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.

3,447 results for "Guelb er Richat" — page 115 of 173

Z_3_03 Verified Molecular Biology

Z_3_03 — Ancient Pathogen Genomics — Plague, TB, Smallpox DNA

Ancient pathogen genomics — the recovery and sequencing of disease-causing organism DNA from archaeological remains — has revolutionized understanding of human disease history. Beginning with the landmark reconstruction

ancient pathogen paleomicrobiology Yersinia pestis plague Black Death Justinianic plague
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_04 Verified Molecular Biology

Z_3_04 — Comparative Genomics and Cross-Species Analysis

Comparative genomics — the systematic comparison of genome sequences across species — has become the primary tool for understanding genome evolution, identifying functionally important sequences, and reconstructing the T

comparative genomics genome sequencing synteny ortholog paralog conserved element
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_3_05 Verified 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 Verified 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_03 Verified 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 Verified 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_18 Verified Molecular Biology

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

pharmacogenomics precision-medicine drug-metabolism cyp450 warfarin adverse-drug-reactions
Z_2_09 Verified Molecular Biology

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

mitochondrial genetics mtDNA mitochondrial DNA mitochondrial disease oxidative phosphorylation OXPHOS
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_00 Molecular Biology

Z_2_00 — Medical Genetics Health: Subfolder Summary

Z_2_07 Verified Molecular Biology

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

disease resistance natural selection pathogen-driven selection sickle cell malaria resistance HbS
Z_2_23 Verified Molecular Biology

Z_2_23 — Immune System & Immunology

The immune system is a multi-layered defense network that protects organisms against pathogens including bacteria, viruses, fungi, and parasites. It comprises two interconnected arms: innate immunity, which provides rapi

immune system innate immunity adaptive immunity T cells B cells antibodies
Z_1_08 Verified Molecular Biology

Z_1_08 — Transposons and Mobile Genetic Elements

Transposable elements (TEs, transposons) — segments of DNA that can move or copy themselves to new genomic locations — are among the most abundant and influential components of eukaryotic genomes. Discovered by Barbara M

transposon mobile genetic element transposable element jumping gene Barbara McClintock retrotransposon
Z_1_02 Verified Molecular Biology

Z_1_02 — Human Chromosome 2 Fusion — Evidence of Primate Ancestry

Humans possess 46 chromosomes (23 pairs), while all other great apes — chimpanzees, gorillas, and orangutans — possess 48 chromosomes (24 pairs). This discrepancy was explained in the 1980s–1990s when molecular cytogenet

chromosome 2 chromosome fusion telomere-telomere ancestral chromosomes primate karyotype great ape
Z_1_16 Verified Molecular Biology

Z_1_16 — Transposable Elements: Jumping Genes and Genome Evolution

Transposable elements (TEs) — sequences of DNA capable of moving ("jumping") from one genomic location to another — constitute approximately 45% of the human genome and up to 85% of the maize genome, making them the sing

transposable elements jumping genes Barbara McClintock retrotransposons DNA transposons Alu elements
Z_1_04 Verified Molecular Biology

Z_1_04 — Gene Expression and Regulation

Gene expression regulation — the molecular mechanisms controlling when, where, and how much each gene is active — is the central process that enables a single genome to produce ~200 distinct cell types, orchestrate embry

gene expression regulation transcription factors promoter enhancer epigenetics
Z_1_01 Verified Molecular Biology

Z_1_01 — ENCODE Project, Non-Coding DNA & Epigenetics

The human genome is ~3.2 billion base pairs long, but only ~1.5% encodes proteins. The remaining ~98.5% was once dismissed as "junk DNA." The ENCODE Project (2003–present) revealed that at least 80% of the genome has bio

ENCODE non-coding DNA junk DNA epigenetics regulatory elements endogenous retrovirus