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Genetic defects in the glucocorticoid receptor gene can cause conditions with abnormal sensitivity to stress hormones, and other factors may also affect this sensitivity.

A woman with a unique syndrome similar to TRPS has a genetic change near the TRPS1 gene, affecting its regulation.

Researchers found a gene in hamsters that responds to male hormones and may be indirectly controlled by them.

Fish teeth and taste bud densities are linked and can change between types due to shared genetic and molecular factors.

The article concludes that studying how skin forms is key to understanding skin diseases and improving regenerative medicine.

Heredity and hormones cause common hair loss, and topical minoxidil is the first recommended treatment.

Ayme-Gripp Syndrome was confirmed in a woman through genetic testing, highlighting the need to consider rare genetic conditions in diagnoses.

New treatments for alopecia areata show promise, but standardized guidelines are needed.

The document suggests more research is needed to understand the link between baldness and prostate cancer.

The cancer gene c-Myc increases harmful chemicals that damage DNA and can lead to cancer, but antioxidants can reduce this damage.

Four genetic risk areas related to male-pattern baldness were identified, with WNT signaling playing a role in its development.

The project aimed to understand how genetic test results affect patients' actions and feelings in dermatology.

The B2 genes are crucial for hair growth in rats.

Researchers identified a new variant of the FGF5 gene in sheep that affects hair length.

The Asiatic lion has very low genetic diversity and unique genetic traits, highlighting the need for its conservation.

Vitamin D receptor is crucial for skin wound healing.

Men and women respond differently to drugs for COVID-19, high cholesterol, and diabetes, which suggests a need for personalized treatments.

ATP-dependent chromatin-remodeling complexes are crucial for gene regulation, cell differentiation, and organ development in mammals.

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

Advanced human skin models improve drug development and could replace animal testing.

There's no significant link between the D19S884 marker at the insulin receptor gene and polycystic ovary syndrome.

Retinoids increase steroid sulfatase activity in leukemia cells through RARα/RXR and involves certain pathways like phosphoinositide 3-kinase and ERK-MAP kinase.

Researchers developed a cost-effective 66 K SNP chip for cashmere goats that is accurate and useful for genetic studies.

Testosterone makes the connections in the uterus lining simpler and lowers certain protein levels, which might lead to infertility.

BMP4-related anomalies can cause a wide range of eye, brain, and hand/foot problems, and new cases show this variability.

Gene differences found in hair follicles linked to male baldness.

Using SNP array testing helped quickly find the gene causing Woodhouse-Sakati syndrome in two related individuals.

A specific genetic change is linked to mental disorders, intellectual disability, and possibly autoimmune disease in a family.

The document concludes that sex hormones are crucial for mammalian reproduction, health, and behavior, and require more research for therapeutic use.

Most adrenal cortex tumors are benign and non-secreting, but proper diagnosis and treatment are important due to the rare possibility of cancer.