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Overexpressing NSD3 in mice causes breast cancer-like tumors and gland abnormalities.

Laminin 332 is essential for normal skin cell behavior and structure.

Spt4 and Spt6 are essential for fat cell development.

The new patch made of cell matrix and a polymer improves wound healing and supports blood vessel growth.

Mutations in the DSG4 gene can cause a rare hair disorder similar to monilethrix.

Mutations in the LSS gene cause hair loss and may affect brain development, with varying severity.

Scientists identified a unique type of human skin stem cell that could help with tissue repair.

A gene mutation in Lama3 is linked to a common type of hair loss.

A Chinese male with a new genetic mutation has a skin condition and severe urinary issues, with treatments having mixed success.

The demineralized bone matrix scaffold is better for cell attachment than the mineralized bone allograft.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

Different PADI isoforms help cells develop diverse functions.

Carriers of a specific gene mutation have subtle skin changes without visible symptoms.

Kdm6b is crucial for skin cell differentiation.

The study concluded that changing the culture conditions can cause sika deer skin cells to switch from a flat to a 3D pattern, which is important for creating hair follicles.

Mutations in the enzyme don't significantly change how it binds to its specific substances.

Researchers created hair-inducing human cell clusters using a 3D culture method.

The DNMT3B -579G>T polymorphism may increase the risk of colorectal cancer.

Sentinel lymph node biopsy is recommended for all types of desmoplastic melanoma due to higher rates of nodal metastasis.

Sentinel lymph node biopsy is recommended for all types of desmoplastic melanoma due to higher rates of nodal metastasis.

BBS7 is crucial for maintaining healthy periodontal ligaments by supporting Shh signaling.

HLD10 can include increased body hair and Mongolian spots.

New SRD5A2 variants may disrupt protein function, aiding diagnosis and treatment of related disorders.

A new mutation in the DCAF17 gene was found in a Chinese family, causing Woodhouse-Sakati syndrome and diabetes.

MPZL3 is important for controlling the hair growth cycle in mice and humans.

Mutations in the DSG4 gene cause fragile, sparse hair in humans, mice, and rats.

Mice with a Gsdma3 gene mutation have thicker skin and longer hair follicle openings due to increased β-catenin levels.

The ZIP13 variant is linked to abnormal hair quality.

Mrp3 may aid in wound healing and hair growth.

Mutations in Plcd1 and Plcd3 together cause severe hair loss in mice.