Palestinian-Arab patients with Glanzmann thrombasthenia

artículo científico publicado en 2005

A Putative Mechanism for Downregulation of the Catalytic Activity of the EGF Receptor via Direct Contact between Its Kinase and C-Terminal Domains

scientific article published on 01 December 2004

A Small Molecule Inhibitor of Bruton’s Tyrosine Kinase Involved in B-Cell Signaling

artículo científico publicado en 2017

A novel factor XI missense mutation (Val371Ile) in the activation loop is responsible for a case of mild type II factor XI deficiency

artículo científico publicado en 2007

A unique interaction between alphaIIb and beta3 in the head region is essential for outside-in signaling-related functions of alphaIIbbeta3 integrin

artículo científico

Atomic View of a Toxic Amyloid Small Oligomer

artículo científico publicado en 2012

Characterization of seven novel mutations causing factor XI deficiency

artículo científico publicado en 2007

Compound heterozygosity of HLA-DRB301:01 and HLA-DRB401:01 as a potential predictor of fetal neonatal alloimmune thrombocytopenia

artículo científico publicado en 2012

ConSurf 2005: the projection of evolutionary conservation scores of residues on protein structures

artículo científico publicado en 2005

Congenital dilated cardiomyopathy caused by biallelic mutations in Filamin C.

artículo científico publicado en 2016

Crystal structures of truncated alphaA and alphaB crystallins reveal structural mechanisms of polydispersity important for eye lens function

artículo científico publicado en 2010

Disulfide bond disruption by a β3-Cys549Arg mutation in six Jordanian families with Glanzmann thrombasthenia causes diminished production of constitutively active αIIbβ3

Dynamic equilibrium between multiple active and inactive conformations explains regulation and oncogenic mutations in ErbB receptors

artículo científico publicado en 2007

Extreme Amyloid Polymorphism inStaphylococcus aureusVirulent PSMα Peptides

Extreme amyloid polymorphism in Staphylococcus aureus virulent PSMα peptides

artículo científico publicado en 2018

Formation of amyloid fibers by monomeric light chain variable domains

artículo científico publicado en 2014

Functional evaluation of autism-associated mutations in NHE9.

artículo científico publicado en 2013

Getting in charge of β-synuclein fibrillation

artículo científico publicado en 2017

Lipid Bilayers Significantly Modulate Cross-Fibrillation of Two Distinct Amyloidogenic Peptides ⬇️

artículo científico publicado el 28 de agosto de 2013

Mimicking cross-α amyloids

scholarly article by Meytal Landau published in August 2018

Model structure of the Na+/H+ exchanger 1 (NHE1): functional and clinical implications

artículo científico publicado en 2007

Molecular basis for amyloid- polymorphism

artículo científico publicado en 2011

Molecular diversity of Glanzmann thrombasthenia in southern India: new insights into mRNA splicing and structure-function correlations of alphaIIbbeta3 integrin (ITGA2B, ITGB3).

artículo científico publicado en 2006

Molecular insight into human platelet antigens: structural and evolutionary conservation analyses offer new perspective to immunogenic disorders

artículo científico publicado en 2010

Molecular mechanisms for protein-encoded inheritance

artículo científico publicado en 2009

Mutations in TAX1BP3 cause dilated cardiomyopathy with septo-optic dysplasia

artículo científico publicado en 2015

Of four mutations in the factor VII gene in Tunisian patients, one novel mutation (Ser339Phe) in three unrelated families abrogates factor X activation

artículo científico publicado en 2005

Preparation of Crystalline Samples of Amyloid Fibrils and Oligomers

artículo científico publicado en 2016

Reciprocal Interactions between Membrane Bilayers and S. aureus PSMα3 Cross-α Amyloid Fibrils Account for Species-Specific Cytotoxicity

artículo científico publicado en 2018

Seven novel mutations in the factor XIII A-subunit gene causing hereditary factor XIII deficiency in 10 unrelated families

article

Severe factor XI deficiency caused by a Gly555 to Glu mutation (factor XI-Glu555): a cross-reactive material positive variant defective in factor IX activation.

artículo científico publicado en 2004

Single point mutations in the zinc finger motifs of the human immunodeficiency virus type 1 nucleocapsid alter RNA binding specificities of the gag protein and enhance packaging and infectivity

artículo científico publicado en 2005

Sodium-Proton (Na(+)/H(+)) Antiporters: Properties and Roles in Health and Disease

artículo científico publicado en 2016

Specific cysteines in beta3 are involved in disulfide bond exchange-dependent and -independent activation of alphaIIbbeta3.

artículo científico publicado en 2008

Staphylococcus aureus PSMα3 Cross-α Fibril Polymorphism and Determinants of Cytotoxicity

scientific article published on 06 January 2020

Structural Insights into Curli CsgA Cross-β Fibril Architecture Inspire Repurposing of Anti-amyloid Compounds as Anti-biofilm Agents

artículo científico publicado en 2019

Structural Insights into Curli CsgA Cross-β Fibril Architecture Inspired Repurposing of Anti-amyloid Compounds as Anti-biofilm Agents

article

Structure-based discovery of fiber-binding compounds that reduce the cytotoxicity of amyloid beta

artículo científico publicado en 2013

The GPSM2/LGN GoLoco motifs are essential for hearing

artículo científico publicado en 2015

The Human LL-37(17-29) antimicrobial peptide reveals a functional supramolecular structure

scientific article published on 04 August 2020

The cytotoxic Staphylococcus aureus PSMα3 reveals a cross-α amyloid-like fibril

artículo científico publicado en 2017

Three residues at the interface of factor XI (FXI) monomers augment covalent dimerization of FXI.

