A novel mutation in collagen transport protein, MIA3 gene, detected in a patient with clinical symptoms of Ehlers-Danlos hypermobile syndrome
Junkiert-Czarnecka, Anna, Pilarska-Deltow, Maria, Bąk, Aneta, Heise, Marta, Haus, Olga
Published in Advances in clinical and experimental medicine : official organ Wroclaw Medical University (01.07.2023)
Published in Advances in clinical and experimental medicine : official organ Wroclaw Medical University (01.07.2023)
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Germline mutations among Polish patients with acute myeloid leukemia
BÄk, Aneta, Skonieczka, Katarzyna, JaÅkowiec, Anna, Junkiert-Czarnecka, Anna, Heise, Marta, Pilarska-Deltow, Maria, Potoczek, StanisÅaw, Czyżewska, Maria, Haus, Olga
Published in Hereditary cancer in clinical practice (12.10.2021)
Published in Hereditary cancer in clinical practice (12.10.2021)
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The role of gene encoding collagen secretion protein (SERPINH1) in the pathogenesis of a hypermobile type of Ehlers-Danlos syndrome
Junkiert-Czarnecka, Anna, Pilarska-Deltow, Maria, Bąk, Aneta, Heise, Marta, Haus, Olga
Published in Postȩpy dermatologii i alergologii (01.02.2023)
Published in Postȩpy dermatologii i alergologii (01.02.2023)
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Clinical Significance of Gene Mutations and Polymorphic Variants and their Association with Prostate Cancer Risk in Polish Men
Heise, Marta, Jarzemski, Piotr, Nowak, Dagmara, Bąk, Aneta, Junkiert-Czarnecka, Anna, Pilarska-Deltow, Maria, Borysiak, Maciej, Pilarska, Beata, Haus, Olga
Published in Cancer control (01.01.2022)
Published in Cancer control (01.01.2022)
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Searching for germline mutations in the RUNX1 gene among Polish patients with acute myeloid leukemia
Bąk, Aneta, Skonieczka, Katarzyna, Jaśkowiec, Anna, Junkiert-Czarnecka, Anna, Heise, Marta, Pilarska-Deltow, Maria, Potoczek, Stanisław, Czyżewska, Maria, Haus, Olga
Published in Leukemia & lymphoma (07.06.2021)
Published in Leukemia & lymphoma (07.06.2021)
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Constitutional mutations of the CHEK2 gene are a risk factor for MDS, but not for de novo AML
Janiszewska, Hanna, Bąk, Aneta, Skonieczka, Katarzyna, Jaśkowiec, Anna, Kiełbiński, Marek, Jachalska, Anna, Czyżewska, Maria, Jaźwiec, Bożena, Kuliszkiewicz-Janus, Małgorzata, Czyż, Jarosław, Kuliczkowski, Kazimierz, Haus, Olga
Published in Leukemia research (01.07.2018)
Published in Leukemia research (01.07.2018)
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Next-Generation Sequencing of Connective Tissue Genes in Patients with Classical Ehlers-Danlos Syndrome
Junkiert-Czarnecka, Anna, Pilarska-Deltow, Maria, Bąk, Aneta, Heise, Marta, Latos-Bieleńska, Anna, Zaremba, Jacek, Bartoszewska-Kubiak, Alicja, Haus, Olga
Published in Current issues in molecular biology (25.03.2022)
Published in Current issues in molecular biology (25.03.2022)
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A multilocus sequence typing scheme for Mycobacterium abscessus complex (MAB-multilocus sequence typing) using whole-genome sequencing data
Wuzinski, Michelle, Bak, Aneta, Petkau, Aaron, B. Demczuk, Walter, Soualhine, Hafid, Sharma, Meenu
Published in International journal of mycobacteriology (01.07.2019)
Published in International journal of mycobacteriology (01.07.2019)
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Clinical significance of PON1 L55M, Q192R and I102V polymorphisms and their association with prostate cancer risk in Polish men
Heise, Marta, Jarzemski, Piotr, Bąk, Aneta, Junkiert-Czarnecka, Anna, Pilarska-Deltow, Maria, Borysiak, Maciej, Haus, Olga
Published in Polish journal of pathology (01.01.2020)
Published in Polish journal of pathology (01.01.2020)
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The germline mutations of the CHEK2 gene are associated with an increased risk of polycythaemia vera
Janiszewska, Hanna, Bąk, Aneta, Hartwig, Martyna, Kuliszkiewicz‐Janus, Małgorzata, Całbecka, Małgorzata, Jaźwiec, Bożena, Kuliczkowski, Kazimierz, Haus, Olga
Published in British journal of haematology (01.04.2016)
Published in British journal of haematology (01.04.2016)
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A risk of breast cancer in women - carriers of constitutional CHEK2 gene mutations, originating from the North - Central Poland
Bąk, Aneta, Janiszewska, Hanna, Junkiert-Czarnecka, Anna, Heise, Marta, Pilarska-Deltow, Maria, Laskowski, Ryszard, Pasińska, Magdalena, Haus, Olga
Published in Hereditary cancer in clinical practice (08.04.2014)
Published in Hereditary cancer in clinical practice (08.04.2014)
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A risk of essential thrombocythemia in carriers of constitutional CHEK2 gene mutations
JANISZEWSKA, Hanna, BAK, Aneta, HAUS, Olga, PILARSKA, Maria, HEISE, Marta, JUNKIERT-CZARNECKA, Anna, KULISZKIEWICZ-JANUS, Małgorzata, CALBECKA, Małgorzata, JAZWIEC, Bożena, WOLOWIEC, Dariusz, KULICZKOWSKI, Kazimierz
Published in Haematologica (Roma) (01.03.2012)
Published in Haematologica (Roma) (01.03.2012)
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Frequency of CYP1B1 homozygous genotype 355T/T in prostate cancer families from Poland
Schab, Marta, Janiszewska, Hanna, Jarzemski, Piotr, Bak, Aneta, Junkiert-Czarnecka, Anna, Pilarska, Maria, Słupski, Piotr, Haus, Olga
Published in European journal of cancer prevention (01.01.2010)
Published in European journal of cancer prevention (01.01.2010)
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Prevalence of the BRCA1 c.68_69delAG (BIC: 185delAG) mutation in women with breast cancer from north-central Poland and a review of the literature on other regions of the country
Hartwig, Martyna, Janiszewska, Hanna, Bąk, Aneta, Pilarska, Maria, Heise, Marta, Junkiert-Czarnecka, Anna, Laskowski, Ryszard, Haus, Olga
Published in Contemporary oncology (Poznan, Poland) (01.01.2013)
Published in Contemporary oncology (Poznan, Poland) (01.01.2013)
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The NOD2 3020insC Mutation in Women with Breast Cancer from the Bydgoszcz Region in Poland. First Results
Janiszewska, Hanna, Haus, Olga, Lauda-Swieciak, Anna, Bak, Aneta, Mierzwa, Tomasz, Sir, Jan, Laskowski, Ryszard
Published in Hereditary cancer in clinical practice (15.01.2006)
Published in Hereditary cancer in clinical practice (15.01.2006)
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