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DHT affects bone growth by altering gene activity in osteoblasts, potentially complicating steroid use.

The Hairless gene is crucial for hair cell development, affecting whether skin cells become hair or skin and oil gland cells.

The congress highlighted new gene therapy techniques and cell transplantation methods for treating diseases.

Identifying nonclassic congenital adrenal hyperplasia and carriers of CYP21 mutations is challenging, and genetic counseling is recommended due to their prevalence.

Plucked hairs can be used instead of skin biopsies to study hair traits because they contain specific cells related to hair.

New tools show that in fish, NPY increases feeding and somatostatin decreases it.

Genetic mutations can affect female sexual development, requiring personalized medical care.

EDA2R gene linked to hair loss.

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

FoxN1 gene is essential for proper thymus structure and preventing hair loss.

Researchers found a new gene variant linked to a rare bone disease, which doesn't always cause symptoms in carriers.

A gene deletion in mice causes weak protein, immune issues, hair loss, airway problems, and wasting disease.

The C-allele and CC-genotype in the PTPN22 gene lower the risk of alopecia areata.

The length of CAG repeats in the androgen receptor gene is linked to ovarian reserve but does not affect how the ovaries respond to stimulation.

Certain gene patterns in breast cancer are linked to how active hormone receptors are and could affect patient survival.

Keratin protein production in cells is controlled by a complex system that changes with cell type, health, and conditions like injury or cancer.

The TRPV3 ion channel is important for skin and hair health and could be a target for treating skin conditions.

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

The gene Prss53 affects hair shape and bone development in rabbits.

The tumor suppressor gene FLCN affects mitochondrial function and energy use in cells.

The document describes a woman with familial Parkinson's disease due to a genetic mutation, showing severe symptoms and poor response to treatment, and suggests finasteride may help reduce symptoms in Tourette syndrome.

A new gene location for Keratosis follicularis squamosa was found on chromosome 7p14.3-7p12.1.

Blood tests for tumor cells could improve prostate cancer diagnosis and treatment; hair loss severity linked to a gene affecting prostate conditions.

The research found that a complex gene network, controlled by microRNAs, is important for hair growth in cashmere goats.

A genetic variant in the androgen receptor gene increases heart disease risk in women but not in men.

Keratin proteins are crucial for healthy skin, but mutations can cause skin disorders with no effective treatments yet.

The severity of symptoms in nonclassical congenital adrenal hyperplasia is not determined by CYP21A2 gene variations.

Finasteride irreversibly affects human steroid 5α-reductase 2, providing insight into its catalytic mechanism and disease-related mutations.

The study found that certain mutations in the vitamin D receptor can cause rickets and potentially affect hair growth.

Keratin mutations cause skin diseases and could lead to new treatments.