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.

3,436 results for "mtDNA haplogroup B" — page 106 of 172

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_12 Verified 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_06 Credible Molecular Biology

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

nutrigenomics nutrigenetics diet-gene interaction lactase persistence alcohol metabolism folate metabolism
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_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_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_06 Verified Molecular Biology

Z_1_06 — Sex Determination Genetics

Sex determination — the biological process that establishes whether an organism develops as male, female, or an alternative reproductive type — employs remarkably diverse mechanisms across the tree of life. In placental

sex determination sex chromosomes X chromosome Y chromosome SRY gene X-inactivation
Z_1_17 Verified Molecular Biology

Z_1_17 — Environmental Epigenetics & Toxicogenomics

Environmental epigenetics examines how chemical exposures, nutritional states, and ecological stressors modify gene expression without altering DNA sequence — through DNA methylation, histone modifications, and non-codin

epigenetics toxicogenomics endocrine disruptors PFAS transgenerational inheritance DNA methylation
Z_1_18 Verified Molecular Biology

Z_1_18 — Junk DNA & the ENCODE Controversy: Function, Noise, and the Human Genome

The term "junk DNA" — coined by Susumu Ohno (1972) to describe non-coding DNA sequences in eukaryotic genomes that appeared to have no functional role — ignited one of the most contentious debates in modern genomics: how

junk DNA ENCODE non-coding DNA transposable elements selfish DNA C-value paradox
Z_1_05 Verified Molecular Biology

Z_1_05 — Genomic Imprinting and Parent-of-Origin Effects

Genomic imprinting is an epigenetic phenomenon in which a gene's expression depends on whether it was inherited from the mother or the father — violating the standard Mendelian assumption that both parental copies functi

genomic imprinting parent-of-origin effect epigenetics DNA methylation imprinting control region ICR
Z_1_03 Verified Molecular Biology

Z_1_03 — Human Genome Project and Its Legacy

The Human Genome Project (HGP), launched in 1990 and completed in 2003, was the largest coordinated biological research effort in history — a $3 billion, 13-year international collaboration to sequence all ~3.2 billion b

Human Genome Project HGP genome sequencing Francis Collins Craig Venter Celera
Z_1_00 Molecular Biology

Z_1_00 — Genome Structure Organization: Subfolder Summary

Z_1_10 Verified Molecular Biology

Z_1_10 — Chromosome Evolution and Karyotype

Karyotype — the number, size, and morphology of chromosomes in a cell — varies enormously across species, from n=1 in the ant Myrmecia pilosula to n=630 in the fern Ophioglossum reticulatum. Humans have 2n=46 (23 pairs),

chromosome evolution karyotype chromosome number Robertsonian translocation chromosome fusion human chromosome 2
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_00 Molecular Biology

Z_4_00 — RNA Protein Cell Biology: Subfolder Summary

Z_4_02 Verified Molecular Biology

Z_4_02 — Stem Cells and Pluripotency

Stem cells — defined by the dual capacity for self-renewal (division producing at least one daughter cell retaining stemness) and differentiation (specialization into distinct cell types) — are the foundational building

stem cell pluripotency embryonic stem cell induced pluripotent stem cell iPSC Yamanaka factors