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A new gene mutation linked to Olmsted syndrome may increase cancer risk, suggesting the need for ongoing patient monitoring.

Researchers found a new mutation causing total hair loss from birth.

The condition is linked to chromosome 12, but no mutations were found in the known genes.

Mutations in the p63 gene affect skin adhesion, barrier integrity, and hair growth.

Sebocytes play a key role in controlling androgen levels in human skin.

The enzyme 17β-HSD type 2 mainly performs oxidation in human sebaceous glands, which may help protect against acne.

17β-estradiol can reduce inflammation in the skin.

CCCA in women of African ancestry may be caused by PADI3 gene mutations and intense hair grooming.

A new mRNA variant of the SCF gene in sheep skin produces a shorter, different protein.

PF-998425 is a new, effective, and non-phototoxic treatment for skin conditions related to androgens.

A new HRAS gene variant may cause a range of symptoms including intellectual disability and psychiatric issues.

Certain gene variations and different levels of BDNF and CRH hormones are linked to vitiligo.

Pesticides can cause reproductive and adrenal health issues.

Advancements in understanding, diagnosing, and managing congenital adrenal hyperplasia have improved treatment and long-term outcomes.

Nonclassic 21-hydroxylase deficiency is a common, treatable genetic disorder causing reversible symptoms like acne and hair loss.

A specific ATR gene mutation is linked to a hereditary oropharyngeal cancer syndrome.

The process effectively regenerates the Pd/C catalyst for finasteride synthesis.

Different genes are linked to various types of hair loss.

TACE/ADAM17 is essential for maintaining healthy hair and hair follicle stem cells.

The length of the CAG repeat in the androgen receptor gene affects the risk and progression of prostate cancer, BPH, infertility, and undermasculinized genitalia.

Women with non-classical congenital adrenal hyperplasia have higher levels of certain steroids, which can be reduced by treatment.

A new mutation in the CDH3 gene causes hair loss and vision problems in a young girl.

Changes in KRT17 gene activity linked to wool production in Angora rabbits.

Testing for CAG repeat polymorphism in the androgen receptor gene is not currently recommended for managing hypogonadism.

Deleting vitamin D and calcium receptors in skin cells increases skin cancer risk by reducing DNA repair and stress response.

A new genetic model may improve treatment and diagnosis for certain inherited skin diseases.

Three new gene mutations cause rickets and hair loss, treatable with high calcium and calcidol, but hair regrowth is rare.

Older parental age, rural living, and specific genetic mutations increase hypospadias risk in children.

ALRN-6924 may prevent hair loss caused by chemotherapy.