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Melatonin affects when and how goat hair follicle genes turn on and off during growth cycles.

The conclusion is that genetic changes in the glucocorticoid receptor can lead to conditions affecting stress response, immunity, and metabolism, requiring personalized treatment.

A new gene variant causes glucocorticoid resistance in a mother and son.

Certain proteins, Lgr5 and Lgr6, are important markers of adult stem cells and are involved in tissue repair and cancer development.

The review suggests thorough evaluation and genetic testing for proper diagnosis and treatment of Chrousos syndrome.

Genotyping for NUDT15 p.Arg139Cys can help predict thiopurine side effects in Japanese IBD patients.

ARL15 is important for fat cell development and the release of the hormone adiponectin.

ILK is essential for skin development, pigmentation, and healing.

Chrousos Syndrome is caused by mutations that make the body less sensitive to glucocorticoids, leading to various symptoms and requiring high-dose treatment.

DNA methylation and long non-coding RNAs are key in controlling hair growth in Cashmere goats.

Scientists found a specific group of itch-sensing nerve cells in mice important for feeling itch but not for sensing heat or touch.

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

A newly found RNA in Cashmere goats may play a role in hair growth and development.

A new mutation in the K6b gene caused a girl's late-appearing nail condition.

The human type II 5α-reductase gene, linked to certain male health conditions, has a specific structure and low similarity to other related genes.

The human type II 5α-reductase gene has a specific structure important for understanding certain medical conditions.

New genetic mutations causing hair loss were found in a Chinese family.

A specific gene change in APCDD1 increases the risk of hair loss.

Genetic variation in the androgen receptor gene mainly causes early-onset hair loss, with maternal inheritance playing a key role.

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

Gene therapy has potential as a future treatment for Hutchinson-Gilford progeria syndrome.

The study concluded that specific proteins are necessary to maintain the structure that holds epithelial cells tightly together.

New mutations in the SLC39A4 gene found in twins help understand the genetic cause of acrodermatitis enteropathica.

A new mutation in the KRT86 gene was found to cause the hair disorder monilethrix in a Han family.

Certain mutations in the H6PD gene cause Cortisone Reductase Deficiency by affecting hormone production.

CK 5/6 expression in breast cancer is linked to negative hormone receptor status and higher tumor grade.

Mouse skin can produce and process serotonin, with variations depending on hair cycle, body location, and mouse strain.

Laser hair-comb therapy doesn't improve male-pattern hair loss.

A new mouse mutation causes skin and hair defects due to a gene change.

The methylation of the HOXC8 gene's exon 1 affects cashmere fiber length in goats.