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The ID2 gene can help distinguish between sensitizers and irritants in skin cells.

KAP genes show significant genetic variability, but its impact on hair traits is unclear.

A specific RNA, circNlgn, contributes to heart damage and scarring caused by the cancer drug doxorubicin.

Certain SPINK5 gene mutations are common in Israeli families with Comèl-Netherton syndrome.

A new gene, JMJD1C, may affect testosterone levels in men.

The type of tumor suppressor gene lost affects the behavior of skin cancer.

New therapies for Birt–Hogg–Dubé syndrome are being developed based on understanding the FLCN gene's role.

The protein CTCF is essential for skin development, maintaining hair follicles, and preventing inflammation.

lncRNA XLOC_008679 and gene KRT35 affect cashmere fineness in goats.

Hox genes control hair growth patterns in mammals by regulating stem cell activity in the skin.

CXXC5 is a protein that controls cell growth and healing processes, and changes in its activity can lead to diseases like cancer and hair loss.

A new mutation in the KRT86 gene causes a hair disorder with variable expression.

Key genes affect cashmere quality differences between Jiangnan and Changthangi goats.

The study showed that a specific DNA sequence can control gene expression in hair growth areas of mice.

Tet2 and Tet3 enzymes are important for controlling hair growth and shape by affecting gene activity and DNA structure in hair follicles.

A specific DNA sequence caused hair loss in male mice by activating immune cells and increasing a certain immune signal.

Mutations in hKAP1 genes may cause hereditary hair disorders.

SETDB1 is essential for controlling DNA methylation, silencing retrotransposons, and maintaining skin cell health, with its absence leading to skin inflammation and hair loss.

Hoxc13 regulates specific hair protein genes on mouse chromosome 16.

A variant in the KRT31 gene causes a rare hereditary hair disorder called monilethrix.

The study found nine new hair protein genes in human hair follicles.

The 4C32 gene may help in mouse skin development and differentiation.

The protein folliculin, involved in a rare disease, works with another protein to control how cells stick together and their organization, and changes in this interaction can lead to disease symptoms.

61 functional keratin genes were identified in dogs and horses, leading to updated gene annotations.

SP1 promotes and KROX20 inhibits hair cell growth by affecting the CUX1 gene.

Two specific hair keratin genes are active during hair growth and decline as hair transitions to rest.

A new mutation in the FLCN gene linked to Birt-Hogg-Dube syndrome was found, suggesting people with certain lung collapse should be tested for this mutation and screened for kidney and colon cancer.

JMJD3 and NF-κB activate Notch1, which is essential for skin cell movement and wound healing.

Lack of functional CYLD in mice leads to early aging and cancer.

KAP genes are crucial for hair development and show both shared and unique traits in humans, chimpanzees, and baboons.