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AcD scaffolds improve tissue repair and regeneration by combining stem cells with a supportive matrix.

The protein aPKCλ is crucial for keeping hair follicle stem cells inactive and for hair growth and regeneration.

Different STUB1 gene mutations cause varied symptoms in autosomal recessive ataxias.

A Japanese patient with a rare genetic disorder had a less severe case than others, suggesting other factors may affect symptoms.

Over a third of women thought to have non-classical congenital adrenal hyperplasia didn't have it confirmed by genetic tests.

New genetic mutations causing hair loss were found in a Chinese family.

circRNA-1926 helps goat stem cells turn into hair follicles by affecting miR-148a/b-3p and CDK19.

A specific RNA molecule, circCOL1A1, affects the growth and quality of goat hair by interacting with miR-149-5p and influencing cell growth pathways.

Near-infrared probes can safely and effectively image cysteine protease activity for disease diagnosis.

Enhancing Tregs can protect against alopecia areata.

CCN1 may aid wound healing, but more research with larger samples is needed.

A new genetic variant causes trichothiodystrophy in two brothers, but their mother may carry it without showing symptoms.

A specific gene change is linked to severe hair loss.

Screening for the NUDT15 gene variant can prevent severe side effects from thiopurine drugs in East-Asian people.

MOF controls skin development by regulating genes for mitochondria and cilia.

CircAGK affects cell death in hair cells by controlling the miR-3180-5p/BAX pathway, which can lead to hair loss.

Astrotactin2 affects hair follicle orientation and skin cell polarity.

Blocking certain proteins in mouse skin can reduce and shrink skin tumors.

Upadacitinib effectively improved severe atopic dermatitis and alopecia universalis in a 29-year-old man.

The tumor suppressor gene FLCN affects mitochondrial function and energy use in cells.

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 protein called CBP is found in prostate cancer and can increase the effectiveness of certain prostate cancer treatments.

A Chinese male with a new genetic mutation has a skin condition and severe urinary issues, with treatments having mixed success.

The DQB1*03 allele is linked to higher alopecia areata risk in Italians.

CK 15, follistatin, and Bmi-1 can help differentiate basal cell carcinoma from squamous cell carcinoma.

27 out of 32 candidates passed the hair restoration surgery exam.

Scientists found a gene in mice that causes early hearing loss.