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

BioPlex-11 improves DNA profiling from telogen hair roots in forensic work.

Blocking a protein called prostaglandin D2 might help treat hair loss.

Researchers found a new mutation in the EDA gene that likely causes missing teeth and mild skin symptoms in one family.

The HtrA1L364P mutation causes brain dysfunction and blood vessel damage.

The TIP1 gene is crucial for normal plant cell growth in Arabidopsis.

SSAT is a key enzyme affecting cell growth and metabolism, with potential but risky use in disease treatment.

Dynamet Technology won an award for its advanced titanium technology.

Carriers of a specific gene mutation have subtle skin changes without visible symptoms.

hsa_circ_0002980 can help stop liver cancer cells from growing and spreading.

A girl with excessive hair growth had a genetic change on chromosome 17 that reduced the activity of two genes linked to hair growth.

S100A4 promotes aggressive ovarian cancer and is a potential treatment target.

Personalized sonidegib dosing can effectively treat Gorlin-Goltz syndrome with fewer side effects.

RU 58841 may treat acne, hair loss, and excessive hair growth.

A specific gene variation in goats is linked to better growth traits.

TTD hair brittleness is caused by multiple structural abnormalities.

The document confirms the structures of major metabolites of the CRTh2 antagonist Setipiprant and identifies minor metabolites.

The SNP rs6457452 is linked to a higher risk of alopecia areata in Koreans.

KAP8.1 protein is crucial for hair structure and interacts with keratin 85.

Using human recombinant hyaluronidase in donor strip harvesting may improve the procedure.

The document's conclusion cannot be summarized as it is not provided in a language I can understand.

A new genetic change causing early stop in the androgen receptor gene was found in a patient with androgen insensitivity syndrome.

A genetic mutation in a specific gene causes a salt-wasting condition in a Pakistani girl and her family.

Dacomitinib can cause nail and skin issues, but these can be managed without stopping the drug.

The document's conclusion cannot be determined because the content is not available.

A new type of hereditary hair loss in a Chinese family is linked to chromosome 2p25.1–2p23.2.