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LPR1 regulates root growth under low phosphate stress independently of SIZ1 in Arabidopsis thaliana.

Mutations in β1 integrins cause embryonic death but have milder effects on skin.

A gene network led by RSL4 is crucial for early root hair growth in response to cold in Arabidopsis thaliana.

Brg1 is crucial for hair growth and skin repair by maintaining stem cells and promoting regeneration.

A specific protein complex increases the activity of a plant enzyme, but this action is not required for plant root hair growth.

Patients with certain FoxN1 gene mutations have severe immune issues but normal skin and hair.

The Foxn1 gene is essential for normal nail and hair development.

Patients with the same vitamin D receptor mutation showed different symptoms due to other factors.

A new genetic disorder caused by an ODC1 mutation can be treated with DFMO.

A mutation in the iRhom2 gene causes hairless mice due to abnormal hair follicle development.

Hair growth-related cells need the enzyme SCD1 to help maintain the area that supports hair growth.

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

Folliculin deficiency causes problems with cell division and positioning due to disrupted RhoA signaling and interaction with p0071.

NLRP1 helps melanoma tumors grow by boosting inflammasome activation and reducing caspase-3 activity.

A new mutation in the TRPS1 gene was found in a Ukrainian girl with Trichorhinophalangeal syndrome type I.

The research found how GPCR Class A Rhodopsin receptors are related and suggested possible substances they interact with.

Double-stranded RNA activates a pathway that causes a skin protein to be expressed in the wrong place.

Researchers found a new ABCD1 gene mutation linked to a rare brain and nerve disorder with unusual brain changes.

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

Different Hairless isoforms affect Vitamin D receptor activity in hair regulation, with one repressing and the other stimulating it.

Mutations in the AP1B1 gene cause a new syndrome with skin, hearing, and developmental issues.

Krtap11-1 is important for hair strength and structure.

The mutant HR bmh protein mis-localizes in cells, affecting skin and hair development.

Hairless protein helps control hair growth by regulating vitamin D receptor activity.

Scientists created a cell model to study and find treatments for a skin disease called RDEB.

Orai1 protein is crucial for tooth development and affects enamel thickness and mineralization.

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

TRM21 helps control flavonoid production and root hair growth in Arabidopsis thaliana.

A genetic variant in "Blonde d'Aquitaine" calves causes death at birth due to a missing protein.

A new gene mutation causes vitamin D resistance and rickets, treatable with calcium therapy.