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"THE GOD WITH CLAY": THE IDEA OF DEEP INCARNATION AND THE INFORMATIONAL UNIVERSE: with Finley I. Lawson, "The Science and Religion Forum Discuss Information and Reality: Questions for Religions and Science"; Niels Henrik Gregersen, "'The God with Clay': The Idea of Deep Incarnation and the Informational Universe"; Michael Burdett and King‐Ho Leung, "The Machine in the Ghost: Transhumanism and the Ontology of Information"; Marius Dorobantu and Fraser Watts, "Spiritual Intelligence: Processing Different Information or Processing Information Differently ?"; Matthew Kuan Johnson and Rachel Siow Robertson, "A Co‐Liberatory Framework for Big Data"; Peter M. Phillips, "Digital Theology and a Potential Theological Approach to a Metaphysics of Information"; and Andrew Jackson, "Peacocke Prize Essay—Towards an Eastern Orthodox Contemplation of Evolution: Maximus the Confessor's Vision of the Phylogenetic Logoi."
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- Zygon: Journal of Religion & Science, 2023, v. 58, n. 3, p. 683, doi. 10.1111/zygo.12881
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- Article
THE EXPLORATION OF ECOSPACE: EXTENDING OR SUPPLEMENTING THE NEO-DARWINIAN PARADIGM?
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- Zygon: Journal of Religion & Science, 2017, v. 52, n. 2, p. 561, doi. 10.1111/zygo.12344
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- Article
PROSPECTS FOR THE FIELD OF SCIENCE AND RELIGION: AN OCTOPUS VIEW.
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- Zygon: Journal of Religion & Science, 2014, v. 49, n. 2, p. 419, doi. 10.1111/zygo.12091
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- Article
Risk and Religion: Toward a Theology of Risk Taking.
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- Zygon: Journal of Religion & Science, 2003, v. 38, n. 2, p. 355, doi. 10.1111/1467-9744.00504
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- Article
Autopoeisis: Less than self-constitution, more than self-organization.
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- Zygon: Journal of Religion & Science, 1999, v. 34, n. 1, p. 117, doi. 10.1111/0591-2385.1971999197
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- Article
The idea of creation and the theory of autopoietic processes.
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- Zygon: Journal of Religion & Science, 1998, v. 33, n. 3, p. 333, doi. 10.1111/0591-2385.00154
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- Article
Prevalent mutations in fatty acid oxidation disorders: diagnostic considerations.
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- European Journal of Pediatrics, 2000, v. 159, n. 15, p. S213, doi. 10.1007/PL00014406
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- Article
A novel missense mutation (402C → T) in exon 1 in the EDA gene in a family with X-linked hypohidrotic ectodermal dysplasia.
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- Clinical Genetics, 1998, v. 53, n. 3, p. 205, doi. 10.1111/j.1399-0004.1998.tb02678.x
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- Publication type:
- Article
Biomarker Discovery by Mass Spectrometry in Cerebrospinal Fluid and Plasma after Global Hypoxia-Ischemia in Newborn Piglets.
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- Neonatology (16617800), 2018, v. 114, n. 4, p. 307, doi. 10.1159/000490393
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- Publication type:
- Article
The frequency of a disease-causing point mutation in the gene coding for medium-chain acyl-CoA dehydrogenase in sudden infant death syndrome.
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- Acta Paediatrica, 1993, v. 82, n. 6/7, p. 544, doi. 10.1111/j.1651-2227.1993.tb12749.x
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- Publication type:
- Article
A novel mutation of the ACADM gene (c.145C>G) associated with the common c.985A>G mutation on the other ACADM allele causes mild MCAD deficiency: a case report.
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- 2010
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- Publication type:
- Case Study
Riboflavin Deficiency—Implications for General Human Health and Inborn Errors of Metabolism.
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- International Journal of Molecular Sciences, 2020, v. 21, n. 11, p. 3847, doi. 10.3390/ijms21113847
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- Article
Tailoring polarization in WSe<sub>2</sub> quantum emitters through deterministic strain engineering.
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- NPJ 2D Materials & Applications, 2024, v. 8, n. 1, p. 1, doi. 10.1038/s41699-024-00497-2
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- Article
Protein Quality Control in the Endoplasmic Reticulum.
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- APMIS, 2003, v. 111, p. 86
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- Publication type:
- Article
Single-nucleotide variations in the genes encoding the mitochondrial Hsp60/Hsp10 chaperone system and their disease-causing potential.
