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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.

Molecular diagnostics help identify genetic defects causing endocrine diseases, improving diagnosis and treatment options.

Bexxar treatment led to a high response rate in patients with advanced-stage, treatment-resistant follicular lymphoma.

A 19-year-old male had two rare skin conditions causing scarring and permanent hair loss.

A new mutation in the TMEM173 gene and a risk allele in IFIH1 cause a unique set of immune-related symptoms.

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.

Not having enough or having too much of the protein Grainyhead-like 3 leads to various developmental problems.

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.

The document concludes that Borrelia afzelii causes a skin condition in France, a gene is linked to hair loss in Caucasian women, and various genetic mutations affect skin diseases.

Hair follicle development is controlled by interactions between skin tissues and specific molecular signals.

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.

Hair loss and aging are caused by the breakdown of a key protein in hair stem cells.

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.

Hair loss in men treated best with early medication or transplant, new treatments researched.

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.

Human beard hair medulla contains a unique and complex mix of keratins not found in other human tissues.

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

Wnt signaling is crucial for skin and hair development and its disruption can cause skin tumors.

Fetal skin cells from a cell bank heal wounds faster and with less scarring than adult cells.

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