Lista de obras - Monika Jasek - Dominio Público Uruguay

6.7-kbp deletion in LILRA3 (ILT6) gene is associated with later onset of the multiple sclerosis in a Polish population

artículo científico publicado en 2012

ALCAM and CD6--multiple sclerosis risk factors.

artículo científico publicado en 2014

ALCAM--novel multiple sclerosis locus interfering with HLA-DRB1*1501.

artículo científico publicado en 2013

Are single nucleotide polymorphisms of the immunoglobulin A Fc receptor gene associated with allergic asthma?

artículo científico publicado en 2004

Association of Common Variants of TNFSF13 and TNFRSF13B Genes with CLL Risk and Clinical Picture, as Well as Expression of Their Products-APRIL and TACI Molecules

artículo científico publicado en 2020

Association of PTPN22 single nucleotide polymorphism with rheumatoid arthritis but not with allergic asthma

artículo científico publicado en 2007

Association of variants in BAFF (rs9514828 and rs1041569) and BAFF-R (rs61756766) genes with the risk of chronic lymphocytic leukemia.

artículo científico publicado en 2016

Bronchial asthma as a multifactorial disease

artículo científico publicado el 1 de enero de 2003

CTLA-4 gene polymorphisms and natural soluble CTLA-4 protein in psoriasis vulgaris

article

Characterization of chromosome arm 20q abnormalities in myeloid malignancies using genome-wide single nucleotide polymorphism array analysis

scientific article published on 01 April 2010

Clonal hematopoiesis in Philadelphia chromosome-negative bone marrow cells of chronic myeloid leukemia patients receiving dasatinib.

artículo científico publicado en 2009

Distribution of CTLA-4 polymorphisms in allergic asthma

artículo científico publicado en 2006

Distribution of LILRA3 (ILT6/LIR4) deletion in psoriatic patients and healthy controls.

artículo científico publicado en 2003

Distribution of the CTLA-4 single nucleotide polymorphisms CT60G>A and +49A>G in psoriasis vulgaris patients and control individuals from a Polish Caucasian population

artículo científico publicado en 2007

Gene for the activating natural killer cell receptor, KIR2DS1, is associated with susceptibility to psoriasis vulgaris.

artículo científico publicado en 2004

Graft-versus-host disease: role of inflammation in the development of chromosomal abnormalities of keratinocytes

artículo científico publicado en 2010

Haplotype dependent association of rs7927894 (11q13.5) with atopic dermatitis and chronic allergic rhinitis: A study in ECAP cohort.

artículo científico publicado en 2017

Inhibitory and activatory KIR gene frequencies in the Polish population

artículo científico publicado en 2006

Intragenic Variations in BTLA Gene Influence mRNA Expression of BTLA Gene in Chronic Lymphocytic Leukemia Patients and Confer Susceptibility to Chronic Lymphocytic Leukemia

artículo científico publicado en 2016

Investigation of gene-gene interactions between CD40 and CD40L in Polish multiple sclerosis patients

artículo científico publicado en 2014

Is the TAP2 single nucleotide polymorphism rs241447 truly associated with psoriasis in Poles?

scientific article published on 31 January 2020

MICA polymorphism identified by whole genome array associated with NKG2D-mediated cytotoxicity in T-cell large granular lymphocyte leukemia

artículo científico publicado en 2010

MS risk allele rs1883832T is associated with decreased mRNA expression of CD40

artículo científico publicado en 2015

Molecular lesions in childhood and adult acute megakaryoblastic leukaemia

scientific article published on 28 November 2011

Polymorphism of the TGFB1 gene is not associated with bronchial allergic asthma in a Polish population.

artículo científico publicado en 2009

Polymorphisms in CD28, CTLA-4, CD80 and CD86 genes may influence the risk of multiple sclerosis and its age of onset

article

Polymorphisms in genes of the BAFF/APRIL system may constitute risk factors of B-CLL--a preliminary study on a Polish population.

artículo científico publicado en 2015

Possible association of cytotoxic T-lymphocyte antigen 4 gene promoter single nucleotide polymorphism with acute rejection of allogeneic kidney transplant

article

Preliminary Study on the Role of TMEM39A Gene in Multiple Sclerosis.

