Search

everythinglearnresearchcommunity

for

Search:↓

A new mutation in the STS gene causes X-linked ichthyosis, even in rare female cases.

The research found that compound 6, a newly created steroid, is more effective at inhibiting 5α-reductase (an enzyme) than current treatments, suggesting it could be a better option for treating urinary tract symptoms in men.

Genotyping for NUDT15 p.Arg139Cys can help predict thiopurine side effects in Japanese IBD patients.

β‐thymosins, especially thymosin β4, help in heart protection, wound healing, and hair growth by stabilizing actin in cells.

The enzyme 5α-reductase type 1 is important for blood vessel development and fertility in the uterus.

Methylated gene parts may cause finasteride-resistance in some enlarged prostate patients.

New compounds were found to help increase hair growth and decrease hair loss.

Arabidopsis Formin 2 stabilizes actin filaments to aid cell-to-cell trafficking.

Two new gene mutations cause a rare hair disorder.

The study found stem cells in minor salivary glands that can differentiate and are involved in tumor formation when exposed to tobacco.

The human keratin 6a gene's specific sequences trigger expression in skin layers after injury.

Testosterone in our bodies helps increase insulin secretion from the pancreas.

RSPO1 mutations in certain patients lead to skin cells that don't develop properly and are more likely to become invasive, increasing the risk of skin cancer.

Compound 6 is a promising candidate for better wound healing.

Two specific genes are more active during hair growth in mice.

PROTACs offer new ways to treat hard-to-target diseases, with promising drugs for cancer in advanced trials.

IL-19 and IL-24 help cells respond to DNA damage and could be targeted for cancer and age-related disease treatments.

TAT-GILZ peptide promotes hair growth by boosting stem cell activity.

FCE 28260 is a stronger and longer-lasting inhibitor of 5α-reductase than finasteride, which may make it a better treatment for certain medical conditions.

Truncated hHb1 keratin may play a role in breast cancer cell transformation.

Inhibiting AP-1 changes skin tumor types and affects tumor cell identity.

Inhibiting AP-1 changes skin tumor types and affects tumor cell identity.

A new mutation in the TRPS1 gene caused Trichorhinophalangeal syndrome in a 17-year-old, highlighting the need for genetic testing.

JAK inhibitors can be safely used in alopecia areata patients with latent hepatitis B or tuberculosis, with proper monitoring.

A new mouse mutation causes skin and hair defects due to a gene change.

Targeting METTL1 may help slow papillary thyroid cancer growth and spread.

Increased methylation of the Filip1l gene may contribute to aggressive skin cancer.

A patient with Satoyoshi syndrome improved with a treatment combining several medications, including carbamazepine and methotrexate.

New genes and pathways are important for testosterone production and male sexual development.

A young Russian girl with Meier-Gorlin syndrome has two new mutations in the CDC6 gene.