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lncRNAs may regulate hair follicle development in Hu sheep.

Patients with Shwachman-Diamond syndrome often get misdiagnosed due to a wide range of symptoms, including immune system problems and bone abnormalities.

AGA progression involves increased lipid synthesis, electron transport, and hair follicle miniaturization.

People with Myotonic Dystrophy type 1 are more likely to have certain skin conditions, but not more likely to get skin cancer.

A specific RNA in cashmere goats helps improve hair growth by interacting with certain molecules.

The document concludes that various childhood hair and nail disorders exist, some may improve on their own, and advances in genetics and immunology could enhance treatment and counseling.

The Itpr3 gene causes a specific hair pattern in mice.

A specific RNA molecule, circCOL1A1, affects the growth and quality of goat hair by interacting with miR-149-5p and influencing cell growth pathways.

Young HS patients often have other physical and mental health issues, and research on HS covers a wide range of topics including genetics, triggers, treatments, and the need for more data.

A rare genetic disease caused severe, worsening hair loss from early childhood with poor treatment results.

The study concluded that changing the culture conditions can cause sika deer skin cells to switch from a flat to a 3D pattern, which is important for creating hair follicles.

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

A new MTX2 gene mutation caused a severe genetic disorder in a young Chinese girl.

Histone modification is key in treating chronic inflammatory skin diseases.

The conclusion is that the nuclear lamina and LINC complex in skin cells respond to mechanical signals, affecting gene expression and cell differentiation, which is important for skin health and can impact skin diseases.

Some Greek melanoma patients have gene mutations linked to increased cancer risk, a new color feature helps diagnose melanoma, the incidence of a skin condition in the Netherlands is rare, and a gene possibly affects male-pattern baldness.

Nonclassic congenital adrenal hyperplasia is a common genetic disorder that can cause a range of symptoms and requires personalized treatment.

Metformin helps with menstrual cycles and insulin levels in PCOS but is less effective for hair growth, diabetes prevention, and weight loss, and may improve fertility and reduce diabetes risk.

Increasing mir-302 turns human hair cells into stem cells by changing gene regulation and demethylation.

Patients with certain skin symptoms and high ANA titers should be monitored for potential systemic lupus.

GABRA2 gene variations impact alcohol response, and hair loss medication finasteride reduces some effects.

New treatments for Alopecia Areata show promise but need to be more effective and affordable.

The document concludes that early diagnosis and treatment of Congenital Adrenal Hyperplasia are crucial for preventing serious health issues and improving patient outcomes.

Targeted cancer therapies often cause skin reactions, so dermatologists must manage these effects.

TCDD speeds up skin barrier formation by increasing certain gene expressions.

Natural 5AR inhibitors effectively improve mild to moderate hair loss in men.

Plant extracts effectively reduce hair loss and increase growth, offering a safe alternative treatment.

Researchers found 15 new genetic links to skin traits in Japanese women.

Prolactin may play a significant role in skin and hair health and could be a target for treating skin and hair disorders.

Recognizing oral symptoms can help diagnose and treat blood and nutritional diseases early.