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New liposome treatment successfully delivers CRISPR to deactivate a key enzyme in androgen-related disorders.

More research is needed to understand how testosterone is maintained in adult males.

The document concludes that inflammation markers can be used in diabetes, vitamin D3 affects immune pathways, hyperthyroidism changes hormone levels, androgen levels help diagnose Adrenocortical Carcinoma, erectile dysfunction is linked to diabetes, hypogonadism is common in HIV-infected males, and hormones can be biomarkers for various conditions.

RNA editing significantly affects hair growth and follicle cycling in the Tianzhu white yak.

Efficient delivery systems are needed for the clinical use of CRISPR-Cas9 gene editing.

Some lesser-known causes of PCOS include autoimmune issues, genetic mutations, and changes in the body's microbiome.

A woman was diagnosed with porphyria cutanea tarda and improved with phlebotomy and lifestyle changes.

Certain genes are linked to type 1 and type 2 diabetes in kids, and changes in these genes can also cause other diabetes-related conditions.

A boy with severe immune deficiency and Epstein-Barr virus died from high-grade B-cell lymphoma.

A patient with Wilson's disease showed hair-pulling behavior as an initial symptom.

Corticosteroids are the most effective treatment for Satoyoshi syndrome.

Early diagnosis and treatment of hereditary vitamin D-resistant rickets (HVDRR) are crucial to prevent growth issues and other health problems.

A genetic mutation in the DCAF17 gene caused Woodhouse-Sakati syndrome in a Chinese patient from a related family.

A child with ectodermal dysplasia-syndactyly syndrome has a new mutation in the NECTIN4 gene.

A child with a rare vitamin D-resistant condition improved with treatment.

A patient with a new PLEC gene mutation showed symptoms of both muscular dystrophy and myasthenia gravis, which improved with steroid treatment.

A new mutation in the LIPH gene was found to cause a rare hair disorder in a Japanese boy.

Genetically modified sheep with more β-catenin grew more wool without changing the wool's length or thickness.

Bone marrow stem cells and their medium help hair regrowth.

Certain skin proteins can form anchoring structures without the protein AMACO.

The L412F variant of TLR3 is linked to skin infections, more viral infections, and autoimmune issues.

The rs231775 genetic variant is linked to a higher risk and severity of Alopecia Areata in males.

The N363S gene variant does not cause higher adrenal androgen levels in women with polycystic ovary syndrome.

The PON1 192R gene variant is linked to a higher risk of psoriasis and heart disease in Western Mexico.

Genetic testing for EGFR mutations is crucial in similar cases.

Haplogroup X found in Altaian population supports Amerindian origin.

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

OsUEV1B protein is essential for controlling phosphate levels in rice.

Blond hair in Solomon Islanders is due to a unique genetic variant, not European ancestry.

Mexican patients had a lower incidence of skin reactions to drugs and no significant link between these reactions and the TNF2 gene variant.