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Mitochondrial problems in tooth cells lead to bad enamel and dentin development in mice.

Changes in the SREBF1 gene cause a rare genetic skin and hair disorder.

The transcription factor Meis2 is essential for touch sensation and proper nerve development in touch receptors.

Diet changes can protect against harmful environmental effects on fetal development.

Frog skin cells need the protein desmoplakin for proper development and cell layer formation.

A protein called IL-36γ causes skin side effects from certain cancer treatments when combined with a common skin bacteria.

Fibrosis causes loss of important fat cells, affecting tissue function.

Alkaline Ceramidase 1 prevents early hair loss in mice by keeping hair follicle stem cells balanced.

Acneiform follicular mucinosis can be controlled with systemic corticosteroids.

IFNγ-primed MSC secretomes can improve joint health by reducing inflammation and supporting tissue repair.

Monkeys with hair loss during pregnancy showed higher stress hormone levels and invested differently in their offspring.

CRISPR gene editing reduces harmful molecules in cells from Emery–Dreifuss Muscular Dystrophy patients.

Mesenchymal stiffness affects sweat gland cell development.

Eating glucoraphanin can help prevent psychosis in offspring whose mothers had immune system activation.

Abnormal Wnt signaling in hair follicle stem cells can lead to acne-like cysts.

Kremen is crucial for proper development and preventing tumors by regulating Wnt signaling.

Estrogen affects how vitamin A is processed in mouse skin, which may impact acne treatment, hair growth, and skin defense.

A mother and daughter had severe skin, hair, and eye issues linked to IFAP.

Mutations in specific keratin genes cause improper hair structure in mice due to faulty keratin protein assembly.

PCOS is linked to low-grade chronic inflammation.

Researchers found a new gene variant linked to a rare bone disease, which doesn't always cause symptoms in carriers.

Ets2 gene is crucial for placental development in mice.

Blocking SCD1 in the skin with XEN103 shrinks sebaceous glands in mice.

EGFR helps mouse hair follicles stop growing by reducing certain growth regulators.

The PI's development is closely linked to skin and hair pigmentation in macaques.

The flaky skin mouse mutation is a natural model for studying human psoriasis.

Mitochondriopathy may cause eyelash loss.

Human dermal fibroblast proteins help restore nerves during healing.

Fadrozole and finasteride change gene expression related to sex hormones and thyroid hormones in frog larvae development.

New lipid/fiber microplexes improve mRNA therapy for degenerative diseases by enhancing cell function and treatment effectiveness.