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Binding Chromium(III) to Form Mixed Cr(III),Fe(III) Serum Transferrins.
- Published in:
- Biological Trace Element Research, 2024, v. 202, n. 7, p. 3377, doi. 10.1007/s12011-023-03917-4
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- Publication type:
- Article
Editorial.
- Published in:
- 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?
- Published in:
- Biological Trace Element Research, 2024, v. 202, n. 4, p. 1335, doi. 10.1007/s12011-023-03809-7
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- Publication type:
- 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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- Publication type:
- 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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- Publication type:
- Article
Effects of Bitter Melon and a Chromium Propionate Complex on Symptoms of Insulin Resistance and Type 2 Diabetes in Rat Models.
- Published in:
- Biological Trace Element Research, 2021, v. 199, n. 3, p. 1013, doi. 10.1007/s12011-020-02202-y
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- Publication type:
- Article
Systematic Review of the Effects of Chromium(III) on Chickens.
- Published in:
- Biological Trace Element Research, 2019, v. 188, n. 1, p. 99, doi. 10.1007/s12011-018-1575-8
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- Publication type:
- 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.
- Published in:
- Biological Trace Element Research, 2018, v. 183, n. 2, p. 342, doi. 10.1007/s12011-017-1132-x
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- Publication type:
- 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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- Publication type:
- 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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- Publication type:
- 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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- Publication type:
- 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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- Publication type:
- Article
Immobilization of conalbumin onto polystyrene/divinylbenzene co-polymers: Towards finding the best support for MAMC.
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- Journal of Molecular Recognition, 1996, v. 9, n. 5/6, p. 558, doi. 10.1002/(SICI)1099-1352(199634/12)9:5/6<558::AID-JMR300>3.0.CO;2-A
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- Publication type:
- 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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- Publication type:
- 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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- Publication type:
- 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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- Publication type:
- 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. 9, p. 2447, doi. 10.1093/hmg/ddt640
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- Publication type:
- Article
Association analysis of DAOA and DAO in bipolar disorder: results from two independent case-control studies.
- Published in:
- 2010
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- Publication type:
- Letter
Structure, Magnetochemistry and Biological Relevance of [Mn<sub>4</sub>O<sub>3</sub>Cl<sub>4</sub>(OAc)<sub>3</sub>(py)<sub>3</sub>], a Complex with S = 9/2 Ground State.
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- Angewandte Chemie International Edition, 1988, v. 27, n. 12, p. 1731, doi. 10.1002/anie.198817311
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- Publication type:
- Article
Salicylate-Mediated Assembly of the Diserete Mixed-Valence Nonanuclear Manganese Complex [Mn<sub>9</sub>O<sub>4</sub>(O<sub>2</sub>CPh)<sub>8</sub>(sal)<sub>4</sub>(salH)<sub>2</sub>(py)<sub>4</sub>] (salH<sub>2</sub> = salicylic acid, py = pyridine).
- Published in:
- Angewandte Chemie International Edition, 1987, v. 26, n. 9, p. 915, doi. 10.1002/anie.198709151
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- Publication type:
- Article
Not quite free yet: clarifying UAV regulatory progress for ecologists.
- Published in:
- 2015
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- Publication type:
- Letter to the Editor
Barriers to adding UAVs to the ecologist's toolbox.
- Published in:
- 2015
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- Publication type:
- Letter to the Editor
Oral administration of the biomimetic [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>]<sup>+</sup> increases insulin sensitivity and improves blood plasma variables in healthy and type 2 diabetic rats.
- Published in:
- 2005
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- Publication type:
- Correction notice
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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- Publication type:
- 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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- Publication type:
- Article
Genetic diversity and population structure of the fall armyworm, Spodoptera frugiperda (J.E. Smith) (Lepidoptera: Noctuidae) in the Philippines.
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- Journal of Applied Entomology, 2024, v. 148, n. 8, p. 983, doi. 10.1111/jen.13307
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- Publication type:
- 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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- Publication type:
- 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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- Publication type:
- 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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- Publication type:
- 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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- Publication type:
- Article
Meta-analysis of genome-wide association data identifies a risk locus for major mood disorders on 3p21.1.
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- Nature Genetics, 2010, v. 42, n. 2, p. 128, doi. 10.1038/ng.523
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- Publication type:
- Article
Mapping autism risk loci using genetic linkage and chromosomal rearrangements.
