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A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

Some children in Malaysia with symptoms have either profound or partial biotinidase deficiency, and early testing and treatment are important.

Exosomes are crucial for protecting sensory hair cells in the inner ear.

Certain changes in the VEGF gene can increase or decrease the risk of polycystic ovary syndrome.

Adjusting the medication tacrolimus resolved a boy's red nail beds after a stem cell transplant.

Two siblings had a rare immune disorder caused by a FOXN1 gene mutation.

Vitamin D and its receptor may help prevent skin cancer.

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

TGM3 is important for skin and hair structure and may help diagnose cancer.

Mice with extra human KLK14 had hair and skin problems, including weaker cell bonds and inflammation, linked to Netherton syndrome.

Female pattern hair loss has multiple causes and treatments, with new therapies showing promise.

The research found genes that change during cashmere goat hair growth and could help determine the best time to harvest cashmere.

Certain gene variations in the Vitamin D Receptor are linked to higher risk of female hair loss.

Lichen Planopilaris is a hair loss condition best treated early with various medications, including hydroxychloroquine, to prevent permanent baldness.

The first Japanese family with Marie Unna hereditary hypotrichosis showed hair condition improvement in a child and highlighted the risk of misdiagnosis.

Hairless protein affects hair follicle structure by regulating the Dlx3 gene.

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

Certain gene variations are not a major cause of male infertility in Nigerian men.

Oncogenic K-ras causes rapid cancerous changes in the mouth's lining.

A male with aromatase deficiency improved bone health with estradiol treatment.

Msx2 and Foxn1 are both crucial for hair growth and health.

Alopecia areata has a complex genetic basis that was not fully understood as of 2001.

Researchers found a new mutation in the EDA gene that likely causes missing teeth and mild skin symptoms in one family.

Tandem repeats significantly influence hair color, especially darker shades, across different ancestries.

Skin lesions in Carney complex are likely caused by a specific group of skin cells that promote pigment production due to a genetic mutation.

Four-amino acid part makes enzyme sensitive to finasteride.

Distinct β-catenin patterns are linked to cell growth, not cell death, in lung cancer.

Mice without the Sp6 gene have problems developing several body parts, including hair, teeth, limbs, and lungs.

Finasteride works better for baldness in people with shorter gene repeats.

A new PAX9 gene mutation causes missing teeth and hair problems, but not skin or nail issues.