Conner D. Reynolds

ORCID: 0000-0001-6320-1131
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About
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Research Areas
  • Genetics and Neurodevelopmental Disorders
  • Autism Spectrum Disorder Research
  • Child Development and Digital Technology
  • PI3K/AKT/mTOR signaling in cancer
  • Neuroendocrine regulation and behavior
  • Infant Health and Development
  • Memory and Neural Mechanisms
  • Neuroscience and Neuropharmacology Research
  • Child and Adolescent Psychosocial and Emotional Development
  • Neurotransmitter Receptor Influence on Behavior
  • RNA regulation and disease
  • Traumatic Ocular and Foreign Body Injuries
  • Neuroblastoma Research and Treatments
  • Congenital heart defects research
  • Gallbladder and Bile Duct Disorders
  • Vascular Malformations Diagnosis and Treatment
  • Antifungal resistance and susceptibility
  • Agricultural safety and regulations
  • Protein Tyrosine Phosphatases
  • Medical Malpractice and Liability Issues
  • Foreign Body Medical Cases
  • Esophageal and GI Pathology
  • Pancreatic function and diabetes
  • Health Policy Implementation Science
  • Attention Deficit Hyperactivity Disorder

University of Arizona
2023-2024

Baylor University
2015-2023

Banner - University Medical Center Tucson
2023

University of North Texas
2016-2022

Texas College
2017-2022

University of North Texas Health Science Center
2016-2022

John Peter Smith Hospital
2021

Health Net
2021

Institute of Biomedical Science
2016

Abstract Objective In this study, we used a systemic Fmr1 knockout in order to investigate both genotype‐ and sex‐specific differences across multiple measures of sociability, repetitive behaviors, activity levels, anxiety, fear‐related learning memory. Background Fragile X syndrome is the most common monogenic cause intellectual disability autism. Few studies date have examined sex mouse model syndrome, though clinical data support idea overall prevalence phenotype between sexes. Methods...

10.1002/brb3.800 article EN cc-by Brain and Behavior 2017-08-25

Fragile X syndrome is a neurodevelopmental disorder caused by trinucleotide (CGG) hyperexpansion in the FMR1 gene, functionally silencing transcription of fragile mental retardation protein (FMRP). This characterized impaired cognition, communication, and social behavior. The aim this study was to investigate development ultrasonic vocalization (USV) behavior Fmr1-deficient mouse model. On postnatal days (PD) 9-14, separate cohorts FVB/NJ pups were removed from their homecage...

10.1097/wnr.0000000000000701 article EN Neuroreport 2016-11-08

Dysregulation of the PI3K/Akt/mTOR signaling cascade has been associated with pathology neurodegenerative disorders, specifically Alzheimer's disease (AD). Both in-vivo models and post-mortem brain samples individuals AD have commonly shown hyperactivation pathway. In present study, we examine how neuron subset-specific deletion Pten (NS-Pten) in mice, which presents hyperactive mammalian target rapamycin (mTOR) activity, affects hippocampal protein levels key neuropathological hallmarks AD....

10.1097/wnr.0000000000001081 article EN Neuroreport 2018-06-30

Infant crying is a series of innate vocal patterns intended to elicit the attention adult caregivers for fulfillment specific needs such as pain, hunger, or hypostimulation. It one earliest forms observable communication. In neonatal rodents, this behavior has recently been investigated potential early behavioral marker neural deficits in neurodevelopmental disorders. However, few studies have examined effects seizures on vocalization during period. The purpose study investigate effect...

10.1111/epi.13450 article EN Epilepsia 2016-07-05

The mechanistic target of rapamycin (mTOR) pathway is a signaling system integral to neural growth and migration. In both patients rodent models, mutations the phosphatase tensin homolog gene (PTEN) on chromosome 10 results in hyperactivation mTOR pathway, as well seizures, intellectual disabilities autistic behaviors. Rapamycin, an inhibitor mTOR, can reverse epileptic phenotype subset specific Pten knockout (NS-Pten KO) mice, but its impact behavior not known. To determine behavioral...

10.1111/gbb.12854 article EN cc-by Genes Brain & Behavior 2023-06-28

The purpose of this investigation was to examine cerebellar levels several molecular signaling pathways, including PI3K/AKT/mammalian target rapamycin (mTOR) and markers neuronal migration, following loss the phosphatase tensin homolog (PTEN) gene in a subset neurons, as well accompanying behavior phenotype mice. Motor coordination learning were measured by sticker removal task accelerating rotarod. Western blots conducted on tissue samples. We demonstrated that neuron subset-specific...

