Lista de obras - Joanna Jakóbkiewicz-Banecka

A bacterial model for studying effects of human mutations in vivo: Escherichia coli strains mimicking a common polymorphism in the human MTHFR gene

artículo científico publicado en 2005

A modified procedure for quantitative analysis of mtDNA, detecting mtDNA depletion

artículo científico publicado en 2005

Abnormal Sphingolipid World in Inflammation Specific for Lysosomal Storage Diseases and Skin Disorders

artículo científico publicado en 2018

Abnormalities in the hair morphology of patients with some but not all types of mucopolysaccharidoses

scientific article published on 15 March 2007

Activities of genes controlling sphingolipid metabolism in human fibroblasts treated with flavonoids

artículo científico publicado en 2015

Atypical microbial infections of digestive tract may contribute to diarrhea in mucopolysaccharidosis patients: a MPS I case study

artículo científico publicado en 2005

Biodegradation of nodularin and effects of the toxin on bacterial isolates from the Gulf of Gdańsk

artículo científico publicado en 2009

Cell cycle is disturbed in mucopolysaccharidosis type II fibroblasts, and can be improved by genistein

artículo científico publicado en 2016

Changes in hair morphology of mucopolysaccharidosis I patients treated with recombinant human alpha-L-iduronidase (laronidase, Aldurazyme)

artículo científico publicado en 2005

Clinical parameters of inflammatory bowel disease in children do not correlate with four common polymorphisms of the transforming growth factor β1 gene

scientific article published on 03 December 2011

Combined Therapies for Lysosomal Storage Diseases

artículo científico

Comparison of siRNA-mediated silencing of glycosaminoglycan synthesis genes and enzyme replacement therapy for mucopolysaccharidosis in cell culture studies.

artículo científico publicado en 2012

Correction: Bocheńska, K. et al. Lysosome Alterations in the Human Epithelial Cell Line HaCaT and Skin Specimens: Relevance to Psoriasis. Int. J. Mol. Sci. 2019, 20, 2255

scientific article published on 16 January 2020

Correlation between severity of mucopolysaccharidoses and combination of the residual enzyme activity and efficiency of glycosaminoglycan synthesis

scientific article published on 30 November 2008

Corrigendum: Modulation of expression of genes involved in glycosaminoglycan metabolism and lysosome biogenesis by flavonoids

artículo científico publicado en 2016

Corrigendum: Modulation of expression of genes involved in glycosaminoglycan metabolism and lysosome biogenesis by flavonoids

artículo científico publicado en 2016

Different amounts of isoflavones in various commercially available soy extracts in the light of gene expression-targeted isoflavone therapy

artículo científico publicado en 2010

Drug-resistant epilepsia and fulminant valproate liver toxicity. Alpers-Huttenlocher syndrome in two children confirmed post mortem by identification of p.W748S mutation in POLG gene

artículo científico publicado en 2011

Effect of silicone on the collagen fibrillogenesis and stability

artículo científico publicado en 2015

Effects of flavonoids on expression of genes involved in cell cycle regulation and DNA replication in human fibroblasts

artículo científico publicado en 2015

Effects of flavonoids on glycosaminoglycan synthesis: implications for substrate reduction therapy in Sanfilippo disease and other mucopolysaccharidoses

artículo científico publicado en 2011

Erratum to: Activities of genes controlling sphingolipid metabolism in human fibroblasts treated with flavonoids.

artículo científico publicado en 2017

Erratum to: Effects of flavonoids on expression of genes involved in cell cycle regulation and DNA replication in human fibroblasts.

artículo científico publicado en 2016

Evidence for interactions between homocysteine and genistein: insights into stroke risk and potential treatment

artículo científico publicado en 2017

Factors and processes modulating phenotypes in neuronopathic lysosomal storage diseases

artículo científico publicado en 2014

False positive results of mitochondrial DNA depletion/deletion due to single nucleotide substitutions causing appearance of additional PvuII restriction sites

artículo científico publicado en 2007

Female Fabry disease patients and X-chromosome inactivation

artículo científico publicado en 2017

Female Hunter syndrome caused by a single mutation and familial XCI skewing: implications for other X-linked disorders

artículo científico publicado en 2010

Genistein inhibits activities of methylenetetrahydrofolate reductase and lactate dehydrogenase, enzymes which use NADH as a substrate

artículo científico publicado en 2015

Genistein reduces lysosomal storage in peripheral tissues of mucopolysaccharide IIIB mice

artículo científico publicado en 2009

Genistein-mediated inhibition of glycosaminoglycan synthesis as a basis for gene expression-targeted isoflavone therapy for mucopolysaccharidoses

artículo científico publicado en 2006

Genistein-mediated inhibition of glycosaminoglycan synthesis, which corrects storage in cells of patients suffering from mucopolysaccharidoses, acts by influencing an epidermal growth factor-dependent pathway.

