Search details
1.
Dnmt3L antagonizes DNA methylation at bivalent promoters and favors DNA methylation at gene bodies in ESCs.
Cell
; 155(1): 121-34, 2013 Sep 26.
Article
in English
| MEDLINE | ID: mdl-24074865
2.
Functional studies associate novel DUOX2 gene variants detected in heterozygosity to Crohn's disease.
Mol Biol Rep
; 51(1): 399, 2024 Mar 08.
Article
in English
| MEDLINE | ID: mdl-38456993
3.
Histone crosstalk between H3S10ph and H4K16ac generates a histone code that mediates transcription elongation.
Cell
; 138(6): 1122-36, 2009 Sep 18.
Article
in English
| MEDLINE | ID: mdl-19766566
4.
Intragenic DNA methylation prevents spurious transcription initiation.
Nature
; 543(7643): 72-77, 2017 03 02.
Article
in English
| MEDLINE | ID: mdl-28225755
5.
Establishment and evaluation of module-based immune-associated gene signature to predict overall survival in patients of colon adenocarcinoma.
J Biomed Sci
; 29(1): 81, 2022 Oct 14.
Article
in English
| MEDLINE | ID: mdl-36229806
6.
Zimmermann-Laband syndrome in monozygotic twins with a mild neurobehavioral phenotype lacking gingival overgrowth-A case report of a novel KCNN3 gene variant.
Am J Med Genet A
; 188(4): 1083-1087, 2022 04.
Article
in English
| MEDLINE | ID: mdl-34907639
7.
The long intergenic non-coding RNA CCR492 functions as a let-7 competitive endogenous RNA to regulate c-Myc expression.
Biochim Biophys Acta
; 1859(10): 1322-32, 2016 10.
Article
in English
| MEDLINE | ID: mdl-27344374
8.
TET1 is controlled by pluripotency-associated factors in ESCs and downmodulated by PRC2 in differentiated cells and tissues.
Nucleic Acids Res
; 43(14): 6814-26, 2015 Aug 18.
Article
in English
| MEDLINE | ID: mdl-25925565
9.
A novel heterozygous RIT1 mutation in a patient with Noonan syndrome, leukopenia, and transient myeloproliferation-a review of the literature.
Eur J Pediatr
; 175(4): 587-92, 2016 Apr.
Article
in English
| MEDLINE | ID: mdl-26518681
10.
Analysis of FOXL2 detects three novel mutations and an atypical phenotype of blepharophimosis-ptosis-epicanthus inversus syndrome.
Clin Exp Ophthalmol
; 44(9): 757-762, 2016 Dec.
Article
in English
| MEDLINE | ID: mdl-27283035
11.
Odontogenic keratocysts in the Basal Cell Nevus (Gorlin-Goltz) Syndrome associated with paresthesia of the lower jaw: Case report, retrospective analysis of a representative Czech cohort and recommendations for the early diagnosis.
Neuro Endocrinol Lett
; 37(4): 269-276, 2016 Sep.
Article
in English
| MEDLINE | ID: mdl-27857042
12.
Polymorphisms of the receptor for advanced glycation end-products and glyoxalase I in patients with renal cancer.
Tumour Biol
; 36(3): 2121-6, 2015 Mar.
Article
in English
| MEDLINE | ID: mdl-25407489
13.
High-throughput single nucleotide variant discovery in E14 mouse embryonic stem cells provides a new reference genome assembly.
Genomics
; 104(2): 121-7, 2014 Aug.
Article
in English
| MEDLINE | ID: mdl-25004115
14.
A novel frameshift mutation in the AFG3L2 gene in a patient with spinocerebellar ataxia.
Cerebellum
; 13(3): 331-7, 2014 Jun.
Article
in English
| MEDLINE | ID: mdl-24272953
15.
Coarctation of the aorta in Noonan-like syndrome with loose anagen hair.
Am J Med Genet A
; 164A(5): 1218-21, 2014 May.
Article
in English
| MEDLINE | ID: mdl-24458596
16.
Spinocerebellar ataxias type 8, 12, and 17 and dentatorubro-pallidoluysian atrophy in Czech ataxic patients.
Cerebellum
; 12(2): 155-61, 2013 Apr.
Article
in English
| MEDLINE | ID: mdl-22872568
17.
Schimke immunoosseous dysplasia: an ultra-rare disease. a 20-year case series from the tertiary hospital in the Czech Republic.
Ital J Pediatr
; 49(1): 11, 2023 Jan 19.
Article
in English
| MEDLINE | ID: mdl-36658659
18.
DNMT3B supports meso-endoderm differentiation from mouse embryonic stem cells.
Nat Commun
; 14(1): 367, 2023 01 23.
Article
in English
| MEDLINE | ID: mdl-36690616
19.
IFNγ-Stat1 axis drives aging-associated loss of intestinal tissue homeostasis and regeneration.
Nat Commun
; 14(1): 6109, 2023 09 30.
Article
in English
| MEDLINE | ID: mdl-37777550
20.
Single-cell atlas of the aging mouse colon.
iScience
; 25(5): 104202, 2022 May 20.
Article
in English
| MEDLINE | ID: mdl-35479413