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Certain HSD3B1 gene types are linked to worse prostate cancer outcomes and affect treatment response and other health conditions.

Two siblings have a rare hair condition caused by a new genetic variant.

Certain genetic changes in the LSS gene cause a rare skin and hair condition.

PP2Acα is essential for proper hair and skin development.

Certain genetic variations are linked to higher liver enzyme levels in patients treated for chronic hepatitis C with specific drugs.

A new gene mutation may allow some piebaldism patients to regain skin color in white patches.

The environment around the time of conception can change the VTRNA2-1 gene in a way that lasts for years and may affect disease risk.

New mutations in the DSG4 gene cause a rare hair condition.

Early and accurate diagnosis is crucial for managing rare genetic disorders like this localized variant of junctional epidermolysis bullosa.

Patients with a specific genetic variant have more severe alopecia areata and higher recurrence rates.

Researchers found a new area on chromosome 2 linked to a genetic hair loss condition.

lncRNA2919 slows down rabbit hair growth by stopping cell growth and causing cell death.

A deficiency in the TTC7A gene causes immune problems, gut issues, and hair loss.

The P133R mutation in AKR1D1 enzyme causes harmful bile acid buildup, explaining related health issues.

Certain mutations in a hair growth-related gene cause a type of genetic hair loss.

The AR gene is linked to male-pattern baldness, TNFSF4 to heart disease, SLC19A3 to BBGD, MCT8 to a syndrome, and segmental duplications to genetic variation.

SQSTM1 gene issues may increase the risk of alopecia areata.

A new syndrome, Teelwani Syndrome, combines features of two rare genetic disorders.

SQSTM1 is linked to increased risk of alopecia areata.

Some cases of short anagen hair syndrome are linked to specific genetic variations that are also connected to male pattern baldness.

Graham-Little Piccardi Lassueur Syndrome is a rare skin condition with specific hair loss and skin symptoms.

Frontal fibrosing alopecia is linked to four genetic areas, especially the HLA-B*07:02 allele.

A new mutation in the TMEM173 gene and a risk allele in IFIH1 cause a unique set of immune-related symptoms.

Protoporphyrin IX is useful in cancer treatment but can cause health problems if not properly regulated.

The CTLA-4 gene change studied does not affect Polycystic Ovarian Syndrome in the women tested.

G allele of AR Stul polymorphism linked to higher hair loss risk, especially in white people.

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

Targeting mitophagy may help treat alopecia areata by reducing inflammasome activation.

Longer CAG repeats in gene linked to more severe hair loss in females.

Your genes, especially IL-1a, can predict how well a hair growth treatment with platelet rich plasma will work for you.