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Biomaterials|May 27, 2008
Observations on the microvasculature of bone defects filled with biodegradable nanoparticulate hydroxyapatiteOlaf Kilian, Sabine Wenisch, Srikanth Karnati, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 8, 2015
Compromised peroxisomes in idiopathic pulmonary fibrosis, a vicious cycle inducing a higher fibrotic response via TGF-β signalingGani Oruqaj, Srikanth Karnati, Vijith Vijayan, et al.
The American Journal of Pathology|December 15, 2022
Transforming Growth Factor-β1 Regulates Peroxisomal Genes/Proteins via Smad Signaling in Idiopathic Pulmonary Fibrosis Fibroblasts and Transgenic Mouse ModelsGani Oruqaj, Srikanth Karnati, Lakshmi Kanth Kotarkonda, et al.
Frontiers in Physiology|December 13, 2021
Excessive Accumulation of Intracellular Ca2+ After Acute Exercise Potentiated Impairment of T-cell FunctionRenyi Liu, Karsten Krüger, Christian Pilat, et al.
Plos One|September 14, 2018
PPARα-mediated peroxisome induction compensates PPARγ-deficiency in bronchiolar club cellsSrikanth Karnati, Gani Oruqaj, Harshavardhan Janga, et al.
Annals of Anatomy = Anatomischer Anzeiger : Official Organ of the Anatomische Gesellschaft|June 6, 2021
Peroxisomes in the mouse parotid glands: An in-depth morphological and molecular analysisChristoph Watermann, Malin T Meyer, Klaus P Valerius, et al.
Plos One|July 26, 2012
Cre-mediated stress affects sirtuin expression levels, peroxisome biogenesis and metabolism, antioxidant and proinflammatory signaling pathwaysYu Xiao, Srikanth Karnati, Guofeng Qian, et al.
Fertility and Sterility|April 15, 2014
Acute epididymitis induces alterations in sperm protein compositionAdrian Pilatz, Guenter Lochnit, Srikanth Karnati, et al.
Oxidative Medicine and Cellular Longevity|February 13, 2018
Differential Alterations of the Mitochondrial Morphology and Respiratory Chain Complexes during Postnatal Development of the Mouse LungNatalia El-Merhie, Eveline Baumgart-Vogt, Adrian Pilatz, et al.
Disease Models & Mechanisms|October 21, 2010
PEX13 deficiency in mouse brain as a model of Zellweger syndrome: abnormal cerebellum formation, reactive gliosis and oxidative stressC Catharina Müller, Tam H Nguyen, Barbara Ahlemeyer, et al.
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