RESEARCH BASE

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

3,721 Documents 34 Sections 43,623 Citations 34,854 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.

1,680 results for "po tolo" — page 36 of 84

Z_3_14 Verified Molecular Biology

Z_3_14 — Behavioral Genetics and the Genetics of Aggression

Behavioral genetics investigates the relative contributions of genetic and environmental factors to variation in behavior — including aggression, impulsivity, risk-taking, anxiety, sociability, and cognitive traits. Twin

behavioral genetics aggression MAOA warrior gene serotonin dopamine
Z_3_07 Molecular Biology

Z_3_07 — Gene Drive Technology

Gene drives are genetic systems that bias their own inheritance to spread through a population at rates exceeding normal Mendelian expectations (~50% → ~99% transmission). Natural selfish genetic elements (transposons, m

gene drive CRISPR gene drive selfish genetic element meiotic drive super-Mendelian inheritance Anopheles
Z_3_12 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_16 Verified Molecular Biology

Z_3_16 — Genomic Conflict and Selfish Genetic Elements

Selfish genetic elements (SGEs) — sequences of DNA that promote their own transmission at the expense of the host organism or other genes in the genome — reveal that the genome is not a cooperating community of genes but

selfish-genetic-elements genomic-conflict transposable-elements meiotic-drive gene-drive intragenomic-conflict
Z_3_02 Molecular Biology

Z_3_02 — Epigenetic Inheritance & Transgenerational Effects

Epigenetic inheritance refers to the transmission of phenotypic information across generations through mechanisms other than changes in DNA sequence. The three primary molecular mechanisms — DNA methylation, histone modi

epigenetics transgenerational inheritance DNA methylation histone modification Dutch Hunger Winter Överkalix
Z_3_09 Molecular Biology

Z_3_09 — Conservation Genetics and Endangered Species

Conservation genetics applies population genetics, genomics, and molecular biology to the preservation of biological diversity. At its core is the recognition that genetic diversity — the raw material for adaptation to c

conservation genetics endangered species genetic diversity inbreeding depression effective population size genetic drift
Z_3_10 Molecular Biology

Z_3_10 — Genetics of Athletic Performance

Athletic performance is a highly polygenic trait with substantial heritability — twin studies estimate heritability of VO2max (maximal oxygen uptake) at ~50% (Bouchard et al., 1999, HERITAGE Family Study), muscle fiber c

sports genetics ACTN3 alpha-actinin-3 ACE angiotensin converting enzyme VO2max heritability
Z_3_11 Molecular Biology

Z_3_11 — Genetic Mosaicism and Chimerism

A fundamental assumption of genetics — that every cell in an individual's body carries the same genome — is wrong. Genetic mosaicism (the presence of two or more genetically distinct cell populations within an individual

genetic mosaicism somatic mosaicism chimerism tetragametic chimera microchimerism fetal microchimerism
Z_3_05 Molecular Biology

Z_3_05 — Viral Integration and Endogenous Retroviruses

Approximately 8% of the human genome consists of human endogenous retroviruses (HERVs) — the remnants of ancient retroviral infections that integrated into germline cells and were subsequently inherited vertically like a

endogenous retrovirus ERV HERV viral integration retrovirus reverse transcriptase
Z_3_01 Molecular Biology

Z_3_01 — Genetics of Brain Development — ASPM, Microcephalin, HAR1

The human brain is approximately three times larger than expected for a primate of our body size, with a vastly expanded cerebral cortex containing ~86 billion neurons. Identifying the genetic basis for this extraordinar

ASPM microcephalin MCPH1 HAR1 human accelerated regions brain evolution
Z_2_15 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_13 Molecular Biology

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

pharmacogenomics pharmacogenetics personalized medicine precision medicine CYP2D6 CYP2C_5_04
Z_2_03 Molecular Biology

Z_2_03 — Pharmacogenomics & Ethnobotanical Genetics

Pharmacogenomics — the study of how genetic variation affects drug response — has revealed that enzymes governing drug metabolism, particularly the cytochrome P450 (CYP) superfamily, show extraordinary population-specifi

pharmacogenomics ethnobotany CYP2D6 cytochrome P450 drug metabolism traditional medicine
Z_2_08 Molecular Biology

Z_2_08 — Prion Genetics and Misfolded Proteins

Prions are infectious agents composed entirely of misfolded protein — the only known pathogen that contains no nucleic acid (no DNA, no RNA). The protein-only hypothesis (Stanley Prusiner, 1982 — Nobel Prize 1997) states

prion PRNP PrP PrPSc PrPC prion diseases
Z_2_17 Verified Molecular Biology

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

prion PrPSc PrPC transmissible spongiform encephalopathy Stanley Prusiner mad cow disease
Z_2_12 Molecular Biology

Z_2_12 — Genetics of Pain Perception

Pain perception — the subjective experience triggered by actual or potential tissue damage — varies enormously across individuals, with genetic factors accounting for 25–50% of the variance in pain sensitivity (twin stud

pain genetics nociception SCN9A Nav1.7 congenital insensitivity to pain TRPV1
Z_2_14 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 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_1_07 Molecular Biology

Z_1_07 — Genetic Recombination and Crossing Over

Genetic recombination — the physical exchange of DNA segments between homologous chromosomes during meiosis — is a fundamental biological process that generates genetic diversity, ensures proper chromosome segregation, a

recombination crossing over meiosis chiasma homologous recombination linkage