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Certain genetic variants are linked to frontal fibrosing alopecia in Spanish patients.

Circle hairs are harmless, spiral-shaped body hairs that don't need medical treatment.

Different ethnic hair types have unique nanoscopic and molecular features despite having the same basic keratin structure.

Cronkhite-Canada syndrome can cause multiple gastrointestinal polyps and various physical symptoms.

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

Enhanced stem cells can reduce fat buildup in eye tissue for Graves' disease.

Understanding monosaccharide composition can improve the development of effective medicinal plant polysaccharides.

The N363S gene variant does not cause higher adrenal androgen levels in women with polycystic ovary syndrome.

The mTurq2-Col4a1 mouse model shows that cells can divide while attached to stable basement membranes during development.

Many high school girls in Zanjan have polycystic ovarian syndrome.

Basement membrane-like ECM supports fibroblast aggregation and cohesion.

A new mutation in the TRPS1 gene caused Trichorhinophalangeal syndrome in a 17-year-old, highlighting the need for genetic testing.

HBCs in the olfactory epithelium can self-renew or differentiate into other cell types, with specific patterns during regeneration.

Early investigation of PCOS in high school girls is necessary due to associated risks and side effects.

The modified hair loss classification is more detailed but less user-friendly.

The report shows that a rare benign tumor was successfully removed from inside the mouth to avoid scarring on the face.

The BASP classification is more reliable than the Norwood-Hamilton for classifying hair loss in men and women.

A 73-year-old woman with Hypopigmented Mycosis Fungoides, a rare skin lymphoma, experienced disease progression despite treatment, emphasizing the need for ongoing monitoring.

Two sisters had rare, widespread cysts and complete hair loss, suggesting a genetic link.

LGR6+ stem cells may improve bone healing.

hHbl gene is active in hair shaft cells and some pilomatricomas.

A rare scalp infection in a child developed into a kerion with additional skin symptoms.

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

A specific genetic marker is linked to male pattern baldness in Han Chinese men.

Syringomas likely start in the upper dermis and form distinct luminal structures.

Albumin and prednisone improved symptoms in a woman with Cronkhite-Canada syndrome, revealing potential genetic causes.

The coronal approach is effective and safe for reducing eye bulging in Graves' eye disease.

The compound was successfully made and shows potential for treating prostate cancer.