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Abnormal keratin expression in mice causes severe oral issues, affecting feeding.

A 15-year-old girl with rare reproductive disorders received hormone therapy to develop secondary sexual traits, but infertility persisted.

Ribonucleotide excision repair is crucial to prevent skin cancer.

Targeting specific molecular pathways may improve treatments for chemoresistant cancers.

Mutations in the SNRPE gene cause hereditary hair loss.

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

Combining genetic and physical data improves diagnosis and treatment for early-onset monogenic diabetes.

A mutation in mice causes hair loss and immune problems.

Bezafibrate treatment improved skin and spleen health in aging mice but didn't extend lifespan.

Dimethyl-fumarate may cause temporary hair loss.

A young boy's uncombable hair is due to a rare genetic condition that usually improves over time.

A six-year-old boy with excessive hair growth and other symptoms may have a genetic link on chromosome 17q, requiring regular medical follow-ups.

Some minoxidil combinations can help differentiate leukemia cells without harming other cells.

A boy with monilethrix has brittle hair that breaks easily due to a genetic condition, which might improve by puberty.

Graying hair is caused by changes in gene expression affecting cell functions.

A specific gene mutation causes hair loss and potential eye issues, even if vision seems normal.

Deleting Smad4 and PTEN genes in mice causes rapid, invasive stomach cancer.

Certain genetic variants reduce enzyme activity, contributing to non-classic congenital adrenal hyperplasia.

Chemotherapy causes permanent hair follicle damage by triggering stem cell loss.

Blocking BACE1 and BACE2 enzymes causes hair color loss in mice.

Increased 14-3-3 proteins may block hair cycle regression, causing hair loss.

Hair analysis could help diagnose and treat schizophrenia more effectively.

Severe genetic variants in children with a specific adrenal condition match predicted symptoms well, but milder variants do not.

A gene mutation in mice causes skin defects and early death.

Melasma's causes include genetics, sun exposure, hormones, and oxidative stress, and understanding these can help create better treatments.

Scientists made a mouse model of a serious skin cancer by changing skin cells with a virus and a specific gene, which is similar to the disease in humans.

Melatonin may help with nerve pain, a hepatitis C drug is effective but has side effects, a treatment for mouth sores works but can cause blood issues, ear reconstruction with an implant is safe, HIV transmission from mother to child in Taiwan is now 0% with treatment, certain blood problems are more common in people with a tongue condition, a gene and being overweight are linked to hair loss in some women, a new technique could reduce radiation for lung nodule patients, a hepatitis treatment may lower cancer recurrence after a procedure, and adding extra screening improves tuberculosis detection in patients with lung infections.

The reconstructed skin model from hair follicles functions like human skin in processing chemicals and can be used to test ingredient safety.

Researchers found markers that can tell if hair has been bleached, which could improve hair test accuracy.

Drosha and Dicer are essential for hair follicle health and preventing DNA damage in skin cells.