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

Green tea extract helps prevent cell death and supports cell survival in hair cells exposed to a chemotherapy drug.

Different stem cells have benefits and challenges for tissue repair, and more research is needed to find the best types for each use.

The cornified envelope is crucial for skin's barrier function and involves key proteins and genetic factors.

Certain long non-coding RNAs are important for the growth of hair follicles in Inner Mongolian cashmere goats.

Genes related to keratin, skin cell differentiation, and immune functions are key in hedgehog skin and spine development.

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

The document concludes that reactivation of herpesviruses, especially HHV-6, is linked to severe symptoms and complications in drug-induced hypersensitivity syndrome.

Some people have a genetic variation that makes them less effective at breaking down drugs.

Diagnosing new systemic lupus during pregnancy is hard but important for the health of the mother and baby.

Stopping finasteride and closing PFO can help prevent strokes in young adults.

LncRNA MTC boosts growth of goat skin cells, improving cashmere quality.

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

AP-2α and AP-2β proteins are essential for healthy adult skin and hair.

There is no cure for myotonic dystrophy type 1, so treatment focuses on managing symptoms and complications.

Researchers found a genetic link for hereditary hair loss but need more analysis to identify the exact gene.

The study found that certain genes are important for hedgehog skin appendage development and immunity, with spines possibly evolving for protection and infection resistance.

A 37-year-old male with severe skin and internal issues has a rare inherited skin condition called dystrophic epidermolysis bullosa.

Understanding normal hair growth and loss in children is key to diagnosing and treating hair disorders.

Accurate diagnosis and timely, tailored treatments improve outcomes in obstetrics and gynecology.

Some blood-thinning medications can increase the risk of bleeding, and certain factors like genetics and other health conditions affect their safety and effectiveness.

The document concludes that Syndromes of Severe Insulin Resistance are rare disorders with limited treatment options.

Age affects how certain proteins involved in COVID-19 infection are expressed in mice, but sex hormones and heart injury do not.

Cantú syndrome is caused by mutations in the ABCC9 gene.

Mutations in the DSG4 gene cause fragile, sparse hair in humans, mice, and rats.

A faulty KLHL24 gene leads to hair loss by damaging hair follicle stem cells.

Targeted anticancer therapies can cause severe side effects similar to traditional chemotherapy, but with different types.

Mutations in the P2RY5 gene cause autosomal recessive woolly hair.

Keratin proteins are increasingly recognized as important for cell health and are linked to many diseases.