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Hair and nail cells share similar proteins, indicating a common differentiation pathway.

Poly(ADP-ribose) synthesis is linked to skin cell differentiation.

Lipocartilage is a new type of tissue that affects hair growth and cartilage regeneration.

A common mutation in the hHb6 gene is linked to monilethrix, but other factors may also play a role.

A new benign nail tumor called onychoblastoma was identified.

A patient with steroid sulfatase deficiency had a unique hair pattern and a brain malformation not previously linked to the condition.

The study found specific skin and cell changes in patients with monkeypox, helping diagnose and understand the disease.

The girl has a genetic hair condition causing thin hair since childhood.

Keratin 17 gene mutations cause both steatocystoma multiplex and pachyonychia congenita type 2.

Identical twins had different symptoms because one had more cells with an extra chromosome fragment in different tissues.

A unique gene mutation was found in a family with monilethrix.

The tumor suppressor gene FLCN affects mitochondrial function and energy use in cells.

Skin-associated cartilage cells can influence hair growth by altering specific signaling pathways.

A new mutation in the FLCN gene linked to Birt-Hogg-Dube syndrome was found, suggesting people with certain lung collapse should be tested for this mutation and screened for kidney and colon cancer.

Woolly hair syndrome is a genetic condition causing frizzy, fragile hair.

Vitamin B12 deficiency can cause darkening of all nails.

The outer root sheath in hair follicles changes during growth, with different keratinization processes in its layers.

Mummy hair from the Taklamakan desert has calcium and phosphorus inside.

The research mapped diverse cell types in mouse lacrimal glands, aiding understanding of gland biology and diseases.

An 80-year-old woman with Cronkhite-Canada syndrome had multiple polyps and symptoms like diarrhea, hair loss, nail issues, and dark skin.

Cholesterol and phospholipids increase in mouse skin during cancer development, with differences between male and female skin.

Mutations in Far2 mice cause hair loss due to sebaceous gland issues.

A 9-year-old boy had a calcium deposit nodule on his earlobe.

A patient with Birt-Hogg-Dubé Syndrome also had choroidal melanoma, suggesting the need for careful eyelid exams in such patients.

The woman has a skin condition involving nodules, scars, and hair loss.

Focal palmoplantar callosities may help diagnose non-Herlitz junctional epidermolysis bullosa.

A rare type of skin lymphoma was identified, affecting hair follicles and sweat glands.

A woman's skin symptoms led to a diagnosis of systemic AL amyloidosis, but she died from sepsis shortly after.

Overexpression of PTHrP in chondrocytes causes short-limbed dwarfism and delayed bone formation in mice.