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Canine epidermal neural crest stem cells could be a promising treatment for spinal cord injuries in dogs.

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

Keratinocytes help keep hair follicle cells and skin cells separate in 3D cultures, which is important for hair growth research.

The Notch signaling pathway helps in mouse hair development through a noncanonical mechanism that does not rely on RBPj or transcription.

The patient was diagnosed with anorexia nervosa and severe malnutrition, requiring urgent refeeding and monitoring.

Stem cell therapy helps heal burn wounds, especially second-degree burns, by promoting blood vessel growth and reducing inflammation.

Minoxidil may cause heart issues in guinea pigs, suggesting potential harm for users with heart conditions.

QR678 treatments were more effective and comfortable for male hair loss than PRP treatments.

A boy's growth and immune problems were caused by a new mutation in the STAT5B gene.

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

Removing myelin protein zero-like 3 in mice leads to better metabolism and resistance to obesity.

The severity of symptoms in nonclassical congenital adrenal hyperplasia is not determined by CYP21A2 gene variations.

Turning scar-forming cells into fat cells can reduce scarring.

Glutamic acid helps increase hair growth in mice.

Allopregnanolone is needed for certain brain processing issues caused by D1 dopamine receptor activation.

Fetal-maternal stem cells in a mother's hair can help with tissue repair and regeneration long after childbirth.

PXX is an effective and affordable photocatalyst for creating new chemical bonds in organic synthesis.

Adipose-derived stem cells show potential for skin rejuvenation and wound healing but require more research to overcome challenges and ensure safety.

Cyproterone acetate with ethinyl estradiol is effective for treating skin symptoms related to high androgen levels, like in PCOS.

Hair microscopy is useful for diagnosing hair disorders, but clear definitions are needed for accurate genetic analysis.

The NUDT15 gene variant causes severe side effects from azathioprine in some Indian patients.

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

Finasteride 5-mg oral disintegrating tablets and standard tablets are bioequivalent in healthy adult male Han Chinese volunteers.

Rare changes in the KRT82 gene are linked to a higher risk of Alopecia Areata.

Different types of fibroblasts play various roles in kidney repair and aging, and may affect chronic kidney disease outcomes.

The STIM1 R304W mutation in mice leads to bone changes and teeth hair growth.

Mutations in the CYP21A2 gene are not a major factor in causing PCOS.

Young women with PCOS and no other heart risk factors have normal heart function.

Mutation in hairless gene may increase hair loss risk.

Selective breeding caused the unique curly hair in Mangalitza pigs.