Lista de obras - Michał Witt - Dominio Público Uruguay

A Closer Look at Frederic Chopin's Cause of Death

artículo científico publicado en 2017

A cystic fibrosis patient homozygous for 621 + 1G-->T mutation has a severe pulmonary disease, mild pancreatic insufficiency and a gastro-esophageal reflux

scientific article published on 01 September 1996

A simplified method for detection of the mutations predominantly causing cystic fibrosis and phenylketonuria in Polish families

scientific article published on 01 July 1993

Aminoglycoside-stimulated readthrough of premature termination codons in selected genes involved in primary ciliary dyskinesia.

artículo científico publicado en 2016

An improved, non-isotopic method of screening cells from patients with abnormalities of sexual differentiation for Y chromosomal DNA content

artículo científico publicado en 1993

An international registry for primary ciliary dyskinesia

artículo científico publicado en 2015

Analysis of exocrine pancreatic function in cystic fibrosis: one mild CFTR mutation does not exclude pancreatic insufficiency

scientific article published on 01 September 2001

Apparent X-linked primary ciliary dyskinesia associated with retinitis pigmentosa and a hearing loss.

artículo científico publicado en 2004

Association of germline genetic variants in RFC, IL15 and VDR genes with minimal residual disease in pediatric B-cell precursor ALL.

artículo científico publicado en 2016

BCL11B, FLT3, NOTCH1 and FBXW7 mutation status in T-cell acute lymphoblastic leukemia patients.

artículo científico publicado en 2012

Best practice guidelines for molecular genetic diagnosis of cystic fibrosis and CFTR-related disorders--updated European recommendations

artículo científico publicado en 2008

Binding specificity and signal transduction of receptors for glucagon-like peptide-1(7-36)amide and gastric inhibitory polypeptide on RINm5F insulinoma cells

artículo científico publicado en 1993

CFAP300: Mutations in Slavic Patients with Primary Ciliary Dyskinesia and a Role in Ciliary Dynein Arms Trafficking

scientific article published on 01 October 2019

CFTR mutations spectrum and the efficiency of molecular diagnostics in Polish cystic fibrosis patients

artículo científico publicado en 2014

Carrier status for 3 most frequent CFTR mutations in Polish PCD/KS patients: lack of association with the primary ciliary dyskinesia phenotype

scientific article published on 01 January 2007

Characterization of a novel 21-kb deletion, CFTRdele2,3(21 kb), in the CFTR gene: a cystic fibrosis mutation of Slavic origin common in Central and East Europe.

artículo científico publicado en 2000

Ciliary genes are down-regulated in bronchial tissue of primary ciliary dyskinesia patients

artículo científico publicado en 2014

Comprehensive Investigation of miRNome Identifies Novel Candidate miRNA-mRNA Interactions Implicated in T-Cell Acute Lymphoblastic Leukemia

scientific article published on 11 February 2019

Correlation between the level of cytogenetic aberrations in cultured human lymphocytes and the age and gender of donors.

artículo científico publicado en 2006

Cost-effective screening of DNMT3A coding sequence identifies somatic mutation in pediatric T-cell acute lymphoblastic leukemia

artículo científico publicado en 2017

Current genetic methodologies in the identification of disaster victims and in forensic analysis

artículo científico publicado en 2011

Cystic fibrosis--a probable cause of Frédéric Chopin's suffering and death

artículo científico publicado en 2003

Cytogenetic perspective of ageing and longevity in men and women

scientific article published on January 2009

DNAI2 mutations cause primary ciliary dyskinesia with defects in the outer dynein arm

artículo científico publicado en 2008

Diagnosis of genetic diseases using DNA recombination technics

scientific article published on 01 September 1988

Disease not genetic but infectious: multiple tuberculomas and fibrinous pericarditis as symptoms pathognomonic for tuberculosis of Frederic Chopin

artículo científico publicado en 2018

Effect of genotype on selected clinical features of Polish cystic fibrosis adults

artículo científico publicado el 1 de enero de 2001

Effects of age and gender on micronucleus and chromosome nondisjunction frequencies in centenarians and younger subjects

artículo científico publicado en 2007

EurEAs_Gplex--A new SNaPshot assay for continental population discrimination and gender identification

artículo científico publicado en 2015

European context of the diversity and phylogenetic position of SARS-CoV-2 sequences from Polish COVID-19 patients

artículo científico publicado en 2021

Feedback of Individual Genetic Results to Research Participants: Is It Feasible in Europe?

