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Certain genetic variants are linked to frontal fibrosing alopecia in Spanish patients.

KRT17 may be a new target for endometrial cancer treatment because it helps cancer cells move and form new blood vessels.

Liver damage in PCOS is linked to iron overload and cell death due to the miR-761-hepcidin/GPX4 pathway.

ETS2 drives cancer progression in squamous cell carcinoma and is linked to poor patient outcomes.

Researchers found that most genes affecting drug responses are not fully covered by commercial SNP chips, suggesting the need for more comprehensive tools to optimize drug selection based on genetics.

A patient with a PLEC mutation has epidermolysis bullosa, muscular dystrophy, and myasthenia gravis, which improved with steroid treatment.

Overexpressing CtBP1 in skin cells causes skin and hair problems.

A patient with a new PLEC gene mutation showed symptoms of both muscular dystrophy and myasthenia gravis, which improved with steroid treatment.

A man with a rare skin condition and a new gene mutation developed high calcium levels due to his treatment.

Using a combination of specific cell cycle regulators is better for safely keeping hair root cells alive indefinitely compared to cancer-related methods.

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

The guidelines aim to find treatable prostate cancer early while avoiding unnecessary tests and treatments.

Ca²⁺-mediated protein citrullination controls cell growth in the CNS and may help treat brain tumors.

Activating β-catenin in different skin stem cells causes various types of hair growth and skin tumors.

ODC expression in mouse skin and tumors is varied and can be inhibited by retinoic acid or cycloheximide.

Disrupting β-catenin signaling in certain cells causes anorectal malformations.

Ponatinib can cause a rare skin reaction that resolves with topical treatment and temporary drug discontinuation.

A mutation in the vitamin D receptor causes severe resistance to vitamin D, affecting bone health but not hair growth.

The LRRK2-G2019S mutation in Parkinson's disease has a lifetime penetrance of 25-35%, and finasteride may help reduce symptoms in adult male Tourette syndrome patients.

Paxillin may help manage androgen-related disorders like PCOS by stabilizing androgen receptor proteins.

Deleting part of a gene in mice causes wavy hair and high pup loss.

Fixing DNA errors is crucial to prevent skin cancer.

Scientists have found specific genes linked to different hair loss conditions, which could lead to new treatments.

Rare changes in the KRT82 gene are linked to a higher risk of Alopecia Areata.

A certain mutation in the fetal alpha 5-reductase gene is linked to a higher risk of late miscarriage.

Researchers found a gene mutation responsible for a rare hair loss condition.

Certain genetic variations are linked to hair loss in Mexican men.

TMPRSS2 is crucial for COVID-19 infection and is a potential target for treatment.

New ABCA12 gene mutations were linked to a skin condition with scaling and hair loss, and a treatment helped with hair loss in a related case.

CCCA can affect both genders and all ages, and it has a genetic component.