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The study concluded that testing hormone levels after stimulation is not reliable for identifying carriers of 21-hydroxylase deficiency; genetic testing is necessary.

Certain genetic markers linked to reproductive potential were identified by their impact on a protein's ability to bind to genes.

No strong genetic link to other skin conditions was found, but some genetic factors may make people more likely to get seborrheic dermatitis.

Researchers found a genetic region that influences the number of coat layers in dogs.

Certain genetic variants in the androgen receptor are linked to higher PSA levels, potentially affecting prostate cancer screening outcomes.

A new genetic area linked to a rare hair loss condition was found on chromosome 13 in a Chinese family.

Myotonic dystrophy should be considered in patients with hair thinning, and genetic counseling is important.

A 12-year-old boy with a rare genetic condition has progressive hair loss with no effective treatment.

New models predict male pattern baldness better than old ones but still need improvement.

A family was found with both Trichorhinophalangeal syndrome and Loose Anagen Syndrome, suggesting a genetic connection.

Different human traits like skin color and hair type vary between populations due to genetic adaptations to the environment.

Genetic screening can help diagnose and manage infertility in Slovenian couples.

A Saudi individual initially identified as a girl had a genetic disorder affecting gender development.

Certain genes may influence hair loss differently in men and women.

Genetic analysis of rabbits identified key genes for traits like coat color, body size, and fertility.

A new MTX2 gene mutation caused a severe genetic disorder in a young Chinese girl.

Genetic risk for PCOS can affect children's growth, metabolism, and development from early life into adulthood.

Different people show different symptoms for genetic diseases because of how sensitive their bodies are to small changes in important factors.

A genetic variant linked to hair thinning in Japanese women was found.

The document concludes that the development of certain tumors is influenced by genetic background and that a specific gene modification can lead to tumor regression and reduced growth.

A new mutation in the CYP11B1 gene was found in a woman with mild hyperandrogenemia, a rare cause of non-classic congenital adrenal hyperplasia.

Mother and son diagnosed with a rare genetic hair loss condition with no effective treatment.

Androgenic alopecia in men is mainly linked to family history, hormonal imbalances, and metabolic issues, but can also be influenced by lifestyle habits, environmental factors, and deficiencies in certain vitamins and microelements like copper.

Certain genetic variations in the AR and ERβ genes can affect androgen levels in women.

New findings explain how genetic changes, body clocks, and certain molecules affect tissue response to stress hormones.

Researchers found 15 new genetic links to skin traits in Japanese women.

Melanoma's complexity requires personalized treatments due to key genetic mutations and tumor-initiating cells.

Nonclassic congenital adrenal hyperplasia is a genetic disorder causing hormone imbalances, affecting fertility and requiring personalized treatment.

Researchers found two new genetic variants linked to Alzheimer's disease.