Search

everythinglearnresearchcommunity

for

Search:↓

The research found a way to identify and study skin cells with stem cell traits, revealing they behave differently in culture and questioning current stemness assessment methods.

Astrotactin2 affects hair follicle orientation and skin cell polarity.

A man with a weakened immune system was diagnosed with a rare skin condition called trichodysplasia spinulosa using skin examination techniques.

Trichodysplasia spinulosa is a rare skin disease in immunocompromised patients caused by a specific virus targeting hair follicle cells.

Researchers found specific genes in the part of hair follicles that could help treat hair disorders.

TMPRSS2 helps viruses enter cells and protects the prostate from inflammation-related cancer.

A 20-year-old woman with a rare form of Turner syndrome showed improvement with hormonal therapy and needs comprehensive care.

Sacituzumab govitecan improves quality of life and symptoms in breast cancer patients, except for causing more diarrhea.

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

GLI1 might protect against the start of skin cancer and is not linked to cancer severity.

LGR6+ stem cells may improve bone healing.

Removing Gata6 causes hair follicle and sebaceous duct enlargement.

In alopecia areata, certain immune cells increase and express a protein linked to immune activation.

Low TRPS1 expression in skin and hair cells is linked to hair problems in Trichorhinophalangeal syndrome.

The research suggests that SFRP2 and PTGDS proteins might be indicators of female pattern hair loss and could contribute to hair loss.

Three genes in Arabidopsis are important for plant growth and development by affecting sugar attachment to proteins.

S100A4 and S100A6 proteins may activate stem cells for hair follicle regeneration and could be potential targets for hair loss treatments.

Patients with Systemic Sclerosis have much higher levels of GDF-15, which could help predict organ involvement and guide treatment.

Trichothiodystrophy is a rare genetic disorder causing hair issues and sometimes linked to DNA repair defects.

Akt2 and SGK3 are both important for normal hair growth and development.

A mutation in the Sgkl gene causes defective hair growth in mice.

New mutations in the DSG4 gene cause a rare hair condition.

Sheep hair follicle transglutaminases are calcium-dependent.

The LTF gene may help predict and manage nonspecific orbital inflammation.

TSPO might help treat anxiety and depression.

Higher TGF-β signaling may increase skin cancer risk in organ transplant recipients.

ERG increases SOX9, promoting prostate cancer growth and invasion.

Mice without the Sp6 gene have problems developing several body parts, including hair, teeth, limbs, and lungs.