List of works - 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

scientific article published on 14 June 2005

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

scientific article published on 01 January 2005

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

scientific article published on 15 January 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

scientific article

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

scientific article

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

scientific article published on 10 April 2009

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

scientific article published on 22 March 2016

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

scientific article published on 01 December 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

scientific article published on 20 September 2015

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

scientific article published on 18 December 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

scientific article published on 09 December 2016

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

scientific article

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

scientific article

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

scientific article published on April 2011

Effect of silicone on the collagen fibrillogenesis and stability

scientific article published on 14 January 2015

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

scientific article

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

scientific article

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

scientific article

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

scientific article published on 28 October 2016

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

scientific article

Factors and processes modulating phenotypes in neuronopathic lysosomal storage diseases

scientific article published on 05 December 2013

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

scientific article published on 01 June 2007

Female Fabry disease patients and X-chromosome inactivation

scientific article

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

scientific article published on 10 November 2010

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

scientific article

Genistein reduces lysosomal storage in peripheral tissues of mucopolysaccharide IIIB mice

scientific article

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

scientific article (publication date: July 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.

scientific article

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

scientific article

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.

scientific article

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

scientific article published on 6 January 2009

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

scientific article published on 14 September 2021

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

scientific article

Improved HPLC method for total plasma homocysteine detection and quantification.

scientific article

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 ⬇️

scientific article published on 20 May 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. ⬇️

scientific article

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

scientific article published in March 2004

Metal and antibiotic resistance of bacteria isolated from the Baltic Sea

scientific article published on 01 September 2012

Models in the Research Process of Psoriasis

scientific article published on 24 November 2017

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

scientific article

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

scientific article published on 14 February 2018

Molecular factors involved in the development of diabetic foot syndrome.

scientific article published on 18 December 2012

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

scientific article published on 23 October 2017

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

scientific article published on 27 February 2017

Osteoprotegerin gene polymorphism in diabetic Charcot neuroarthropathy

scientific article published in June 2012

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

scientific article

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

scientific article

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

scientific article

Putative biological mechanisms of efficiency of substrate reduction therapies for mucopolysaccharidoses

scientific article published on 05 September 2012

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

scientific article published on 01 August 2007

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

scientific article published on 14 May 2012

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

scientific article

Substrate reduction therapies for mucopolysaccharidoses

scientific article

Synthetic genistein derivatives as modulators of glycosaminoglycan storage

scientific article

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

article

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.

scientific article published on 15 May 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

scientific article published on 28 May 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

scientific article

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.

scientific article

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

scientific article published on April 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

List of works by 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]