Lista de obras - Stavros Malas - Dominio Público Uruguay

Aniridia due to a novel microdeletion affecting regulatory enhancers: case report and review of the literature

artículo científico publicado en 2018

Anti-SOX1 antibodies in patients with paraneoplastic and non-paraneoplastic neuropathy

artículo científico publicado en 2010

C1q ablation exacerbates amyloid deposition: A study in a transgenic mouse model of ATTRV30M amyloid neuropathy.

artículo científico publicado en 2017

Cloning and mapping of the human SOX1: a highly conserved gene expressed in the developing brain

artículo científico publicado en 1997

Generation of an ABCG2(GFPn-puro) transgenic line--a tool to study ABCG2 expression in mice.

artículo científico publicado en 2009

Genetic and physical mapping of the murine Sox1 gene.

artículo científico publicado en 1996

Genetic background modifies amyloidosis in a mouse model of ATTR neuropathy.

artículo científico publicado en 2016

Intraperitoneal melatonin is not neuroprotective in the G93ASOD1 transgenic mouse model of familial ALS and may exacerbate neurodegeneration

artículo científico publicado en 2013

Linkage Mapping around the Ragged (Ra) and Wasted (wst) Loci on Distal Mouse Chromosome 2

scientific article published on 01 March 1994

Molecular analysis of Cypriot families with aniridia reveals a novel PAX6 mutation

artículo científico publicado en 2018

Neuronal migration and ventral subtype identity in the telencephalon depend on SOX1

artículo científico publicado en 2005

Omega-3 fatty acids protect retinal neurons in the DBA/2J hereditary glaucoma mouse model

artículo científico publicado en 2017

Pax6 is expressed in subsets of V0 and V2 interneurons in the ventral spinal cord in mice.

artículo científico publicado en 2013

SOX1 links the function of neural patterning and Notch signalling in the ventral spinal cord during the neuron-glial fate switch.

artículo científico publicado en 2009

Sequential Role of SOXB2 Factors in GABAergic Neuron Specification of the Dorsal Midbrain.

artículo científico publicado en 2018

Sox1 is required for the specification of a novel p2-derived interneuron subtype in the mouse ventral spinal cord

scientific journal article

Sox1 maintains the undifferentiated state of cortical neural progenitor cells via the suppression of Prox1-mediated cell cycle exit and neurogenesis

artículo científico publicado en 2011

Spatially distinct functions of PAX6 and NKX2.2 during gliogenesis in the ventral spinal cord

scientific journal article

The genes for endothelin 3, vitamin D 24-hydroxylase, and melanocortin 3 receptor map to distal mouse Chromosome 2, in the region of conserved synteny with human Chromosome 20

article

The isolation and high-resolution chromosomal mapping of human SOX14 and SOX21; two members of the SOX gene family related to SOX1, SOX2, and SOX3

artículo científico publicado en 1999

The isolation and mapping of PCR markers specific to mouse Chromosome 2

scientific article published on 01 February 1996

Two loci for tuberous sclerosis: one on 9q34 and one on 16p13.

artículo científico publicado en 1994

Vsx1 Transiently Defines an Early Intermediate V2 Interneuron Precursor Compartment in the Mouse Developing Spinal Cord.

artículo científico publicado en 2016

Lista de obras de Stavros Malas

Aniridia due to a novel microdeletion affecting regulatory enhancers: case report and review of the literature

Anti-SOX1 antibodies in patients with paraneoplastic and non-paraneoplastic neuropathy

C1q ablation exacerbates amyloid deposition: A study in a transgenic mouse model of ATTRV30M amyloid neuropathy.

Cloning and mapping of the human SOX1: a highly conserved gene expressed in the developing brain

Generation of an ABCG2(GFPn-puro) transgenic line--a tool to study ABCG2 expression in mice.

Genetic and physical mapping of the murine Sox1 gene.

Genetic background modifies amyloidosis in a mouse model of ATTR neuropathy.

Intraperitoneal melatonin is not neuroprotective in the G93ASOD1 transgenic mouse model of familial ALS and may exacerbate neurodegeneration

Linkage Mapping around the Ragged (Ra) and Wasted (wst) Loci on Distal Mouse Chromosome 2

Molecular analysis of Cypriot families with aniridia reveals a novel PAX6 mutation

Neuronal migration and ventral subtype identity in the telencephalon depend on SOX1

Omega-3 fatty acids protect retinal neurons in the DBA/2J hereditary glaucoma mouse model

Pax6 is expressed in subsets of V0 and V2 interneurons in the ventral spinal cord in mice.

SOX1 links the function of neural patterning and Notch signalling in the ventral spinal cord during the neuron-glial fate switch.

Sequential Role of SOXB2 Factors in GABAergic Neuron Specification of the Dorsal Midbrain.

Sox1 is required for the specification of a novel p2-derived interneuron subtype in the mouse ventral spinal cord

Sox1 maintains the undifferentiated state of cortical neural progenitor cells via the suppression of Prox1-mediated cell cycle exit and neurogenesis

Spatially distinct functions of PAX6 and NKX2.2 during gliogenesis in the ventral spinal cord

The genes for endothelin 3, vitamin D 24-hydroxylase, and melanocortin 3 receptor map to distal mouse Chromosome 2, in the region of conserved synteny with human Chromosome 20

The isolation and high-resolution chromosomal mapping of human SOX14 and SOX21; two members of the SOX gene family related to SOX1, SOX2, and SOX3

The isolation and mapping of PCR markers specific to mouse Chromosome 2

Two loci for tuberous sclerosis: one on 9q34 and one on 16p13.

Vsx1 Transiently Defines an Early Intermediate V2 Interneuron Precursor Compartment in the Mouse Developing Spinal Cord.