W
Wesley S. Haynie Data-verified
Affiliation confirmed via AI analysis of OpenAlex, ORCID, and web sources.
Researcher
faculty
13 h-index
38 pubs
741 cited
Research Areas
Links
Biography and Research Information
OverviewAI-generated summary
Wesley S. Haynie's research investigates the biological mechanisms underlying skeletal muscle atrophy and regeneration, with a particular focus on sex-based differences in these processes. His work has explored the development of cachexia in both male and female mice, examining metabolic and contractile alterations, as well as the progression of skeletal muscle fibrosis in rodent models. Haynie has also studied mitochondrial aberrations during disuse atrophy and the effects of interventions such as voluntary wheel running on muscle recovery following volumetric muscle loss. His publications include investigations into the impact of PGC-1α overexpression on skeletal muscle regeneration and the influence of diet-induced obesity on extracellular matrix remodeling. Haynie has a publication record of 38 papers, with an h-index of 13 and 729 citations. He has collaborated extensively with researchers at the University of Arkansas at Fayetteville, including Tyrone A. Washington, Megan E. Rosa‐Caldwell, Nicholas P. Greene, and Eleanor R. Schrems.
Metrics
- h-index: 13
- Publications: 38
- Citations: 741
Selected Publications
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Leucine Supplementation Exacerbates Morbidity in Male but Not Female Mice with Colorectal Cancer-Induced Cachexia (2023)
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Development of skeletal muscle fibrosis in a rodent model of cancer cachexia (2023)
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Biological Sex Differences of Fibrosis During the Development of Cancer Cachexia (2023)
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Effects of PGC-1α overexpression on the myogenic response during skeletal muscle regeneration (2022)
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Development of metabolic and contractile alterations in development of cancer cachexia in female tumor-bearing mice (2021)
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Mitochondrial aberrations during the progression of disuse atrophy differentially affect male and female mice (2021)
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Female mice may have exacerbated catabolic signalling response compared to male mice during development and progression of disuse atrophy (2021)
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The effect of autologous repair and voluntary wheel running on force recovery in a rat model of volumetric muscle loss (2021)
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The effect of diet-induced obesity on extracellular matrix remodeling during skeletal muscle regeneration (2021)
Collaboration Network
Top Collaborators
Tyrone A. Washington
University of Arkansas at Fayetteville
7 shared publications
In database
- Mitochondrial aberrations during the progression of disuse atrophy differentially affect male and female mice
- Development of metabolic and contractile alterations in development of cancer cachexia in female tumor-bearing mice
- The effect of autologous repair and voluntary wheel running on force recovery in a rat model of volumetric muscle loss
- Development of skeletal muscle fibrosis in a rodent model of cancer cachexia
- Effects of PGC-1α overexpression on the myogenic response during skeletal muscle regeneration
Showing 5 of 7 shared publications
Nicholas P. Greene
University of Arkansas at Fayetteville
6 shared publications
In database
- Mitochondrial aberrations during the progression of disuse atrophy differentially affect male and female mice
- Development of metabolic and contractile alterations in development of cancer cachexia in female tumor-bearing mice
- The effect of autologous repair and voluntary wheel running on force recovery in a rat model of volumetric muscle loss
- Development of skeletal muscle fibrosis in a rodent model of cancer cachexia
- Leucine Supplementation Exacerbates Morbidity in Male but Not Female Mice with Colorectal Cancer-Induced Cachexia
Showing 5 of 6 shared publications
Megan E. Rosa‐Caldwell
University of Arkansas at Fayetteville
6 shared publications
In database
- Mitochondrial aberrations during the progression of disuse atrophy differentially affect male and female mice
- Development of metabolic and contractile alterations in development of cancer cachexia in female tumor-bearing mice
- Development of skeletal muscle fibrosis in a rodent model of cancer cachexia
- Effects of PGC-1α overexpression on the myogenic response during skeletal muscle regeneration
- Leucine Supplementation Exacerbates Morbidity in Male but Not Female Mice with Colorectal Cancer-Induced Cachexia
Showing 5 of 6 shared publications
Richard Perry
University of Arkansas at Fayetteville (US)
5 shared publications
- The effect of autologous repair and voluntary wheel running on force recovery in a rat model of volumetric muscle loss
- Development of skeletal muscle fibrosis in a rodent model of cancer cachexia
- Effects of PGC-1α overexpression on the myogenic response during skeletal muscle regeneration
- Leucine Supplementation Exacerbates Morbidity in Male but Not Female Mice with Colorectal Cancer-Induced Cachexia
