Genetics
100 videos • 28,458 views • by Medicosis Perfectionalis
Medicosis Genetics Playlist (Video Lectures). Genetic Diseases Lectures...Congenital Diseases, Inherited Diseases
1
Introduction to Genetics - Biology
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2
How your Chromosomes are Numbered | Genetics 🧬
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3
DNA & RNA | Molecular Biology 🧬
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4
DNA is the genetic material | The Evidence! | Biology Lectures
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5
1st & 2nd Mendelian Laws | Genetics 🧬
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6
Punnett Squares (Monohybrid Cross, Dihybrid Cross) | Genetics
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7
Types of Mutations | Changes in the Gene Pool | Genetic Drift | Biology 🧬
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8
Sex-linked Crosses and Gene maps | Biology
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9
Hardy-Weinberg Equation | Genetics | Biology
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10
DNA 🧬 Structure & Function - Nucleosides & Nucleotides - Biochemistry & Biology Series
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11
DNA, RNA (mRNA, tRNA, rRNA), and the Genetic Code | Molecular Biology
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12
Purines, Pyrimidines, Nucleotides, Nucleosides, DNA, RNA, Denaturation & Annealing
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13
Telomeres, Centromeres, Telomerase, Hererochromatin, Euchromatin, Histones | Molecular Biology
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14
DNA replication in Prokaryotes & Eukaryotes (DETAILED) | Molecular Biology 🧬 & Biochemistry 🧪
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15
How DNA Repairs Itself (Proofreading, Oncogenes, Tumor Suppressor Genes, Mismatch, Excision Repair)
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16
DNA Transcription (Converting DNA to RNA)
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17
Posttranscriptional modification (hnRNA to mRNA) Splicesome, Splicing, Cap, Tail, Introns, Exons
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18
RNA (mRNA, tRNA, rRNA) & Genetic Mutations | Molecular Biology 🧬
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19
Translation (mRNA to Proteins) & Ribosomes (rER) | Post-translational Modification 🧬
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20
Recombinant DNA technology (Biotechnology) | Molecular Biology 🧬 & Biochemistry
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21
Lac Operon & Trp operon - Regulator, Promotor, Operator - A Comprehensive Explanation from A to Z
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22
Control of Gene Expression | Transcription Factors, Enhancers, Promotor, Acetylation vs Methylation
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23
Pharyngeal Arches, Pouches, and Clefts (Grooves).
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24
VACTERL Association with a Mnemonic 😉 - Embryology and Pathology
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25
Genetic Diseases 🧬 and Cataracts 👁
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26
Duchenne Muscular Dystrophy
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27
Duchenne Muscular Dystrophy (The D Mnemonic) 📖
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28
Duchenne VS Becker Muscular Dystrophy
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29
Gower Sign | Duchenne Muscular Dystrophy (DMD) | Signs in Medicine.
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30
Fanconi Anemia Mnemonic
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31
DiGeorge Syndrome Mnemonic
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32
Phenylketonuria (PKU) — A True Story 🥺
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33
Genetic Diseases (Down, Edwards, Patau, Cri-du-chat, and Williams Syndromes).
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34
When a Doctor 👨⚕️ goes to a Bookstore 📚 🤣
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35
Noonan Syndrome - The Mushroom mnemonic
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36
IgA Nephropathy (Berger’s Disease) | Nephrology 🩸
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37
Silver-Russell Syndrome | Mnemonic | Genetics 🧬
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38
Familial Hypocalcuric Hypercalcemia (FHH)
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39
Amino Acid Profiles | Inborn Errors of Metabolism Diagnosis | Blood & Urine Tests | Labs 🧪
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40
Lynch Syndrome (Hereditary Nonpolyposis Colorectal cancer or HNPCC) | Pathology | 5-Minute-Review
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41
All Biochemistry In 45 Minutes | Ultimate Biochemistry Quick Review
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42
Growth Hormone (GH) - Somatotropin - Dwarfism, Gigantism, Acromegaly - Endocrine Physiology
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43
Insulin-like growth factor (IGF-1) - Somatomedin C - GH- Dwarfism, Gigantism, Acromegaly - Endocrine
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44
Thrombotic Thrombocytopenic Purpura (TTP)
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45
HUS vs TTP
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46
Atypical Hemolytic Uremic Syndrome (aHUS) vs Thrombotic Thrombocytopenic Purpura (TTP)
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47
Immune Thrombocytopenia (ITP) vs Hemolytic Uremic Syndrome (HUS)
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48
ITP vs TTP (Immune Thrombocytopenic purpura vs Thrombotic Theombocytopenic Purpura)
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49
HUS vs aHUS vs TTP
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50
Henoch-Schönlein Purpura (HSP) Mnemonic
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51
Congenital Adrenal Hyperplasia (CAH) | 11, 17, and 21-hydroxylase deficiencies Endocrine Physiology
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52
Do you want to (Join) my Youtube membership program? Member-only videos!
