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

The research provides a gene-based framework for hair biology, highlighting the Hippo pathway's importance and suggesting links between hair disorders, cancer pathways, and the immune system.

Alk1 in specific cells is crucial for proper nerve branching and hair function.

Scientists created cell lines from balding patients and found that cells from the front of the scalp are more affected by hormones that cause hair loss than those from the back.

Msx2 deficiency in mice leads to bone growth and organ development problems.

The Wnt/β-catenin pathway is important for body functions and diseases, and targeting it may treat conditions like cancer, but with safety challenges.

Mutations in the P2RY5 gene cause autosomal recessive woolly hair.

Genetic variations greatly affect individual metabolism and can impact health and disease risk.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

A gene mutation in Lama3 is linked to a common type of hair loss.

Gene therapy helped rats with a specific type of rickets grow hair without severe inflammation.

FAGA diagnosis uses blood tests and trichoscopy, with treatments like topical minoxidil, oral anti-androgens, and hormone-modulating drugs.

Malassezia yeast linked to hair loss; ketoconazole helps treat it.

Two siblings have a rare genetic condition causing curly, coarse hair.

Using minoxidil on balding scalps can stimulate hair regrowth and increase blood flow. It's an effective treatment for early hair loss.

Finasteride 1 mg effectively and safely increases hair growth in Japanese men with hair loss.

Androgens may block hair growth signals, targeting this could treat hair loss.

LLLT helps treat hair loss by increasing blood flow, reducing inflammation, and stimulating growth factors.

The best animal model for studying male-pattern baldness is the stumptailed macaque, not rats or mice.

The document reports findings on genetic research, including ethical concerns about genome editing, improved diagnosis of mitochondrial mutations, solving inherited eye diseases, confirming gene roles in epilepsy, linking a gene to aneurysms, and identifying genes associated with age-related macular degeneration.

Topical minoxidil improved hair loss in a patient when used consistently.

The document suggests that for better patient satisfaction in hair transplants, high-quality photos are needed, and using a narrow donor strip might lead to fewer grafts and dissatisfaction, but filling the scar with FUE grafts and using tranexamic acid can improve results.

The research shows that a gene called Wnt3 affects hair growth and structure, causing short hair and balding when overactive.

Pregnancy can cause various skin changes and diseases, with PUPPP being the most common skin condition specific to pregnancy.

In Italian patients with lupus, the most common skin issue was chronic cutaneous lupus, especially discoid lesions, and nonspecific skin problems occurred in about a third of those with systemic lupus, mainly during active disease.

Effective management of children's hair loss involves accurate diagnosis, various treatments, and supportive care.

Most Hairless gene mutations reduce its ability to work with the Vitamin D Receptor, which might explain a certain type of hair loss.

EVG staining is a valuable, simple, and cost-effective method for diagnosing various skin conditions in dermatopathology.

Minoxidil helps treat eyebrow thinning, monilethrix, early hair loss, and shortens chemo-related hair loss.

Platelet-Rich Plasma (PRP) treatment may increase hair growth for genetic hair loss, but more research is needed to confirm this.