artículo científico publicado en 2009

Genistein: a lysosomal stimulator for treatment of various lysosomal diseases

article published in 2017

Genistein: a natural isoflavone with a potential for treatment of genetic diseases

artículo científico publicado en 2010

Genistin-rich soy isoflavone extract in substrate reduction therapy for Sanfilippo syndrome: An open-label, pilot study in 10 pediatric patients

scientific article published on April 2008

Glycosaminoglycans and mucopolysaccharidosis type III.

artículo científico publicado en 2016

Homocysteine level and metabolism in ischemic stroke in the population of Northern Poland

artículo científico publicado en 2009

Impact of isoflavone genistein on psoriasis in in vivo and in vitro investigations

artículo científico publicado en 2021

Impairment of glycosaminoglycan synthesis in mucopolysaccharidosis type IIIA cells by using siRNA: a potential therapeutic approach for Sanfilippo disease

artículo científico publicado en 2009

Improved HPLC method for total plasma homocysteine detection and quantification.

artículo científico publicado en 2008

Improvement in the range of joint motion in seven patients with mucopolysaccharidosis type II during experimental gene expression-targeted isoflavone therapy (GET IT)

scientific article published on 10 August 2011

Lipids and Lipid Mediators Associated with the Risk and Pathology of Ischemic Stroke ⬇️

artículo científico publicado en 2020

Lipophagy and Lipolysis Status in Lipid Storage and Lipid Metabolism Diseases

scientific article published on 25 August 2020

Lysosome Alterations in the Human Epithelial Cell Line HaCaT and Skin Specimens: Relevance to Psoriasis. ⬇️

artículo científico publicado en 2019

MDM2 gene amplification: a new independent factor of adverse prognosis in non-small cell lung cancer (NSCLC).

artículo científico publicado en 2004

Metal and antibiotic resistance of bacteria isolated from the Baltic Sea

artículo científico publicado en 2012

Models in the Research Process of Psoriasis

artículo científico publicado en 2017

Modulation of expression of genes involved in glycosaminoglycan metabolism and lysosome biogenesis by flavonoids

artículo científico publicado en 2015

Molecular action of isoflavone genistein in the human epithelial cell line HaCaT.

artículo científico publicado en 2018

Molecular factors involved in the development of diabetic foot syndrome.

artículo científico

Non-steroidal anti-inflammatory drugs are safe with respect to the transcriptome of human dermal fibroblasts

artículo científico publicado en 2017

Nonsteroidal anti-inflammatory drugs modulate cellular glycosaminoglycan synthesis by affecting EGFR and PI3K signaling pathways

artículo científico publicado en 2017

Osteoprotegerin gene polymorphism in diabetic Charcot neuroarthropathy

artículo científico publicado en 2012

P53 and K-ras mutations are frequent events in microscopically negative surgical margins from patients with nonsmall cell lung carcinoma.

artículo científico publicado en 2004

Post mortem identification of deoxyguanosine kinase (DGUOK) gene mutations combined with impaired glucose homeostasis and iron overload features in four infants with severe progressive liver failure

artículo científico publicado en 2010

Prevalence of polymorphisms in OPG, RANKL and RANK as potential markers for Charcot arthropathy development

artículo científico publicado en 2017

Putative biological mechanisms of efficiency of substrate reduction therapies for mucopolysaccharidoses

artículo científico publicado en 2012

Rapid deterioration of a patient with mucopolysaccharidosis type I during interruption of enzyme replacement therapy

artículo científico publicado en 2007

Simultaneous siRNA-mediated silencing of pairs of genes coding for enzymes involved in glycosaminoglycan synthesis

artículo científico publicado en 2012

Substrate deprivation therapy: a new hope for patients suffering from neuronopathic forms of inherited lysosomal storage diseases

artículo científico publicado en 2007

Substrate reduction therapies for mucopolysaccharidoses

artículo científico publicado en 2011

Synthetic genistein derivatives as modulators of glycosaminoglycan storage

artículo científico publicado en 2012

The Role of Dimethyl Sulfoxide (DMSO) in Gene Expression Modulation and Glycosaminoglycan Metabolism in Lysosomal Storage Disorders on an Example of Mucopolysaccharidosis ⬇️

artículo científico

The mRNA level of the transforming growth factor β1 gene, but not the amount of the gene product, can be considered as a potential prognostic parameter in inflammatory bowel diseases in children.

