Search

everythinglearnresearchcommunity

for

Search:↓

A genetic mutation in the LIPH gene causes tightly curled hair that stops growing in some Japanese individuals.

The muscle damage was caused by T-cell large granular lymphocytic leukemia, not dermatomyositis.

Measuring 24-OHase induction helps identify defects in vitamin D processing and predict treatment response.

Hemoglobin α acts as an antioxidant in skin cells, especially protecting hair follicle stem cells from UV damage.

Researchers found a new genetic mutation causing a rare hair loss condition in the first Japanese child studied.

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

LRIG1 is linked to better survival in Merkel cell carcinoma.

SLHA can be hard to diagnose and needs teamwork between specialists.

The study suggests that a specific type of immune cell, memory-like NK cells, may increase during active hair loss in Alopecia areata.

A gene called APCDD1, which controls hair growth, is found to be faulty in a type of hair loss called hereditary hypotrichosis simplex.

A specific mutation in the K25 gene causes a rare genetic disorder with curly hair at birth and later hair loss, along with dental issues.

A new mutation in the PLEC gene causes a rare condition with skin blistering, muscle weakness, and hair loss.

The research found genetic differences in identical twins that could explain why one twin has a disease while the other does not.

A 589 nm laser increases IL-2 and IFN-y gene expression in human T-cells.

The Brazilian version of the Alopecia Areata Quality of Life Index is reliable for assessing patients' quality of life.

A deletion in the CDH3 gene causes a rare disorder with short hair and vision loss.

Focal palmoplantar callosities may help diagnose non-Herlitz junctional epidermolysis bullosa.

Variation in the TCHH gene affects wool curliness in sheep.

Mutations in the LSS gene cause hair loss and may affect brain development, with varying severity.

A point mutation in the androgen receptor gene causes complete androgen insensitivity.

IFN-γ production by CD4 T cells is crucial for causing alopecia areata.

MILL molecules are unique immune proteins in mice that don't need TAP to appear on cell surfaces.

CDH3-related disease causes worsening eye and hair issues.

The HSD3B1 variant increases hair loss risk in overweight women with PCOS.

The treatments stopped hair regrowth in mice.

Genetic testing is crucial for diagnosing and treating acrodermatitis enteropathica effectively.

HHV-6 reactivation may be linked to psychiatric disorders and can improve with antiviral treatment.

The new skin-targeted COVID-19 vaccine creates strong immune responses and could improve vaccination methods.

Both induced and spontaneous AA lymphocytes can cause alopecia areata in mice.