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A new mutation in the CYP11B1 gene was found in a woman with mild hyperandrogenemia, a rare cause of non-classic congenital adrenal hyperplasia.

GBP1 is a key target for treating Epstein-Barr virus-related kidney cancer, and finasteride may help.

Patients with Shwachman-Diamond syndrome often get misdiagnosed due to a wide range of symptoms, including immune system problems and bone abnormalities.

The role of γδT-cells in causing alopecia areata remains unclear.

A new tool helps study hair follicle cells to develop better treatments for hair disorders.

Arteannuin might work against cancer and Alzheimer's by targeting neprilysin.

New genes linked to male pattern baldness were found on chromosome 20p11.

Trichohyalin may trigger the immune response causing alopecia areata.

The near-naked hairless mutation causes hair loss but is not due to a mutation in the hairless gene itself.

B blood type has the highest growth factors and cytokines in umbilical cord blood-derived PRP.

Hedgehog signaling is crucial for hair development, cadherins affect cell adhesion, neutrophils play a role in skin lesions, and BP230 autoantibodies impact skin stability.

Two rare genetic diseases cause severe rickets in children due to defects in vitamin D metabolism.

Higher DKK-1 levels found in hair loss patients; L-ascorbic acid 2-phosphate, L-threonate, and ginsenoside F2 may help promote hair growth.

Giving a special protein to dogs with a certain genetic disease improved their symptoms but didn't help with hair growth.

Lrig1 could be a marker for advanced sebaceous carcinoma.

The AIRE gene variant rs2075876 is linked to a higher risk of alopecia areata in males.

New therapies for Birt–Hogg–Dubé syndrome are being developed based on understanding the FLCN gene's role.

Genetically repaired stem cells may treat certain genetic diseases, Th17 cells are key in fighting systemic fungal infections, hair loss in AGA is due to progenitor cell loss, and α-synuclein transfer might contribute to Parkinson's disease progression.

Certain RNAs may help diagnose alopecia areata by affecting keratin genes.

A specific gene mutation causes complete hair loss in an Irish Traveller family.

pdHGF speeds up wound healing and hair growth.

Skin changes help detect graft-versus-host reaction early after bone marrow transplants.

Organ transplant recipients have a higher risk of skin cancer over time, atopic dermatitis skin shows unusual bacterial and fungal patterns, a new tool for measuring hidradenitis suppurativa severity was created, and gene expression changes in male baldness suggest new treatments.

KRT14 gene variants cause dermatopathia pigmentosa reticularis, affecting nails, teeth, and hair.

Hair loss treatment caused more hair loss in a man.

Cinacalcet may help treat hereditary vitamin D resistant rickets safely.

Human placenta extract reduces inflammation and symptoms in atopic dermatitis.

Chronic graft-versus-host disease in the skin shows strong Th1 immune response and unique barrier issues.

Myoblast transplantation shows promise for treating various muscle and heart conditions.

Plucked hair follicles can help diagnose scalp lupus.