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New mutations in hair keratin genes cause the rare hair disorder monilethrix.

The MtAnn3 gene affects root hair growth and is influenced by cytokinin.

The C-allele and CC-genotype in the PTPN22 gene lower the risk of alopecia areata.

Trapa bispinosa Roxb. extract may help reduce prostate size and cell growth in BPH.

hHbl gene is active in hair shaft cells and some pilomatricomas.

Identical p53 gene mutations in different cancers suggest the need for careful treatment.

Tsc2-deficient stem cells can help understand and treat TSC-related tumors.

Betamethasone activates and increases the growth of certain skin cells from hair follicles.

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

β1 integrin is essential for the survival, growth, and movement of human epithelial progenitor cells.

BMP2 and BMP7 have opposite roles in feather formation.

A new genetic mutation in the ODC1 gene causes developmental delay and other symptoms in a young girl.

miR-124 helps mouse hair follicle stem cells become nerve cells by blocking Ptbp1 and Sox9.

CaBP1 and 2 are necessary for maintaining calcium currents and hearing in inner ear cells.

Gene expression in milk cells and blood can help detect illegal rbST use in cows.

Birt–Hogg–Dubé syndrome is a rare genetic condition causing skin lesions, lung cysts, and a higher chance of kidney cancer.

BMP signaling is crucial for skin and hair growth.

Targeting ATM could help manage heart cell enlargement due to pressure overload.

Budesonide and N-acetylcysteine reduced tumors and alopecia in mice, regardless of FHIT gene status.

A new mutation in the STING protein causes a range of symptoms and its severity may be affected by other genetic variations; treatment with a specific inhibitor showed improvement in one patient.

BMPs are important for hair growth and can counteract the negative effects of androgens on hair follicle stem cells.

A new mutation in the Hr gene causes hair loss in mice, similar to a human hair disorder.

The gene for Clouston syndrome in a large Indian family is located in the 13q11-q12.1 region.

Pyruvate Kinase M2 helps hair grow by linking energy production and a key hair growth pathway.

Too much thymosin beta4 causes weird teeth and more hair growth in mice.

mEphA1 receptor tyrosine kinase is important for skin and hair development and may play a role in certain diseases.

Hoxc8 gene helps start mammary gland development by controlling specific signals.

A specific genetic mutation causes POMC deficiency, leading to symptoms like weight gain and red hair.