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The review shows that skin symptoms like chronic fungal infections, hair loss, and skin depigmentation are key for early detection and management of APECED.

New hair loss treatments could be improved by using combined biological markers.

Eclipta prostrata is a medicinal plant that helps treat diseases, protects the liver and nerves, and promotes hair growth.

Experts recommend personalized treatment plans for best outcomes in managing Alopecia Areata.

Different types of fibroblasts play specific roles in wound healing and cancer, which could help improve treatments.

The research found that PCOS has common genetic factors regardless of how it is diagnosed and is linked to metabolic and reproductive issues.

Certain mutations in a hair growth-related gene cause a type of genetic hair loss.

Mutations in the HEPHL1 gene cause abnormal hair and cognitive issues.

Certain gene variations increase the risk of alopecia areata in Koreans.

Beige and leaden pigment genes act within melanocytes, affecting pigment patterns.

The EDAR gene mutation leads to thinner and more deformed hair shafts.

Different proteins are linked to the varying thickness of sheep and goat hair types.

Turing patterns are now recognized as important in developmental biology.

Hair loss gene found on chromosome 3q26.

FOXN1 gene variants cause low T cells and immune issues from birth.

Certain DNA variants can predict straight hair in Europeans but are not highly specific.

Boys with less severe EDA mutations in XLHED have milder symptoms and better sweat and hair production.

The VEGF +405G allele may increase the risk of PCOS in South Indian women.

People with X-linked hypohidrotic ectodermal dysplasia have no sweat ducts and less, thinner hair.

Certain gene variations are linked to higher male hormone levels in Chinese women with PCOS and insulin resistance.

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

Using SNP array testing helped quickly find the gene causing Woodhouse-Sakati syndrome in two related individuals.

A new type of pachyonychia congenita linked to a specific keratin gene mutation was found in two Pakistani families.

The document concludes that the fast-growing direct-to-consumer genetic testing market lacks sufficient regulation, posing risks to consumers due to questionable test quality and accuracy.

Pegvaliase effectively reduces blood phenylalanine levels in most PKU patients, but requires personalized plans and good communication to manage side effects.

The study found two new mutations in a Chinese patient with severe biotinidase deficiency.

The research found specific genes and proteins that affect how fast chickens' feathers grow, which is not solely determined by traditional inheritance patterns.

A woman with a unique syndrome similar to TRPS has a genetic change near the TRPS1 gene, affecting its regulation.

Mutations in the RBPJ gene cause Adams-Oliver Syndrome.

A person got uncombable hair syndrome from two copies of chromosome 1 from their mother.