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Fossil Evidence
Fossil Evidence
Ancient Proteins Reveal Sex of Australopithecus africanus
January 29, 2026
Source: South African Journal of Science | February 07, 2025 The Scientific Breakthrough In a land[...]
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Early Humans Began Wiping Out Elephant Relatives 1.8 Million Years Ago
January 23, 2026
Source: New Scientist | July 24, 2024 The Research Finding A recent study reported in New Scientis[...]
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6-Million-Year-Old Human Footprints: A Discovery That Rewrites History
December 05, 2025
A Find That Challenges the Textbook Story of Human Origins 30 May 2025 , The Greek Herald In 2[...]
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CHILD FROM THE WORLD’S OLDEST BURIAL WAS A HUMAN–NEANDERTHAL HYBRID
November 26, 2025
New Fossil Study | Skhul Cave | l’Anthropologie, 2025 Introduction A groundbreaking reassess[...]
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The Diet That Shaped Human Evolution
November 18, 2025
Based on Luke D. Fannin et al., Science, 31 July 2025 Human evolution is written most clearly in ou[...]
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Early Humans Used Fire 1 Million Years Ago
November 15, 2025
Dr. Miki Ben-Dor and Professor Ran Barkai — 16 May 2025, Frontiers in Nutrition Observations [...]
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Featured Posts
Improved Prime Editing System Enables Gene-Sized Edits in Human Cells at Therapeutic Levels
The largest and most diverse study on recessive genetic changes in developmental disorders reveals that over 80% of cases caused by recessive variants are linked to known genes. Researchers analyzed data from nearly 30,000 families and found that a shift in focus from gene discovery to interpreting changes in known genes could double diagnosis rates. • The study highlights the importance of genetic background in diagnosis and suggests that some patients may have multiple contributing genetic factors. These findings could lead to more personalized and accurate diagnoses for families affected by developmental disorders. • They include Joubert syndrome, Bardet-Biedl syndrome and TaySachs disease. Until now, overall quantification of these recessive genetic causes across diverse populations has not been done. • The team found the number of patients affected by recessive genetic variants varied greatly between different ancestry groups, ranging from two to 19 per cent of cases. This variation is strongly linked to the prevalence of unions between close relatives – consanguinity – in these groups.
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Stone Tools Created 400,000 Years Ago Reveal Major Technological Advancement in Humans
Union Budget 2026–27 Explained: Kartavya-Based Growth Strategy, Key Highlights & UPSC Analysis
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