Krepelova A - Search Results

Year	Number of Results
1987	1
1992	2
1993	1
1998	2
2000	1
2002	1
2003	6
2004	5
2005	6
2006	2
2007	7
2008	1
2009	9
2010	6
2011	7
2012	8
2013	6
2014	7
2015	8
2016	10
2017	3
2018	2
2019	2
2021	7
2022	6
2023	5
2024	1

1

Establishment of a fluorescent reporter of RNA-polymerase II activity to identify dormant cells.

Freter R, Falletta P, Omrani O, Rasa M, Herbert K, Annunziata F, Minetti A, Krepelova A, Adam L, Käppel S, Rüdiger T, Wang ZQ, Goding CR, Neri F. Freter R, et al. Among authors: krepelova a. Nat Commun. 2021 Jun 3;12(1):3318. doi: 10.1038/s41467-021-23580-4. Nat Commun. 2021. PMID: 34083536 Free PMC article.

2

[Birt-Hogg-Dubé syndrome].

Křepelová A, Puchmajerová A, Vasovčák P, Chocholatý M. Křepelová A, et al. Klin Onkol. 2012;25 Suppl:S18-20. Klin Onkol. 2012. PMID: 22920201 Czech.

3

A novel heterozygous RIT1 mutation in a patient with Noonan syndrome, leukopenia, and transient myeloproliferation-a review of the literature.

Nemcikova M, Vejvalkova S, Fencl F, Sukova M, Krepelova A. Nemcikova M, et al. Among authors: krepelova a. Eur J Pediatr. 2016 Apr;175(4):587-92. doi: 10.1007/s00431-015-2658-6. Epub 2015 Oct 31. Eur J Pediatr. 2016. PMID: 26518681 Review.

4

Low-Input Whole-Genome Bisulfite Sequencing.

Krepelova A, Neri F. Krepelova A, et al. Methods Mol Biol. 2021;2351:353-368. doi: 10.1007/978-1-0716-1597-3_20. Methods Mol Biol. 2021. PMID: 34382200

5

[Pregnancy and delivery in a patient with pure 46,XY karyotype. Summary of actual knowledge about XY women].

Poláková M, Alexander D, Sulc J, Zetová L, Vlk R, Křepelová A, Zantová D. Poláková M, et al. Among authors: krepelova a. Ceska Gynekol. 2013 Nov;78(5):443-7. Ceska Gynekol. 2013. PMID: 24313430 Review. Czech.

6

DNMT3B supports meso-endoderm differentiation from mouse embryonic stem cells.

Lauria A, Meng G, Proserpio V, Rapelli S, Maldotti M, Polignano IL, Anselmi F, Incarnato D, Krepelova A, Donna D, Levra Levron C, Donati G, Molineris I, Neri F, Oliviero S. Lauria A, et al. Among authors: krepelova a. Nat Commun. 2023 Jan 23;14(1):367. doi: 10.1038/s41467-023-35938-x. Nat Commun. 2023. PMID: 36690616 Free PMC article.

7

IFNγ-Stat1 axis drives aging-associated loss of intestinal tissue homeostasis and regeneration.

Omrani O, Krepelova A, Rasa SMM, Sirvinskas D, Lu J, Annunziata F, Garside G, Bajwa S, Reinhardt S, Adam L, Käppel S, Ducano N, Donna D, Ori A, Oliviero S, Rudolph KL, Neri F. Omrani O, et al. Among authors: krepelova a. Nat Commun. 2023 Sep 30;14(1):6109. doi: 10.1038/s41467-023-41683-y. Nat Commun. 2023. PMID: 37777550 Free PMC article.

8

Zimmermann-Laband syndrome in monozygotic twins with a mild neurobehavioral phenotype lacking gingival overgrowth-A case report of a novel KCNN3 gene variant.

Schwarz M, Ryba L, Křepelová A, Moslerová V, Zelinová M, Turnovec M, Martinková J, Kratochvílová L, Drahanský M, Macek M Jr, Havlovicová M. Schwarz M, et al. Among authors: krepelova a. Am J Med Genet A. 2022 Apr;188(4):1083-1087. doi: 10.1002/ajmg.a.62616. Epub 2021 Dec 14. Am J Med Genet A. 2022. PMID: 34907639

9

[Li-Fraumeni syndrome - a proposal of complex prevention care for carriers of TP53 mutation with total-body MRI].

Foretová L, Stěrba J, Opletal P, Mach V, Lisý J, Petráková K, Palácová M, Navrátilová M, Gaillyová R, Puchmajerová A, Křepelová A, Macháčková E. Foretová L, et al. Among authors: krepelova a. Klin Onkol. 2012;25 Suppl:S49-54. Klin Onkol. 2012. PMID: 22920207 Review. Czech.

10

A novel frameshift mutation in the AFG3L2 gene in a patient with spinocerebellar ataxia.

Musova Z, Kaiserova M, Kriegova E, Fillerova R, Vasovcak P, Santava A, Mensikova K, Zumrova A, Krepelova A, Sedlacek Z, Kanovsky P. Musova Z, et al. Among authors: krepelova a. Cerebellum. 2014 Jun;13(3):331-7. doi: 10.1007/s12311-013-0538-z. Cerebellum. 2014. PMID: 24272953

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