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53
Wilms Tumor (Nephroblastoma) | Kidney Tumors (Neoplasms) | Renal Pathology | Nephrology Series
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54
Neuroblastoma…A tumor of sympathetic chain (N-myc Oncogene) | Pathology | Pediatrics
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55
Horseshoe Kidney 🧲…Congenital Anomalies | Renal Pathology | Nephrology Playlist
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56
Cystic Kidney Diseases (ARPKD, ADPKD, Medullary, Sponge Kidney,…etc)
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57
Wilms Tumor (Nephroblastoma) | A Mnemonic | Renal Pathology | Nephrology Playlist
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58
Neuroblastoma vs Nephroblastoma (Wilms Tumor) | A Comparison | Pathology | Nephrology | Pediatrics
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59
Galactosemia
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60
Glycogen Storage Diseases
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61
Cystinuria
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62
Cystinosis
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63
Marfan Syndrome
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64
Marfan Syndrome vs Homocystinemia
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65
Marfan Syndrome Mnemonic
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66
Homocystinemia (Homocystinuria)
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67
Hereditary Mitochondrial Diseases (Leber, MELAS, MERRF)
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68
Leber Hereditary Optic Neuropathy | Mitochondrial disease
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69
MELAS Syndrome | Mitochondrial Disease
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70
MERRF Syndrome | Ragged-Red Fibers | Mitochondrial Disease
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71
Kearns-Sayre Syndrome | Mitochondrial Disease
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72
Osteogenesis Imperfecta
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73
Osteogenesis Imperfecta Mnemonic
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74
Ehlers-Danlos Syndrome
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75
Ehlers-Danlos Syndrome Mnemonic
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76
Marfan Syndrome vs Ehlers-Danlos Syndrome
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77
Pyruvate Dehydrogenase (PDH) Complex Deficiency
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78
Pyruvate Kinase Deficiency (Hemolytic Anemia)
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79
Alkaptonuria
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80
Disorders of Fructose Metabolism (Fructose Intolerance & Fructosuria)
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81
Tyrosinemia (3 Types)
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82
Propionic Acidemia vs Methymalonic acidemia
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83
Maple Syrup Urine Disease
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84
Albinism
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85
Porphyria cutanea tarda
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86
Congenital Erythropoietic Porphyria
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87
Acute Intermittent Porphyria | Disorders of Heme Synthesis | Biochemistry & Hematology
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88
Aceruloplasminemia (Copper Disorder)
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89
Abetalipoproteinemia | Inherited lipid disorders (Dyslipidemia) | Biochemistry & Genetics
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90
Hyperlipidemia (Type I, II, III, IV, and V) | Biochemistry & Genetics
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91
Hyperammonemia & Urea Cycle Disorders (CPS I, OTC, NAGS, ASS, ASL deficiency) | Biochemistry Series
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92
Orotic Aciduria, CPS I deficiency & OTC deficiency | Biochemistry & Genetics
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93
Fatty Acid Metabolism defects (Carnitine, MCAD deficiency, Refsum, Adrenoleukodystrophy, Zellwegar)
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94
Lysosomal Storage Diseases (Sphingolipidoses) | Tay-Sachs, Neimann-Pick, Gaucher, Krabbe, Fabry
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95
Mucopolysaccharidoses (Hurler & Hunter diseases)...MPS I & MPS II...Lysosomal Storage Diseases
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96
Lennox-Gastaut syndrome (LGS) - visual mnemonic
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97
CRISPR / Cas9 Gene Therapy and CAR T-cell therapy (CART) - Promising?
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98
Inclusion-Cell Disease (I-cell disease) | Lysosomal Storage Diseases | Biochemistry & Genetics
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99
Urea Cycle (The Most Comprehensive Explanation) | Protein metabolism | Biochemistry series
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100
McArdle disease- Glycogen Storage Disease type V (GSD-V) - Clinical Biochemistry & Genetics
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