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The wavy coat in NCT mice is caused by multiple genes, including a mutation in the Prss53 gene.

Iron deficiency in mothers causes hair loss in their baby mice.

Deleting the CD271 gene in mouse skin cells leads to disorganized skin and increased hair growth, suggesting CD271 is important for skin health.

Rushton's hyaline bodies form from hair keratin and blood substances.

Removing HIF-P4H-2 from certain skin cells in mice causes hair loss on the body but not the head.

Gremlin proteins help regulate hair growth by balancing signals in hair follicles.

DPR can cause skin, hair, and nail issues, sometimes appearing later in life.

A gene called HDAC9 might be a new factor in male-pattern baldness.

A gene in Arabidopsis thaliana, AtPRPL1, affects root hair length but not cell wall composition.

The study found genetic diversity in coat color dilution among Czech pointers in Slovakia.

A new gene mutation may cause cyclic thrombocytopenia by affecting platelet production.

A new DSG4 gene mutation causes hair defects in a young girl.

A specific gene mutation causes varying hair loss severity in a Pakistani family.

The study concluded that testing hormone levels after stimulation is not reliable for identifying carriers of 21-hydroxylase deficiency; genetic testing is necessary.

A genetic hair protein variant is more common in Japanese people and is inherited.

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

The updated NPRT system now covers different types of hair loss in men and women.

Researchers found two new genetic variants linked to Alzheimer's disease.

A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

A Korean baby with nevus sebaceus syndrome was found to have a KRAS gene mutation.

Neprilysin is important for hair growth regulation.

A gene mutation causes a rare hereditary hair loss, offering potential for new treatments.

Ring Chromosome 11 may be linked to conditions like early puberty, excessive hair growth, hair loss, and type 2 diabetes.

NISCH syndrome is a rare genetic disorder affecting skin and liver, with variable symptoms and limited treatment options.

A specific mutation in the K25 gene causes a rare genetic disorder with curly hair at birth and later hair loss, along with dental issues.

Basonuclin 1 (BNC1) helps skin cells multiply and move, which is crucial for wound healing.

The man has a genetic skin condition called pachyonychia congenita.

Studying rare genetic disorders can help us understand and treat common diseases better.

Netherton syndrome is a genetic skin disorder causing severe skin issues and requires careful treatment to protect the skin barrier.