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Three specific mutations in the LIPH gene can cause hair loss by damaging the protein's structure and function.

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

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

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

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

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

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

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

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

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

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

Nelfb is essential for dermal fat development and survival.

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

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

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

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

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

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

The Notch signaling pathway helps in mouse hair development through a noncanonical mechanism that does not rely on RBPj or transcription.

A new mutation in the LIPH gene was found to cause a rare hair disorder in a Japanese boy.

BFNB could be a promising treatment for hair growth.

Targeting NMMHC IIA may help treat blood-brain barrier damage.

A rare ITGB6 gene variant causes intellectual disability, hair loss, and dental issues.

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

The report expanded knowledge of MBTPS1-related disorders by identifying new symptoms.

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

A new gene mutation linked to a skin condition was found in a Spanish family.