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The research found that people's hair proteins vary, especially by ethnicity and body part, which could help identify individuals in forensic science.

The research found that people's hair proteins vary by individual and body part, with some differences between ethnic groups, which could help in forensics.

Hair relaxers are linked to reduced cystine levels and potential hair damage.

The research found that PCOS has common genetic factors regardless of how it is diagnosed and is linked to metabolic and reproductive issues.

A WNT10A gene mutation leads to ectodermal dysplasia by disrupting cell growth and differentiation.

A new mutation in the STING protein causes a range of symptoms and its severity may be affected by other genetic variations; treatment with a specific inhibitor showed improvement in one patient.

Finasteride for hair loss may cause long-lasting side effects like impotence and low libido, but trials lack proper safety reporting.

Genetic variations affecting skin structure play a key role in severe acne.

Surface Plasmon Resonance is a useful tool for studying protein interactions and has potential for future technological advancements.

Basal cell carcinomas have much higher levels of Vitamin D3 receptors compared to healthy skin.

G allele of AR Stul polymorphism linked to higher hair loss risk, especially in white people.

Early onset hair loss linked to genetics and androgen levels.

African American men with prostate cancer have more androgen receptor mutations, which may lead to more aggressive cancer compared to Caucasian American men.

Certain variations of the HDAC9 gene can increase or decrease stroke risk in the Chinese population.

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

A Turkish family with sparse hair and eyebrow loss has a mutation in the U2HR gene linked to Marie Unna hereditary hypotrichosis.

A mutation in the FAM83G gene is linked to skin and hair abnormalities in two related individuals.

A new gene mutation may allow some piebaldism patients to regain skin color in white patches.

Filaggrin mutations are linked to atopic dermatitis and help explain how genetics and environment affect the disease.

Inherited color dilution in Rex rabbits is linked to DNA methylation changes in hair follicles.

A new mutation in the TMEM173 gene and a risk allele in IFIH1 cause a unique set of immune-related symptoms.

Androgen receptors in the mouse brain may explain cognitive and mood changes in prostate cancer treatment.

A TNFAIP3 gene mutation can cause unusual and varied symptoms of lupus and Sjogren's syndrome.

Certain mutations in the KLHL24 gene cause a skin disorder by breaking down an important skin protein.

Pregnancies in a woman with the Donohue mutation were managed with genetic testing, resulting in three healthy infants.

Finasteride's stability and safety confirmed through precise analytical methods.

People with alopecia areata often have other health issues like skin diseases, metabolic syndrome, stomach infections, lupus, anemia, thyroid problems, mental health issues, vitamin D deficiency, and hearing and eye problems.

Fatty acid transport protein 4 is essential for skin and hair development.

Signaling pathways are crucial for hair growth in goats.

A new mutation in the XEDAR gene might cause a rare skin condition called hypohidrotic ectodermal dysplasia.