- Biological Sex Differences of Fibrosis During the Development of Cancer Cachexia
Eleanor R. Schrems
University of Arkansas at Fayetteville
5 shared publications
In database
- Development of metabolic and contractile alterations in development of cancer cachexia in female tumor-bearing mice
- Development of skeletal muscle fibrosis in a rodent model of cancer cachexia
- Effects of PGC-1α overexpression on the myogenic response during skeletal muscle regeneration
- Leucine Supplementation Exacerbates Morbidity in Male but Not Female Mice with Colorectal Cancer-Induced Cachexia
- Biological Sex Differences of Fibrosis During the Development of Cancer Cachexia
Seongkyun Lim
University of Arkansas at Fayetteville
4 shared publications
In database
- Mitochondrial aberrations during the progression of disuse atrophy differentially affect male and female mice
- Development of metabolic and contractile alterations in development of cancer cachexia in female tumor-bearing mice
- Development of skeletal muscle fibrosis in a rodent model of cancer cachexia
- Biological Sex Differences of Fibrosis During the Development of Cancer Cachexia
Jacob L. Brown
University of Arkansas at Fayetteville (US)
4 shared publications
- Mitochondrial aberrations during the progression of disuse atrophy differentially affect male and female mice
- Development of skeletal muscle fibrosis in a rodent model of cancer cachexia
- Effects of PGC-1α overexpression on the myogenic response during skeletal muscle regeneration
- Biological Sex Differences of Fibrosis During the Development of Cancer Cachexia
David E. Lee
University of Arkansas at Fayetteville (US)
3 shared publications
- Mitochondrial aberrations during the progression of disuse atrophy differentially affect male and female mice
- Development of skeletal muscle fibrosis in a rodent model of cancer cachexia
- Effects of PGC-1α overexpression on the myogenic response during skeletal muscle regeneration
Landen W. Saling
University of Arkansas at Fayetteville
3 shared publications
In database
- Development of metabolic and contractile alterations in development of cancer cachexia in female tumor-bearing mice
- Development of skeletal muscle fibrosis in a rodent model of cancer cachexia
- Biological Sex Differences of Fibrosis During the Development of Cancer Cachexia
Lemuel A. Brown
University of Arkansas at Fayetteville
3 shared publications
In database
- Development of skeletal muscle fibrosis in a rodent model of cancer cachexia
- Effects of PGC-1α overexpression on the myogenic response during skeletal muscle regeneration
- Biological Sex Differences of Fibrosis During the Development of Cancer Cachexia
Kirsten R. Dunlap
University of Arkansas at Fayetteville (US)
2 shared publications
- Mitochondrial aberrations during the progression of disuse atrophy differentially affect male and female mice
- Development of metabolic and contractile alterations in development of cancer cachexia in female tumor-bearing mice
Lisa T. Jansen
University of Arkansas at Fayetteville
2 shared publications
In database
- Mitochondrial aberrations during the progression of disuse atrophy differentially affect male and female mice
- Development of metabolic and contractile alterations in development of cancer cachexia in female tumor-bearing mice
Michael P. Wiggs
Baylor University (US)
2 shared publications
- Mitochondrial aberrations during the progression of disuse atrophy differentially affect male and female mice
- Development of metabolic and contractile alterations in development of cancer cachexia in female tumor-bearing mice
Francielly Morena da Silva
University of Arkansas at Fayetteville
2 shared publications
In database
- Development of metabolic and contractile alterations in development of cancer cachexia in female tumor-bearing mice
- Leucine Supplementation Exacerbates Morbidity in Male but Not Female Mice with Colorectal Cancer-Induced Cachexia
Ana Regina Cabrera
University of Arkansas at Fayetteville
2 shared publications
In database
- Development of metabolic and contractile alterations in development of cancer cachexia in female tumor-bearing mice
- Leucine Supplementation Exacerbates Morbidity in Male but Not Female Mice with Colorectal Cancer-Induced Cachexia
Similar Researchers
Based on overlapping research topics
Eleanor Schrems
University of Arkansas at Fayetteville
Muscle Physiology and Disorders
Mitochondrial Function and Pathology
Cancer-related molecular mechanisms research
Nathan Serrano
University of Arkansas at Fayetteville
Muscle Physiology and Disorders
Mitochondrial Function and Pathology
Diet and metabolism studies
Seongkyun Lim
University of Arkansas at Fayetteville
Muscle Physiology and Disorders
Mitochondrial Function and Pathology
Cancer-related molecular mechanisms research
Tyrone A. Washington
University of Arkansas at Fayetteville
Muscle Physiology and Disorders
Mitochondrial Function and Pathology
Cancer-related molecular mechanisms research
Landen W. Saling
University of Arkansas at Fayetteville
Muscle Physiology and Disorders
Mitochondrial Function and Pathology
Cancer-related molecular mechanisms research
KiranKumar Adepu
University of Arkansas for Medical Sciences
Muscle Physiology and Disorders
Mitochondrial Function and Pathology
Diet and metabolism studies