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Chromosome Mutation Books

Human Genetics, 12th edition

Author: Ricki Lewis

School: National Open University of Nigeria

Department: Agriculture and Veterinary Medicine

Course Code: ANP312

Topics: Human Genetics, genomics, genomes, cells, cell components, cell division, cell death, stem cells, human microbiome, transmission genetics, meiosis, development, aging, reproductive system, gametes, prenatal development, birth defects, maturation, pedigree analysis, Mendel's law, mitochondrial genes, Sex-influenced traits, DNA structure, DNA replication, Sequencing DNA, multifactorial traits, genes, behavior, sleep, intelligence, intellectual disability, drug addiction, mood disorders, Schizophrenia, autism, Gene action, protein translation, gene expression, epigenetics, gene mutation, allelic diseases, population genetics, Constant Allele Frequencies, Nonrandom Mating, genetic drift, mutation, natural selection, eugenics, human ancestry, human origins, immunity genetics, human immune system, altering immunity, abnormal immunity, patenting DNA, modifying DNA, monitoring gene function, gene silencing, genome edition, genetic technology, genetic testing, genetic treatment, genetic counselling, Treating Genetic Disease, cancer genetics, reproductive technologies, infertility, subfertility, assisted reproductive technologies, extra embryos, personal genome sequencing

Principles of genetics and genetic counselling

Author: Mohammed Abdulkadir

School: University of Ilorin

Department: Medical, Pharmaceutical and Health science

Course Code: PAEDIATRICS

Topics: Character, trait, phenotype, genotype, locus, alleles, mutation, polymorphism, Homozygote, Heterozygote, Hemizygote, Medical Genetics, Medical Genetics, Chromosomes, Genes, mitosis, meiosis, cell division, Mendelian Genetics, Gregor Mendel, pedigree analysis, Heredity, Achondroplasia, autosomal recessive diseases, X-linked Recessive, X-linked dominant inheritance

Inherited Haemolytic Anaemia Sickle cell disease

Author: Haematology

School: University of Ilorin

Department: Medical, Pharmaceutical and Health science

Course Code: HAEMATOLOGY

Topics: Sickle Mutation, HAPLOTYPE DISTRIBUTION, KUWAITI BETA S CHROMOSOMES, HAND AND FOOT SYNDROME, Painful vaso-occlusive crisis, Visceral sequestration crises, Aplastic crises, Bone marrow transplantation, Allogeneic bone marrow transplantation, Gene therapy, Hydroxyurea, Sickling test, Priapism

