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Men with hair loss have more DNA changes in back-of-head hair follicles, possibly protecting them from thinning.

Four patients with a type of rickets and hair loss had different mutations in their vitamin D receptor gene, causing it to not work properly.

The tropical legume Sesbania rostrata can form nodules in waterlogged conditions using a different method that involves plant hormones and specific genes.

A new gene, mrp4, is found in mice and may play a unique role in hair follicle development in tails and ears.

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

A certain gene variant may increase the risk of polycystic ovary syndrome in Chinese women.

Hairless gene not strongly linked to baldness.

Certain gene variations are linked to higher male hormone levels in Chinese women with PCOS and insulin resistance.

Hair loss gene linked to prostate issues.

A new mutation in the hairless gene causes hair loss and skin wrinkling in mice.

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

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

Certain gene variations are linked to better memory in healthy Chinese women.

Finasteride affects SRD5A2 gene pattern, possibly causing lasting side effects.

HSD3B1 gene variant and being overweight linked to hair loss in women with polycystic ovary syndrome.

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

New and known mutations in the hairless gene cause a hair loss condition called Atrichia with papular lesions.

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.

Guasha changed rat skin appearance and blood vessels temporarily without affecting certain nerve proteins or fiber structure.

Longer TA repeats in the SRD5A2 gene may increase acne risk in Chinese people.

MendelVar is a tool that helps identify important genes by combining GWAS data with Mendelian disease information.

A new gene variant in the DSP gene is linked to a unique type of hair loss.

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

Certain gene variations may increase the risk and severity of alopecia areata.

CT60 polymorphism might increase the risk of Alopecia Areata.

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

The study suggests that a specific gene variation and higher gene activity are linked to increased baldness in Egyptian men.

The ZIP7 gene helps control zinc levels in cells by moving zinc from the Golgi apparatus to the cytoplasm.