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Finasteride side effects in young men may be linked to specific gene variations.

A gene in Sebekia benihana, CYP-sb21, is needed for a specific reaction on the drug Cyclosporine A, which could be important for hair growth without affecting the immune system.

A gene mutation causes woolly hair in a Syrian patient.

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

A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

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

Changes in the HR gene have influenced hair growth and may lead to hair loss conditions in humans.

Mutation in hairless gene may increase hair loss risk.

Researchers found a new mutation in the FERMT1 gene in a Spanish family with Kindler syndrome.

Researchers found a new ABCD1 gene mutation linked to a rare brain and nerve disorder with unusual brain changes.

A specific gene mutation is linked to a hereditary form of dystonia that responds well to certain medications.

The R343H mutation in the VDR gene causes vitamin D-resistant rickets with alopecia by impairing specific gene activity.

SA linked to mitochondrial issues and oxidative stress, while AGA involves disrupted hair growth genes.

A new mutation in the DCAF17 gene was found in a Chinese family, causing Woodhouse-Sakati syndrome and diabetes.

A Taiwanese patient had hair loss and skin bumps without the usual gene mutation, suggesting other genetic factors might be involved.

Mutation in hairless gene may increase hair loss risk.

Certain genetic variants are linked to frontal fibrosing alopecia in Spanish patients.

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

The gene Ascl4 is not necessary for the development of hair, teeth, or mammary glands.

A baby from an Indian family had a rare genetic disorder causing no scalp or body hair due to a specific gene deletion.

A new genetic change in the DSC3 gene is linked to a rare condition causing hair loss and skin blisters in a child.

Certain gene variations in AKT2 are more common in women with PCOS and are linked to higher levels of specific hormones and symptoms.

New treatments targeting specific genes show promise for treating keratin disorders.

The study identified and characterized new keratin genes linked to hair follicles and epithelial tissues.

Researchers found a new gene, hacl-1, that is active in mouse hair follicles during hair growth and may be important for hair biology.

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

A specific microRNA, chi-miR-30b-5p, slows down the growth of hair-related cells by affecting the CaMKIIδ gene in cashmere goats.

Researchers found that most genes affecting drug responses are not fully covered by commercial SNP chips, suggesting the need for more comprehensive tools to optimize drug selection based on genetics.

Maize hybrids show better early growth due to complex gene interactions from their parent strains.

Some parents have a mild form of congenital adrenal hyperplasia without symptoms, and they usually don't need treatment.