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Screening for the NUDT15 gene variant can prevent severe side effects from thiopurine drugs in East-Asian people.

Trodelvy™ helped some patients with advanced breast cancer, but had side effects.

Some treatments can improve skin's defense against damage, but overuse may cause other skin problems.

Prenatal diagnosis of trichothiodystrophy is possible in the second trimester using fetal eyebrow biopsy, with sulfur content analysis being more reliable.

The girl had a rare disorder causing mental and physical symptoms, with weak hair and unclear neurological issues.

Trimethoprim-sulfamethoxazole can cause aseptic meningitis.

The E2 protein affects gene activity in hair follicles of mice.

The TRPV3 gene variant may cause the long-haired suri alpaca coat.

UVFT helps diagnose hair and scalp diseases by showing different fluorescence patterns.

Enterobacter sp. SA187 helps tomato plants grow better in salt and heat by boosting stress-related responses.

Antiviral medication valganciclovir may improve skin and hair in Trichodysplasia Spinulosa patients.

A genetic mutation in a specific gene causes a salt-wasting condition in a Pakistani girl and her family.

TTNPB helps turn stem cells into neural stem cells, improving depression-like behaviors in rats.

The Trichodysplasia spinulosa virus protein can cause abnormal hair growth in mice.

PRMT5 inhibitors effectively fight adenoid cystic carcinoma in salivary glands.

K_ATP channel gene mutations are linked to heart diseases, but more research is needed to understand the connection and treatment potential.

Lowering homocyst(e)ine levels can reverse skin and hair lightening by restoring enzyme activity needed for pigmentation.

Transgenic sheep cells with spider silk gene were successfully created for future sheep hair expression.

Thioglycolic acid and L-cysteine change hair structure differently during perms, affecting hair strength and curling efficiency.

Tacrolimus and corticosteroids can improve symptoms of Satoyoshi syndrome.

Finasteride significantly reduced tics and obsessive-compulsive symptoms in Tourette syndrome patients.

Early diagnosis, stopping the suspected drug, and supportive care are crucial for treating Stevens-Johnson Syndrome and Toxic Epidermal Necrolysis.

The frizzy mouse and hairless rat mutations are due to changes in the Prss8 gene.

PEGylated flavonoid Aspasomes improve brain protection and memory in stress-related disorders.

ATP-sensitive K+ channel subunits, particularly Sur2A, play a significant role in various cancers.

A 90-year-old man was diagnosed with heart failure due to wild-type transthyretin cardiac amyloidosis.

TMPRSS2 affects COVID-19 severity and treatment options.