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Computational tools identified 29 drugs that could potentially target 19 genes involved in chemotherapy-induced hair loss, which could lead to more effective treatments.

SQSTM1 is linked to increased risk of alopecia areata.

iEdgePathDDA effectively finds new drug-disease links, outperforming other methods.

Two specific SNPs in the TRPS1 gene cause excessive hair growth by altering the protein's structure.

The study identified key genes involved in goat hair growth.

MendelVar is a tool that helps identify important genes by combining GWAS data with Mendelian disease information.

A new gene variant in the DSP gene is linked to a unique type of hair loss.

A boy with Pachyonychia congenita has a confirmed gene mutation, highlighting the need for a local genetic database in India.

Keratin gene regulation was emerging, with a key transcription factor found to influence hair growth and gene expression.

The document concludes that computational methods using networks and various data can improve the process of finding new uses for existing drugs.

ELL is crucial for gene transcription related to skin cell growth.

The study identified unique genes in hair follicle cells and their environment, suggesting these genes help organize cells for hair growth.

A certain smell receptor in hair follicles can affect hair growth when activated by a synthetic sandalwood scent.

Researchers made a detailed map of gene activity for different parts of human hair follicles to help create targeted hair disorder treatments.

A new tool helps study hair follicle cells to develop better treatments for hair disorders.

Scientists created a detailed map of gene activity in different parts of human hair follicles.

A specific mutation in the K25 gene causes a rare genetic disorder with curly hair at birth and later hair loss, along with dental issues.

A new mutation in the XEDAR gene might cause a rare skin condition called hypohidrotic ectodermal dysplasia.

A new IL6ST gene variant may cause a unique form of hyper-IgE syndrome with skin abscesses and high IgE levels.

A rare genetic deletion in the KRT1 gene causes unique skin symptoms in a family.

Olmsted syndrome can be inherited as an autosomal recessive trait due to a rare TRPV3 gene mutation.

Three new types of a skin blistering disease were found, caused by specific gene mutations.

61 functional keratin genes were identified in dogs and horses, leading to updated gene annotations.

More research is needed to improve wool and cashmere quality through genetics.

The study found that diseases can be grouped by symptoms and that the accuracy of predicting disease-related genes varies with the data source.

Collagen peptides may promote hair growth by activating certain genes in the skin.

3D-oxy exosomes may significantly boost hair growth, offering new treatment options for hair loss.

Found 32 genes linked to male baldness, affecting hair growth and stress-related pathways.

A second domain of high sulfur KAP genes on chromosome 21q23 is crucial for hair structure.

Signaling pathways are crucial for hair growth in goats.