RESEARCH BASE

Search 3,721 documents across 34 fields — every claim tier-rated by evidence

3,721 Documents 34 Sections 43,625 Citations 34,852 Keywords Indexed 4 Evidence Tiers

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.

1,426 results for "Su Song" — page 28 of 72

ZF_1_17 Credible Oceanography

ZF_1_17 — Abyssal Trench Biogeography

Hadal trenches — oceanic depressions exceeding 6,000 m depth, formed by tectonic subduction — represent Earth's deepest and least explored biomes, harboring unique ecosystems under extreme pressures (600–1,100 atm), perp

hadal-zone ocean-trenches abyssal-ecology deep-sea-biogeography barophiles piezophiles
ZF_1_03 Verified Oceanography

ZF_1_03 — Seafloor Spreading, Plate Tectonics and Marine Geology

The discovery that the ocean floor is not ancient and static but young, dynamic, and continuously recycled revolutionized Earth science in the 20th century. Seafloor spreading — proposed by Harry Hess (1962) and confirme

seafloor spreading plate tectonics mid-ocean ridge subduction zone Mariana Trench seamount
Z_5_13 Verified Molecular Biology

Z_5_13 — Molecular Clocks: Timing Evolution at the Sequence Level

Molecular clocks — the observation that DNA and protein sequences accumulate substitutions (mutations that become fixed in a lineage) at approximately regular rates over long periods of evolutionary time, enabling the es

molecular clock neutral theory substitution rate Zuckerkandl Pauling calibration
Z_5_04 Verified Molecular Biology

Z_5_04 — Structural Biology: Seeing Molecules at Atomic Resolution

Structural biology — the determination of the three-dimensional atomic structures of biological macromolecules (proteins, nucleic acids, and their complexes) — has been one of the most transformative disciplines in moder

structural biology X-ray crystallography cryo-EM NMR spectroscopy protein structure resolution revolution
Z_5_23 Verified Molecular Biology

Z_5_23 — Gene Drives: CRISPR-Based Inheritance Manipulation and Ecological Engineering

A gene drive is a genetic engineering technology that biases inheritance in sexually reproducing organisms, causing a modified gene to spread through a population at rates far exceeding normal Mendelian inheritance (~50%

gene drive CRISPR mutagenic chain reaction malaria Anopheles population suppression
Z_5_07 Verified Molecular Biology

Z_5_07 — Epigenome Mapping: Charting the Chemical Modifications of DNA and Chromatin

Epigenome mapping — the systematic, genome-wide identification and quantification of epigenetic modifications (chemical marks on DNA and histone proteins that regulate gene expression without changing the underlying DNA

epigenome DNA methylation bisulfite sequencing ATAC-seq ChIP-seq histone modification
Z_3_12 Verified Molecular Biology

Z_3_12 — Genetics of Alcohol Metabolism

The genetics of alcohol metabolism provides one of the clearest examples of how specific genetic variants influence behavior and disease risk at a population scale. Ethanol is metabolized primarily through a two-step oxi

alcohol metabolism ADH1B ALDH2 acetaldehyde Asian flush alcohol dehydrogenase
Z_3_08 Verified Molecular Biology

Z_3_08 — Genetics of Taste and Smell

Taste and smell perception are profoundly shaped by genetics, with variation in chemosensory receptor genes producing dramatically different sensory worlds between individuals. The olfactory receptor (OR) gene family — d

taste genetics olfactory genetics olfactory receptor OR genes gustatory receptor TAS2R
Z_3_06 Verified Molecular Biology

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

circadian rhythm clock genes CLOCK BMAL1 PER CRY
Z_2_15 Verified Molecular Biology

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

future genomics personalized medicine precision medicine polygenic risk scores whole genome sequencing newborn screening
Z_2_10 Verified Molecular Biology

Z_2_10 — Genetics of Aging and Progeria

Aging — the progressive decline in physiological function leading to increased vulnerability to disease and death — has a substantial genetic component: twin studies estimate heritability of human lifespan at ~25–30% (He

aging genetics progeria Hutchinson-Gilford progeria HGPS LMNA lamin A
Z_2_14 Verified Molecular Biology

Z_2_14 — Genetics of Longevity and Blue Zones

The genetics of human longevity — why some individuals live past 100 while most do not — is a field where heritability is modest, effect sizes are small, and environmental factors dominate, yet several genetic pathways h

longevity genetics aging centenarians Blue Zones telomeres telomerase
Z_2_11 Verified Molecular Biology

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

major histocompatibility complex MHC HLA human leukocyte antigen adaptive immunity antigen presentation
Z_2_16 Verified Molecular Biology

Z_2_16 — Cancer Genomics & Precision Oncology

Cancer genomics — the comprehensive analysis of the genetic alterations that drive cancer initiation, progression, and resistance to therapy — has transformed oncology from a tissue-of-origin classification system into a

cancer genomics precision oncology tumor sequencing oncogene tumor suppressor somatic mutation
Z_2_01 Verified Molecular Biology

Z_2_01 — HLA System & Archaic Immune Inheritance

The Human Leukocyte Antigen (HLA) system is the most polymorphic region of the human genome, encoding cell-surface proteins critical to adaptive immune function. Located on chromosome 6p21.3, the Major Histocompatibility

HLA human leukocyte antigen MHC major histocompatibility complex archaic introgression Denisovan
Z_1_13 Verified Molecular Biology

Z_1_13 — DNA Repair Mechanisms and Genome Stability

Every human cell sustains an estimated 10,000–100,000 DNA lesions per day from endogenous sources alone — oxidative metabolism, spontaneous hydrolysis, replication errors, and reactive metabolites — while environmental m

DNA repair base excision repair nucleotide excision repair mismatch repair double-strand break homologous recombination
Z_1_12 Verified Molecular Biology

Z_1_12 — Genome Architecture and 3D Organization

The human genome — approximately 6.4 billion base pairs of DNA — is packed into a nucleus only ~6 μm in diameter. If stretched end-to-end, the DNA of a single human cell would extend about 2 meters, yet it is packaged an

genome architecture 3D genome chromatin organization topologically associating domains TADs chromosome territories
Z_1_11 Verified Molecular Biology

Z_1_11 — Polyploidy and Genome Duplication

Polyploidy — the possession of more than two complete sets of chromosomes — is a major force in genome evolution, particularly in plants and some animal lineages. Susumu Ohno (1970) proposed that whole genome duplication

polyploidy genome duplication whole genome duplication WGD autopolyploidy allopolyploidy
Z_4_21 Verified Molecular Biology

Z_4_21 — Autophagy Mechanisms

Autophagy (from Greek, "self-eating") is a fundamental cellular process by which eukaryotic cells degrade and recycle their own components — damaged organelles, protein aggregates, intracellular pathogens, and surplus cy

autophagy autophagosomes lysosome Ohsumi ATG genes mTOR
Z_4_12 Verified Molecular Biology

Z_4_12 — Autophagy: The Cell's Self-Eating Recycling System

Autophagy (from Greek auto "self" + phagein "to eat") — the process by which cells degrade and recycle their own components — is a fundamental cellular quality control and survival mechanism conserved from yeast to human

autophagy Ohsumi lysosome mTOR autophagosome protein degradation