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

Esrp1 is important for skin health by helping form and maintain the skin barrier.

ANE syndrome is caused by a mutation in the RBM28 protein that disrupts ribosome assembly.

Nexin 1 may help control hair growth.

CAP1/Prss8 does not activate PAR2 or inhibit PN-1.

Neuronatin is found in specific cells within rat testis, hair follicles, tongue, and pancreas, suggesting it has various roles in tissue development and function.

Nexin 1 helps control hair growth in young rats.

NAC1 controls certain enzymes that reduce root hair growth in Arabidopsis.

Targeting NCoR1 can help treat heart enlargement and dysfunction.

NDRG1 protein helps infantile hemangioma, a common infant tumor, to grow, and its mismanagement by FOXO1 protein plays a big role in causing the tumor.

The enzyme Dgat1 is essential for healthy hair and skin by controlling retinoid levels.

RXR and RAR proteins in skin may help with cell growth, hair growth, and gland function.

Neuronatin is found in various cells of rat tissues and has a unique location in sperm cells.

LRIG1 protein affects hair growth by regulating skin receptors, leading to hair loss when overexpressed.

RTA 408 cream protects mice from radiation skin damage.

TRPS1 is crucial for bone, kidney, and hair follicle development.

A new genetic mutation in the TRPS1 gene causes Trichorhinophalangeal Syndrome, leading to specific hair, dental, and bone issues.

Certain genetic changes in the KRT82 gene may cause patchy skin in New Zealand rabbits.

DS-2325a is safe and well-tolerated, supporting further development for Netherton Syndrome treatment.

RD26 controls root hair growth during drought by repressing key genes, helping plants save energy.

Krt15+ cells in the mouse intestine resist radiation and can start tumors.

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

Some HIV treatments can harm mitochondria, potentially causing side effects like lactic acidosis and nerve damage.

A rare genetic deletion in the KRT1 gene causes unique skin symptoms in a family.

KRT2.13 gene is similar to KRT2.9 but not expressed in hair follicles.

Oral Acitretin effectively resolved symptoms in a child with Netherton syndrome.

ATR12-351 ointment safely delivers LEKTI protein to the skin, reducing enzyme activity in Netherton syndrome.

Genotyping for NUDT15 p.Arg139Cys can help predict thiopurine side effects in Japanese IBD patients.