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- Journal of Human Genetics, 2007, v. 52, n. 1, p. 56, doi. 10.1007/s10038-006-0080-7
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- Article
A Novel Synonymous Variant in the <bold>AVP</bold> Gene Associated with Autosomal Dominant Familial Neurohypophyseal Diabetes Insipidus Causes Partial RNA Missplicing.
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- Neuroendocrinology, 2018, v. 107, n. 2, p. 167, doi. 10.1159/000491579
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- Article
The Novel Ser18del AVP Variant Causes Inherited Neurohypophyseal Diabetes Insipidus by Mechanisms Shared with Other Signal Peptide Variants.
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- Neuroendocrinology, 2018, v. 106, n. 2, p. 167, doi. 10.1159/000477246
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- Publication type:
- Article
Novel and recurrent variants in AVPR2 in 19 families with X-linked congenital nephrogenic diabetes insipidus.
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- 2018
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- Publication type:
- journal article
Actin mutations in hypertrophic and dilated cardiomyopathy cause inefficient protein folding and perturbed filament formation.
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- FEBS Journal, 2005, v. 272, n. 8, p. 2037, doi. 10.1111/j.1742-4658.2005.04630.x
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- Publication type:
- Article
Harnessing Light with Photonic Nanowires: Fundamentals and Applications to Quantum Optics.
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- ChemPhysChem, 2013, v. 14, n. 11, p. 2393, doi. 10.1002/cphc.201300033
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- Article
Cover Picture: Harnessing Light with Photonic Nanowires: Fundamentals and Applications to Quantum Optics (ChemPhysChem 11/2013).
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- ChemPhysChem, 2013, v. 14, n. 11, p. 2353, doi. 10.1002/cphc.201390051
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- Publication type:
- Article
Association Between Low Self-Rated Health and Heterozygosity for -110A > C Polymorphism in the Promoter Region of HSP70-1 in Aged Danish Twins.
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- Biogerontology, 2004, v. 5, n. 3, p. 169, doi. 10.1023/B:BGEN.0000031154.57176.4f
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- Publication type:
- Article
Prenatal diagnosis of medium-chain acyl-CoA dehydrogenase (MCAD) deficiency in a family with a previous fatal case of sudden unexpected death in childhood.
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- 1995
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- Publication type:
- journal article
Functional testing of keratin 14 mutant proteins associated with the three major subtypes of epidermolysis bullosa simplex.
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- Experimental Dermatology, 2003, v. 12, n. 4, p. 472, doi. 10.1034/j.1600-0625.2002.120416.x
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- Publication type:
- Article
High-throughput quantum photonic devices emitting indistinguishable photons in the telecom C-band.
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- Nature Communications, 2024, v. 15, n. 1, p. 1, doi. 10.1038/s41467-024-47551-7
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- Publication type:
- Article
Large-Scale Proteomics Differentiates Cholesteatoma from Surrounding Tissues and Identifies Novel Proteins Related to the Pathogenesis.
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- PLoS ONE, 2014, v. 9, n. 8, p. 1, doi. 10.1371/journal.pone.0104103
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- Article
Quantitative Proteomics Reveals Cellular Targets of Celastrol.
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- PLoS ONE, 2011, v. 6, n. 10, p. 1, doi. 10.1371/journal.pone.0026634
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- Publication type:
- Article
Vulnerability to Oxidative Stress In Vitro in Pathophysiology of Mitochondrial Short-Chain Acyl-CoA Dehydrogenase Deficiency: Response to Antioxidants.
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- PLoS ONE, 2011, v. 6, n. 4, p. 1, doi. 10.1371/journal.pone.0017534
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- Publication type:
- Article
Differential Cellular Handling of Defective Arginine Vasopressin (AVP) Prohormones in Cells Expressing Mutations of the AVP Gene Associated with Autosomal Dominant and Recessive Familial Neurohypophyseal Diabetes Insipidus.
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- Journal of Clinical Endocrinology & Metabolism, 2004, v. 89, n. 9, p. 4521, doi. 10.1210/jc.2003-031813
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- Article
Autosomal Dominant Neurohypophyseal Diabetes Insipidus due to Substitution of Histidine for Tyrosine<sub>2</sub> in the Vasopressin Moiety of the Hormone Precursor.
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- Journal of Clinical Endocrinology & Metabolism, 2002, v. 87, n. 7, p. 3351, doi. 10.1210/jcem.87.7.8677
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- Article
Clinical and Molecular Evidence of Abnormal Processing and Trafficking of the Vasopressin Preprohormone in a Large Kindred with Familial Neurohypophyseal Diabetes Insipidus due to A Signal Peptide Mutation.
