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Genetic diversity and population structure of the fall armyworm, Spodoptera frugiperda (J.E. Smith) (Lepidoptera: Noctuidae) in the Philippines.
- Published in:
- Journal of Applied Entomology, 2024, v. 148, n. 8, p. 983, doi. 10.1111/jen.13307
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- Article
Binding Chromium(III) to Form Mixed Cr(III),Fe(III) Serum Transferrins.
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- Biological Trace Element Research, 2024, v. 202, n. 7, p. 3377, doi. 10.1007/s12011-023-03917-4
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- Article
Biallelic variants identified in 36 Pakistani families and trios with autism spectrum disorder.
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- Scientific Reports, 2024, v. 14, n. 1, p. 1, doi. 10.1038/s41598-024-57942-x
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- Article
Editorial.
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- 2024
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- Publication type:
- Editorial
What Are the Implications of Cr(III) Serving as an Inhibitor of the Beta Subunit of Mitochondrial ATP Synthase?
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- Biological Trace Element Research, 2024, v. 202, n. 4, p. 1335, doi. 10.1007/s12011-023-03809-7
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- Article
Morpho-molecular characterization of golden potato cyst nematode population from Bauko, Mountain Province, Philippines.
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- Journal of Plant Diseases & Protection, 2024, v. 131, n. 2, p. 631, doi. 10.1007/s41348-023-00831-8
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- Article
Nonsynonymous Mutations in Intellectual Disability and Autism Spectrum Disorder Gene PTCHD1 Disrupt N -Glycosylation and Reduce Protein Stability.
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- Cells (2073-4409), 2024, v. 13, n. 2, p. 199, doi. 10.3390/cells13020199
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- Article
MeCP2 ubiquitination and sumoylation, in search of a function.
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- Human Molecular Genetics, 2024, v. 33, n. 1, p. 1, doi. 10.1093/hmg/ddad150
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- Article
Examining the Potential Formation of Ternary DNA Complexes with Chromium‑Cysteine, Chromium-Ascorbate, and Chromium-Glutathione and Implications for Their Carcinogenicity.
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- Biological Trace Element Research, 2023, v. 201, n. 10, p. 5053, doi. 10.1007/s12011-023-03573-8
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- Article
Wide spectrum of neuronal and network phenotypes in human stem cell-derived excitatory neurons with Rett syndrome-associated MECP2 mutations.
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- Translational Psychiatry, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41398-022-02216-1
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- Article
Biallelic Loss of Function Mutation in Sodium Channel Gene SCN10A in an Autism Spectrum Disorder Trio from Pakistan.
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- Genes, 2022, v. 13, n. 9, p. 1633, doi. 10.3390/genes13091633
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- Article
Mutation Analysis of a Pakistani Oculocutaneous Albinism Family Identifies a Novel Splice Site Defect in OCA2 Gene.
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- Pakistan Journal of Zoology, 2022, v. 54, n. 3, p. 1215, doi. 10.17582/journal.pjz/20200501060515
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- Article
Examining the Potential Formation of Ternary Chromium-Histidine-DNA Complexes and Implications for Their Carcinogenicity.
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- Biological Trace Element Research, 2022, v. 200, n. 3, p. 1473, doi. 10.1007/s12011-021-02743-w
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- Article
PTCHD1 : Identification and Neurodevelopmental Contributions of an Autism Spectrum Disorder and Intellectual Disability Susceptibility Gene.
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- Genes, 2022, v. 13, n. 3, p. 527, doi. 10.3390/genes13030527
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- Article
Heterozygous De Novo Truncating Mutation of Nucleolin in an ASD Individual Disrupts Its Nucleolar Localization.
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- Genes, 2022, v. 13, n. 1, p. 51, doi. 10.3390/genes13010051
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- Article
Biallelic inheritance in a single Pakistani family with intellectual disability implicates new candidate gene RDH14.
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- Scientific Reports, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41598-021-02599-z
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- Article
Exome sequencing identifies novel and known mutations in families with intellectual disability.
