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Staphylococcus epidermidis A/C strains are more antibiotic-resistant and infection-adapted, while B strains thrive in hair follicles.

Genetic variations greatly affect individual metabolism and can impact health and disease risk.

Human hair keratin might be good for filtering out harmful substances from water.

Hair's strength and flexibility come from its protein structure and molecular interactions.

A Jordanian family with Clouston syndrome has a common GJB6 gene mutation.

Genetic testing is crucial before giving azathioprine to avoid severe side effects.

A young Russian girl with Meier-Gorlin syndrome has two new mutations in the CDC6 gene.

A new goat gene affects cashmere fiber thickness; certain variations can make the fibers coarser.

Different harmful mutations in the CDH3 gene cause HJMD, but symptoms vary among individuals.

FGF9 controls which receptors it binds to through a process where two FGF9 molecules join, and changes in FGF9 can lead to incorrect receptor activation.

A rare genetic mutation caused unusual skin symptoms in a man with Blau syndrome.

Researchers found a new mutation in the EDA gene that likely causes missing teeth and mild skin symptoms in one family.

Hair thinning and loss in a girl with a rare metabolic disorder was linked to her condition.

Mutations in the KRT85 gene cause hair and nail problems.

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 L457(3.43)R mutation in the human lutropin receptor causes increased activity and hormone insensitivity, leading to precocious puberty.

Understanding the genetics of rare inherited ichthyosis syndromes is key for better treatments and genetic counseling.

Primary care doctors should address female sexual dysfunctions to improve women's sexual health and life quality.

Jumonji genes are important for development and their mutations can cause abnormalities, especially in the heart and brain.

Minoxidil helps hair cells live longer and grow longer.

A rare ITGB6 gene variant causes intellectual disability, hair loss, and dental issues.

Researchers found 617 genes that behave differently in cashmere goat hair follicles, which could help understand hair growth.

Two different mutations in the vitamin D receptor gene cause different symptoms and responses to treatment in Lebanese patients with hereditary rickets.

Two specific SNPs in the TRPS1 gene cause excessive hair growth by altering the protein's structure.

A new mutation linked to partial Androgen Insensitivity Syndrome and prostate cancer was found in a patient unhappy with their female gender assignment.

The CORIN gene variant causes the golden color in Siberian cats.

Trichohyalin-like proteins are essential for the development of skin structures like hair, nails, and feathers.

Scaffoldin helps form hard skin structures in chicken embryos.

Mutations in three genes cause Uncombable Hair Syndrome, leading to frizzy hair that can't be combed flat.