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Skin biopsy samples were excised and cut into >2 portions.
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Ten to 14 cores from each biopsy sample were excised, and the pathology of each core was determined based on the H&E staining of the two adjacent sections.
Skeletal muscle samples were excised using the percutaneous needle biopsy technique [ 28] modified to include suction [ 29] from the vastus lateralis of healthy young males, in accordance with the Deakin University Ethics Committee, where written and verbal informed consent was obtained.
The skin samples were excised from the paws of rats after washing with 70% ethanol.
Lung samples were excised, snap frozen in liquid N2 and stored at −80°C.
Tissue samples were excised using sterile technique and placed in chilled Hanks Buffered Saline Solution (HBSS).
Skin samples were excised from DDR2-/ and DDR2+/+ mice.
Punch biopsies removed from the patient were immediately sent to Laboratoire BIO-EC (Longjumeau, France), where the hypodermis was removed from the skin and circular samples were excised using a punch instrument.
The samples were excised and washed with sterile water.
Tissue samples were excised and stored in liquid nitrogen.
Total RNA and protein were extracted directly as soon as the liver samples were excised.
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