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Clouston syndrome is inherited in an autosomal dominant pattern and caused by a specific gene mutation, with no current treatment available.

A Persian cat and its owner fully recovered from Cheyletiellosis after treatment.

The article suggests that hair transplant surgery may not be purely cosmetic because it treats a disease and calls for clearer guidelines on its classification.

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

BMP signaling is crucial for skin and hair growth.

Certain genes on chromosomes 6, 10, 16, and 18 may increase the risk of alopecia areata.

The Hedgehog signaling pathway is important for skin and hair growth and can lead to cancer if it doesn't work right.

Human hair proteins vary by individual, body site, and ethnicity, useful for forensics.

HOXC13 is essential for hair and nail development by regulating Foxn1.

Certain mouse strains develop a skin condition similar to a human hair loss disease due to genetic defects.

Future hair cosmetics will be safer and more effective.

Lysophospholipids like LPA and S1P are important for hair growth, immune responses, and vascular development, and could be targeted for treating diseases.

Primary cicatricial alopecia, a rare disorder causing permanent hair loss, is hard to diagnose and treat, with treatments like anti-inflammatory drugs and steroids offering varied results and no guaranteed cure. Psychological support for patients is important, and future research should aim to identify causes of the condition.

LPA3 signaling in the uterus is crucial for placental formation and fetal development.

Poliosis circumscripta is a patch of white hair caused by lack of melanin, linked to genetic and acquired conditions.

Female pattern hair loss is caused by multiple factors and while treatments like topical minoxidil, hormone therapy, and low-level light therapy can help, none can fully cure it.

Trichoscopy is useful for diagnosing different types of hair loss.

Desmoglein 4 is controlled by specific proteins that affect hair growth.

Early detection of specific skin lesions can help identify Birt-Hogg-Dube syndrome and prevent serious complications.

Alopecia areata is an incurable autoimmune condition causing hair loss, with research aiming for better treatments.

Prostasin has two roles in skin: one for normal skin development without needing activation, and another for proper hair growth that requires activation.

Mutations in specific keratin genes cause improper hair structure in mice due to faulty keratin protein assembly.

Scalp cooling can help prevent hair loss from chemotherapy, but treatment should be tailored to the individual and more research is needed.

Tailored treatments for alopecia areata are recommended based on severity and patient needs.

The document suggests a possible link between FAM111B gene mutations and increased cancer risk, particularly pancreatic cancer.

Prostaglandin analogs like Latanoprost might help grow hair on the scalp and body.

Researchers found genes and microRNAs that control curly fleece in Chinese Tan sheep.

Mice with extra human KLK14 had hair and skin problems, including weaker cell bonds and inflammation, linked to Netherton syndrome.

Key genes crucial for sheep hair follicle development were identified, aiding fine wool breeding and human hair loss research.

Growth hormone levels affect hair growth and loss, with too much causing excess hair and too little leading to hair loss.