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Scientists identified three genes important for processing certain brain chemicals, thyroid hormones, and medications.

Environmental factors affect reproductive traits by altering the SRD5A1 gene.

A 195 bp duplication in the HOXC10 gene causes crests in domestic chickens.

CCC1 is essential for pH balance and normal cell function in plants.

A new type of nerve cell involved in itch perception was discovered.

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

Truncated hHb1 keratin may play a role in breast cancer cell transformation.

Legumes use flavonoids to start a process with rhizobia for nitrogen fixation, involving specific genes and proteins.

A new mutation in the FLCN gene linked to Birt-Hogg-Dube syndrome was found, suggesting people with certain lung collapse should be tested for this mutation and screened for kidney and colon cancer.

miR-29 is a key factor that accelerates aging.

TRPV3 in skin cells causes inflammation and cell death.

A rare genetic disorder causes sparse hair and vision loss due to a CDH3 gene mutation.

Researchers found a new mutation in the HR gene causing hair loss and skin bumps in a Pakistani family.

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

A specific RNA in cashmere goats helps improve hair growth by interacting with certain molecules.

Ptprq has multiple forms that change during inner ear development.

Two rare genetic diseases cause severe rickets in children due to defects in vitamin D metabolism.

A circular RNA helps cashmere goat hair cells become hair follicles by blocking a molecule to boost a gene important for hair growth.

Lack of Cisd2 disrupts calcium balance in cells, leading to poorly functioning neutrophils.

Deleting the Trf1 protein in mice is safe and may help prevent cancer without major side effects.

Double-stranded RNA causes inflammation in hair follicle cells, which may help understand and treat alopecia areata.

Dermal EZH2 controls skin cell development and hair growth in mice.

A mutation in the Sgkl gene causes defective hair growth in mice.

Protease Nexin-1 is found in human hair growth cells and is affected by male hormones.

A mutation in the vitamin D receptor causes severe resistance to vitamin D, affecting bone health but not hair growth.

Stat3 activation increases hair follicle progenitors but reduces bulge region stem cells.

GasderminA3 is important for normal hair cycle transitions by controlling Wnt signaling.

Isolation stress in rats reduces brain enzyme levels, affecting dopamine function.

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