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Leukocyte-endothelial cell interaction is enhanced in podocalyxin-deficient mice

The international journal of biochemistry & cell biology, 2018-06, Vol.99, p.72-79

2018

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Loss of endothelial barrier integrity in mice with conditional ablation of podocalyxin (Podxl) in endothelial cells

European journal of cell biology, 2016-08, Vol.95 (8), p.265-276

2016

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Human endoglin as a potential new partner involved in platelet–endothelium interactions

Cellular and molecular life sciences : CMLS, 2018-04, Vol.75 (7), p.1269-1284

2018

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Role of CD34 family members in lumen formation in the developing kidney

Developmental biology, 2016-10, Vol.418 (1), p.66-74

2016

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Possible role for cellular FXIII in monocyte-derived dendritic cell motility

European journal of cell biology, 2009-08, Vol.88 (8), p.423-431

2009

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C3G transgenic mouse models with specific expression in platelets reveal a new role for C3G in platelet clotting through its GEF activity

Biochimica et biophysica acta, 2012-08, Vol.1823 (8), p.1366-1377

2012

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Generation of mice with conditional ablation of the Cd40lg gene: new insights on the role of CD40L

Transgenic research, 2014-02, Vol.23 (1), p.53-66

2014

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Ventricular enlargement associated with the panneural ablation of the podocalyxin gene

Molecular and cellular neuroscience, 2010, Vol.43 (1), p.90-97

2010

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Type II Glanzmann thrombasthenia in a compound heterozygote for the alpha IIb gene. A novel missense mutation in exon 27

Haematologica (Roma), 2006-10, Vol.91 (10), p.1352-1359

2006

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alpha-Adrenergic-mediated activation of human reconstituted fibrinogen receptor (integrin alphaIIbbeta3) in Chinese hamster ovary cells

Thrombosis and haemostasis, 2004-12, Vol.92 (6), p.1368-1376

2004

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Integrating magnetic capabilities to intracellular chips for cell trapping

Scientific reports, 2021-09, Vol.11 (1), p.18495-18495, Article 18495

2021

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Control of cell adhesion and migration by podocalyxin. Implication of Rac1 and Cdc42

Biochemical and biophysical research communications, 2013-03, Vol.432 (2), p.302-307

2013

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A novel (288delC) mutation in exon 2 of GPIIb associated with type I Glanzmann's thrombasthenia

British journal of haematology, 2000-10, Vol.111 (1), p.96-103

2000

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Functional and molecular characterization of inherited platelet disorders in the Iberian Peninsula: results from a collaborative study

Orphanet journal of rare diseases, 2014-12, Vol.9 (1), p.213-213, Article 213

2014

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L718P mutation in the membrane-proximal cytoplasmic tail of β3 promotes abnormal αIIbβ3 clustering and lipid microdomain coalescence, and associates with a thrombasthenia-like phenotype

Haematologica (Roma), 2010-07, Vol.95 (7), p.1158-1166

2010

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A mutant (Arg327-->His) GPIIb associated to thrombasthenia exerts a dominant negative effect in stably transfected CHO cells

Thrombosis and haemostasis, 1996, Vol.76 (3), p.292-301

1996

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Activin-A inhibits proopiomelanocortin messenger RNA accumulation and adrenocorticotropin secretion of AtT20 cells

Molecular endocrinology (Baltimore, Md.), 1991-10, Vol.5 (10), p.1389-1395

1991

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Allogeneic hematopoietic cell transplantation in an adult patient with Glanzmann thrombasthenia

Clinical case reports, 2017-11, Vol.5 (11), p.1887-1890

2017

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Involvement of ERK1/2, p38 and PI3K in megakaryocytic differentiation of K562 cells

European journal of haematology, 2010-05, Vol.84 (5), p.430-440

2010

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Diminished thrombogenic responses by deletion of the Podocalyxin Gene in mouse megakaryocytes

PloS one, 2011-10, Vol.6 (10), p.e26025

2011

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Nonsense mutation in exon-19 of GPIIb associated with thrombasthenic phenotype. Failure of GPIIb(delta597-1008) to form stable complexes with GPIIIa

Thrombosis and haemostasis, 2002-04, Vol.87 (4), p.684-691

2002

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Compound Heterozygosity of the GPIbα Gene Associated with Bernard-Soulier Syndrome

Thrombosis and haemostasis, 2001, Vol.86 (12), p.1385-1391

2001

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Disruption of the β3 663-687 disulfide bridge confers constitutive activity to β3 integrins

Blood, 2003-10, Vol.102 (7), p.2491-2497

2003

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Activin-A, inhibin and transforming growth factor-β modulate growth of two gonadal cell lines

Endocrinology (Philadelphia), 1989-09, Vol.125 (3), p.1666-1672

1989

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Role of transcription factor Sp1 and CpG methylation on the regulation of the human podocalyxin gene promoter

BMC molecular biology, 2006-05, Vol.7 (1), p.17-17, Article 17

2006

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Leukocyte-endothelial cell interaction is enhanced in podocalyxin-deficient mice

Loss of endothelial barrier integrity in mice with conditional ablation of podocalyxin (Podxl) in endothelial cells

Human endoglin as a potential new partner involved in platelet–endothelium interactions

Role of CD34 family members in lumen formation in the developing kidney

Possible role for cellular FXIII in monocyte-derived dendritic cell motility

C3G transgenic mouse models with specific expression in platelets reveal a new role for C3G in platelet clotting through its GEF activity

Generation of mice with conditional ablation of the Cd40lg gene: new insights on the role of CD40L

Ventricular enlargement associated with the panneural ablation of the podocalyxin gene

Type II Glanzmann thrombasthenia in a compound heterozygote for the alpha IIb gene. A novel missense mutation in exon 27

alpha-Adrenergic-mediated activation of human reconstituted fibrinogen receptor (integrin alphaIIbbeta3) in Chinese hamster ovary cells

Integrating magnetic capabilities to intracellular chips for cell trapping

Control of cell adhesion and migration by podocalyxin. Implication of Rac1 and Cdc42

A novel (288delC) mutation in exon 2 of GPIIb associated with type I Glanzmann's thrombasthenia

Functional and molecular characterization of inherited platelet disorders in the Iberian Peninsula: results from a collaborative study

L718P mutation in the membrane-proximal cytoplasmic tail of β3 promotes abnormal αIIbβ3 clustering and lipid microdomain coalescence, and associates with a thrombasthenia-like phenotype

A mutant (Arg327-->His) GPIIb associated to thrombasthenia exerts a dominant negative effect in stably transfected CHO cells

Activin-A inhibits proopiomelanocortin messenger RNA accumulation and adrenocorticotropin secretion of AtT20 cells

Allogeneic hematopoietic cell transplantation in an adult patient with Glanzmann thrombasthenia

Involvement of ERK1/2, p38 and PI3K in megakaryocytic differentiation of K562 cells

Diminished thrombogenic responses by deletion of the Podocalyxin Gene in mouse megakaryocytes

Nonsense mutation in exon-19 of GPIIb associated with thrombasthenic phenotype. Failure of GPIIb(delta597-1008) to form stable complexes with GPIIIa

Compound Heterozygosity of the GPIbα Gene Associated with Bernard-Soulier Syndrome

Disruption of the β3 663-687 disulfide bridge confers constitutive activity to β3 integrins

Activin-A, inhibin and transforming growth factor-β modulate growth of two gonadal cell lines

Role of transcription factor Sp1 and CpG methylation on the regulation of the human podocalyxin gene promoter

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