Search

everythinglearnresearchcommunity

for

Search:↓

OCIAD2 and DCN genes affect hair growth in goats by having opposite effects on a growth signaling pathway and inhibiting each other.

Clonally expanded CD8+ T cells cause alopecia areata.

The boy's severe skin disorder is caused by two new mutations in his TGM1 gene.

A specific gene region can control targeted and responsive gene expression in mice, useful for skin disorder treatments.

WNT10A mutations cause varied symptoms in patients with odonto-onycho-dermal dysplasia.

The HoxC gene cluster and its enhancers are essential for developing hair and nails in mammals.

PON1 levels might indicate hair loss severity, but other health factors can affect this.

A gene mutation worsens skin irritation in mice due to a lack of certain fats.

Higher CRHR1 levels in AA patients lead to increased inflammation.

A specific gene mutation causes a rare hair loss condition in a Chinese patient.

A specific gene mutation causes complete hair loss without other health issues.

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

miR-5110 affects alpaca pigmentation by altering specific gene expressions.

A new gene mutation linked to Olmsted syndrome may increase cancer risk, suggesting the need for ongoing patient monitoring.

A new genetic mutation linked to CARASIL syndrome and small artery disease was found in a Chinese family.

SOCS1 and SOCS3 help control skin inflammation and are important for developing treatments for skin diseases.

Targeting the p300/AR axis may help treat polycystic ovary syndrome.

P-cadherin is important for hair growth and health, and its problems can cause hair and skin disorders.

A potential treatment for atopic dermatitis could be to increase PADI1 expression to improve skin barrier function.

More PDCD4 is linked to obesity, insulin problems, and cell death in ovaries for those with polycystic ovary syndrome.

CRISPR/Cas9 and prime editing can potentially fix skin disorder genes safely and effectively.

Removing MCPIP1 from myeloid cells in mice leads to hair loss and prevents skin tumors but causes pigmented spots.

A woman with a new PTCH gene mutation has both Gorlin syndrome and severe hair loss.

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

New hair regrowth model introduced, imiquimod kills skin cancer cells, T-cadherin loss makes skin cancer more invasive, no strong link between PTCH1 gene and skin cancer after transplant, and male teens more likely to have hereditary hair loss.

A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

The cancer gene c-Myc increases harmful chemicals that damage DNA and can lead to cancer, but antioxidants can reduce this damage.

Two gene variations, rs6493497 and rs7176005, may be linked to female hair loss in Chinese people.

Increased ODC expression makes normally tumor-resistant mice more prone to tumor development.

Hoxc13 gene affects wool length in Gansu alpine fine-wool sheep.