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PIKFyve is essential for normal platelet function and its deficiency causes organ issues and macrophage infiltration.

A 16-year-old girl with a hair-eating disorder needed surgery to remove a hairball from her stomach and small bowel.

Advocacy groups should avoid marketing partnerships that may imply drug endorsements.

Dkk4 protein is necessary for the proper development and arrangement of hair follicles.

Hoxc13 gene is essential for hair, nail, and papilla development.

Rabbit hair color is influenced by the shape and distribution of pigment granules.

A genetic mutation in the EDA gene causes hypohidrotic ectodermal dysplasia in cats.

The Foxn1(-/-) nude mouse shows disrupted and expanded skin stem cell areas due to high Lhx2 levels.

Chemotherapy caused the patient's hair to have alternating thick and thin segments.

Keratinous tissues have multiple structural layers, including ordered keratin and lipid granules.

Abnormal scalp whorls can indicate brain development issues but may also be seen in neurologically normal people.

The junction of the inner and outer prepuce with good blood flow is ideal for surgical flaps.

Dermoscopy may not show hookworms clearly, and comparing it with tissue studies could improve diagnosis accuracy for skin conditions caused by parasites.

Tiger tail bands in hair are caused by wavy hair fibers with melanin, unlike straight fibers in normal hair.

The HGCA tool helps identify genes that work together by analyzing their co-expression patterns.

A new method effectively visualizes keratin in hair without harsh chemicals.

Overexpressing ornithine decarboxylase and v-Ha-ras in keratinocytes leads to invasiveness and malignancy.

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

A new mutation in the XEDAR gene might cause a rare skin condition called hypohidrotic ectodermal dysplasia.

The new composite scaffold may effectively treat chronic and deep wounds.

Certain scalp patterns can indicate the severity and activity of hair loss in Turkish alopecia patients.

The dense fine speckled pattern in ANA tests is common in autoimmune diseases, challenging previous beliefs that it was unrelated.

Clouston syndrome is inherited in an autosomal dominant pattern and caused by a specific gene mutation, with no current treatment available.

Mice hair growth patterns get more complex with age and can change with events like pregnancy or injury.

A KRT71 mutation in Hereford cattle in Uruguay causes thin, curly hair and scaly skin.

Activated β-catenin affects hair growth and skin thickness, and changes are reversible.

The mouse hairy ears mutation causes longer ear hair due to changes in gene expression.

Tamsulosin may slightly increase dementia risk compared to other treatments for enlarged prostate.