10.1097/wnr.0000000000001241 article EN Neuroreport 2019-03-26

<ns4:p><ns4:bold>Background</ns4:bold>: The piracetam analog, aniracetam, has recently received attention for its cognition enhancing potential, with minimal reported side effects. Previous studies report the drug to be effective in both human and non-human models pre-existing cognitive dysfunction, but few have evaluated efficacy healthy subjects. A previous study performed our laboratory found no effects of oral aniracetam administration 1-hour prior behavioral testing naïve C57BL/6J...

10.12688/f1000research.11023.3 preprint EN cc-by F1000Research 2018-06-22

The piracetam analog, aniracetam, has recently received attention for its cognition enhancing potential, with minimal reported side effects. Previous studies report the drug to be effective in both human and non-human models pre-existing cognitive dysfunction, but few have evaluated efficacy healthy subjects. A previous study performed our laboratory found no effects of oral aniracetam administration 1-hour prior behavioral testing naïve C57BL/6J mice.The current aims further evaluate this...

10.12688/f1000research.11023.1 preprint EN cc-by F1000Research 2017-08-14

Fragile X syndrome (FXS) develops from excessive trinucleotide CGG repeats in the 5’-untranslated region at Xq27.3 of Fmr-1 gene, which functionally silences its expression and prevents transcription protein. This disorder is most prominent form heritable intellectual deficiency, affecting roughly 1 5,000 males 10,000 females globally. Antibody specificity selectivity are essential for investigating changes intracellular protein signaling phosphorylation status Mental Retardation Protein...

10.1371/journal.pone.0143134 article EN cc-by PLoS ONE 2015-11-18

In this review, we present a case report of an immunocompetent 58-year-old male who presented with disseminated histoplasmosis (DH) outside the known endemic regions. Due to his atypical clinical presentation that did not fit classical picture DH, diagnosis was delayed. addition, researched DH in hosts as these cases are common and leave patient population vulnerable delayed diagnosis. The literature supports considering differential among patients possible exposures regions immunocompetent.

10.3390/jof10110756 article EN cc-by Journal of Fungi 2024-10-31

Plasmacytomas are rare monoclonal neoplastic plasma cell proliferations in soft tissue or bone, with clival plasmacytomas being extremely and occasionally presenting light chain deposition disease (LCDD). While imaging findings for have shown variable T2 signal characteristics, complete loss has not been previously reported. We present a case of 61-year-old female found to 1.9 cm expansile lytic lesion the clivus on CT. MRI revealed intermediate T1 near-complete loss. Histopathology...

10.7759/cureus.76289 article EN Cureus 2024-12-23

Individuals on immunosuppressive therapies experience greater morbidity and mortality due to vaccine-preventable illnesses, but there are low rates of adherence immunization guidelines within this population.To determine the effectiveness clinician-led education, patient-centered dialogue, immediately available influenza vaccination uptake in patients taking therapies.We used a controlled before-and-after quasi-experimental design evaluate our quality improvement intervention occurring from...

10.1097/md.0000000000029786 article EN cc-by-nc Medicine 2022-07-29

Focal cortical dysplasia (FCD) accounts for nearly half of all cases medically refractory epilepsy in the pediatric and adult patient populations. This neurological disorder stems from localized malformations brain tissue due to impaired neuronal proliferation, differentiation, migration patterns. Recent studies animal models have highlighted potential role Fragile X mental retardation protein (FMRP) levels FCD. The purpose this study was investigate status FMRP activation tissues surgically...

10.1097/wnr.0000000000001517 article EN Neuroreport 2020-08-24

Preventable healthcare-associated harm results in significant morbidity and mortality the United States, costing nearly 400 000 patient lives annually. The Institute for Healthcare Improvement provides high-quality educational resources tailored working healthcare professionals. One such resource is Certified Professional Patient Safety (CPPS™) review course, which equips professionals with advanced proficiency 5 core safety domains. CPPS™ certification only interprofessional, science...

10.1177/23821205211025854 article EN cc-by-nc Journal of Medical Education and Curricular Development 2021-01-01

<ns4:p><ns4:bold>Background</ns4:bold>: The piracetam analog, aniracetam, has recently received attention for its cognition enhancing potential, with minimal reported side effects. Previous studies report the drug to be effective in both human and non-human models pre-existing cognitive dysfunction, but few have evaluated efficacy healthy subjects. A previous study performed our laboratory found no effects of oral aniracetam administration 1-hour prior behavioral testing naïve C57BL/6J...

10.12688/f1000research.11023.2 preprint EN cc-by F1000Research 2017-12-15
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