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FER and TOR signaling help root hair growth in low temperature and low nitrate conditions.

A new keratin, hK6irs1, is found in all layers of the hair follicle's inner root sheath.

The 736T>A mutation in the LIPH gene is common in Japanese people with autosomal recessive woolly hair.

Keratin 17 gene mutations cause both steatocystoma multiplex and pachyonychia congenita type 2.

Changing protein kinase levels in pituitary cells affects calcium flow and beta-endorphin release.

The study found two new mutations in a Chinese patient with severe biotinidase deficiency.

A heterozygous mutation in HTRA1 can cause severe CARASIL symptoms.

A new genetic region, 17q21.31, is linked to higher ovarian cancer risk.

TRPA1 is crucial for mechanical sensitivity in skin sensory neurons.

KIF18B is important for correctly positioning cell division machinery in skin cells, affecting hair follicle development.

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

Rhizobacterial strain RT3 helps lettuce survive drought by producing protective substances like proline.

FTase and GGTase-I are essential for skin keratinocyte health.

The peach gene CTG134 helps control the interaction between auxin and ethylene, which could lead to new agricultural chemicals.

Too much keratin 16 in mice skin causes abnormal skin thickening and structure.

Potassium channel modulators mostly increase the activity of rat whisker mechanoreceptors.

The AR gene is linked to male-pattern baldness, TNFSF4 to heart disease, SLC19A3 to BBGD, MCT8 to a syndrome, and segmental duplications to genetic variation.

The protein RSL4 is crucial for making root hairs longer by controlling genes related to cell growth.

CT-707 is effective and safe for treating certain Chinese lung cancer patients.

TB and BCC tumors show similar follicular differentiation patterns.

A rare EGFR mutation in newborns leads to severe health issues and early death.

Ruxolitinib helped a woman with a genetic mutation regrow her hair and improved her health.

New mutations in the DSG4 gene cause a rare hair condition.

A new genetic mutation linked to CARASIL syndrome and small artery disease was found in a Chinese family.