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Uncombable hair syndrome causes frizzy hair and can affect the nervous system, eyes, and ears, often co-occurring with other hair, skin, nail, and teeth conditions, and is linked to three specific gene mutations.

Meis1 is crucial for skin health and tumor development.

Mutations in the vitamin D receptor cause hereditary vitamin D-resistant rickets, leading to poor bone health and requiring high calcium doses for treatment.

Different fields of expertise must work together to better understand hair growth and create effective hair loss treatments.

The study found that a specific area of the hair follicle helps start hair growth by reducing the blocking effects on certain cells and controlling growth signals.

Platelet-rich plasma may help hair follicle cells grow by affecting certain genes and pathways.

The research provides insights into hair follicle growth in forest musk deer by identifying key genes and pathways involved.

Molecular diagnostics help identify genetic defects causing endocrine diseases, improving diagnosis and treatment options.

Interleukin-1 increases keratin K6 production in skin cells.

The stiffness of a wound affects hair growth during healing, with less stiff areas growing more hair.

Skin tumor regression is helped by retinoic acid signaling blocking Wnt signaling.

The rash on the infant indicated a serious underlying condition.

Researchers identified genes that may affect hair growth in Cashmere goats.

Eating a high-fat fish oil diet caused mice to lose hair due to a specific immune cell activity in the skin linked to a protein called E-FABP.

ELL is crucial for gene transcription related to skin cell growth.

A new mutation in the Hairless gene causes hair loss in two Pakistani families.

PRX102 is essential for rice root hair growth by helping transport substances to the tips.

AE can have varied symptoms and genetic causes, but zinc therapy helps.

A new mutation in the AGPAT2 gene causes severe fat tissue loss and related health issues by reducing the protein's levels.

Biotin and biotinidase are essential to prevent health issues, and deficiencies require lifelong supplementation.

Researchers found a new mutation causing total hair loss from birth.

Oxidative stress and immune dysfunction are linked to both Hashimoto's thyroiditis and polycystic ovary syndrome, with diet and specific treatments important for managing these conditions.

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

Mutations in the NR3C1 gene cause a rare condition that affects hormone signaling and can lead to various symptoms, with dexamethasone as a treatment option.

Mutations in certain receptors can cause diseases and offer new treatment options.

The KRTAP21-1 gene affects wool yield and can help improve wool production.

The enzyme steroid sulfatase is linked to breast cancer and other conditions, and inhibitors are being developed for treatment.

Drug repositioning is becoming more targeted and efficient with new technologies, offering personalized treatment options and growing interest in the field.

The AIRE gene variant rs2075876 is linked to a higher risk of alopecia areata in males.

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