artículo científico publicado en 2016

GLP-1/GIP chimeric peptides define the structural requirements for specific ligand-receptor interaction of GLP-1

artículo científico publicado en 1996

Gene expression studies in cells from primary ciliary dyskinesia patients identify 208 potential ciliary genes.

artículo científico publicado en 2010

HLA expression on human germinal cells

artículo científico publicado en 1987

Hematopoietic chimerism after allogeneic stem cell transplantation: a comparison of quantitative analysis by automated DNA sizing and fluorescent in situ hybridization

artículo científico publicado en 2005

Identification of Endogenous Control miRNAs for RT-qPCR in T-Cell Acute Lymphoblastic Leukemia

scientific article published on 20 September 2018

Immunoglobulin/T-cell receptor gene rearrangements in the diagnostic paradigm of pediatric patients with T-cell acute lymphoblastic leukemia

artículo científico publicado en 2012

Impact of SNPs on methylation readouts by Illumina Infinium HumanMethylation450 BeadChip Array: implications for comparative population studies.

artículo científico publicado en 2015

Implementation of the standard strategy for identification of Ig/TCR targets for minimal residual disease diagnostics in B-cell precursor ALL pediatric patients: Polish experience

artículo científico publicado en 2008

In vitro culturing of ciliary respiratory cells--a model for studies of genetic diseases

artículo científico publicado en 2011

Infant acute bilineal leukemia

artículo científico publicado en 2009

Longitudinal follow-up of exocrine pancreatic function in pancreatic sufficient cystic fibrosis patients using the fecal elastase-1 test

artículo científico publicado en 2003

Manifestations of ageing at the cytogenetic level

artículo científico publicado en 2003

Molecular assessment of post-BMT chimerism using various biologic specimens and automated DNA sizing technology

artículo científico

Molecular follow up of donor lymphocyte infusion in CML children after allogeneic bone marrow transplantation

artículo científico publicado el 1 de enero de 2001

Mutations in radial spoke head genes and ultrastructural cilia defects in East-European cohort of primary ciliary dyskinesia patients

artículo científico publicado en 2012

PCD and RP: X-linked inheritance of both disorders?

artículo científico publicado en 2004

PTEN abnormalities predict poor outcome in children with T-cell acute lymphoblastic leukemia treated according to ALL IC-BFM protocols

artículo científico publicado en 2019

Partial CFTR genotyping and characterisation of cystic fibrosis patients with myocardial fibrosis and necrosis

scientific article published on 01 January 2000

Partial purification, characterization and cell-free translation of mRNAs coding for H-2d antigens

artículo científico publicado en 1982

Pattern of immunoglobulin and T-cell receptor (Ig/TCR) gene rearrangements in Polish pediatric acute lymphoblastic leukemia patients--implications for RQ-PCR-based assessment of minimal residual disease

artículo científico publicado en 2006

Polymerase chain reactions with alphoid-repeat primers in combination with Alu or LINEs primers, generate chromosome-specific DNA fragments ⬇️

artículo científico publicado el 1 de julio de 1991

Population specificity of the DNAI1 gene mutation spectrum in primary ciliary dyskinesia (PCD).

artículo científico publicado en 2010

Primary ciliary dyskinesia: genes, candidate genes and chromosomal regions

artículo científico publicado en 2004

RPGR mutations might cause reduced orientation of respiratory cilia

artículo científico publicado en 2012

Recent advances in primary ciliary dyskinesia genetics.

artículo científico publicado en 2014

SRY gen--primary "switch" in human sex determination?

artículo científico publicado en 1995

Sequence analysis of 21 genes located in the Kartagener syndrome linkage region on chromosome 15q

article

Simultaneous transplantation of two allogeneic units of cord blood in an adult patient with acute myeloblastic leukemia: a case report.

