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1.
Gene-specific somatic epigenetic mosaicism of FDFT1 underlies a non-hereditary localized form of porokeratosis.
Am J Hum Genet
; 111(5): 896-912, 2024 May 02.
Artículo
en Inglés
| MEDLINE | ID: mdl-38653249
2.
Systematic molecular analyses for 115 karyotypically normal men with isolated non-obstructive azoospermia.
Hum Reprod
; 39(5): 1131-1140, 2024 May 02.
Artículo
en Inglés
| MEDLINE | ID: mdl-38511217
3.
Identification of unique DNA methylation sites in Kabuki syndrome using whole genome bisulfite sequencing and targeted hybridization capture followed by enzymatic methylation sequencing.
J Hum Genet
; 67(12): 711-720, 2022 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-36167771
4.
Epitranscriptomic profiling in human placenta: N6-methyladenosine modification at the 5'-untranslated region is related to fetal growth and preeclampsia.
FASEB J
; 34(1): 494-512, 2020 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-31914637
5.
DNA methylation changes involved in the tumor increase in F2 males born to gestationally arsenite-exposed F1 male mice.
Cancer Sci
; 110(8): 2629-2642, 2019 Aug.
Artículo
en Inglés
| MEDLINE | ID: mdl-31215104
6.
Integrated genetic and epigenetic analysis revealed heterogeneity of acute lymphoblastic leukemia in Down syndrome.
Cancer Sci
; 110(10): 3358-3367, 2019 Oct.
Artículo
en Inglés
| MEDLINE | ID: mdl-31385395
7.
Creatine enhances the duration of sperm capacitation: a novel factor for improving in vitro fertilization with small numbers of sperm.
Hum Reprod
; 33(6): 1117-1129, 2018 06 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-29635630
8.
The DNA methylation profile of liver tumors in C3H mice and identification of differentially methylated regions involved in the regulation of tumorigenic genes.
BMC Cancer
; 18(1): 317, 2018 03 22.
Artículo
en Inglés
| MEDLINE | ID: mdl-29566670
9.
Placental Development and Nutritional Environment.
Adv Exp Med Biol
; 1012: 63-73, 2018.
Artículo
en Inglés
| MEDLINE | ID: mdl-29956195
10.
Molecular mechanisms of transcriptional regulation by the nuclear zinc-finger protein Zfat in T cells.
Biochim Biophys Acta
; 1859(11): 1398-1410, 2016 11.
Artículo
en Inglés
| MEDLINE | ID: mdl-27591365
11.
DNA methylation analysis of human myoblasts during in vitro myogenic differentiation: de novo methylation of promoters of muscle-related genes and its involvement in transcriptional down-regulation.
Hum Mol Genet
; 24(2): 410-23, 2015 Jan 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-25190712
12.
Human cytomegalovirus downregulates SLITRK6 expression through IE2.
J Neurovirol
; 23(1): 79-86, 2017 02.
Artículo
en Inglés
| MEDLINE | ID: mdl-27530937
13.
Adverse parenting is associated with blunted salivary cortisol awakening response and altered expression of glucocorticoid receptor ß and ß2-adrenergic receptor mRNAs in leukocytes in Japanese medical students.
Stress
; 20(2): 159-166, 2017 03.
Artículo
en Inglés
| MEDLINE | ID: mdl-28285561
14.
Loss of NSD2 causes dysregulation of synaptic genes and altered H3K36 dimethylation in mice.
Front Genet
; 15: 1308234, 2024.
Artículo
en Inglés
| MEDLINE | ID: mdl-38419783
15.
Cytokine profiling in 128 patients with transient abnormal myelopoiesis: a report from the JPLSG TAM-10 trial.
Blood Adv
; 2024 May 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-38691583
16.
Associations between chronotype and salivary endocrinological stress markers.
Endocr Res
; 38(1): 1-7, 2013.
Artículo
en Inglés
| MEDLINE | ID: mdl-22591393
17.
Identification of a KDM6A somatic mutation responsible for Kabuki syndrome by excluding a conflicting KMT2D germline variant through episignature analysis.
Eur J Med Genet
; 66(8): 104806, 2023 Aug.
Artículo
en Inglés
| MEDLINE | ID: mdl-37379880
18.
Prevalence of pathogenic variants in cancer-predisposing genes in second cancer after childhood solid cancers.
Cancer Med
; 12(10): 11264-11273, 2023 05.
Artículo
en Inglés
| MEDLINE | ID: mdl-37021926
19.
Pre-procedural glucose levels and the risk for contrast-induced acute kidney injury in patients undergoing emergency coronary intervention.
Circ J
; 76(8): 1848-55, 2012.
Artículo
en Inglés
| MEDLINE | ID: mdl-22572459
20.
A familial case of periodontal Ehlers-Danlos syndrome lacking skin extensibility and joint hypermobility with a missense mutation in C1R.
J Dermatol
; 49(7): 714-718, 2022 Jul.
Artículo
en Inglés
| MEDLINE | ID: mdl-35365885