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1.
Gene expression variability in long-term survivors of childhood cancer and cancer-free controls in response to ionizing irradiation.
Mol Med
; 29(1): 41, 2023 03 30.
Artículo
en Inglés
| MEDLINE | ID: mdl-36997855
2.
Radiation-response in primary fibroblasts of long-term survivors of childhood cancer with and without second primary neoplasms: the KiKme study.
Mol Med
; 28(1): 105, 2022 09 06.
Artículo
en Inglés
| MEDLINE | ID: mdl-36068491
3.
Comparison of time and dose dependent gene expression and affected pathways in primary human fibroblasts after exposure to ionizing radiation.
Mol Med
; 26(1): 85, 2020 09 09.
Artículo
en Inglés
| MEDLINE | ID: mdl-32907548
4.
Homozygous variants in the gene SCAPER cause syndromic intellectual disability.
Am J Med Genet A
; 179(7): 1214-1225, 2019 07.
Artículo
en Inglés
| MEDLINE | ID: mdl-31069901
5.
A boy with homozygous microdeletion of NEUROG1 presents with a congenital cranial dysinnervation disorder [Moebius syndrome variant].
Behav Brain Funct
; 9: 7, 2013 Feb 18.
Artículo
en Inglés
| MEDLINE | ID: mdl-23419067
6.
The original family revisited after 37 years: odontoma-dysphagia syndrome is most likely caused by a microduplication of chromosome 11q13.3, including the FGF3 and FGF4 genes.
Clin Oral Investig
; 17(1): 123-30, 2013 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-22297612
7.
Searching for gene expression differences in primary fibroblasts between patients with one and two neoplasms in childhood.
Pediatr Hematol Oncol
; 30(1): 33-45, 2013 Feb.
Artículo
en Inglés
| MEDLINE | ID: mdl-23140311
8.
Replication stress drives chromosomal instability in fibroblasts of childhood cancer survivors with second primary neoplasms.
DNA Repair (Amst)
; 122: 103435, 2023 02.
Artículo
en Inglés
| MEDLINE | ID: mdl-36549044
9.
Self-administered questionnaire assessing childhood cancer treatments and associated risks for adverse health outcomes - The KiKme study.
Front Oncol
; 13: 1150629, 2023.
Artículo
en Inglés
| MEDLINE | ID: mdl-37124517
10.
Identification of lncRNAs involved in response to ionizing radiation in fibroblasts of long-term survivors of childhood cancer and cancer-free controls.
Front Oncol
; 13: 1158176, 2023.
Artículo
en Inglés
| MEDLINE | ID: mdl-37182169
11.
Novel clinical findings in the first Egyptian case of Sotos syndrome caused by complete deletion of the NSD1 gene.
Am J Med Genet A
; 173(4): 1090-1093, 2017 04.
Artículo
en Inglés
| MEDLINE | ID: mdl-28328121
12.
Spatial, temporal and interindividual epigenetic variation of functionally important DNA methylation patterns.
Nucleic Acids Res
; 38(12): 3880-90, 2010 Jul.
Artículo
en Inglés
| MEDLINE | ID: mdl-20194112
13.
Late health effects and changes in lifestyle factors after cancer in childhood with and without subsequent second primary cancers - the KiKme case-control study.
Front Oncol
; 12: 1037276, 2022.
Artículo
en Inglés
| MEDLINE | ID: mdl-36324589
14.
Hypermethylation of RAD9A intron 2 in childhood cancer patients, leukemia and tumor cell lines suggest a role for oncogenic transformation.
EXCLI J
; 21: 117-143, 2022.
Artículo
en Inglés
| MEDLINE | ID: mdl-35221838
15.
Δ133p53α enhances metabolic and cellular fitness of TCR-engineered T cells and promotes superior antitumor immunity.
J Immunother Cancer
; 9(6)2021 06.
Artículo
en Inglés
| MEDLINE | ID: mdl-34112738
16.
Identification of Genetic Predispositions Related to Ionizing Radiation in Primary Human Skin Fibroblasts From Survivors of Childhood and Second Primary Cancer as Well as Cancer-Free Controls: Protocol for the Nested Case-Control Study KiKme.
JMIR Res Protoc
; 10(11): e32395, 2021 Nov 11.
Artículo
en Inglés
| MEDLINE | ID: mdl-34762066
17.
Spontaneous and Radiation-Induced Chromosome Aberrations in Primary Fibroblasts of Patients With Pediatric First and Second Neoplasms.
Front Oncol
; 10: 1338, 2020.
Artículo
en Inglés
| MEDLINE | ID: mdl-32850427
18.
Correction to: Molecular karyotyping and gene expression analysis in childhood cancer patients.
J Mol Med (Berl)
; 98(11): 1657, 2020 Nov.
Artículo
en Inglés
| MEDLINE | ID: mdl-32978668
19.
De novo t(12;17)(p13.3;q21.3) translocation with a breakpoint near the 5' end of the HOXB gene cluster in a patient with developmental delay and skeletal malformations.
Eur J Hum Genet
; 15(5): 570-7, 2007 May.
Artículo
en Inglés
| MEDLINE | ID: mdl-17327879
20.
Single-chain antibodies against a plant viral RNA-dependent RNA polymerase confer virus resistance.
Nat Biotechnol
; 22(7): 856-62, 2004 Jul.
Artículo
en Inglés
| MEDLINE | ID: mdl-15195103