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Researchers fixed gene mutations causing a skin disease in stem cells, which then improved skin grafts in mice.

Prostate cancer cells can make their own androgens to activate the androgen receptor, and treatments like abiraterone may increase this ability, suggesting new therapies should target the entire steroid-making pathway.

Early diagnosis and treatment of hereditary hemochromatosis can prevent serious complications.

TRPV1 is involved in pain, various body functions, and diseases, but targeting it for treatment is challenging.

CCL5 is important for the hair growth potential of human dermal papilla cells.

A gene in Sebekia benihana, CYP-sb21, is needed for a specific reaction on the drug Cyclosporine A, which could be important for hair growth without affecting the immune system.

Crataegi Fructus water extract helps hair grow better and thicker.

Prenatal THC exposure may harm ovarian health and fertility.

Inhibiting ornithine decarboxylase may help prevent certain skin cancers.

A specific DNA duplication in Polish chickens affects feather shape by altering gene expression.

A substance from Caulerpa racemosa seaweed may protect against skin damage caused by air pollution by reducing oxidative stress and cell death.

The study created a mouse model to mimic degenerative diseases for testing tissue repair and new therapies.

Recombinant thrombomodulin can effectively treat severe complications in Cronkhite-Canada syndrome.

Involucrin is a useful marker for keratinocyte differentiation in mice.

Mutations in the vitamin D receptor cause hereditary vitamin D-resistant rickets, leading to poor bone health and requiring high calcium doses for treatment.

The method accurately and reliably detects residual solvents in Finasteride.

Live vaccines can be safely given to infants with a FOXN1 variant if their immune function improves over time.

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.

Alpha-difluoromethylornithine prevents cancer in mice but causes hair loss.

A novel CLDN1 mutation in a 2-month-old with NISCH showed improvement with symptom management.

The hairless (hr) gene is essential for normal hair follicle function and its mutation leads to hair loss.

Cepharanthine may help treat gastric cancer by causing cancer cell death and affecting energy use.

Cancer-associated fibroblasts promote tumor growth in skin cancer.

A new Wnt surrogate specifically targets the Frizzled7 receptor, promoting organoid formation and hair growth.

Ca_v1.2 affects hair growth and could be a target for hair loss treatments.

CGRP may help protect hair follicles from immune system attacks, potentially slowing hair loss.

A new gene mutation causes complete androgen insensitivity in a 16-year-old with a female appearance.

Keratin structure changes during keratinization, but the exact model remains uncertain.