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Published in 2020 at "Acta histochemica"
DOI: 10.1016/j.acthis.2020.151595
Abstract: Spermatogenesis involves mitosis, meiosis, growth, and differentiation of spermatogonial stem cells (SSCs), which are capable of self-renewal and differentiation into spermatozoa. Markers of spermatogonia and other spermatogenic cells have been extensively studied in rodents, whereas…
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Keywords:
box protein;
protein pax7;
boar;
expression ... See more keywords
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Published in 2019 at "Translational Oncology"
DOI: 10.1016/j.tranon.2019.07.001
Abstract: Gliomas present the most common type of brain tumors in adults, characterized by high morbidity and mortality. In search of potential molecular targets, members of paired box (PAX) family have been found expressed in neural…
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Keywords:
gliomas;
glioma;
pax3;
emerging pathogenic ... See more keywords
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Published in 2022 at "Histopathology"
DOI: 10.1111/his.14853
Abstract: A distinct subset of lung adenocarcinomas (LADs), arising from a series of peripheral lung cells defined as the terminal respiratory unit (TRU), is characterised by thyroid transcription factor 1 (TTF‐1) expression. The clinical relevance of…
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Keywords:
lung;
subset lung;
paired box;
expression paired ... See more keywords
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Published in 2017 at "International journal of ophthalmology"
DOI: 10.18240/ijo.2017.08.06
Abstract: AIM To identify the potentially pathogenic gene variants that contributes to the etiology of strabismus. METHODS A Chinese pedigree with strabismus was collected and the exomes of two affected individuals were sequenced using the next-generation…
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Keywords:
exome sequencing;
rare paired;
identification rare;
whole exome ... See more keywords
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Published in 2019 at "Translational cancer research"
DOI: 10.21037/31896
Abstract: Background: Paired box 2 gene promoted the progression of subsequent epithelial-mesenchymal transition (EMT) in malignant melanoma, which is the most dangerous type of skin cancer. We aimed to investigate the functional role of miR-204-3p in…
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Keywords:
melanoma;
375 cells;
box gene;
mir 204 ... See more keywords
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Published in 2018 at "Molecular Medicine Reports"
DOI: 10.3892/mmr.2018.9469
Abstract: Congenital aniridia is a rare genetic disorder characterized by a variable degree of hypoplasia or absence of iris. It is frequently associated with keratopathy, cataract, juvenile-onset glaucoma and foveal and optic nerve hypoplasia. Mutations in…
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Keywords:
aniridia cataract;
aniridia;
classic congenital;
congenital aniridia ... See more keywords