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1.
The Differential Translation Capabilities of the Human DHFR2 Gene Indicates a Developmental and Tissue-Specific Endogenous Protein of Low Abundance.
Mol Cell Proteomics
; 23(3): 100718, 2024 Mar.
Artículo
en Inglés
| MEDLINE | ID: mdl-38224738
2.
A one-step reverse transcription recombinase polymerase amplification assay for lateral flow-based visual detection of PVY.
Anal Biochem
; 642: 114526, 2022 04 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-34922917
3.
Assessment of candidate folate sensitive-differentially methylated regions in a randomised controlled trial of continued folic acid supplementation during the second and third trimesters of pregnancy.
Ann Hum Genet
; 83(1): 23-33, 2019 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-30175844
4.
Evidence from a Randomized Trial That Exposure to Supplemental Folic Acid at Recommended Levels during Pregnancy Does Not Lead to Increased Unmetabolized Folic Acid Concentrations in Maternal or Cord Blood.
J Nutr
; 146(3): 494-500, 2016 Mar.
Artículo
en Inglés
| MEDLINE | ID: mdl-26817717
5.
A dihydrofolate reductase 2 (DHFR2) variant is associated with risk of neural tube defects in an Irish cohort but not in a United Kingdom cohort.
Am J Med Genet A
; 185(4): 1307-1311, 2021 04.
Artículo
en Inglés
| MEDLINE | ID: mdl-33544972
6.
The Dihydrofolate Reductase 19 bp Polymorphism Is Not Associated with Biomarkers of Folate Status in Healthy Young Adults, Irrespective of Folic Acid Intake.
J Nutr
; 145(10): 2207-11, 2015 Oct.
Artículo
en Inglés
| MEDLINE | ID: mdl-26269242
7.
An NTD-associated polymorphism in the 3' UTR of MTHFD1L can affect disease risk by altering miRNA binding.
Hum Mutat
; 35(1): 96-104, 2014 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-24123340
8.
Replication and exploratory analysis of 24 candidate risk polymorphisms for neural tube defects.
BMC Med Genet
; 15: 102, 2014 Oct 08.
Artículo
en Inglés
| MEDLINE | ID: mdl-25293959
9.
The former annotated human pseudogene dihydrofolate reductase-like 1 (DHFRL1) is expressed and functional.
Proc Natl Acad Sci U S A
; 108(37): 15157-62, 2011 Sep 13.
Artículo
en Inglés
| MEDLINE | ID: mdl-21876184
10.
Vitamin B12 status and folic acid supplementation influence mitochondrial heteroplasmy levels in mice.
PNAS Nexus
; 3(4): pgae116, 2024 Apr.
Artículo
en Inglés
| MEDLINE | ID: mdl-38560530
11.
Automated solid phase DNA extraction on a lab-on-a-disc with two-degrees of freedom instrumentation.
Anal Chim Acta
; 1280: 341859, 2023 Nov 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-37858565
12.
Genotyping of a tri-allelic polymorphism by a novel melting curve assay in MTHFD1L: an association study of nonsyndromic Cleft in Ireland.
BMC Med Genet
; 13: 29, 2012 Apr 20.
Artículo
en Inglés
| MEDLINE | ID: mdl-22520921
13.
Evaluation of common genetic variants in 82 candidate genes as risk factors for neural tube defects.
BMC Med Genet
; 13: 62, 2012 Aug 02.
Artículo
en Inglés
| MEDLINE | ID: mdl-22856873
14.
Mito-SiPE is a sequence-independent and PCR-free mtDNA enrichment method for accurate ultra-deep mitochondrial sequencing.
Commun Biol
; 5(1): 1269, 2022 11 19.
Artículo
en Inglés
| MEDLINE | ID: mdl-36402890
15.
Methods to Study Translated Pseudogenes: Recombinant Expression and Complementation, Targeted Proteomics, and RNA Profiling.
Methods Mol Biol
; 2324: 239-254, 2021.
Artículo
en Inglés
| MEDLINE | ID: mdl-34165719
16.
A review of pharmaceutical occurrence and pathways in the aquatic environment in the context of a changing climate and the COVID-19 pandemic.
Anal Methods
; 13(5): 575-594, 2021 02 07.
Artículo
en Inglés
| MEDLINE | ID: mdl-33507166
17.
Monitoring of emerging contaminants of concern in the aquatic environment: a review of studies showing the application of effect-based measures.
Anal Methods
; 13(43): 5120-5143, 2021 11 11.
Artículo
en Inglés
| MEDLINE | ID: mdl-34726207
18.
A common variant in MTHFD1L is associated with neural tube defects and mRNA splicing efficiency.
Hum Mutat
; 30(12): 1650-6, 2009 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-19777576
19.
Analysis of the MTHFD1 promoter and risk of neural tube defects.
Hum Genet
; 125(3): 247-56, 2009 Apr.
Artículo
en Inglés
| MEDLINE | ID: mdl-19130090
20.
The application of CRISPR-Cas for single species identification from environmental DNA.
Mol Ecol Resour
; 19(5): 1106-1114, 2019 Sep.
Artículo
en Inglés
| MEDLINE | ID: mdl-31177615