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The FTO gene hinders stem cells in hair follicles from becoming pigment cells.

Ambras syndrome's genetic cause is unknown, as it isn't linked to androgen levels.

Certain genetic variants increase the risk of aggressive prostate cancer.

PRSS35 enzyme may help start skin tumors and could be a target for cancer treatment.

Understanding the APCDD1 gene can lead to new hair loss treatments.

Genetic testing for cancer risk can lead to early and life-saving treatments in people without symptoms.

Blocking CRF1 receptors improved male hormone levels and reduced testicular tumor size in men with a specific adrenal condition.

A new gene mutation linked to KID syndrome was found, expanding genetic knowledge.

Oral contraceptive use may increase the risk of frontal fibrosing alopecia in women with a specific CYP1B1 gene variant.

Scientists developed a new way to study mutations in a skin condition using blood cells, which may help diagnose and treat the disease.

The Megsin-Cre transgene is a new tool for genetic manipulation in the skin and upper digestive tract.

Activated β-catenin affects hair growth and skin thickness, and changes are reversible.

Pachyonychia congenita is linked to a keratin gene on chromosome 17.

PCR genotyping in cre-loxP mice can be inaccurate due to unintended gene deletions in non-target tissues.

The TCL1 transgenic mouse model is useful for understanding human B-cell leukemia and testing new treatments.

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

Activating β-catenin and inactivating PTEN cause follicular tumors, not papillomas, similar to those in Cowden’s Disease.

Specific gene variants affect wool traits in Chinese Tan sheep.

Cantu syndrome, which causes excessive hair growth and skin issues, is due to a mutation in the ABCC9 gene, and understanding this could help develop new treatments for hair diseases.

STK11 gene polymorphism does not predict metformin response in PCOS.

Mutations in the androgen receptor gene cause different levels of androgen insensitivity, making it hard to create simple tests for the condition.

A specific gene mutation causes severe skin and nail issues and hair loss.

A mutation in the HOXC13 gene causes hair and nail problems in a Syrian family.

Increasing SSAT makes skin more prone to cancer.

The IRS-2 Asp/Asp genotype may increase the risk of PCOS in Chinese women, especially if they are not obese.

Severe CCCA may be biologically and clinically different from milder forms.

Certain gene variations might help protect against insulin resistance and glucose intolerance in people with Polycystic Ovary Syndrome.

A rabbit gene important for hair development was identified and detailed.

Researchers found a non-functional sheep keratin gene due to mutations.