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We assessed gonadal histology using standard histological techniques as described by Jobling et al. (2006).
Histology samples were processed using standard histological techniques and stained with haematoxylin and eosin (H&E) at the Norwegian School of Veterinary Science.
Sections were stained with haematoxylin and eosin (H&E) using standard histological techniques.
Sections were stained with haematoxylin and eosin or stained for Nissl substance using standard histological techniques.
Lungs were inflated and maintained in formalin for 24 h before being processed into paraffin using standard histological techniques.
Samples were collected at 2, 3, and 4 weeks after implantation and processed using standard histological techniques.
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Hematoxylin and eosin staining was performed using standard histological technique.
The first section was stained with H&E, using standard histological technique.
Specimens were processed after 48 hours using standard histological technique [ 22].
Morphological analysis in patient and mouse skeletal muscle tissue was carried out on 8 µm cryostat sections using standard histological and histochemical techniques (Dubowitz et al. 1973).
Paraffin‐embedded sections were dewaxed using standard histological procedures.
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