Lista de obras - Salla Keskitalo - Dominio Público Uruguay

A Family With A20 Haploinsufficiency Presenting With Novel Clinical Manifestations and Challenges for Treatment

artículo científico publicado en 2020

Alteration of prolyl oligopeptidase and activated α-2-macroglobulin in multiple sclerosis subtypes and in the clinically isolated syndrome.

artículo científico publicado en 2013

An Activating STAT3 Mutation Causes Neonatal Diabetes through Premature Induction of Pancreatic Differentiation

artículo científico publicado en 2017

Anagrelide for Gastrointestinal Stromal Tumor

scientific article published on 07 December 2018

Colonic metaproteomic signatures of active bacteria and the host in obesity.

artículo científico publicado en 2015

Combined immunodeficiency and hypoglycemia associated with mutations in hypoxia upregulated 1.

artículo científico publicado en 2016

Deletion of vascular endothelial growth factor C (VEGF-C) and VEGF-D is not equivalent to VEGF receptor 3 deletion in mouse embryos

artículo científico publicado en 2008

Disturbed keratinocyte differentiation in transgenic mice and organotypic keratinocyte cultures as a result of spermidine/spermine N-acetyltransferase overexpression.

artículo científico publicado en 2005

Dominant TOM1 mutation associated with combined immunodeficiency and autoimmune disease

artículo científico publicado en 2019

Enhanced capillary formation stimulated by a chimeric vascular endothelial growth factor/vascular endothelial growth factor-C silk domain fusion protein

artículo científico publicado en 2007

Functional Analysis of FLT4 Mutations Associated with Nonne–Milroy Lymphedema

article

Functional interaction of VEGF-C and VEGF-D with neuropilin receptors

artículo científico publicado en 2006

Gain-of-function CEBPE mutation causes noncanonical autoinflammatory inflammasomopathy

scientific article published on 13 June 2019

Haploinsufficiency of A20 impairs protein-protein interactome and leads into caspase-8-dependent enhancement of NLRP3 inflammasome activation

artículo científico publicado en 2018

Navigating through metaproteomics data: a logbook of database searching

artículo científico publicado en 2015

Novel TMEM173 Mutation and the Role of Disease Modifying Alleles

artículo científico publicado en 2019

Pool-seq driven proteogenomic database for Group G Streptococcus

scientific article published on 20 April 2019

Rapid genome editing by CRISPR-Cas9-POLD3 fusion

artículo científico publicado en 2021

SARS-CoV-2-host proteome interactions for antiviral drug discovery

artículo científico publicado en 2021

Somatic MED12 Nonsense Mutation Escapes mRNA Decay and Reveals a Motif Required for Nuclear Entry

artículo científico publicado en 2017

Somatic MED12 mutations in prostate cancer and uterine leiomyomas promote tumorigenesis through distinct mechanisms.

artículo científico publicado en 2015

The tyrosine kinase inhibitor cediranib blocks ligand-induced vascular endothelial growth factor receptor-3 activity and lymphangiogenesis

artículo científico publicado en 2008

The variant methylenetetrahydrofolate reductase c.1298A>C (p.E429A) is associated with multiple sclerosis in a German case-control study.

artículo científico publicado en 2009

Uterine leiomyoma-linked MED12 mutations disrupt mediator-associated CDK activity.

artículo científico publicado en 2014

Vascular endothelial growth factor-angiopoietin chimera with improved properties for therapeutic angiogenesis

artículo científico publicado en 2013

Lista de obras de Salla Keskitalo

A Family With A20 Haploinsufficiency Presenting With Novel Clinical Manifestations and Challenges for Treatment

Alteration of prolyl oligopeptidase and activated α-2-macroglobulin in multiple sclerosis subtypes and in the clinically isolated syndrome.

An Activating STAT3 Mutation Causes Neonatal Diabetes through Premature Induction of Pancreatic Differentiation

Anagrelide for Gastrointestinal Stromal Tumor

Colonic metaproteomic signatures of active bacteria and the host in obesity.

Combined immunodeficiency and hypoglycemia associated with mutations in hypoxia upregulated 1.

Deletion of vascular endothelial growth factor C (VEGF-C) and VEGF-D is not equivalent to VEGF receptor 3 deletion in mouse embryos

Disturbed keratinocyte differentiation in transgenic mice and organotypic keratinocyte cultures as a result of spermidine/spermine N-acetyltransferase overexpression.

Dominant TOM1 mutation associated with combined immunodeficiency and autoimmune disease

Enhanced capillary formation stimulated by a chimeric vascular endothelial growth factor/vascular endothelial growth factor-C silk domain fusion protein

Functional Analysis of FLT4 Mutations Associated with Nonne–Milroy Lymphedema

Functional interaction of VEGF-C and VEGF-D with neuropilin receptors

Gain-of-function CEBPE mutation causes noncanonical autoinflammatory inflammasomopathy

Haploinsufficiency of A20 impairs protein-protein interactome and leads into caspase-8-dependent enhancement of NLRP3 inflammasome activation

Navigating through metaproteomics data: a logbook of database searching

Novel TMEM173 Mutation and the Role of Disease Modifying Alleles

Pool-seq driven proteogenomic database for Group G Streptococcus

Rapid genome editing by CRISPR-Cas9-POLD3 fusion

SARS-CoV-2-host proteome interactions for antiviral drug discovery

Somatic MED12 Nonsense Mutation Escapes mRNA Decay and Reveals a Motif Required for Nuclear Entry

Somatic MED12 mutations in prostate cancer and uterine leiomyomas promote tumorigenesis through distinct mechanisms.

The tyrosine kinase inhibitor cediranib blocks ligand-induced vascular endothelial growth factor receptor-3 activity and lymphangiogenesis

The variant methylenetetrahydrofolate reductase c.1298A>C (p.E429A) is associated with multiple sclerosis in a German case-control study.

Uterine leiomyoma-linked MED12 mutations disrupt mediator-associated CDK activity.

Vascular endothelial growth factor-angiopoietin chimera with improved properties for therapeutic angiogenesis