artículo científico publicado en 2005

T-cell acute lymphoblastic leukaemia: recent molecular biology findings

artículo científico

The 102-year old woman with translocation (7;12) and infertility in anamnesis

artículo científico publicado en 2003

Transcriptomic population markers for human population discrimination

artículo científico publicado en 2018

Truncating mutations in exons 20 and 21 of OFD1 can cause primary ciliary dyskinesia without associated syndromic symptoms

artículo científico publicado en 2019

Ullrich-Turner syndrome with a small ring X chromosome and presence of mental retardation

artículo científico publicado el 1 de agosto de 1992

ZMYND10--Mutation Analysis in Slavic Patients with Primary Ciliary Dyskinesia

artículo científico publicado en 2016

[A model of genetic therapy of selected disease entities]

scientific article published on 01 November 1987

[Cystic fibrosis diagnosed in 36-year old man]

scientific article published on 01 January 2004

[Frequency of mutations and genotypes of the CFTR gene in cystic fibrosis adults in Poland]

artículo científico publicado en 1999

[Identification of immunoglobulin and T-cell receptor gene rearrangements--prerequisite for monitoring of minimal residual disease in Polish acute lymphoblastic leukemia patients based on European standards. Preliminary results]

scientific article published on 01 January 2006

[International Institute of molecular and cell biology in Warsaw]

artículo científico publicado en 2005

[Molecular genetics of the major histocompatibility complex]

scientific article published on 01 January 1985

[Molecular methods for diagnostics and assessment of treatment effectiveness in modern pediatric hematooncology]

scientific article published on 01 January 2006

hsa-miR-20b-5p and hsa-miR-363-3p Affect Expression of PTEN and BIM Tumor Suppressor Genes and Modulate Survival of T-ALL Cells In Vitro

scientific article published on 05 May 2020

Lista de obras de Michał Witt

A Closer Look at Frederic Chopin's Cause of Death

A cystic fibrosis patient homozygous for 621 + 1G-->T mutation has a severe pulmonary disease, mild pancreatic insufficiency and a gastro-esophageal reflux

A simplified method for detection of the mutations predominantly causing cystic fibrosis and phenylketonuria in Polish families

Aminoglycoside-stimulated readthrough of premature termination codons in selected genes involved in primary ciliary dyskinesia.

An improved, non-isotopic method of screening cells from patients with abnormalities of sexual differentiation for Y chromosomal DNA content

An international registry for primary ciliary dyskinesia

Analysis of exocrine pancreatic function in cystic fibrosis: one mild CFTR mutation does not exclude pancreatic insufficiency

Apparent X-linked primary ciliary dyskinesia associated with retinitis pigmentosa and a hearing loss.

Association of germline genetic variants in RFC, IL15 and VDR genes with minimal residual disease in pediatric B-cell precursor ALL.

BCL11B, FLT3, NOTCH1 and FBXW7 mutation status in T-cell acute lymphoblastic leukemia patients.

Best practice guidelines for molecular genetic diagnosis of cystic fibrosis and CFTR-related disorders--updated European recommendations

Binding specificity and signal transduction of receptors for glucagon-like peptide-1(7-36)amide and gastric inhibitory polypeptide on RINm5F insulinoma cells

CFAP300: Mutations in Slavic Patients with Primary Ciliary Dyskinesia and a Role in Ciliary Dynein Arms Trafficking

CFTR mutations spectrum and the efficiency of molecular diagnostics in Polish cystic fibrosis patients

Carrier status for 3 most frequent CFTR mutations in Polish PCD/KS patients: lack of association with the primary ciliary dyskinesia phenotype

Characterization of a novel 21-kb deletion, CFTRdele2,3(21 kb), in the CFTR gene: a cystic fibrosis mutation of Slavic origin common in Central and East Europe.

Ciliary genes are down-regulated in bronchial tissue of primary ciliary dyskinesia patients

Comprehensive Investigation of miRNome Identifies Novel Candidate miRNA-mRNA Interactions Implicated in T-Cell Acute Lymphoblastic Leukemia

Correlation between the level of cytogenetic aberrations in cultured human lymphocytes and the age and gender of donors.

Cost-effective screening of DNMT3A coding sequence identifies somatic mutation in pediatric T-cell acute lymphoblastic leukemia

Current genetic methodologies in the identification of disaster victims and in forensic analysis

Cystic fibrosis--a probable cause of Frédéric Chopin's suffering and death

Cytogenetic perspective of ageing and longevity in men and women

DNAI2 mutations cause primary ciliary dyskinesia with defects in the outer dynein arm

Diagnosis of genetic diseases using DNA recombination technics

Disease not genetic but infectious: multiple tuberculomas and fibrinous pericarditis as symptoms pathognomonic for tuberculosis of Frederic Chopin

Effect of genotype on selected clinical features of Polish cystic fibrosis adults

Effects of age and gender on micronucleus and chromosome nondisjunction frequencies in centenarians and younger subjects

EurEAs_Gplex--A new SNaPshot assay for continental population discrimination and gender identification

European context of the diversity and phylogenetic position of SARS-CoV-2 sequences from Polish COVID-19 patients

Feedback of Individual Genetic Results to Research Participants: Is It Feasible in Europe?