Essentials of Medical Biochemistry ,Second Edition With Clinical Cases

Author: NV Bhagavan, Chung-Eun Ha

School: University of Ilorin

Department: Medical, Pharmaceutical and Health science

Course Code: BCH303

Topics: Organ Systems, Cells, Organelles, Microbiota, Organ Systems, Water, Acids, Bases, Buffers, H+ Concentration, Disorders of Protein Misfolding, Protein Structure, Precursor Proteins, active protein, Proteolysis, Protease Inhibitors, Protein Folding, Autophagy, Protein Misfolding, Fibrillogenic Diseases, Chemical Kinetics, Thermodynamics, Enzymes, Enzyme RegulationActive Site, Enzyme–Substrate Complex, Michaelis–Menten Model, Enzyme-Catalyzed Reactions, Irreversible Inhibition, Inhibition, Clinical Enzymology, Biomarkers of Tissue Injury, Tissue Injury, Serum, Plasma Markers, Tissue Damage, Simple Carbohydrates, Simple Carbohydrates, Heteropolysaccharides, Glycoconjugates, Glycoproteins, Glycolipids, Cell Membrane Constituents, Cell-Surface Glycoproteins, Serum Glycoproteins, Connective Tissue, Fibrous Protein, Nonfibrous Protein, Proteoglycan, Gastrointestinal Digestion, Gastrointestinal Absorption, Gastrointestinal Tract, Gastrointestinal Hormones, Carbohydrate Metabolism, Glycolysis, Tricarboxylic Acid Cycle, Glycolysis, Pyruvate Metabolism, Tricarboxylic Acid Cycle, Electron Transport Chain, Oxidative Phosphorylation, Oxygen-Consuming Systems, Mitochondrial Structure, Mitochondrial Genome, Respiratory Chain Expression, Mitochondrial Diseases, Gluconeogenesis, Glycogen Synthesis, glycogen Breakdown, Alternative Pathways, Hexose Interconversion, Amino Acid Metabolism, Metabolism of Ammonia, Lipid, fatty acid, Eicosanoid, Fatty Acid Oxidation, Unsaturated Fatty Acid, Trans-Fatty Acid, Essential Fatty Acid, Phospholipids, Glycosphingolipids, Cholesterol, Phosphatidylcholine, Phosphosphingolipid, Catabolism, Storage Disorders of Sphingolipids, Sphingolipids, Acetyl-Coa, Hmg-Coa, Plasma Lipoprotein, Contractile Systems, Muscle Systems, Nonmuscle Systems, Energy Metabolism, Obesity, Diabetes Mellitus, Chromosomes, Chromatin, DNA, Recombinant DNA Technology, DNA Replication, DNA Repair, DNA Mutation, Protein Synthesis, RNA, Messenger RNA, Prokaryotic Transcription, Genetic Code, tRNA Molecule, Ribosomes, Gene Expression, mRNA Synthesis, Gene Regulation, Nucleotide Metabolism

Bacterial genetics and variation

Author: IN Nwafia

School: University of Nigeria, Nsukka

Department: Medical, Pharmaceutical and Health science

Course Code: MIC301

Topics: Gene, Genetic variation, Heredity, Genome, Phenotype, Genotype, Genotypic variation, DNA structure, RNA Structure, DNA, RNA, Bacterial chromosome.Transposons, Jumping genes, plasmid, Gene Expression, Protein synthesis, GENETIC VARIATION, mutation, GENETIC EXCHANGE, Mutagenes

Principles of genetics

Author: TNAU

School: University of Nigeria, Nsukka

Department: Science and Technology

Course Code: BIO101

Topics: Genetics, Mendel’s laws of inheritance, gene action, multiple alleles, Multiple factor hypothesis, Quantitative traits, Qualitative traits, Cytoplasmic inheritance, mutation, Regulation Gene expression, Lac operon, Fine structure of Gene, chromosome structure, mitosis, meiosis, DNA, RNA, DNA Transcription, DNA Translation, Genetic code, protein synthesis, Numerical chromosomal aberrations, Polyploidy, Structural chromosomal aberrations

Principles of Genetics, 7th edition

Author: Robert Tamarin

School: University of Nigeria, Nsukka

Department: Science and Technology

Course Code: BIO101

Topics: Genetics, Mendelism, chromosomal theory, mitosis, meiosis, sex determination, sex linkage, pedigree analysis, cytogenetics, molecular genetics, gene expression, DNA,DNA mutation, genomics, DNA recombination, DNA repair, biotechnology, recombinant DNA, Gene expression, Eukaryotic chromosome, Non-Mendelian inheritance, Quantitative genetic, evolutionary genetics, Quantitative inheritance, population genetics, Hardy Weinberg Equilibrium, mating systems, evolution, speciation

The genetic (Cell biology ) Basis of cancer

Author: Pharmacology

School: University of Ilorin

Department: Medical, Pharmaceutical and Health science

Course Code: PHARMACOLOGY400

Topics: cancerous cells, Hematoxylin stain, eosin stain, Cell Cycle Checkpoints, Cyclins, Tumor Cells, Programmed Cell Death, Oncogenes, Tumor-Inducing Retroviruses, Viral Oncogenes, Rous sarcoma virus, Proto-Oncogenes, Viral Oncogenes, Normal Ras Protein Signaling, Mutant Ras Protein, Chromosome Rearrangements, Philadelphia Chromosome, Burkitt’s Lymphoma, Knudson’s Two-Hit Hypothesis, Tumor Suppressor Proteins, Apoptosis, T-DNA transfer

