Search

everythinglearnresearchcommunity

for

Search:↓

The conclusion is that genetic changes in the glucocorticoid receptor can lead to conditions affecting stress response, immunity, and metabolism, requiring personalized treatment.

Genetic research has advanced our understanding of skin diseases, but complex conditions require an integrative approach for deeper insight.

Over 67 genes linked to ichthyosis help improve diagnosis and treatment.

New treatments for skin conditions related to the sebaceous gland are being developed based on current research.

THA is a rare condition with no significant clinical consequences if thyroid function is normal.

Chicken feather gene mutation helps understand human hair disorders.

The conference highlighted new dermatological treatments and emphasized early intervention and addressing conditions lacking evidence-based treatments.

The congress highlighted new gene therapy techniques and cell transplantation methods for treating diseases.

Pangolins have lost some skin-related genes, but kept others, leading to their unique scales and skin features.

Different amounts of daylight affect cashmere growth in goats by changing the activity of certain genes and molecules.

Vitamin D is crucial for skin health and managing skin diseases.

Diagnosing sex development disorders requires combining medical history, physical exams, imaging, lab tests, and genetic data.

A new mutation in the ST14 gene broadens the understanding of ichthyosis-hypotrichosis syndrome.

A specific genetic change is linked to mental disorders, intellectual disability, and possibly autoimmune disease in a family.

The study found that the hair loss condition in Cesky Fousek dogs is influenced by multiple genes affecting skin and muscle structure, fat metabolism, and immunity.

The study concludes that regulating apoptosis could lead to new treatments for various skin and hair conditions.

Damaging mutations in NFKB2 cause a severe and distinct form of primary immunodeficiency with early-onset and often ACTH-deficiency.

The conclusion is that genetic testing is important for diagnosing and treating various genetic hair disorders.

Rare changes in the KRT82 gene are linked to a higher risk of Alopecia Areata.

Bimatoprost, a glaucoma medication, may also help treat hair loss.

A gene called Gk5 controls lipid production in the skin and affects hair growth.

A genetic mutation in the EDA gene causes hypohidrotic ectodermal dysplasia in cats.

Lower levels of certain brain chemicals are linked to worse PTSD symptoms in men.

Understanding and manipulating epigenetic changes can potentially lead to human organ regeneration therapies, but more research is needed to improve these methods and minimize risks.

TRP channels in the skin are important for sensation and health, and targeting them could help treat skin disorders.

Some growth factors, while important for normal body functions, can cause diseases when not regulated properly.

Potassium channel openers are effective in treating heart conditions, high blood pressure, pulmonary diseases, bladder issues, and hair loss, but more selective drugs are needed.

Changes to the Foxp3 protein affect how well regulatory T cells can control the immune system, which could help treat immune diseases and cancer.

Steroid sex hormones activate matriptase in prostate cancer cells but not in breast cancer cells.

Eph/ephrin signaling is important for skin cell behavior and could be targeted to treat skin diseases.