Paul A. Watkins mainly focuses on Biochemistry, Fatty acid, Peroxisome, Adrenoleukodystrophy and Genetics. His research in Fatty acid intersects with topics in Fatty Acid Transport Proteins, Internal medicine and Endocrinology. He combines subjects such as Molecular biology, Peptide sequence and ATP-binding cassette transporter with his study of Peroxisome.
His work deals with themes such as Mutation and Very long chain fatty acid, which intersect with Molecular biology. His studies examine the connections between Adrenoleukodystrophy and genetics, as well as such issues in Pathology, with regards to Neurological disorder. In general Genetics, his work in Complementation, Gene, Mitochondrial DNA and Neuronal ceroid lipofuscinosis is often linked to Human genome linking many areas of study.
His primary areas of study are Biochemistry, Peroxisome, Fatty acid, Adrenoleukodystrophy and Internal medicine. His research is interdisciplinary, bridging the disciplines of Molecular biology and Biochemistry. His work on Zellweger syndrome, Peroxisomal disorder, Phytanic acid and Rhizomelic chondrodysplasia punctata as part of general Peroxisome study is frequently connected to Plasmalogen, therefore bridging the gap between diverse disciplines of science and establishing a new relationship between them.
His work on Free fatty acid receptor, adipocyte protein 2 and Fatty acid synthesis as part of his general Fatty acid study is frequently connected to Coenzyme A, thereby bridging the divide between different branches of science. His study focuses on the intersection of Adrenoleukodystrophy and fields such as Very long chain fatty acid with connections in the field of Beta oxidation. His study on Internal medicine is mostly dedicated to connecting different topics, such as Endocrinology.
Paul A. Watkins spends much of his time researching Biochemistry, Peroxisome, Metabolic pathway, Cell growth and Pharmacology. His studies in Fatty acid, Cytoplasm, Metabolism, Acyl-CoA synthetase and Lipid droplet are all subfields of Biochemistry research. While working in this field, Paul A. Watkins studies both Fatty acid and Secretory pathway.
Paul A. Watkins does research in Peroxisome, focusing on Adrenoleukodystrophy specifically. In his study, which falls under the umbrella issue of Adrenoleukodystrophy, Heterozygote advantage and Immunology is strongly linked to Blood plasma. As part of the same scientific family, Paul A. Watkins usually focuses on Cell growth, concentrating on Molecular biology and intersecting with Lung cancer and Saturated fatty acid.
Paul A. Watkins focuses on Biochemistry, Metabolic pathway, Cytoplasm, Enzyme and Metabolite. His Biochemistry study focuses mostly on Lipid droplet, Fatty acid, Protease and RNA. The various areas that Paul A. Watkins examines in his Metabolic pathway study include Peroxisomal disorder, Peroxisome and Lipid metabolism.
His Cytoplasm study combines topics in areas such as Transport protein, Cell culture and Chlamydia trachomatis. Enzyme is closely attributed to SLC27A2 in his study. His Metabolite study integrates concerns from other disciplines, such as Malonate, Succinate dehydrogenase and Metabolism.
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Probiotics and antibodies to TNF inhibit inflammatory activity and improve nonalcoholic fatty liver disease
Zhiping Li;Shiqi Yang;Huizhi Lin;Jiawen Huang.
Hepatology (2003)
Mutations in the PTS1 receptor gene, PXR1, define complementation group 2 of the peroxisome biogenesis disorders
Gabriele Dodt;Nancy Braverman;Candice Wong;Ann Moser.
Nature Genetics (1995)
Adrenoleukodystrophy: Incidence, new mutation rate, and results of extended family screening
Lena Bezman;Ann B. Moser;Gerald V. Raymond;Piero Rinaldo.
Annals of Neurology (2001)
Diagnoses of neuronal ceroid-lipofuscinosis by immunochemical methods.
Syed Hosain;Walter E. Kaufmann;Gisela Negrin;Paul A. Watkins;Paul A. Watkins.
American Journal of Medical Genetics (1995)
Bone marrow-derived mesenchymal stem cells remain host-derived despite successful hematopoietic engraftment after allogeneic transplantation in patients with lysosomal and peroxisomal storage diseases
Omer N. Koç;Charles Peters;Patrick Aubourg;Shrini Raghavan.
Experimental Hematology (1999)
Evidence for 26 distinct acyl-coenzyme A synthetase genes in the human genome
Paul A. Watkins;Dony Maiguel;Zhenzhen Jia;Jonathan Pevsner.
Journal of Lipid Research (2007)
Insulin control of glucose metabolism in man: a new kinetic analysis.
Paul A. Insel;John E. Liljenquist;Jordan D. Tobin;Robert S. Sherwin.
Journal of Clinical Investigation (1975)
A mouse model for X-linked adrenoleukodystrophy
Jyh Feng Lu;Ann M. Lawler;Paul A. Watkins;James M. Powers.
Proceedings of the National Academy of Sciences of the United States of America (1997)
Gene redundancy and pharmacological gene therapy: Implications for X-linked adrenoleukodystrophy
Stephan Kemp;He Ming Wei;Jyh Feng Lu;Lelita T. Braiterman.
Nature Medicine (1998)
Identification of PAHX, a Refsum disease gene.
Stephanie J. Mihalik;James C. Morrell;Do Kim;Katherine A. Sacksteder.
Nature Genetics (1997)
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