artículo científico publicado en 2012

The model homologue of the partially defective human 5,10-methylenetetrahydrofolate reductase, considered as a risk factor for stroke due to increased homocysteine level, can be protected and reactivated by heat shock proteins

artículo científico publicado en 2016

The molecular mechanism of genistein action in lysosomal storage diseases: A transcriptomic approach

The phytoestrogen genistein modulates lysosomal metabolism and transcription factor EB (TFEB) activation

artículo científico publicado en 2014

The role of genetic factors and monocyte-to-osteoclast differentiation in the pathogenesis of Charcot neuroarthropathy

scientific article published on 21 July 2020

Transforming growth factor β1 protein and mRNA levels in inflammatory bowel diseases: towards solving the contradictions by longitudinal assessment of the protein and mRNA amounts.

artículo científico publicado en 2013

Two-year follow-up of Sanfilippo Disease patients treated with a genistein-rich isoflavone extract: assessment of effects on cognitive functions and general status of patients

artículo científico publicado en 2011

Why are behaviors of children suffering from various neuronopathic types of mucopolysaccharidoses different?

scientific article published on 21 August 2010

[Gene polymorphism of transforming growth factor beta1 (TGF-beta1) in the pathogenesis and clinical course of chronic hepatitis in children]

scientific article published on 01 July 2009

Lista de obras de Joanna Jakóbkiewicz-Banecka

A bacterial model for studying effects of human mutations in vivo: Escherichia coli strains mimicking a common polymorphism in the human MTHFR gene

A modified procedure for quantitative analysis of mtDNA, detecting mtDNA depletion

Abnormal Sphingolipid World in Inflammation Specific for Lysosomal Storage Diseases and Skin Disorders

Abnormalities in the hair morphology of patients with some but not all types of mucopolysaccharidoses

Activities of genes controlling sphingolipid metabolism in human fibroblasts treated with flavonoids

Atypical microbial infections of digestive tract may contribute to diarrhea in mucopolysaccharidosis patients: a MPS I case study

Biodegradation of nodularin and effects of the toxin on bacterial isolates from the Gulf of Gdańsk

Cell cycle is disturbed in mucopolysaccharidosis type II fibroblasts, and can be improved by genistein

Changes in hair morphology of mucopolysaccharidosis I patients treated with recombinant human alpha-L-iduronidase (laronidase, Aldurazyme)

Clinical parameters of inflammatory bowel disease in children do not correlate with four common polymorphisms of the transforming growth factor β1 gene

Combined Therapies for Lysosomal Storage Diseases

Comparison of siRNA-mediated silencing of glycosaminoglycan synthesis genes and enzyme replacement therapy for mucopolysaccharidosis in cell culture studies.

Correction: Bocheńska, K. et al. Lysosome Alterations in the Human Epithelial Cell Line HaCaT and Skin Specimens: Relevance to Psoriasis. Int. J. Mol. Sci. 2019, 20, 2255

Correlation between severity of mucopolysaccharidoses and combination of the residual enzyme activity and efficiency of glycosaminoglycan synthesis

Corrigendum: Modulation of expression of genes involved in glycosaminoglycan metabolism and lysosome biogenesis by flavonoids

Corrigendum: Modulation of expression of genes involved in glycosaminoglycan metabolism and lysosome biogenesis by flavonoids

Different amounts of isoflavones in various commercially available soy extracts in the light of gene expression-targeted isoflavone therapy

Drug-resistant epilepsia and fulminant valproate liver toxicity. Alpers-Huttenlocher syndrome in two children confirmed post mortem by identification of p.W748S mutation in POLG gene

Effect of silicone on the collagen fibrillogenesis and stability

Effects of flavonoids on expression of genes involved in cell cycle regulation and DNA replication in human fibroblasts

Effects of flavonoids on glycosaminoglycan synthesis: implications for substrate reduction therapy in Sanfilippo disease and other mucopolysaccharidoses

Erratum to: Activities of genes controlling sphingolipid metabolism in human fibroblasts treated with flavonoids.

Erratum to: Effects of flavonoids on expression of genes involved in cell cycle regulation and DNA replication in human fibroblasts.

Evidence for interactions between homocysteine and genistein: insights into stroke risk and potential treatment

Factors and processes modulating phenotypes in neuronopathic lysosomal storage diseases

False positive results of mitochondrial DNA depletion/deletion due to single nucleotide substitutions causing appearance of additional PvuII restriction sites

Female Fabry disease patients and X-chromosome inactivation

Female Hunter syndrome caused by a single mutation and familial XCI skewing: implications for other X-linked disorders

Genistein inhibits activities of methylenetetrahydrofolate reductase and lactate dehydrogenase, enzymes which use NADH as a substrate

Genistein reduces lysosomal storage in peripheral tissues of mucopolysaccharide IIIB mice

Genistein-mediated inhibition of glycosaminoglycan synthesis as a basis for gene expression-targeted isoflavone therapy for mucopolysaccharidoses

Genistein-mediated inhibition of glycosaminoglycan synthesis, which corrects storage in cells of patients suffering from mucopolysaccharidoses, acts by influencing an epidermal growth factor-dependent pathway.

