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Targeted siRNA therapy may be a promising treatment for KID syndrome by reducing mutant gene expression and improving cell communication.

A 6-year-old girl was diagnosed with a rare hair disorder called monilethrix.

A man with kidney tumors and lung cysts was diagnosed with Birt–Hogg–Dubé syndrome and treated successfully, with genetic testing confirming the diagnosis.

A new mutation in the TRPS1 gene was found in a Ukrainian girl with Trichorhinophalangeal syndrome type I.

Blocking the enzyme that turns testosterone into DHT can safely and effectively treat enlarged prostate.

Cantú syndrome is caused by mutations in the ABCC9 gene.

New treatments targeting specific genes show promise for treating keratin disorders.

The study found that Keratosis Pilaris Atrophicans is a genetic skin condition that starts in childhood, involves inflammation and scarring, and current treatments are only somewhat effective.

New therapies are being developed that target integrin pathways to treat various diseases.

RXRα is crucial for proper immune response and links diet to immune function.

Different skin stem cells help heal wounds, with hair follicle cells becoming more important over time.

A girl had rickets due to a gene mutation affecting vitamin D response.

KFSD is a genetic disorder causing hair loss and skin issues, with no effective treatment.

Recent genetic insights show that low-renin hypertension includes a range from essential hypertension to secondary or familial forms, affecting diagnosis and treatment.

Ca_v1.2 affects hair growth and could be a target for hair loss treatments.

Retinoids increase steroid sulfatase activity in leukemia cells through RARα/RXR and involves certain pathways like phosphoinositide 3-kinase and ERK-MAP kinase.

Tigason improved hair growth in a boy with monilethrix without side effects.

Keratosis pilaris is often linked to genetic mutations and causes skin and hair abnormalities, regardless of those mutations.

Dermatopathia pigmentosa reticularis causes skin discoloration, hair loss, and nail problems.

Polish medical societies recommend personalized treatment for PCOS based on the patient's specific symptoms and use the Rotterdam criteria for diagnosis.

New techniques have enhanced our understanding of how stem cells function and the role of mutations in aging tissues, which may influence future cancer therapies.

Plant-based ingredients in hair care are being replaced by synthetic alternatives.

About 21.3% of young, healthy Chinese men experience hair loss. Hairlines are mostly linear or have a central protrusion. Hair is densest on the top and back of the head, and hair follicles usually have 1 or 2 hairs. This information can help in designing hair restoration procedures.

New gene variants linked to a rare inherited hair loss disorder were found in three Chinese families.

Chronic scalp lesions with crusts and pus that heal with strong topical steroids suggest Erosive Pustular Dermatosis, confirmed by biopsy showing specific immune cells.

Monilethrix is a genetic hair disorder causing fragile, beaded hair with no effective treatment.

A new type of pachyonychia congenita linked to a specific keratin gene mutation was found in two Pakistani families.

Wound healing can help prevent hair loss from chemotherapy in young rats by increasing interleukin-1β signaling.

New drug shows promise for better hair growth in baldness treatment.

Targeting CXCL10 may help treat alopecia areata.