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A 70-year-old woman with bronchiectasis developed a rare immune disease due to a bacterial infection, requiring a difficult balance of treatments.

B2m-free HLA variants may be a new class of HLA important in immune responses and diseases.

Tetrathiomolybdate reduces hair growth marker in skin cells by boosting harmful oxygen molecules, but effects can be reversed.

Transplant success has improved with better immunosuppressive drugs and donor matching.

Skin aging is a complex process influenced by various factors, leading to wrinkles and sagging, and should be considered a disease due to its health impacts.

The document concludes that future heart disease research should account for sex-specific differences to improve diagnosis, treatment, and outcomes.

Testosterone may influence COVID-19 severity and outcomes.

KRT80 may worsen cancer by increasing growth and spread, but its full effects on treatment and outcomes need more research.

Origanum vulgare leaf extract reduces liver and kidney damage caused by finasteride in mice.

Long-term use of finasteride in women can cause hormonal changes, DNA damage, and menstrual issues.

New genetic discoveries may lead to better treatments for alopecia areata.

Loss of a specific protein in skin cells causes symptoms similar to psoriasis.

Diabetes can lead to blindness and skin problems, and managing blood sugar and blood pressure is crucial to prevent these complications.

Computational tools identified 29 drugs that could potentially target 19 genes involved in chemotherapy-induced hair loss, which could lead to more effective treatments.

Bioinspired polymers are promising for advanced medical treatments and tissue repair.

Identified genes linked to male-pattern baldness may help develop new treatments.

Skin cells and certain hair follicle areas produce hemoglobin, which may help protect against oxidative stress like UV damage.

A woman in Sri Lanka was diagnosed with lupus after presenting with protein loss from the gut and other symptoms.

Psoriasis is linked to a higher risk of autoimmune diseases and other health conditions.

FOXN1 mutations cause severe immunodeficiency, hair loss, nail issues, and thymus defects.

Plet-1 protein helps hair follicle cells move and stick to tissues.

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

Mushroom beta-glucans from Ganoderma lucidum can reduce tumor size and metastasis in cancer.

Early genetic testing and JAK inhibitors can help treat systemic inflammation in SAVI patients.

Afatinib, neratinib, and zanubrutinib could be effective against KRASG12C-mutant tumors.

Folliculin deficiency causes problems with cell division and positioning due to disrupted RhoA signaling and interaction with p0071.

μ-Crystallin may help hair growth by affecting thyroid hormone levels in mouse hair follicles.

A patient with Birt-Hogg-Dubé Syndrome also had choroidal melanoma, suggesting the need for careful eyelid exams in such patients.

Stem cell therapy is promising for treating various health conditions, but more research is needed to understand its full potential and address challenges.

Genetic defects in the glucocorticoid receptor gene can cause conditions with abnormal sensitivity to stress hormones, and other factors may also affect this sensitivity.