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- Nature Genetics, 2007, v. 39, n. 3, p. 319, doi. 10.1038/ng1985
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- Publication type:
- Article
A previously unidentified MECP2 open reading frame defines a new protein isoform relevant to Rett syndrome.
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- Nature Genetics, 2004, v. 36, n. 4, p. 339, doi. 10.1038/ng1327
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- Publication type:
- Article
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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- Publication type:
- 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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- Publication type:
- 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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- Publication type:
- Article
Copy number variant study of bipolar disorder in Canadian and UK populations implicates synaptic genes.
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- American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2014, v. 165B, n. 4, p. 303, doi. 10.1002/ajmg.b.32232
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- Publication type:
- Article
Genetic studies of multiple consanguineous Pakistani families segregating oculocutaneous albinism identified novel and reported mutations.
- Published in:
- Annals of Human Genetics, 2019, v. 83, n. 4, p. 278, doi. 10.1111/ahg.12307
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- Publication type:
- Article
The Human Homologue of Flamingo, EGFL2, Encodes a Brain-Expressed Large Cadherin-Like Protein with Epidermal Growth Factor-Like Domains, and Maps to Chromosome 1p13.3-p21.1.
- Published in:
- DNA Research, 2000, v. 7, n. 3, p. 233, doi. 10.1093/dnares/7.3.233
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- Publication type:
- Article
Quest for the molecular mechanism of chromium action and its relationship to diabetes.
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- Nutrition Reviews, 2000, v. 58, n. 3, p. 67
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- Publication type:
- Article
Homozygosity mapping of autosomal recessive intellectual disability loci in 11 consanguineous Pakistani families.
- Published in:
- Acta Neuropsychiatrica, 2015, v. 27, n. 1, p. 38, doi. 10.1017/neu.2014.37
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- Publication type:
- Article
Over-Expression of Either MECP2_e1 or MECP2_e2 in Neuronally Differentiated Cells Results in Different Patterns of Gene Expression.
- Published in:
- PLoS ONE, 2014, v. 9, n. 4, p. 1, doi. 10.1371/journal.pone.0091742
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- Publication type:
- Article
Recent advances in the nutritional biochemistry of trivalent chromium.
- Published in:
- Proceedings of the Nutrition Society, 2004, v. 63, n. 1, p. 41, doi. 10.1079/PNS2003315
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- Publication type:
- Article
GPT2 mutations in autosomal recessive developmental disability: extending the clinical phenotype and population prevalence estimates.
- Published in:
- Human Genetics, 2019, v. 138, n. 10, p. 1183, doi. 10.1007/s00439-019-02057-x
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- Publication type:
- Article
From Function to Phenotype: Impaired DNA Binding and Clustering Correlates with Clinical Severity in Males with Missense Mutations in MECP2.
- Published in:
- Scientific Reports, 2016, p. 38590, doi. 10.1038/srep38590
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- Publication type:
- Article
DO TRADE-OFFS HAVE EXPLANATORY POWER FOR THE EVOLUTION OF ORGANISMAL INTERACTIONS?
- Published in:
- Evolution, 2012, v. 66, n. 5, p. 1297, doi. 10.1111/j.1558-5646.2011.01573.x
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- Publication type:
- Article
Ectomycorrhizal fungal diversity and saprotrophic fungal diversity are linked to different tree community attributes in a field-based tree experiment.
- Published in:
- Molecular Ecology, 2016, v. 25, n. 16, p. 4032, doi. 10.1111/mec.13719
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- Publication type:
- Article
Relative importance of abiotic, biotic, and disturbance drivers of plant community structure in the sagebrush steppe.
- Published in:
- Ecological Applications, 2017, v. 27, n. 3, p. 756, doi. 10.1002/eap.1479
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- Publication type:
- Article
A synonymous change, p.Gly16Gly in MECP2 Exon 1, causes a cryptic splice event in a Rett syndrome patient.
- Published in:
- Orphanet Journal of Rare Diseases, 2013, v. 8, n. 1, p. 1, doi. 10.1186/1750-1172-8-108
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- Publication type:
- Article
A synonymous change, p.Gly16Gly in MECP2 Exon 1, causes a cryptic splice event in a Rett syndrome patient.
- Published in:
- 2013
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- Publication type:
- journal article