Junkiert-Czarnecka A - Search Results

1

The role of gene encoding collagen secretion protein (SERPINH1) in the pathogenesis of a hypermobile type of Ehlers-Danlos syndrome.

Junkiert-Czarnecka A, Pilarska-Deltow M, Bąk A, Heise M, Haus O. Junkiert-Czarnecka A, et al. Postepy Dermatol Alergol. 2023 Feb;40(1):102-106. doi: 10.5114/ada.2022.124107. Epub 2023 Jan 13. Postepy Dermatol Alergol. 2023. PMID: 36909907 Free PMC article.

2

New variants in COL5A1 gene among Polish patients with Ehlers-Danlos syndrome: analysis of nine cases.

Junkiert-Czarnecka A, Pilarska-Deltow M, Bąk A, Heise M, Haus O. Junkiert-Czarnecka A, et al. Postepy Dermatol Alergol. 2019 Feb;36(1):29-33. doi: 10.5114/ada.2018.79440. Epub 2019 Feb 22. Postepy Dermatol Alergol. 2019. PMID: 30858776 Free PMC article.

3

Next-Generation Sequencing of Connective Tissue Genes in Patients with Classical Ehlers-Danlos Syndrome.

Junkiert-Czarnecka A, Pilarska-Deltow M, Bąk A, Heise M, Latos-Bieleńska A, Zaremba J, Bartoszewska-Kubiak A, Haus O. Junkiert-Czarnecka A, et al. Curr Issues Mol Biol. 2022 Mar 25;44(4):1472-1478. doi: 10.3390/cimb44040099. Curr Issues Mol Biol. 2022. PMID: 35723357 Free PMC article.

4

A novel mutation in collagen transport protein, MIA3 gene, detected in a patient with clinical symptoms of Ehlers-Danlos hypermobile syndrome.

Junkiert-Czarnecka A, Pilarska-Deltow M, Bąk A, Heise M, Haus O. Junkiert-Czarnecka A, et al. Adv Clin Exp Med. 2023 Jul;32(7):777-781. doi: 10.17219/acem/158028. Adv Clin Exp Med. 2023. PMID: 36603143 Free article.

5

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 M, Janiszewska H, Bąk A, Pilarska M, Heise M, Junkiert-Czarnecka A, Laskowski R, Haus O. Hartwig M, et al. Contemp Oncol (Pozn). 2013;17(1):34-7. doi: 10.5114/wo.2013.33767. Epub 2013 Mar 15. Contemp Oncol (Pozn). 2013. PMID: 23788959 Free PMC article.

6

A risk of breast cancer in women - carriers of constitutional CHEK2 gene mutations, originating from the North - Central Poland.

Bąk A, Janiszewska H, Junkiert-Czarnecka A, Heise M, Pilarska-Deltow M, Laskowski R, Pasińska M, Haus O. Bąk A, et al. Hered Cancer Clin Pract. 2014 Apr 8;12(1):10. doi: 10.1186/1897-4287-12-10. Hered Cancer Clin Pract. 2014. PMID: 24713400 Free PMC article.

7

G84E germline mutation in HOXB13 gene is associated with increased prostate cancer risk in Polish men.

Heise M, Jarzemski P, Bąk A, Junkiert-Czarnecka A, Pilarska-Deltow M, Haus O. Heise M, et al. Among authors: junkiert czarnecka a. Pol J Pathol. 2019;70(2):127-133. doi: 10.5114/pjp.2019.87103. Pol J Pathol. 2019. PMID: 31556563 Free article.

8

Searching for germline mutations in the RUNX1 gene among Polish patients with acute myeloid leukemia.

Bąk A, Skonieczka K, Jaśkowiec A, Junkiert-Czarnecka A, Heise M, Pilarska-Deltow M, Potoczek S, Czyżewska M, Haus O. Bąk A, et al. Among authors: junkiert czarnecka a. Leuk Lymphoma. 2021 Jul;62(7):1749-1755. doi: 10.1080/10428194.2021.1881503. Epub 2021 Feb 10. Leuk Lymphoma. 2021. PMID: 33563056

9

Germline mutations among Polish patients with acute myeloid leukemia.

Bąk A, Skonieczka K, Jaśkowiec A, Junkiert-Czarnecka A, Heise M, Pilarska-Deltow M, Potoczek S, Czyżewska M, Haus O. Bąk A, et al. Among authors: junkiert czarnecka a. Hered Cancer Clin Pract. 2021 Oct 12;19(1):42. doi: 10.1186/s13053-021-00200-2. Hered Cancer Clin Pract. 2021. PMID: 34641967 Free PMC article.

10

Clinical Significance of Gene Mutations and Polymorphic Variants and their Association with Prostate Cancer Risk in Polish Men.

Heise M, Jarzemski P, Nowak D, Bąk A, Junkiert-Czarnecka A, Pilarska-Deltow M, Borysiak M, Pilarska B, Haus O. Heise M, et al. Among authors: junkiert czarnecka a. Cancer Control. 2022 Jan-Dec;29:10732748211062342. doi: 10.1177/10732748211062342. Cancer Control. 2022. PMID: 35638715 Free PMC article.

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