artículo científico publicado en 2009

Towards a Pharmacophore for Amyloid

artículo científico publicado en 2011

Toxic Determinants of Staphylococcus aureus PSMα3 Cross-α Amyloid

article

Two conflicting NHE1 model structures: compatibility with experimental data and implications for the transport mechanism

artículo científico publicado en 2011

Unique disulfide bonds in epidermal growth factor (EGF) domains of β3 affect structure and function of αIIbβ3 and αvβ3 integrins in different manner

artículo científico publicado en 2012

Lista de obras de Meytal Landau

A 13-bp deletion in alpha(IIb) gene is a founder mutation that predominates in Palestinian-Arab patients with Glanzmann thrombasthenia

A Putative Mechanism for Downregulation of the Catalytic Activity of the EGF Receptor via Direct Contact between Its Kinase and C-Terminal Domains

A Small Molecule Inhibitor of Bruton’s Tyrosine Kinase Involved in B-Cell Signaling

A novel factor XI missense mutation (Val371Ile) in the activation loop is responsible for a case of mild type II factor XI deficiency

A unique interaction between alphaIIb and beta3 in the head region is essential for outside-in signaling-related functions of alphaIIbbeta3 integrin

Atomic View of a Toxic Amyloid Small Oligomer

Characterization of seven novel mutations causing factor XI deficiency

Compound heterozygosity of HLA-DRB3*01:01 and HLA-DRB4*01:01 as a potential predictor of fetal neonatal alloimmune thrombocytopenia

ConSurf 2005: the projection of evolutionary conservation scores of residues on protein structures

Congenital dilated cardiomyopathy caused by biallelic mutations in Filamin C.

Crystal structures of truncated alphaA and alphaB crystallins reveal structural mechanisms of polydispersity important for eye lens function

Disulfide bond disruption by a β3-Cys549Arg mutation in six Jordanian families with Glanzmann thrombasthenia causes diminished production of constitutively active αIIbβ3

Dynamic equilibrium between multiple active and inactive conformations explains regulation and oncogenic mutations in ErbB receptors

Extreme Amyloid Polymorphism inStaphylococcus aureusVirulent PSMα Peptides

Extreme amyloid polymorphism in Staphylococcus aureus virulent PSMα peptides

Formation of amyloid fibers by monomeric light chain variable domains

Functional evaluation of autism-associated mutations in NHE9.

Getting in charge of β-synuclein fibrillation

Lipid Bilayers Significantly Modulate Cross-Fibrillation of Two Distinct Amyloidogenic Peptides ⬇️

Mimicking cross-α amyloids

Model structure of the Na+/H+ exchanger 1 (NHE1): functional and clinical implications

Molecular basis for amyloid- polymorphism

Molecular diversity of Glanzmann thrombasthenia in southern India: new insights into mRNA splicing and structure-function correlations of alphaIIbbeta3 integrin (ITGA2B, ITGB3).

Molecular insight into human platelet antigens: structural and evolutionary conservation analyses offer new perspective to immunogenic disorders

Molecular mechanisms for protein-encoded inheritance

Mutations in TAX1BP3 cause dilated cardiomyopathy with septo-optic dysplasia

Of four mutations in the factor VII gene in Tunisian patients, one novel mutation (Ser339Phe) in three unrelated families abrogates factor X activation

Preparation of Crystalline Samples of Amyloid Fibrils and Oligomers

Reciprocal Interactions between Membrane Bilayers and S. aureus PSMα3 Cross-α Amyloid Fibrils Account for Species-Specific Cytotoxicity

Seven novel mutations in the factor XIII A-subunit gene causing hereditary factor XIII deficiency in 10 unrelated families

Severe factor XI deficiency caused by a Gly555 to Glu mutation (factor XI-Glu555): a cross-reactive material positive variant defective in factor IX activation.

Single point mutations in the zinc finger motifs of the human immunodeficiency virus type 1 nucleocapsid alter RNA binding specificities of the gag protein and enhance packaging and infectivity

Sodium-Proton (Na(+)/H(+)) Antiporters: Properties and Roles in Health and Disease

Specific cysteines in beta3 are involved in disulfide bond exchange-dependent and -independent activation of alphaIIbbeta3.

Staphylococcus aureus PSMα3 Cross-α Fibril Polymorphism and Determinants of Cytotoxicity

Structural Insights into Curli CsgA Cross-β Fibril Architecture Inspire Repurposing of Anti-amyloid Compounds as Anti-biofilm Agents

Structural Insights into Curli CsgA Cross-β Fibril Architecture Inspired Repurposing of Anti-amyloid Compounds as Anti-biofilm Agents

Structure-based discovery of fiber-binding compounds that reduce the cytotoxicity of amyloid beta

The GPSM2/LGN GoLoco motifs are essential for hearing

The Human LL-37(17-29) antimicrobial peptide reveals a functional supramolecular structure

The cytotoxic Staphylococcus aureus PSMα3 reveals a cross-α amyloid-like fibril

Three residues at the interface of factor XI (FXI) monomers augment covalent dimerization of FXI.

Towards a Pharmacophore for Amyloid

Toxic Determinants of Staphylococcus aureus PSMα3 Cross-α Amyloid

Two conflicting NHE1 model structures: compatibility with experimental data and implications for the transport mechanism

Unique disulfide bonds in epidermal growth factor (EGF) domains of β3 affect structure and function of αIIbβ3 and αvβ3 integrins in different manner

Compound heterozygosity of HLA-DRB301:01 and HLA-DRB401:01 as a potential predictor of fetal neonatal alloimmune thrombocytopenia