Browsing by Author "Chalkley, Mary Bronwen"

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    • Investigating the Requirement for the Gene TSC2 in Early Human Neurodevelopment 
      Chalkley, Mary Bronwen; 0000-0001-7136-3034 (2024-03-18)
      Department: Cell & Developmental Biology
      Tuberous sclerosis complex (TSC) is a multi-organ genetic disorder caused by mutations in either TSC1 or TSC2 which encode hamartin and tuberin, respectively. Hamartin and tuberin form a protein complex that indirectly, ...
    • Investigating the Requirement for the Gene TSC2 in Early Human Neurodevelopment 
      Chalkley, Mary Bronwen; 0000-0001-7136-3034 (2024-03-18)
      Department: Cell & Developmental Biology
      Tuberous sclerosis complex (TSC) is a multi-organ genetic disorder caused by mutations in either TSC1 or TSC2 which encode hamartin and tuberin, respectively. Hamartin and tuberin form a protein complex that indirectly, ...