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Patients with the same genetic mutation for vitamin D-resistant rickets showed different symptoms but all improved with treatment except for hair loss.

Using special RNA to target a mutant gene fixed hair problems in mice.

Different hair loss types need accurate diagnosis for proper treatment.

Certain genetic variants increase the risk of resistance to hormone therapy in prostate cancer patients.

Hyperadrenocorticism in ferrets is linked to neutering and indoor housing, and is best treated with surgery and a deslorelin implant.

Researchers found a new genetic mutation causing a rare hair loss condition in the first Japanese child studied.

A man with KID syndrome developed a rare cancer in a long-term skin infection.

The research linked PLCD1 gene variants to the development of trichilemmal cysts.

Deleting the Trf1 protein in mice is safe and may help prevent cancer without major side effects.

Genetic defects in testosterone production can cause hormonal and developmental disorders, and more research is needed to understand androgen regulation and develop safer treatments.

Iron deficiency might contribute to hair loss in women.

Dermatologists diagnose and manage melanoma more effectively than general practitioners.

The conclusion is that certain genetic factors and blood types may affect COVID-19 severity, but changes in ACE2 and TMPRSS2 genes are not clearly linked to it.

Genetically modified sheep with more β-catenin grew more wool without changing the wool's length or thickness.

Two different mutations in the vitamin D receptor gene cause different symptoms and responses to treatment in Lebanese patients with hereditary rickets.

The document explains the difficulty in diagnosing and treating brain diseases caused by the immune system and stresses the need for quick and accurate tests.

Genetic differences within ethnic groups may affect prostate cancer treatment effectiveness.

A 12-year-old boy with a rare genetic condition has progressive hair loss with no effective treatment.

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

A new mutation in the K6b gene caused a girl's late-appearing nail condition.

Certain transcription factors are key in controlling skin stem cell behavior and could impact future treatments for skin repair and hair loss.

The unique coat of lykoi cats is likely caused by new variants in the Hairless gene.

A mutation in the HR gene causes a rare form of irreversible hair loss in two Kashmiri families. Whole exome sequencing is effective for finding such mutations.

Genetic variations affect dutasteride treatment response for male pattern hair loss.

Longer TA repeats in the SRD5A2 gene may increase acne risk in Chinese people.

Some domesticated animals have the same genetic skin diseases as humans, which can help doctors understand human genetic mutations.

CaV1.2 helps activate hair follicle stem cells without calcium flux.

Certain proteins help nerve cells branch, and other findings relate to cancer, stem cell behavior, and cell division.

A new mutation in the KRT86 gene was found to cause the hair disorder monilethrix in a Han family.

A Taiwanese patient had hair loss and skin bumps without the usual gene mutation, suggesting other genetic factors might be involved.