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- BMC Medical Genomics, 2021, v. 14, n. 1, p. 1, doi. 10.1186/s12920-021-01066-y
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- Article
Homozygosity mapping coupled with whole-exome sequencing and protein modelling identified a novel missense mutation in GUCY2D in a consanguineous Pakistani family with Leber congenital amaurosis.
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- Journal of Genetics, 2021, v. 100, n. 2, p. 1, doi. 10.1007/s12041-021-01310-5
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- Article
Cytochrome C Oxidase Subunit I and II (COI and COII) Sequences Support Recognition of Papilio chikae Igarashi and Papilio hermeli Nuyda as Distinct Species.
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- Philippine Journal of Science, 2021, v. 150, p. 111
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- Article
MeCP2: latest insights fundamentally change our understanding of its interactions with chromatin and its functional attributes.
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- BioEssays, 2021, v. 43, n. 3, p. 1, doi. 10.1002/bies.202000281
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- Article
Effects of Bitter Melon and a Chromium Propionate Complex on Symptoms of Insulin Resistance and Type 2 Diabetes in Rat Models.
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- Biological Trace Element Research, 2021, v. 199, n. 3, p. 1013, doi. 10.1007/s12011-020-02202-y
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- Article
Intraspecific trait variation across elevation predicts a widespread tree species' climate niche and range limits.
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- Ecology & Evolution (20457758), 2020, v. 10, n. 9, p. 3856, doi. 10.1002/ece3.5969
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- Article
Cover Feature: Molecular Structure of Binary Chromium(III)–DNA Adducts (ChemBioChem 5/2020).
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- ChemBioChem, 2020, v. 21, n. 5, p. 575, doi. 10.1002/cbic.202000078
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- Article
Molecular Structure of Binary Chromium(III)–DNA Adducts.
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- ChemBioChem, 2020, v. 21, n. 5, p. 628, doi. 10.1002/cbic.201900436
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- Article
GPT2 mutations in autosomal recessive developmental disability: extending the clinical phenotype and population prevalence estimates.
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- Human Genetics, 2019, v. 138, n. 10, p. 1183, doi. 10.1007/s00439-019-02057-x
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- Article
Genetic studies of multiple consanguineous Pakistani families segregating oculocutaneous albinism identified novel and reported mutations.
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- Annals of Human Genetics, 2019, v. 83, n. 4, p. 278, doi. 10.1111/ahg.12307
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- Article
Systematic Review of the Effects of Chromium(III) on Chickens.
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- Biological Trace Element Research, 2019, v. 188, n. 1, p. 99, doi. 10.1007/s12011-018-1575-8
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- Article
Bears habituate to the repeated exposure of a novel stimulus, unmanned aircraft systems.
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- Conservation Physiology, 2019, p. N.PAG, doi. 10.1093/conphys/coy067
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- Article
Enrichment of pathogenic variants in genes associated with inborn errors of metabolism in psychiatric populations.
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- American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2019, v. 180, n. 1, p. 46, doi. 10.1002/ajmg.b.32702
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- Article
The use of chromium(III) complexes to enhance peptide protonation by electrospray ionization mass spectrometry.
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- Journal of Mass Spectrometry, 2018, v. 53, n. 12, p. 1198, doi. 10.1002/jms.4297
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- Article
[Cr<sub>3</sub>O(O<sub>2</sub>CCH<sub>2</sub>CH<sub>3</sub>)<sub>6</sub>(H<sub>2</sub>O)<sub>3</sub>]NO<sub>3</sub>·H<sub>2</sub>O (Cr3) Toxicity Potential in Bacterial and Mammalian Cells.
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- Biological Trace Element Research, 2018, v. 183, n. 2, p. 342, doi. 10.1007/s12011-017-1132-x
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- Article
MeCP2 AT‐Hook1 mutations in patients with intellectual disability and/or schizophrenia disrupt DNA binding and chromatin compaction in vitro.
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- Human Mutation, 2018, v. 39, n. 5, p. 717, doi. 10.1002/humu.23409
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- Article
Tropical forest dynamics in unstable terrain: a case study from New Guinea.
