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The hair-growth formula with L-cystine helps protect and grow hair cells.

Topical cetirizine may help increase hair length in male pattern baldness and could be an alternative to minoxidil with fewer side effects.

People with alopecia areata have higher levels of a heart disease marker than those without hair loss.

Acitretin effectively treats severe hypertrophic lichen planus.

A patient with alopecia had hair regrowth with tofacitinib but developed a skin reaction, choosing to continue the treatment despite the side effect.

Hidradenitis suppurativa may be more severe in people with Mediterranean fever gene mutations.

A new protein, mK6irs, is found in specific hair layers and may help understand hair growth and diseases.

Alloxan diabetes, methylthiouracil, cortisone, and adrenaline affect how white mice hair follicles use glucose and cystine and their cell division.

Activating β-catenin and inactivating PTEN cause follicular tumors, not papillomas, similar to those in Cowden’s Disease.

DNA methylation changes are linked to skin diseases with inflammation.

Longer TA repeats in the SRD5A2 gene may increase acne risk in Chinese people.

β-Catenin signaling is involved in brain cell growth after injury and could be a therapy target.

Croton membranaceus root extract can change how drugs are processed in the body.

Bleaching hair removes its protective top layer and exposes more hydrophilic groups, changing its chemical surface and affecting how it interacts with products.

Melanocyte-associated antigens may play a key role in alopecia areata and could be targets for new treatments.

Genetic screening for NUDT15 polymorphisms is crucial for patients taking azathioprine, especially in Asians.

Anti-Ku-positive patients often have muscle weakness and autophagy plays a key role in their condition.

ATR12-351 ointment safely delivers LEKTI protein to the skin, reducing enzyme activity in Netherton syndrome.

A specific gene variant is linked to severe insulin resistance and hormone imbalance in a teenage girl.

A new gene mutation causes a rare type of hair loss.

K_ATP channel gene mutations are linked to heart diseases, but more research is needed to understand the connection and treatment potential.

A new method, iSiMPRe, effectively identifies key protein regions in cancer genes, highlighting potential drug targets.

CXXC5 is a protein that controls cell growth and healing processes, and changes in its activity can lead to diseases like cancer and hair loss.

Certain KIR genes in Indian SLE patients are linked to disease severity and could be biomarkers.

Copper and iron cause keratin damage in hair by converting methionine to homocysteine.

Deleting the MAD2L1 gene in mice led to rapid tumor growth despite chromosomal instability.

ASLAN004 was safe and well-tolerated, supporting further development for treating certain diseases.

Corticosteroids improved symptoms in a man with Cronkhite-Canada Syndrome.