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TTNPB helps turn stem cells into neural stem cells, improving depression-like behaviors in rats.

NIPP1 is important for healthy skin and could help treat skin inflammation.

Researchers found a new mutation in the LIPH gene of a woman with a rare hair condition.

Researchers found a new genetic mutation linked to a hair condition in a Japanese boy.

Folliculin helps regulate energy and nutrient sensing, impacting Birt–Hogg–Dubé syndrome.

An American Bully with a genetic skin condition improved significantly with specific topical treatments.

Nelfb is crucial for forming skin fat tissue by regulating genes needed for fat cell development.

BI 2536 had limited effectiveness against several advanced cancers and caused significant side effects.

NIPT can help detect potential maternal cancer, and GIPXplore can identify immune diseases in pregnancies.

ULBP3 could be a marker for diagnosing alopecia areata incognita and may be linked to its cause and development.

MYB30 and EIN3 work against each other to control root hair growth and phosphorus uptake in plants when phosphate is low.

The PIP5K1A gene helps cashmere growth in goats by promoting cell proliferation, and melatonin boosts its expression.

Long-read RNA sequencing can identify complex gene changes in IFAP syndrome.

The type 3 IP3 receptor is important for controlling hair loss and growth.

Beta-trace protein may help diagnose and predict treatment response in certain nerve disorders.

NFIC helps rat dental cells grow and turn into bone-like cells.

A new syndrome was linked to two new genetic changes in the MBTPS1 gene in a 14-year-old girl.

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

The MBTPS2 gene variant c.970+5G>A is a common mutation causing IFAP syndrome.

The Itpr3 gene causes a specific hair pattern in mice.

Nitrate helps plants manage phosphate uptake and starvation responses through NIGT1 proteins.

The PP2A-B55α protein is essential for brain and skin development in embryos.

Mutations in NIPAL4 cause skin issues by disrupting lipid layers, but some improvement is seen with topical treatment.

BAP1 mutations are rare in pediatric melanocytic tumors and may develop later in life.

PNKP is essential for keeping adult mouse progenitor cells healthy and growing normally.

Par3–mInsc and Gαi3 work together to ensure proper cell division orientation in skin development.

The protein called small nuclear ribonucleoprotein polypeptide E is identified as a cause of a type of hair loss without other symptoms.

Nelfb is essential for dermal fat development and survival.

The PER3 rs772027021 SNP may cause mild skin pigmentation changes in a new subtype of dyschromatosis universalis hereditaria.