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CD2 might be a new treatment target for patchy alopecia areata.

Cancer cells often have more copies of TERT and TERC genes, which helps them grow and could affect patient outcomes.

The document concludes that certain genetic mutations and dietary factors are involved in acne development, and treatments like isotretinoin and diet changes can help manage it.

WNT10A helps esophageal cancer cells spread and keep renewing themselves.

Understanding the genetics of rare inherited ichthyosis syndromes is key for better treatments and genetic counseling.

The study found that mouse sweat glands develop before birth, mature after birth, and have specific keratin patterns.

BMP4-related anomalies can cause a wide range of eye, brain, and hand/foot problems, and new cases show this variability.

A man with KID syndrome developed a rare cancer in a long-term skin infection.

Hydroxypinacolone retinoate is a potent anti-aging ingredient for skin that is more effective and less irritating than other forms of retinoids.

Vitiligo is a skin condition causing white spots, more common in women, often starts before age 20, and can affect mental health.

Lichen Planus is a less common condition affecting skin and mucous membranes, with various types and associated risk factors, challenging to diagnose, significantly impacts life quality, and may have a risk of cancerous changes in oral lesions.

The document concludes that accurate diagnosis of ichthyosis is crucial for treatment and genetic advice, and ongoing research is needed for better therapies.

New treatments targeting skin stem cells show promise for skin repair, anti-aging, and cancer therapy.

FOXN1 gene mutations cause a rare, severe immune disease treatable with cell or tissue transplants.

Eyebrow loss has many causes and requires accurate diagnosis for proper treatment.

The research suggests that a specific skin gene can be controlled by signals within and between cells and is wrongly activated in certain skin diseases.

CD61 is important for mouse tooth cell growth and works through Lgr5.

Acitretin helped improve hand mobility and skin condition in a patient.

A high-fat diet may weaken tongue structure by reducing certain protein genes.

The document concludes that patient outcomes for Congenital Adrenal Hyperplasia are often not ideal because of poor management and a need for better diagnosis and treatment methods.

Keratins help protect cells, aid in cancer diagnosis, and influence cancer behavior and treatment.

The study found that sweat glands contain different types of stem cells that help with healing and maintaining healthy skin.

Blood vessels and specific genes help turn cartilage into bone when bones heal.

Fibroblast growth factor receptor signaling controls cell development and repair, and its malfunction can cause disorders and cancer, but it also offers potential for targeted therapies.

Olive oil compounds may help prevent cancer in animals, but human results are mixed.

FGF signaling is a promising target for developing treatments for wounds, metabolic diseases, and cancer.

5α‐reductase isozymes are crucial for prostate development and health, and targeting them can help prevent and treat prostate issues.

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

YAP and TAZ proteins are necessary for the development of two types of skin cancer.

Noggin overexpression delays eyelid opening by affecting cell death and skin cell development.