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The wavy coat in NCT mice is caused by multiple genes, including a mutation in the Prss53 gene.

A mutation in the VDR gene affects hair cycling without needing ligand binding.

Certain gene variations and low adiponectin levels may increase the risk of hair loss in Egyptians.

JAK inhibitors effectively treat severe atopic dermatitis and alopecia areata.

Increasing zinc intake improved skin and hair symptoms in a rare genetic disorder.

Specific mutations in a receptor cause facial abnormalities and hair loss.

The arrector pili muscle attaches to the extracellular matrix using α5β1 integrin and connects muscle cells using α1β1 integrin.

MOF controls skin development by regulating genes for mitochondria and cilia.

Certain gene variations in EGF and EGFR may increase the risk of alopecia areata in Koreans.

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

A PKP1 gene mutation causes skin fragility and hair loss in Chesapeake Bay retriever puppies.

The research showed that CRISPR/Cas9 can fix mutations causing a skin disease in stem cells, which then improved skin grafts in mice, but more work on safety and efficiency is needed.

Reduced SIRT1 in hair cells may cause alopecia areata by triggering immune responses.

Male hormones and reduced plakoglobin can impair heart electrical function and increase arrhythmia risk in males.

High CRP levels could indicate vitamin D deficiency in people with alopecia areata.

Gorab deficiency speeds up skin aging by disrupting protein regulation and reducing collagen.

Phosphatidylinositol 4-kinases are crucial for root growth, defense, and immunity in Arabidopsis thaliana.

Stress in hair follicle cells increases certain immune-related proteins, which might contribute to hair loss conditions.

Genes related to keratin, skin cell differentiation, and immune functions are key in hedgehog skin and spine development.

Upadacitinib effectively treated a patient with multiple inflammatory conditions.

A specific gene mutation causes complete hair loss without other health issues.

Researchers found a new gene, hacl-1, that is active in mouse hair follicles during hair growth and may be important for hair biology.

Certain gene variations are linked to severe acne in Egyptian patients and could guide treatment choices.

Targeting NMMHC IIA may help treat blood-brain barrier damage.

Mutations at Val-889 and Arg-752 disrupt key interactions in androgen receptor dimerization.

p120-catenin helps control skin inflammation by regulating cadherin levels.

Integrin-linked kinase is crucial for melanoblasts to properly colonize the skin.

Activin helps skin growth and healing mainly through stromal cells and affects keratinocytes based on its amount.

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