Kotlas J - Search Results

1

Autosomal dominant polycystic kidney disease in a family with mosaicism and hypomorphic allele.

Reiterová J, Štekrová J, Merta M, Kotlas J, Elišáková V, Lněnička P, Korabečná M, Kohoutová M, Tesař V. Reiterová J, et al. Among authors: kotlas j. BMC Nephrol. 2013 Mar 15;14:59. doi: 10.1186/1471-2369-14-59. BMC Nephrol. 2013. PMID: 23496908 Free PMC article.

2

Bilineal inheritance of pathogenic PKD1 and PKD2 variants in a Czech family with autosomal dominant polycystic kidney disease - a case report.

Elisakova V, Merta M, Reiterova J, Baxova A, Kotlas J, Hirschfeldova K, Obeidova L, Tesar V, Stekrova J. Elisakova V, et al. Among authors: kotlas j. BMC Nephrol. 2018 Jul 4;19(1):163. doi: 10.1186/s12882-018-0978-2. BMC Nephrol. 2018. PMID: 29973168 Free PMC article.

3

Novel APC mutations in Czech and Slovak FAP families: clinical and genetic aspects.

Stekrova J, Sulova M, Kebrdlova V, Zidkova K, Kotlas J, Ilencikova D, Vesela K, Kohoutova M. Stekrova J, et al. Among authors: kotlas j. BMC Med Genet. 2007 Apr 5;8:16. doi: 10.1186/1471-2350-8-16. BMC Med Genet. 2007. PMID: 17411426 Free PMC article.

4

Novel mutations of the APC gene and genetic consequences of splicing mutations in the Czech FAP families.

Schwarzová L, Štekrová J, Florianová M, Novotný A, Schneiderová M, Lněnička P, Kebrdlová V, Kotlas J, Veselá K, Kohoutová M. Schwarzová L, et al. Among authors: kotlas j. Fam Cancer. 2013 Mar;12(1):35-42. doi: 10.1007/s10689-012-9569-8. Fam Cancer. 2013. PMID: 22987206

5

Two Czech patients with familial adenomatous polyposis presenting mosaicism in APC gene.

Urbanova M, Hirschfeldova K, Obeidova L, Janosikova B, Lastuvkova J, Lukas M, Kotlas J, Stekrova J. Urbanova M, et al. Among authors: kotlas j. Neoplasma. 2019 Mar 5;66(2):294-300. doi: 10.4149/neo_2018_180731N559. Epub 2018 Dec 12. Neoplasma. 2019. PMID: 30569724

6

[Hereditary forms of colorectal adenomatous polyposis].

Kohoutová M, Stekrová J, Sulová M, Zidková K, Kleibl Z, Vandrovcová J, Kebrdlová V, Kotlas J, Jirásek V. Kohoutová M, et al. Among authors: kotlas j. Cas Lek Cesk. 2006;145(6):475-9. Cas Lek Cesk. 2006. PMID: 16836001 Czech.

7

[Human gene therapy].

Kohoutová M, Kotlas J. Kohoutová M, et al. Among authors: kotlas j. Cas Lek Cesk. 1994 Mar 21;133(6):164-6. Cas Lek Cesk. 1994. PMID: 8156570 Review. Czech.

8

High proportion of recurrent germline mutations in the BRCA1 gene in breast and ovarian cancer patients from the Prague area.

Pohlreich P, Zikan M, Stribrna J, Kleibl Z, Janatova M, Kotlas J, Zidovska J, Novotny J, Petruzelka L, Szabo C, Matous B. Pohlreich P, et al. Among authors: kotlas j. Breast Cancer Res. 2005;7(5):R728-36. doi: 10.1186/bcr1282. Epub 2005 Jul 19. Breast Cancer Res. 2005. PMID: 16168118 Free PMC article.

9

Screening for genomic rearrangements in BRCA1 and BRCA2 genes in Czech high-risk breast/ovarian cancer patients: high proportion of population specific alterations in BRCA1 gene.

Ticha I, Kleibl Z, Stribrna J, Kotlas J, Zimovjanova M, Mateju M, Zikan M, Pohlreich P. Ticha I, et al. Among authors: kotlas j. Breast Cancer Res Treat. 2010 Nov;124(2):337-47. doi: 10.1007/s10549-010-0745-y. Epub 2010 Feb 5. Breast Cancer Res Treat. 2010. PMID: 20135348

10

Identification of deleterious germline CHEK2 mutations and their association with breast and ovarian cancer.

Kleiblova P, Stolarova L, Krizova K, Lhota F, Hojny J, Zemankova P, Havranek O, Vocka M, Cerna M, Lhotova K, Borecka M, Janatova M, Soukupova J, Sevcik J, Zimovjanova M, Kotlas J, Panczak A, Vesela K, Cervenkova J, Schneiderova M, Burocziova M, Burdova K, Stranecky V, Foretova L, Machackova E, Tavandzis S, Kmoch S, Macurek L, Kleibl Z. Kleiblova P, et al. Among authors: kotlas j. Int J Cancer. 2019 Oct 1;145(7):1782-1797. doi: 10.1002/ijc.32385. Epub 2019 May 20. Int J Cancer. 2019. PMID: 31050813

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