His scientific interests lie mostly in Biochemistry, Cardiolipin, Cell biology, Mitochondrion and Biosynthesis. His Biochemistry study focuses mostly on Phosphatidic acid, Fatty acid, Phosphatidylethanolamine, Phosphatidylcholine and Phospholipid. His Cardiolipin research integrates issues from Molecular biology and ATP synthase, Enzyme.
The study incorporates disciplines such as Mitochondrial carrier and Glycerophospholipids in addition to Cell biology. Grant M. Hatch works mostly in the field of Mitochondrion, limiting it down to concerns involving Tafazzin and, occasionally, Gene expression, Endoplasmic reticulum and Acyltransferase. His Biosynthesis study incorporates themes from Glycerol and Biological membrane.
Grant M. Hatch mainly investigates Biochemistry, Cardiolipin, Internal medicine, Endocrinology and Cell biology. The concepts of his Cardiolipin study are interwoven with issues in Molecular biology and Mitochondrion. Grant M. Hatch focuses mostly in the field of Mitochondrion, narrowing it down to matters related to Programmed cell death and, in some cases, Cancer research.
His studies in Internal medicine integrate themes in fields like AMPK and Streptozotocin. His Endocrinology research incorporates elements of Offspring and Gestational diabetes. His Cell biology research includes themes of Microvessel, Myocardin and Gene knockdown.
His primary scientific interests are in Cell biology, Internal medicine, Endocrinology, Cardiolipin and Tafazzin. His study in the field of Endoplasmic reticulum is also linked to topics like Phosphatidylinositol 3-kinase signaling. The study incorporates disciplines such as Offspring, Gestational diabetes and Type 2 diabetes in addition to Internal medicine.
His study in the fields of Insulin resistance, Cholesterol, Ezetimibe and Sterol under the domain of Endocrinology overlaps with other disciplines such as ABCG8. His Cardiolipin research is multidisciplinary, incorporating perspectives in Molecular biology, Secretion and Inner mitochondrial membrane. Barth syndrome is a subfield of Biochemistry that Grant M. Hatch investigates.
Grant M. Hatch mainly investigates Cell biology, Programmed cell death, Endoplasmic reticulum, Mitochondrion and Barth syndrome. The Cell biology study combines topics in areas such as Glucose transporter and Myocardin. His Endoplasmic reticulum study incorporates themes from Calcium metabolism, Calcium, Gene knockdown, Mitochondrial permeability transition pore and Necrosis.
His studies in Mitochondrion integrate themes in fields like Transcription factor complex, Gene expression, Lipidomics and Alternative splicing, Exon. His Barth syndrome research incorporates themes from Monolysocardiolipin acyltransferase, Molecular biology and Tafazzin. His Cardiolipin study improves the overall literature in Biochemistry.
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Host cell phospholipids are trafficked to and then modified by Chlamydia trachomatis.
John L. Wylie;Grant M. Hatch;Grant Mcclarty.
Journal of Bacteriology (1997)
Activation of Raf/MEK/ERK/cPLA2 Signaling Pathway Is Essential for Chlamydial Acquisition of Host Glycerophospholipids
Heng Su;Grant McClarty;Feng Dong;Grant M. Hatch.
Journal of Biological Chemistry (2004)
Fatty acid transport protein expression in human brain and potential role in fatty acid transport across human brain microvessel endothelial cells
Ryan W. Mitchell;Ngoc H. On;Marc R. Del Bigio;Donald W. Miller.
Journal of Neurochemistry (2011)
Cloning and characterization of murine 1-acyl-sn-glycerol 3-phosphate acyltransferases and their regulation by PPARα in murine heart
Biao Lu;Yan J. Jiang;Yaling Zhou;Fred Y. Xu.
Biochemical Journal (2005)
Cardiolipin metabolism and Barth Syndrome
Kristin D. Hauff;Grant M. Hatch.
Progress in Lipid Research (2006)
Cell biology of cardiac mitochondrial phospholipids.
Grant M Hatch.
Biochemistry and Cell Biology (2004)
Fatty acid transport into the brain: of fatty acid fables and lipid tails.
Ryan W. Mitchell;Grant M. Hatch.
Prostaglandins Leukotrienes and Essential Fatty Acids (2011)
Stomatin-Like Protein 2 Binds Cardiolipin and Regulates Mitochondrial Biogenesis and Function
Darah A. Christie;Caitlin D. Lemke;Isaac M. Elias;Luan A. Chau.
Molecular and Cellular Biology (2011)
Oxidative modification of low density lipoprotein in normal and hyperlipidemic patients: effect of lysophosphatidylcholine composition on vascular relaxation.
L. Chen;B. Liang;D. E. Froese;S. Liu.
Journal of Lipid Research (1997)
Sirtuin-3 (SIRT3) Protein Attenuates Doxorubicin-induced Oxidative Stress and Improves Mitochondrial Respiration in H9c2 Cardiomyocytes
Kyle G. Cheung;Laura K. Cole;Bo Xiang;Keyun Chen.
Journal of Biological Chemistry (2015)
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