Genistein: a lysosomal stimulator for treatment of various lysosomal diseases

Genistein: a natural isoflavone with a potential for treatment of genetic diseases

Genistin-rich soy isoflavone extract in substrate reduction therapy for Sanfilippo syndrome: An open-label, pilot study in 10 pediatric patients

Glycosaminoglycans and mucopolysaccharidosis type III.

Homocysteine level and metabolism in ischemic stroke in the population of Northern Poland

Impact of isoflavone genistein on psoriasis in in vivo and in vitro investigations

Impairment of glycosaminoglycan synthesis in mucopolysaccharidosis type IIIA cells by using siRNA: a potential therapeutic approach for Sanfilippo disease

Improved HPLC method for total plasma homocysteine detection and quantification.

Improvement in the range of joint motion in seven patients with mucopolysaccharidosis type II during experimental gene expression-targeted isoflavone therapy (GET IT)

Lipids and Lipid Mediators Associated with the Risk and Pathology of Ischemic Stroke ⬇️

Lipophagy and Lipolysis Status in Lipid Storage and Lipid Metabolism Diseases

Lysosome Alterations in the Human Epithelial Cell Line HaCaT and Skin Specimens: Relevance to Psoriasis. ⬇️

MDM2 gene amplification: a new independent factor of adverse prognosis in non-small cell lung cancer (NSCLC).

Metal and antibiotic resistance of bacteria isolated from the Baltic Sea

Models in the Research Process of Psoriasis

Modulation of expression of genes involved in glycosaminoglycan metabolism and lysosome biogenesis by flavonoids

Molecular action of isoflavone genistein in the human epithelial cell line HaCaT.

Molecular factors involved in the development of diabetic foot syndrome.

Non-steroidal anti-inflammatory drugs are safe with respect to the transcriptome of human dermal fibroblasts

Nonsteroidal anti-inflammatory drugs modulate cellular glycosaminoglycan synthesis by affecting EGFR and PI3K signaling pathways

Osteoprotegerin gene polymorphism in diabetic Charcot neuroarthropathy

P53 and K-ras mutations are frequent events in microscopically negative surgical margins from patients with nonsmall cell lung carcinoma.

Post mortem identification of deoxyguanosine kinase (DGUOK) gene mutations combined with impaired glucose homeostasis and iron overload features in four infants with severe progressive liver failure

Prevalence of polymorphisms in OPG, RANKL and RANK as potential markers for Charcot arthropathy development

Putative biological mechanisms of efficiency of substrate reduction therapies for mucopolysaccharidoses

Rapid deterioration of a patient with mucopolysaccharidosis type I during interruption of enzyme replacement therapy

Simultaneous siRNA-mediated silencing of pairs of genes coding for enzymes involved in glycosaminoglycan synthesis

Substrate deprivation therapy: a new hope for patients suffering from neuronopathic forms of inherited lysosomal storage diseases

Substrate reduction therapies for mucopolysaccharidoses

Synthetic genistein derivatives as modulators of glycosaminoglycan storage

The Role of Dimethyl Sulfoxide (DMSO) in Gene Expression Modulation and Glycosaminoglycan Metabolism in Lysosomal Storage Disorders on an Example of Mucopolysaccharidosis ⬇️

The mRNA level of the transforming growth factor β1 gene, but not the amount of the gene product, can be considered as a potential prognostic parameter in inflammatory bowel diseases in children.

The model homologue of the partially defective human 5,10-methylenetetrahydrofolate reductase, considered as a risk factor for stroke due to increased homocysteine level, can be protected and reactivated by heat shock proteins

The molecular mechanism of genistein action in lysosomal storage diseases: A transcriptomic approach

The phytoestrogen genistein modulates lysosomal metabolism and transcription factor EB (TFEB) activation

The role of genetic factors and monocyte-to-osteoclast differentiation in the pathogenesis of Charcot neuroarthropathy

Transforming growth factor β1 protein and mRNA levels in inflammatory bowel diseases: towards solving the contradictions by longitudinal assessment of the protein and mRNA amounts.

Two-year follow-up of Sanfilippo Disease patients treated with a genistein-rich isoflavone extract: assessment of effects on cognitive functions and general status of patients

Why are behaviors of children suffering from various neuronopathic types of mucopolysaccharidoses different?

[Gene polymorphism of transforming growth factor beta1 (TGF-beta1) in the pathogenesis and clinical course of chronic hepatitis in children]