RESEARCH BASE
Search 3,721 documents across 34 fields — every claim tier-rated by evidence
3,633 are the core, quality-scored corpus (34 lettered sections — see How We Work); the remaining 88 are cross-corpus synthesis documents (68 InterDocs, 12 Connections, 8 Theories) also indexed here.
2,448 results for "Shang Di" — page 9 of 123
Z_5_10 — Genome Editing Beyond CRISPR: TALENs, Base Editors, Prime Editors, and Next-Generation Tools
While CRISPR-Cas9 (covered in Z_1_02) dominates the genome editing landscape, it is neither the first nor the only precision genome editing technology. The field began with zinc finger nucleases (ZFNs) in the early 2000s
Z_5_08 — Mitochondrial DNA: Maternal Inheritance, Ancient Lineages, and Disease
Mitochondrial DNA (mtDNA) — the small, circular genome (~16,569 base pairs in humans) contained within mitochondria — encodes 37 genes essential for oxidative phosphorylation (13 protein-coding genes, 22 transfer RNAs, 2
Z_3_06 — Genetics of Circadian Rhythms
Circadian rhythms — endogenous ~24-hour oscillations in physiology and behavior — are generated by an intracellular transcription-translation feedback loop (TTFL) encoded by a set of core clock genes conserved across ani
Z_2_15 — Future of Genomics and Personalized Medicine
Genomics is undergoing a transition from research tool to clinical infrastructure. The cost of whole-genome sequencing (WGS) has plummeted from $2.7 billion (Human Genome Project, 1990–2003) to ~$200 per genome (Illumina
Z_2_13 — Pharmacogenomics and Personalized Medicine
Pharmacogenomics — the study of how genetic variation influences drug response — is among the most clinically actionable applications of human genetics. Adverse drug reactions (ADRs) are the 4th–6th leading cause of deat
Z_2_17 — Prion Biology: Self-Propagating Protein Misfolding and Transmissible Encephalopathies
Prions — proteinaceous infectious particles lacking nucleic acid — represent a paradigm-shattering departure from the central dogma that biological information flows from DNA to RNA to protein. The protein-only hypothesi
Z_2_18 — Pharmacogenomics and Precision Medicine
Pharmacogenomics — the study of how genetic variation affects individual responses to drugs — aims to replace the "one-size-fits-all" prescribing model with genotype-guided therapy, selecting the right drug at the right
Z_2_09 — Mitochondrial Genetics and Diseases
Human mitochondrial DNA (mtDNA) is a 16,569-bp circular genome encoding 37 genes: 13 proteins (all subunits of the oxidative phosphorylation/OXPHOS complexes I, III, IV, and V), 22 transfer RNAs, and 2 ribosomal RNAs. Un
Z_2_04 — Genetic Disorders and Inborn Errors of Metabolism
Genetic disorders — diseases caused by mutations in single genes (monogenic) or chromosomal abnormalities — affect ~3–5% of live births and collectively represent thousands of distinct conditions catalogued in the Online
Z_2_06 — Nutrigenomics and Diet-Gene Interactions
Nutrigenomics — the study of how genetic variation influences nutritional requirements, dietary responses, and disease susceptibility — and its complement nutrigenetics (how diet influences gene expression) represent a r
Z_2_11 — Genetics of Immunity and MHC Diversity
The major histocompatibility complex (MHC) — known as the human leukocyte antigen (HLA) system in humans — is the most polymorphic gene region in the human genome, encoding cell-surface glycoproteins essential for adapti
Z_2_07 — Genetics of Disease Resistance
Infectious disease has been the most powerful selective force shaping the human genome, leaving signatures across thousands of loci. The best-understood example is sickle cell disease (HbS, Glu6Val in HBB): heterozygous
Z_1_19 — Non-Coding RNA and Gene Regulation
Non-coding RNAs (ncRNAs) — RNA molecules that are transcribed from the genome but do not encode proteins — have emerged as central regulators of gene expression, challenging the classical "one gene–one protein" paradigm
Z_4_18 — Protein Misfolding and Prion Diseases
Prion diseases — transmissible spongiform encephalopathies (TSEs) — are fatal neurodegenerative disorders caused by the misfolding and self-propagating aggregation of a normal cellular protein (PrPᶜ) into a pathological
Z_4_17 — Non-coding RNA Networks: Regulation Beyond the Genome
Non-coding RNAs (ncRNAs) — RNA molecules that are not translated into protein but perform functional roles in the cell — have emerged since the late 1990s as a vast and previously unsuspected layer of biological regulati
K_3_14 — Consciousness in Octopuses and Distributed Nervous Systems
Octopuses (Octopus vulgaris, O. bimaculoides, Abdopus aculeatus, and ~300 other species in order Octopoda) represent perhaps the most profound natural experiment in the evolution of consciousness: they are the most cogni
K_4_12 — Noosphere — Teilhard de Chardin, Vernadsky, and the Thinking Layer
The noosphere ("sphere of mind") is a concept developed independently by Russian geochemist Vladimir Vernadsky and French paleontologist-priest Pierre Teilhard de Chardin in the 1920s, describing a layer of collective hu
K_2_18 — Meditation Neurophysiology
Neuroimaging studies of meditation have produced a convergent picture: focused attention practices increase prefrontal and anterior cingulate cortex activity, open monitoring practices decrease default mode network (DMN)
K_2_20 — Savant Syndrome — Neuroscience of Extraordinary Ability
Savant syndrome — the coexistence of extraordinary ability in a specific domain with significant cognitive disability or neurodevelopmental condition — was first described medically by J. Langdon Down (the physician who
K_5_11 — Synaesthesia and Consciousness: Cross-Modal Binding
Synaesthesia (British spelling; "synesthesia" in American English) is a neurological condition in which stimulation of one sensory or cognitive pathway automatically triggers an involuntary experience in a second, unstim
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