Search

everythinglearnresearchcommunity

for

Search:↓

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

A rare genetic disorder causes sparse hair and vision loss due to a CDH3 gene mutation.

Repetin is a protein involved in skin and hair development, binding calcium and compensating for other proteins when needed.

Adrenomedullin 2 stops cell growth and causes cell death in human hair follicles.

A boy with severe immune deficiency and Epstein-Barr virus died from high-grade B-cell lymphoma.

The conclusion is that the cornea has two types of stem cells, with Lrig1+ cells being key for renewal in aging corneas, independent of CD44.

The mK6irs1/Krt2-6g gene likely causes wavy hair in mice.

YAP and TAZ proteins are necessary for the development of two types of skin cancer.

AIRE protein, defective in APECED patients, is found in skin and hair cells and interacts with cytokeratin 17.

Reduced Sonic hedgehog signaling leads to increased HPV replication and wart formation.

A rare genetic variant linked to skin cysts was found in blood DNA, suggesting its role in cyst formation.

E6/E7 oncogenes in hair follicles cause continuous hair growth by skipping the resting phase.

Removing β-catenin in certain stem cells causes hair whitening and pigmentation issues.

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

Removing the Crif1 gene in mouse skin disrupts skin balance and hair growth.

The enzyme DHHC13 is essential for healthy hair and skin, and its deficiency leads to hair loss and skin problems.

Damaged hair follicles make mice more prone to skin inflammation and skin cancer after UV exposure.

A specific gene change plus an additional mutation in the same gene cause hereditary trichilemmal cysts.

High ornithine decarboxylase levels may lead to hair loss and cancer by increasing CK2 activity in the nucleus.

Foreskin keratinocytes and SVK14 cells express certain cytochrome P450 enzymes, unlike hair follicle keratinocytes.

Astrotactin2 affects hair follicle orientation and skin cell polarity.

ATP-dependent chromatin-remodeling complexes are crucial for gene regulation, cell differentiation, and organ development in mammals.

Ptch2 plays a key role in controlling stem cell function and the ability to regenerate after birth.

Loss of Ten1 in mice causes telomere shortening and symptoms similar to human dyskeratosis congenita.

Vav2 and Vav3 proteins help control skin stem cell numbers and activity in both healthy and cancerous cells.

The 14-3-3σ gene is essential for preventing hair loss.

PCAT1 helps hair growth by controlling miR-329/Wnt10b.

PDCD4 protein levels, affected by genetics and breastfeeding, may predict breast cancer treatment response.