Detalles de la búsqueda
1.
Germline Variants in MLH1 and ATM Genes in a Young Patient with MSI-H in a Precancerous Colonic Lesion.
Int J Mol Sci
; 24(6)2023 Mar 22.
Artículo
en Inglés
| MEDLINE | ID: mdl-36983044
2.
A Novel εγδß-Thalassemia Deletion Associated with Severe Anemia at Birth and a ß-Thalassemia Intermedia Phenotype Later in Life in Three Generations of a Greek Family.
Hemoglobin
; 45(6): 351-354, 2021 Nov.
Artículo
en Inglés
| MEDLINE | ID: mdl-31829079
3.
Oxidative Stress and ROS-Mediated Signaling in Leukemia: Novel Promising Perspectives to Eradicate Chemoresistant Cells in Myeloid Leukemia.
Int J Mol Sci
; 22(5)2021 Feb 28.
Artículo
en Inglés
| MEDLINE | ID: mdl-33671113
4.
Implications of Splicing Alterations in the Onset and Phenotypic Variability of a Family with Subclinical Manifestation of Peutz-Jeghers Syndrome: Bioinformatic and Molecular Evidence.
Int J Mol Sci
; 21(21)2020 Nov 02.
Artículo
en Inglés
| MEDLINE | ID: mdl-33147782
5.
GATA-1 isoforms differently contribute to the production and compartmentation of reactive oxygen species in the myeloid leukemia cell line K562.
J Cell Physiol
; 234(11): 20829-20846, 2019 11.
Artículo
en Inglés
| MEDLINE | ID: mdl-31049966
6.
Incomplete Segregation of MSH6 Frameshift Variants with Phenotype of Lynch Syndrome.
Int J Mol Sci
; 18(5)2017 May 06.
Artículo
en Inglés
| MEDLINE | ID: mdl-28481244
7.
Role of WT1-ZNF224 interaction in the expression of apoptosis-regulating genes.
Hum Mol Genet
; 22(9): 1771-82, 2013 May 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-23362234
8.
miR-1202 acts as anti-oncomiR in myeloid leukaemia by down-modulating GATA-1S expression.
Open Biol
; 14(2): 230319, 2024 Feb.
Artículo
en Inglés
| MEDLINE | ID: mdl-38350611
9.
Prenatal diagnosis of haemoglobinopathies: our experience of 523 cases.
Clin Chem Lab Med
; 51(12): 2219-25, 2013 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-23612661
10.
KRAB-Zinc Finger Proteins: A Repressor Family Displaying Multiple Biological Functions.
Curr Genomics
; 14(4): 268-78, 2013 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-24294107
11.
Differential expression of PTEN gene correlates with phenotypic heterogeneity in three cases of patients showing clinical manifestations of PTEN hamartoma tumour syndrome.
Hered Cancer Clin Pract
; 11(1): 8, 2013.
Artículo
en Inglés
| MEDLINE | ID: mdl-23886400
12.
Identification and Functional Analysis of Known and New Mutations in the Transcription Factor KLF1 Linked with ß-Thalassemia-like Phenotypes.
Biology (Basel)
; 12(4)2023 Mar 28.
Artículo
en Inglés
| MEDLINE | ID: mdl-37106711
13.
The Epithelial to Mesenchymal Transition in Colorectal Cancer Progression: The Emerging Role of Succinate Dehydrogenase Alterations and Succinate Accumulation.
Biomedicines
; 11(5)2023 May 11.
Artículo
en Inglés
| MEDLINE | ID: mdl-37239099
14.
Over-Expressed GATA-1S, the Short Isoform of the Hematopoietic Transcriptional Factor GATA-1, Inhibits Ferroptosis in K562 Myeloid Leukemia Cells by Preventing Lipid Peroxidation.
Antioxidants (Basel)
; 12(3)2023 Feb 21.
Artículo
en Inglés
| MEDLINE | ID: mdl-36978786
15.
Biochemical and functional interaction between ZNF224 and ZNF255, two members of the Kruppel-like zinc-finger protein family and WT1 protein isoforms.
Hum Mol Genet
; 19(18): 3544-56, 2010 Sep 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-20591825
16.
Beta catenin and cytokine pathway dysregulation in patients with manifestations of the "PTEN hamartoma tumor syndrome".
BMC Med Genet
; 13: 28, 2012 Apr 20.
Artículo
en Inglés
| MEDLINE | ID: mdl-22520842
17.
Significance of rare variants in genes involved in the pathogenesis of Lynch syndrome.
Int J Mol Med
; 49(6)2022 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-35475445
18.
Hereditary Colorectal Cancer: State of the Art in Lynch Syndrome.
Cancers (Basel)
; 15(1)2022 Dec 23.
Artículo
en Inglés
| MEDLINE | ID: mdl-36612072
19.
Association of low-risk MSH3 and MSH2 variant alleles with Lynch syndrome: probability of synergistic effects.
Int J Cancer
; 129(7): 1643-50, 2011 Oct 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-21128252
20.
Coexistence of MLH3 germline variants in colon cancer patients belonging to families with Lynch syndrome-associated brain tumors.
J Neurooncol
; 129(3): 577-578, 2016 09.
Artículo
en Inglés
| MEDLINE | ID: mdl-27401157