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- Journal of Tropical Ecology, 2018, v. 34, n. 3, p. 157, doi. 10.1017/S0266467418000123
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- Article
The Identity of 'Chromium Malate'.
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- Biological Trace Element Research, 2018, v. 181, n. 2, p. 369, doi. 10.1007/s12011-017-1046-7
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- Article
MeCP2_E1 N-terminal modifications affect its degradation rate and are disrupted by the Ala2Val Rett mutation.
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- Human Molecular Genetics, 2017, v. 26, n. 21, p. 4132, doi. 10.1093/hmg/ddx300
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- Article
Relative importance of abiotic, biotic, and disturbance drivers of plant community structure in the sagebrush steppe.
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- Ecological Applications, 2017, v. 27, n. 3, p. 756, doi. 10.1002/eap.1479
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- Article
Investigation of correlations between DNA methylation, suicidal behavior and aging.
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- Bipolar Disorders, 2017, v. 19, n. 1, p. 32, doi. 10.1111/bdi.12466
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- Article
From Function to Phenotype: Impaired DNA Binding and Clustering Correlates with Clinical Severity in Males with Missense Mutations in MECP2.
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- Scientific Reports, 2016, p. 38590, doi. 10.1038/srep38590
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- Article
Ectomycorrhizal fungal diversity and saprotrophic fungal diversity are linked to different tree community attributes in a field-based tree experiment.
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- Molecular Ecology, 2016, v. 25, n. 16, p. 4032, doi. 10.1111/mec.13719
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- Article
Not quite free yet: clarifying UAV regulatory progress for ecologists.
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- 2015
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- Publication type:
- Letter to the Editor
MeCP2-chromatin binding dynamics shows a direct genotype–phenotype correlation in males with single amino acid substitutions.
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- International Journal of Developmental Neuroscience, 2015, v. 47, p. 42, doi. 10.1016/j.ijdevneu.2015.04.120
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- Article
15q11.2 Duplication Encompassing Only the UBE3A Gene Is Associated with Developmental Delay and Neuropsychiatric Phenotypes.
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- Human Mutation, 2015, v. 36, n. 7, p. 689, doi. 10.1002/humu.22800
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- Article
New recessive truncating mutation in LTBP3 in a family with oligodontia, short stature, and mitral valve prolapse.
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- American Journal of Medical Genetics. Part A, 2015, v. 167A, n. 6, p. 1396, doi. 10.1002/ajmg.a.37049
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- Article
Forest carbon in lowland Papua New Guinea: Local variation and the importance of small trees.
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- Austral Ecology, 2015, v. 40, n. 2, p. 151, doi. 10.1111/aec.12187
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- Article
Trophic phylogenetics: evolutionary influences on body size, feeding, and species associations in grassland arthropods.
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- Ecology, 2015, v. 96, n. 4, p. 998, doi. 10.1890/14-0784.1
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- Article
Barriers to adding UAVs to the ecologist's toolbox.
- Published in:
- 2015
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- Publication type:
- Letter to the Editor
Homozygosity mapping of autosomal recessive intellectual disability loci in 11 consanguineous Pakistani families.
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- Acta Neuropsychiatrica, 2015, v. 27, n. 1, p. 38, doi. 10.1017/neu.2014.37
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- Article
Mice with an isoform-ablating Mecp2 exon 1 mutation recapitulate the neurologic deficits of Rett syndrome.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 24, p. 6695, doi. 10.1093/hmg/ddu496
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- Article
A missense mutation in the PISA domain of HsSAS-6 causes autosomal recessive primary microcephaly in a large consanguineous Pakistani family.
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- Human Molecular Genetics, 2014, v. 23, n. 22, p. 5940, doi. 10.1093/hmg/ddu318
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- Article
Disruption of the methyltransferase-like 23 gene METTL23 causes mild autosomal recessive intellectual disability.
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- Human Molecular Genetics, 2014, v. 23, n. 15, p. 4015, doi. 10.1093/hmg/ddu115
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- Article