Lista de obras - David Coelho - Dominio Público Uruguay

APRDX1 mutant allele causes a MMACHC secondary epimutation in cblC patients.

artículo científico publicado en 2018

Brain Susceptibility to Methyl Donor Deficiency: From Fetal Programming to Aging Outcome in Rats

scientific article published on 14 November 2019

Carbon ions-induced apoptosis in hematopoietic tumor cell lines.

artículo científico publicado en 2003

Clinical and molecular heterogeneity in patients with the cblD inborn error of cobalamin metabolism.

artículo científico publicado en 2008

Clinical or ATPase domain mutations in ABCD4 disrupt the interaction between the vitamin B12-trafficking proteins ABCD4 and LMBD1.

artículo científico publicado en 2017

Ex vivo determination of the effect of whole-body exposure to fast neutrons on murine spleen cell viability and apoptosis

scientific article published on 01 September 2000

Gene identification for the cblD defect of vitamin B12 metabolism

artículo científico publicado en 2008

Genetic animal models to decipher the pathogenic effects of vitamin B12 and folate deficiency.

artículo científico publicado en 2016

Inherited disorders of cobalamin metabolism disrupt nucleocytoplasmic transport of mRNA through impaired methylation/phosphorylation of ELAVL1/HuR

scientific article published on 01 September 2018

Interaction between methionine synthase isoforms and MMACHC: characterization in cblG-variant, cblG and cblC inherited causes of megaloblastic anaemia

artículo científico publicado en 2013

Involvement of TP53 in apoptosis induced in human lymphoblastoid cells by fast neutrons.

artículo científico publicado en 2002

Methionine synthase and methionine synthase reductase interact with MMACHC and with MMADHC.

artículo científico publicado en 2016

Modulation of the antiproliferative activity of anticancer drugs in hematopoietic tumor cell lines by the poly(ADP-ribose) polymerase inhibitor 6(5H)-phenanthridinone.

artículo científico publicado en 2000

Mutation Update and Review of Severe Methylenetetrahydrofolate Reductase Deficiency.

artículo científico publicado en 2016

Mutations in ABCD4 cause a new inborn error of vitamin B12 metabolism

artículo científico publicado en 2012

Mutations in MTHFR and POLG impaired activity of the mitochondrial respiratory chain in 46-year-old twins with spastic paraparesis

scientific article published on 23 October 2019

Perturbation by geraniol of cell membrane permeability and signal transduction pathways in human colon cancer cells.

artículo científico publicado en 2002

Prevention of nitrogen mustard-induced apoptosis in normal and transformed lymphocytes by ebselen.

artículo científico publicado en 2000

Publisher Correction: A PRDX1 mutant allele causes a MMACHC secondary epimutation in cblC patients

artículo científico publicado en 2018

SIRT1 activation rescues the mislocalization of RNA-binding proteins and cognitive defects induced by inherited cobalamin disorders

scientific article published on 28 October 2019

Sirt1-PPARS Cross-Talk in Complex Metabolic Diseases and Inherited Disorders of the One Carbon Metabolism

artículo científico publicado en 2020

The cblD defect causes either isolated or combined deficiency of methylcobalamin and adenosylcobalamin synthesis.

artículo científico publicado en 2004

[Vitamin B12 and related genetic disorders]

article published in 2014

Lista de obras de David Coelho

APRDX1 mutant allele causes a MMACHC secondary epimutation in cblC patients.

Brain Susceptibility to Methyl Donor Deficiency: From Fetal Programming to Aging Outcome in Rats

Carbon ions-induced apoptosis in hematopoietic tumor cell lines.

Clinical and molecular heterogeneity in patients with the cblD inborn error of cobalamin metabolism.

Clinical or ATPase domain mutations in ABCD4 disrupt the interaction between the vitamin B12-trafficking proteins ABCD4 and LMBD1.

Ex vivo determination of the effect of whole-body exposure to fast neutrons on murine spleen cell viability and apoptosis

Gene identification for the cblD defect of vitamin B12 metabolism

Genetic animal models to decipher the pathogenic effects of vitamin B12 and folate deficiency.

Inherited disorders of cobalamin metabolism disrupt nucleocytoplasmic transport of mRNA through impaired methylation/phosphorylation of ELAVL1/HuR

Interaction between methionine synthase isoforms and MMACHC: characterization in cblG-variant, cblG and cblC inherited causes of megaloblastic anaemia

Involvement of TP53 in apoptosis induced in human lymphoblastoid cells by fast neutrons.

Methionine synthase and methionine synthase reductase interact with MMACHC and with MMADHC.

Modulation of the antiproliferative activity of anticancer drugs in hematopoietic tumor cell lines by the poly(ADP-ribose) polymerase inhibitor 6(5H)-phenanthridinone.

Mutation Update and Review of Severe Methylenetetrahydrofolate Reductase Deficiency.

Mutations in ABCD4 cause a new inborn error of vitamin B12 metabolism

Mutations in MTHFR and POLG impaired activity of the mitochondrial respiratory chain in 46-year-old twins with spastic paraparesis

Perturbation by geraniol of cell membrane permeability and signal transduction pathways in human colon cancer cells.

Prevention of nitrogen mustard-induced apoptosis in normal and transformed lymphocytes by ebselen.

Publisher Correction: A PRDX1 mutant allele causes a MMACHC secondary epimutation in cblC patients

SIRT1 activation rescues the mislocalization of RNA-binding proteins and cognitive defects induced by inherited cobalamin disorders

Sirt1-PPARS Cross-Talk in Complex Metabolic Diseases and Inherited Disorders of the One Carbon Metabolism

The cblD defect causes either isolated or combined deficiency of methylcobalamin and adenosylcobalamin synthesis.

[Vitamin B12 and related genetic disorders]