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- Journal of Clinical Endocrinology & Metabolism, 1999, v. 84, n. 8, p. 2933, doi. 10.1210/jcem.84.8.5869
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- Article
Heat-Shock Protein 70 Genes and Human Longevity.
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- Annals of the New York Academy of Sciences, 2006, v. 1067, n. 1, p. 301, doi. 10.1196/annals.1354.040
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- Article
Quantitative proteomics suggests metabolic reprogramming during ETHE1 deficiency.
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- Proteomics, 2016, v. 16, n. 7, p. 1166, doi. 10.1002/pmic.201500336
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- Article
A novel variation in the AVP gene resulting in familial neurohypophyseal diabetes insipidus in a large Italian kindred.
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- Pituitary, 2013, v. 16, n. 2, p. 152, doi. 10.1007/s11102-012-0392-x
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- Publication type:
- Article
The ACADS gene variation spectrum in 114 patients with short-chain acyl-CoA dehydrogenase (SCAD) deficiency is dominated by missense variations leading to protein misfolding at the cellular level.
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- Human Genetics, 2008, v. 124, n. 1, p. 43, doi. 10.1007/s00439-008-0521-9
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- Publication type:
- Article
Short/branched-chain acyl-CoA dehydrogenase deficiency due to an IVS3+3A>G mutation that causes exon skipping.
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- Human Genetics, 2006, v. 118, n. 6, p. 680, doi. 10.1007/s00439-005-0070-4
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- Publication type:
- Article
Genomic structure of the human mitochondrial chaperonin genes: HSP60 and HSP10 are localised head to head on chromosome 2 separated by a bidirectional promoter.
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- 2003
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- Publication type:
- Erratum
Genomic structure of the human mitochondrial chaperonin genes: HSP60 and HSP10 are localised head to head on chromosome 2 separated by a bidirectional promoter.
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- Human Genetics, 2003, v. 112, n. 1, p. 71, doi. 10.1007/s00439-002-0837-9
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- Publication type:
- Article
Bioenergetic and Proteomic Profiling of Immune Cells in Myalgic Encephalomyelitis/Chronic Fatigue Syndrome Patients: An Exploratory Study.
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- Biomolecules (2218-273X), 2021, v. 11, n. 7, p. 961, doi. 10.3390/biom11070961
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- Publication type:
- Article
Beyond Secularist Supersessionism: Risk, Religion and Technology.
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- Ecotheology: Journal of Religion, Nature & the Environment, 2006, v. 11, n. 2, p. 137, doi. 10.1558/ecot.2006.11.2.137
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- Publication type:
- Article
Six novel mutations in the arginine vasopressin gene in 15 kindreds with autosomal dominant familial neurohypophyseal diabetes insipidus give further insight into the pathogenesis.
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- European Journal of Human Genetics, 2004, v. 12, n. 1, p. 44, doi. 10.1038/sj.ejhg.5201086
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- Publication type:
- Article
Limb-girdle muscular dystrophy 2I: phenotypic variability within a large consanguineous Bedouin family associated with a novel FKRP mutation.
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- European Journal of Human Genetics, 2004, v. 12, n. 1, p. 38, doi. 10.1038/sj.ejhg.5201087
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- Publication type:
- Article
Deep incarnation: From deep history to post-axial religion.
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- Hervormde Teologiese Studies, 2016, v. 72, n. 4, p. 1, doi. 10.4102/hts.v72i4.3428
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- Article
Resilient selves: A theology of resonance and secularity.
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- Dialog: A Journal of Theology, 2020, v. 59, n. 2, p. 93, doi. 10.1111/dial.12568
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- Article
The corona crisis unmasks prevailing social ideologies.
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- Dialog: A Journal of Theology, 2020, v. 59, n. 2, p. 73, doi. 10.1111/dial.12558
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- Article
Endangered Selves and Societies: Theologies of Tragedy and Disaster.
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- 2017
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- Publication type:
- Editorial
Positive Loss and Tragic Memory: On the Preservation of Community.
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- Dialog: A Journal of Theology, 2017, v. 56, n. 4, p. 361, doi. 10.1111/dial.12356
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- Article
Sola Scriptura: The Inclusive Principle.
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- 2016
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- Publication type:
- Editorial
The Emotional Christ: Bonaventure and Deep Incarnation<sup>1</sup>.
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- Dialog: A Journal of Theology, 2016, v. 55, n. 3, p. 247, doi. 10.1111/dial.12261
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- Publication type:
- Article
Deep Incarnation and Kenosis: In, With, Under, and As: A Response to Ted Peters.
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- Dialog: A Journal of Theology, 2013, v. 52, n. 3, p. 251, doi. 10.1111/dial.12050
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- Publication type:
- Article