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A protein called PCBP2 controls the production of a hair growth protein by interacting with its genetic message and is linked to hair loss when this control is disrupted.

Genetic testing is crucial for diagnosing rare hair loss disorders.

Organoids help study and treat genetic diseases, offering personalized medicine and therapy testing.

Genes related to calcium signaling and lipid metabolism are important for curly hair in Mangalitza pigs.

HtrA2 activity is crucial for normal hair growth by regulating fat cell development.

A girl with a rare genetic disorder had a unique bone condition, highlighting the need for careful diagnosis and suggesting the disorder might be more common than thought.

Chinese domestic goats have unique genetic traits due to domestication and geographic isolation.

Osthole inhibits the TRPV3 channel by binding to specific sites, potentially aiding drug development for skin diseases and cancers.

Hairless protein reduces Msx2 gene activity, affecting hair follicle development.

The research confirms that Hidradenitis Suppurativa is characterized by increased inflammation, disrupted skin cell organization, and abnormal metabolic processes.

Genetic variants in PDE6H and LPAR6 cause vision impairment and hair loss in two Pakistani brothers.

Ectodysplasin signaling is crucial for skin appendage development, requiring specific doses and durations.

Inherited color dilution in rabbits is linked to DNA methylation changes.

A new mRNA variant of the SCF gene in sheep skin produces a shorter, different protein.

Gastric bypass surgery improved a woman's hormonal disorder without the need for medication.

Oral isotretinoin temporarily improved skin symptoms in a child with IFAP syndrome.

The TRPV3 ion channel is important for skin and hair health and could be a target for treating skin conditions.

The study found that specific proteins are markers of hair follicle development in human fetuses.

Diagnosing and managing Glucocorticoid Resistance Syndrome is complex due to genetic differences and varied symptoms.

High levels of ST14 and TMEFF1 proteins in ovarian cancer are linked to worse patient outcomes and may be a new treatment target.

The TRPV3 gene variant may cause the long-haired suri alpaca coat.

Hoxc13 gene affects wool length in Gansu alpine fine-wool sheep.

Six genetic conditions are often linked to complete scalp hair loss in children.

Hair follicle sampling is a practical method for measuring biomarkers in children with and without Fragile X syndrome.

A baby with a skin condition improved with treatment but developed a rare form of the condition affecting only his trunk.

Monilethrix causes fragile, patchy hair loss.

More precise, personalized therapies are needed for autoimmune diseases.

DHT in the human prostate is produced through multiple pathways, not just from testosterone.

Fibroblast Growth Factors (FGFs) are important for tissue repair and regeneration, influencing cell behavior and other factors involved in healing, and are crucial in processes like wound healing, bone repair, and hair growth.

The document concludes that blocking the internal pathways that create androgens might help treat cancers that depend on sex hormones.