Michael T. Williams

Family Medicine

404 S White St
Athens, TN 37303

Last Updated: 09/26/2026

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Found 118 publications

Genetic activation of ERK2 recapitulates core neurodevelopmental features of Rasopathy syndromes in mice.

Genetic activation of ERK2 recapitulates core neurodevelopmental features of Rasopathy syndromes in mice.

Journal: HGG advances

Published: January 06, 2026

Genetic activation of ERK2 recapitulates core neurodevelopmental features of Rasopathy syndromes in mice.

Genetic activation of ERK2 recapitulates core neurodevelopmental features of Rasopathy syndromes in mice.

Journal: HGG advances

Published: January 06, 2026

Genetic activation of ERK2 recapitulates core neurodevelopmental features of Rasopathy syndromes in mice.

Genetic activation of ERK2 recapitulates core neurodevelopmental features of Rasopathy syndromes in mice.

Journal: bioRxiv : the preprint server for biology

Published: December 25, 2025

FMR1 gene therapy restores translationally relevant phenotypes in a mouse model for fragile X syndrome.

FMR1 gene therapy restores translationally relevant phenotypes in a mouse model for fragile X syndrome.

Journal: Gene therapy

Published: November 25, 2025

Dek Loss Induces Sex-Dependent, Task-Specific Cognitive Deficits and Reprograms the Hippocampal Transcriptome in Mice.

Dek Loss Induces Sex-Dependent, Task-Specific Cognitive Deficits and Reprograms the Hippocampal Transcriptome in Mice.

Journal: Research square

Published: November 24, 2025

Gene × environment interaction between latrophilin-3 (Lphn3 or Adgrl3) and developmental permethrin exposure in Sprague Dawley rats.

Gene × environment interaction between latrophilin-3 (Lphn3 or Adgrl3) and developmental permethrin exposure in Sprague Dawley rats.

Journal: Neurotoxicology and teratology

Published: November 05, 2025

A mouse model of a patient derived P544L mutation in the Slc6a8 gene shows hypoactivity and cognitive deficits.

A mouse model of a patient derived P544L mutation in the Slc6a8 gene shows hypoactivity and cognitive deficits.

Journal: Brain research

Published: September 30, 2025

DEK Loss Induces Task-specific Deficits in Learning and Memory and Reprograms the Hippocampal Transcriptome in Mice.

DEK Loss Induces Task-specific Deficits in Learning and Memory and Reprograms the Hippocampal Transcriptome in Mice.

Journal: Molecular neurobiology

Published: September 09, 2025

Auditory Event-Related Potentials in Two Rat Models of Attention-Deficit Hyperactivity Disorder: Evidence of Automatic Attention Deficits in Spontaneously Hypertensive Rats but Not in Latrophilin-3 Knockout Rats.

Auditory Event-Related Potentials in Two Rat Models of Attention-Deficit Hyperactivity Disorder: Evidence of Automatic Attention Deficits in Spontaneously Hypertensive Rats but Not in Latrophilin-3 Knockout Rats.

Journal: Genes

Published: May 05, 2025

Gene × environment interaction between heterozygous deletion of the ADHD risk gene latrophilin-3 (adgrl3) and developmental deltamethrin exposure in Sprague Dawley rats.

Gene × environment interaction between heterozygous deletion of the ADHD risk gene latrophilin-3 (adgrl3) and developmental deltamethrin exposure in Sprague Dawley rats.

Journal: Neurotoxicology and teratology

Published: December 10, 2024

A Randomized Controlled Trial Comparing "Early" Versus "Late" Periosteal Patch Attachment to Knee Chondral Defects in Autologous Chondrocyte Implantation.

A Randomized Controlled Trial Comparing "Early" Versus "Late" Periosteal Patch Attachment to Knee Chondral Defects in Autologous Chondrocyte Implantation.

Journal: Cartilage

Published: October 31, 2024

Comparison of Sprague Dawley with Long Evans rats on a battery of widely used neurobehavioral tests.

Comparison of Sprague Dawley with Long Evans rats on a battery of widely used neurobehavioral tests.

Journal: Physiology & behavior

Published: October 29, 2024

Showing 1-12 of 118

Last Updated: 09/26/2026