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1.
Evaluation of Genetic Variants Associated with the Risk of Thiopurine-Related Pancreatitis: A Case Control Study from ENEIDA Registry.
Dig Dis
; 42(3): 257-264, 2024.
Artículo
en Inglés
| MEDLINE | ID: mdl-38452742
2.
Expanding the clinical and molecular spectrum of FOXG1- and ZBTB18-associated neurodevelopmental disorders.
Cytogenet Genome Res
; 2023 Dec 06.
Artículo
en Inglés
| MEDLINE | ID: mdl-38056433
3.
Food services in times of uncertainty: Remodeling operations, changing trends, and looking into perspectives after the COVID-19 pandemic.
Trends Food Sci Technol
; 120: 301-307, 2022 Feb.
Artículo
en Inglés
| MEDLINE | ID: mdl-35035090
4.
Influence of Kv11.1 (hERG1) K+ channel expression on DNA damage induced by the genotoxic agent methyl methanesulfonate.
Pflugers Arch
; 473(2): 197-217, 2021 02.
Artículo
en Inglés
| MEDLINE | ID: mdl-33452554
5.
Invasion-mediated effects on marine trophic interactions in a changing climate: positive feedbacks favour kelp persistence.
Proc Biol Sci
; 286(1899): 20182866, 2019 03 27.
Artículo
en Inglés
| MEDLINE | ID: mdl-30900532
6.
Novel truncating variants expand the phenotypic spectrum of KAT6B-related disorders.
Am J Med Genet A
; 179(2): 290-294, 2019 02.
Artículo
en Inglés
| MEDLINE | ID: mdl-30569622
7.
New Structures and Gating of Voltage-Dependent Potassium (Kv) Channels and Their Relatives: A Multi-Domain and Dynamic Question.
Int J Mol Sci
; 20(2)2019 Jan 10.
Artículo
en Inglés
| MEDLINE | ID: mdl-30634573
8.
Functional characterization of Kv11.1 (hERG) potassium channels split in the voltage-sensing domain.
Pflugers Arch
; 470(7): 1069-1085, 2018 07.
Artículo
en Inglés
| MEDLINE | ID: mdl-29572566
9.
Gating mechanism of Kv11.1 (hERG) K+ channels without covalent connection between voltage sensor and pore domains.
Pflugers Arch
; 470(3): 517-536, 2018 03.
Artículo
en Inglés
| MEDLINE | ID: mdl-29270671
10.
Moesin expression by tumor cells is an unfavorable prognostic biomarker for oral cancer.
BMC Cancer
; 18(1): 53, 2018 01 08.
Artículo
en Inglés
| MEDLINE | ID: mdl-29310601
11.
Whole exome sequencing approach to analysis of the origin of cancer stem cells in patients with head and neck squamous cell carcinoma.
J Oral Pathol Med
; 47(10): 938-944, 2018 Nov.
Artículo
en Inglés
| MEDLINE | ID: mdl-30067878
12.
Phloroglucinol derivatives from Hypericum species trigger mitochondrial dysfunction in Leishmania amazonensis.
Parasitology
; 145(9): 1199-1209, 2018 08.
Artículo
en Inglés
| MEDLINE | ID: mdl-29482667
13.
Antinociceptive Activity of Phloroglucinol Derivatives Isolated from Southern Brazilian Hypericum Species.
Chem Biodivers
; 15(11): e1800266, 2018 Nov.
Artículo
en Inglés
| MEDLINE | ID: mdl-30156379
14.
Progressive Cervical Myelopathy With Medullary Involvement as a Presentation of Dural Arteriovenous Fistula.
Stroke
; 53(12): e515-e516, 2022 12.
Artículo
en Inglés
| MEDLINE | ID: mdl-36168129
15.
Plasma membrane insertion of epithelial sodium channels occurs with dual kinetics.
Pflugers Arch
; 468(5): 859-70, 2016 05.
Artículo
en Inglés
| MEDLINE | ID: mdl-26876388
16.
Interactions between the N-terminal tail and the gating machinery of hERG K⺠channels both in closed and open/inactive states.
Pflugers Arch
; 467(8): 1747-56, 2015 Aug.
Artículo
en Inglés
| MEDLINE | ID: mdl-25224286
17.
Clinical characterization of a male patient with the recently described 8q21.11 microdeletion syndrome.
Am J Med Genet A
; 167(6): 1369-73, 2015 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-25898976
18.
Female patient with autistic disorder, intellectual disability, and co-morbid anxiety disorder: Expanding the phenotype associated with the recurrent 3q13.2-q13.31 microdeletion.
Am J Med Genet A
; 167A(12): 3121-9, 2015 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-26332054
19.
A maternally inherited 16p13.11-p12.3 duplication concomitant with a de novo SOX5 deletion in a male patient with global developmental delay, disruptive and obsessive behaviors and minor dysmorphic features.
Am J Med Genet A
; 167(6): 1315-22, 2015 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-25847113
20.
Interstitial microdeletions including the chromosome band 4q13.2 and the UBA6 gene as possible causes of intellectual disability and behavior disorder.
Am J Med Genet A
; 167A(12): 3113-20, 2015 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-26284580