GLP-1/GIP chimeric peptides define the structural requirements for specific ligand-receptor interaction of GLP-1

Gene expression studies in cells from primary ciliary dyskinesia patients identify 208 potential ciliary genes.

HLA expression on human germinal cells

Hematopoietic chimerism after allogeneic stem cell transplantation: a comparison of quantitative analysis by automated DNA sizing and fluorescent in situ hybridization

Identification of Endogenous Control miRNAs for RT-qPCR in T-Cell Acute Lymphoblastic Leukemia

Immunoglobulin/T-cell receptor gene rearrangements in the diagnostic paradigm of pediatric patients with T-cell acute lymphoblastic leukemia

Impact of SNPs on methylation readouts by Illumina Infinium HumanMethylation450 BeadChip Array: implications for comparative population studies.

Implementation of the standard strategy for identification of Ig/TCR targets for minimal residual disease diagnostics in B-cell precursor ALL pediatric patients: Polish experience

In vitro culturing of ciliary respiratory cells--a model for studies of genetic diseases

Infant acute bilineal leukemia

Longitudinal follow-up of exocrine pancreatic function in pancreatic sufficient cystic fibrosis patients using the fecal elastase-1 test

Manifestations of ageing at the cytogenetic level

Molecular assessment of post-BMT chimerism using various biologic specimens and automated DNA sizing technology

Molecular follow up of donor lymphocyte infusion in CML children after allogeneic bone marrow transplantation

Mutations in radial spoke head genes and ultrastructural cilia defects in East-European cohort of primary ciliary dyskinesia patients

PCD and RP: X-linked inheritance of both disorders?

PTEN abnormalities predict poor outcome in children with T-cell acute lymphoblastic leukemia treated according to ALL IC-BFM protocols

Partial CFTR genotyping and characterisation of cystic fibrosis patients with myocardial fibrosis and necrosis

Partial purification, characterization and cell-free translation of mRNAs coding for H-2d antigens

Pattern of immunoglobulin and T-cell receptor (Ig/TCR) gene rearrangements in Polish pediatric acute lymphoblastic leukemia patients--implications for RQ-PCR-based assessment of minimal residual disease

Polymerase chain reactions with alphoid-repeat primers in combination with Alu or LINEs primers, generate chromosome-specific DNA fragments ⬇️

Population specificity of the DNAI1 gene mutation spectrum in primary ciliary dyskinesia (PCD).

Primary ciliary dyskinesia: genes, candidate genes and chromosomal regions

RPGR mutations might cause reduced orientation of respiratory cilia

Recent advances in primary ciliary dyskinesia genetics.

SRY gen--primary "switch" in human sex determination?

Sequence analysis of 21 genes located in the Kartagener syndrome linkage region on chromosome 15q

Simultaneous transplantation of two allogeneic units of cord blood in an adult patient with acute myeloblastic leukemia: a case report.

T-cell acute lymphoblastic leukaemia: recent molecular biology findings

The 102-year old woman with translocation (7;12) and infertility in anamnesis

Transcriptomic population markers for human population discrimination

Truncating mutations in exons 20 and 21 of OFD1 can cause primary ciliary dyskinesia without associated syndromic symptoms

Ullrich-Turner syndrome with a small ring X chromosome and presence of mental retardation

ZMYND10--Mutation Analysis in Slavic Patients with Primary Ciliary Dyskinesia

[A model of genetic therapy of selected disease entities]

[Cystic fibrosis diagnosed in 36-year old man]

[Frequency of mutations and genotypes of the CFTR gene in cystic fibrosis adults in Poland]

[Identification of immunoglobulin and T-cell receptor gene rearrangements--prerequisite for monitoring of minimal residual disease in Polish acute lymphoblastic leukemia patients based on European standards. Preliminary results]

[International Institute of molecular and cell biology in Warsaw]

[Molecular genetics of the major histocompatibility complex]

[Molecular methods for diagnostics and assessment of treatment effectiveness in modern pediatric hematooncology]

hsa-miR-20b-5p and hsa-miR-363-3p Affect Expression of PTEN and BIM Tumor Suppressor Genes and Modulate Survival of T-ALL Cells In Vitro