Immunology and Evolution of Infectious Disease

Author: Steven Frank

School: Edo University

Department: Medical, Pharmaceutical and Health science

Course Code: BCH224

Topics: Immunology, Infectious Disease evolution, Vertebrate Immunity, nonspecific immunity, specific immunity, antigens, epitopes, antibodies, Antigenic Variation, Specificity, Cross-Reactivity, Antigens, Antibody Epitopes, Antibody Paratopes, Antibody Affinity Maturation, Natural Antibodies, mutation, hypermutation, Intragenomic Recombination, Immunodominance, Antibody Immunodominance, CTL Immunodominance, Immune Regulation, Immunological Memory, Immunodominance of Memory, Antigenic Linkage Disequilibrium, Antigenicity, Phylogeny, Experimental Evolution, Antibody Escape Mutants, cell binding, cell tropism, Experimental Evolution, influenza, Antibody Escape Mutants

Color Atlas of Clinical Hematology Molecular and Cellular Basis of Disease ,fifth edition

Author: Victor Hoffbrand, Paresh Vyas, Elias Campo, Torsten Haferlach, Keith Gomez

School: University of Nigeria, Nsukka

Department: Medical, Pharmaceutical and Health science

Course Code: HEM301, HEM401, HEM402, HEM403

Topics: Gene Transcription, Messenger RNA, DNA Mutation, gene expression, Lineage Commitment, Micro-RNAs, Regulatory Noncoding RNAs, DNA Replication, Telomeres, Cell Cycle, Apoptosis, Cellular Debris, Lysosomes, Protein Ubiquitination,  Clonal Hematologic Disorders, Erythropoiesis, Bone Marrow, Peripheral Blood, Hypochromic Microcytic Anemias, Iron Metabolism, Iron Absorption, Hepcidin, Iron Homeostasis, Iron‐Deficiency Anemia, Hypochromic Anemias, Sideroblastic Anemia, Lead Poisoning, alchohol, Lead Poisoning, Hematopoiesis, Hematopoietic Niche, growth factor signaling, Congenital Erythropoietic Porphyria, Congenital Erythropoietic Protoporphyria, iron overload, porphyrias, megoblastic anemia, Bone Marrow Appearances, Phagocytic Function, Leukocytosis, Leukoerythroblastic Reaction, Neutropenia, Myelokathexis, Lysosomal Storage Diseases, Hereditary Hemolytic Anemia, Hemolytic Anemia, Acquired Hemolytic Anemia, genetic disorders, Thalassemia, α‐Thalassemia, T Cells, B cells, Natural Killer Cells, Lymphocyte Proliferation, Somatic Hypermutation, Lymphocyte Circulation, Lymphocytosis, Lymphadenopathy, Primary Immunodeficiency Disorders, Granulopoiesis, Monocyte Production, Neutrophils, Polymorphs, Mononuclear Phagocytic System, Reticuloendothelial System, Autoimmune Lymphoproliferative Syndrome, Acquired Immunodeficiency Syndrome, Aplastic Anemia, Red Cell Aplasia, Congenital Dyserythropoietic Anemias, MYELODYSPLASTIC SYNDROMES, molecular genetics, Mirage Syndrome, Clonal Hematopoiesis, HEMATOLOGIC NEOPLASMS, MYELOID LEUKEMIA, Acute Myeloid Leukemia, MYELOPROLIFERATIVE NEOPLASMS, Chronic Myeloid Leukemia, Chronic Neutrophilic Leukemia, Nonleukemic Myeloproliferative Diseases, Polycythemia Vera, Myelofibrosis, Chronic Eosinophilic Leukemia, Myeloproliferative Disorder, ACUTE LYMPHOBLASTIC LEUKEMIA, Mastocytosis, Paraneoplastic Pemphigus, Myeloid Neoplasm, Lymphoid Neoplasm, Myelodysplastic Neoplasm, Myeloproliferative Neoplasm, Ring Sideroblast, Thrombocytosis, Juvenile Myelomonocytic Leukemia, CHRONIC LYMPHOCYTIC LEUKEMIA, Mature B‐Cell Leukemia, Mature T‐C

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