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A new gene mutation linked to Olmsted syndrome may increase cancer risk, suggesting the need for ongoing patient monitoring.

hHb1, hHb3, and hHb6 mRNAs start expressing at the same time in hair follicles.

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Researchers found a new area on chromosome 2 linked to a genetic hair loss condition.

Abnormal Hedgehog signaling in blood cancers may help tumors grow and resist chemotherapy, suggesting potential for targeted treatments.

27 out of 32 candidates passed the hair restoration surgery exam.

Human hair keratin artificial tendon is a safe and effective tendon substitute.

Some patients treated with peginterferon and ribavirin for chronic hepatitis C had mild to moderate skin reactions, but treatment did not need to be stopped.

Alopecia can be reversed with timely steroid treatment in VKH and SO diseases.

Tgm2 helps stabilize dying cells and aids fibroblast attachment to the extracellular matrix.

A new genetic area linked to a rare hair loss condition was found on chromosome 13 in a Chinese family.

Herpes simplex virus infections should be considered in pemphigus patients to avoid unnecessary changes in treatment.

Reticulocyte hemoglobin content is the best indicator of iron deficiency in women with diffuse non-scarring hair loss.

The protein called small nuclear ribonucleoprotein polypeptide E is identified as a cause of a type of hair loss without other symptoms.

Ringworm from Trichophyton verrucosum mainly affects farm workers in Japan, spreading in families and peaking in winter.

Recombinant human TSG-6 speeds up wound healing in diabetic mice.

The conclusion about the value of ABHRS certification cannot be determined from the text provided.

Trichothiodystrophy causes abnormal protein deposits and distortion in hair follicles.

A gene mutation causes a rare hereditary hair loss, offering potential for new treatments.

An 8-year-old boy with Recklinghausen's Disease shows various symptoms and is from a family with close genetic ties.

Human hair keratin may help repair spinal cord injuries.

A young athlete's fragile hair condition improved by cutting hair and using gentle shampoo.

Rac1 is crucial for normal hair structure and pigmentation.

A new gene mutation causes a rare type of hair loss.

Immune cells might contribute to hair loss caused by a specific mutation.

VEGF can boost hair growth in mice with scleroderma.

Vδ1+ T-cells in the skin contribute to hair loss in alopecia areata and could be targeted for treatment.

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