artículo científico publicado en 2017

SNP-SNP Interaction in Genes Encoding PD-1/PD-L1 Axis as a Potential Risk Factor for Clear Cell Renal Cell Carcinoma

artículo científico publicado en 2020

TP53 mutations in myeloid malignancies are either homozygous or hemizygous due to copy number-neutral loss of heterozygosity or deletion of 17p.

artículo científico publicado en 2009

The impact of HLA-G, LILRB1 and LILRB2 gene polymorphisms on susceptibility to and severity of endometriosis.

artículo científico publicado en 2017

Lista de obras de Monika Jasek

6.7-kbp deletion in LILRA3 (ILT6) gene is associated with later onset of the multiple sclerosis in a Polish population

ALCAM and CD6--multiple sclerosis risk factors.

ALCAM--novel multiple sclerosis locus interfering with HLA-DRB1*1501.

Are single nucleotide polymorphisms of the immunoglobulin A Fc receptor gene associated with allergic asthma?

Association of Common Variants of TNFSF13 and TNFRSF13B Genes with CLL Risk and Clinical Picture, as Well as Expression of Their Products-APRIL and TACI Molecules

Association of PTPN22 single nucleotide polymorphism with rheumatoid arthritis but not with allergic asthma

Association of variants in BAFF (rs9514828 and rs1041569) and BAFF-R (rs61756766) genes with the risk of chronic lymphocytic leukemia.

Bronchial asthma as a multifactorial disease

CTLA-4 gene polymorphisms and natural soluble CTLA-4 protein in psoriasis vulgaris

Characterization of chromosome arm 20q abnormalities in myeloid malignancies using genome-wide single nucleotide polymorphism array analysis

Clonal hematopoiesis in Philadelphia chromosome-negative bone marrow cells of chronic myeloid leukemia patients receiving dasatinib.

Distribution of CTLA-4 polymorphisms in allergic asthma

Distribution of LILRA3 (ILT6/LIR4) deletion in psoriatic patients and healthy controls.

Distribution of the CTLA-4 single nucleotide polymorphisms CT60G>A and +49A>G in psoriasis vulgaris patients and control individuals from a Polish Caucasian population

Gene for the activating natural killer cell receptor, KIR2DS1, is associated with susceptibility to psoriasis vulgaris.

Graft-versus-host disease: role of inflammation in the development of chromosomal abnormalities of keratinocytes

Haplotype dependent association of rs7927894 (11q13.5) with atopic dermatitis and chronic allergic rhinitis: A study in ECAP cohort.

Inhibitory and activatory KIR gene frequencies in the Polish population

Intragenic Variations in BTLA Gene Influence mRNA Expression of BTLA Gene in Chronic Lymphocytic Leukemia Patients and Confer Susceptibility to Chronic Lymphocytic Leukemia

Investigation of gene-gene interactions between CD40 and CD40L in Polish multiple sclerosis patients

Is the TAP2 single nucleotide polymorphism rs241447 truly associated with psoriasis in Poles?

MICA polymorphism identified by whole genome array associated with NKG2D-mediated cytotoxicity in T-cell large granular lymphocyte leukemia

MS risk allele rs1883832T is associated with decreased mRNA expression of CD40

Molecular lesions in childhood and adult acute megakaryoblastic leukaemia

Polymorphism of the TGFB1 gene is not associated with bronchial allergic asthma in a Polish population.

Polymorphisms in CD28, CTLA-4, CD80 and CD86 genes may influence the risk of multiple sclerosis and its age of onset

Polymorphisms in genes of the BAFF/APRIL system may constitute risk factors of B-CLL--a preliminary study on a Polish population.

Possible association of cytotoxic T-lymphocyte antigen 4 gene promoter single nucleotide polymorphism with acute rejection of allogeneic kidney transplant

Preliminary Study on the Role of TMEM39A Gene in Multiple Sclerosis.

SNP-SNP Interaction in Genes Encoding PD-1/PD-L1 Axis as a Potential Risk Factor for Clear Cell Renal Cell Carcinoma

TP53 mutations in myeloid malignancies are either homozygous or hemizygous due to copy number-neutral loss of heterozygosity or deletion of 17p.

The impact of HLA-G, LILRB1 and LILRB2 gene polymorphisms on susceptibility to and severity of endometriosis.