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Increased Toll-like receptors in blood cells may contribute to alopecia areata and could be a target for new treatments.

The DNMT3B -579G>T polymorphism may increase the risk of colorectal cancer.

Two siblings had a rare hair condition with banded hair, which doesn't need treatment.

An 87-year-old man showed unusual signs of Hodgkin lymphoma, primarily high calcium levels, which improved after treatment and revealed the disease.

Impaired LEF1 activation speeds up skin cell development in Hutchinson-Gilford Progeria Syndrome.

The immune system can cause permanent skin and hair whitening by attacking pigment cells.

The AR gene is linked to male-pattern baldness, TNFSF4 to heart disease, SLC19A3 to BBGD, MCT8 to a syndrome, and segmental duplications to genetic variation.

Dynlt3 is important for melanosome transport and skin coloration.

A cluster of sulfur-rich hair protein genes was found on chromosome 17.

The study identified key immune cell differences between mild and severe alopecia areata.

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.

TPA strongly increases ODC activity in certain skin cells, potentially aiding tumor growth.

A misdiagnosed case of HAIR-AN syndrome led to unnecessary surgeries and highlighted the importance of correct diagnosis and treatment.

A new EDA gene variant causes X-linked hypohidrotic ectodermal dysplasia in a Chinese family.

The HDDPiW-jSB solution may prevent hair loss caused by docetaxel in rats when applied regularly.

The KRTAP36-1 gene affects wool quality in Chinese Tan lambs.

Some people with chronic hair loss may have thyroid autoimmunity.

Baricitinib helps alopecia areata and may improve psoriasis, but its effect on psoriatic arthritis is unclear.

Frontal fibrosing alopecia shows increased inflammation and JAK-STAT pathway activity without reduced hair proteins.

IL-15 promotes hair growth and protects hair follicles.

TRIV-509 quickly improves skin barrier and cell health in atopic dermatitis.

NBCCS and BFHS might be the same syndrome, helping better identify and manage cases.

A 6-year-old boy's skin condition improved after stopping a specific treatment and starting new medications.

GABEB is a less severe skin condition caused by a gene mutation affecting collagen, leading to blisters and other symptoms.

Botulinum toxin type A injections may help treat hidradenitis suppurativa.

Adults with alopecia areata stick to their medication better than those with atopic dermatitis.

EBV infection increases a specific keratin variant in carcinoma cells, possibly affecting cell structure and cancer progression.

A Turkish family with sparse hair and eyebrow loss has a mutation in the U2HR gene linked to Marie Unna hereditary hypotrichosis.