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Researchers found that most genes affecting drug responses are not fully covered by commercial SNP chips, suggesting the need for more comprehensive tools to optimize drug selection based on genetics.

Keratinocytes can reverse the effects of the GNAQ oncogene, inhibiting melanoma cell growth.

miR-370-3p slows sheep hair cell growth by blocking SMAD4.

The research found that a protein called PPARg is important for the formation and healing of sebaceous glands, which can regenerate independently from hair follicles.

Different types of resting melanocyte stem cells have unique characteristics and vary in their potential to become other cells.

B6.Cg-Tyr c−2J Hr hr /J mice have a stronger delayed sunburn reaction and are good for UV research.

The condition is linked to chromosome 12, but no mutations were found in the known genes.

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

Sfrp2 increases during hair follicle catagen phase and slows keratinocyte growth.

Mutations in the KLHL24 gene cause a skin disorder in some Russian families.

The frizzy mouse and hairless rat mutations are due to changes in the Prss8 gene.

Pigs without the Hairless gene showed skin and thymus changes, useful for studying human hair disorders.

Pekin duck skin quality improves with age, peaking at 5-6 weeks.

Researchers found a new mutation in the FERMT1 gene in a Spanish family with Kindler syndrome.

Type I keratin genes are closely linked to the rex locus on mouse chromosome 11, affecting hair development.

KLHL24-mutant stem cells help understand skin and heart disease.

PRC1 influences skin stem cell development by both turning genes on and off, affecting hair growth and skin cell types.

Skin cell types develop when specific genes are turned on by removing certain chemical tags from DNA.

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

BMP signaling is important for skin color, affecting melanin production, pigment spread, and cell movement.

Mutations in the hHb6 gene cause the hair disorder monilethrix.

SCDSFs from zebrafish embryos are beneficial for treating cancer, regenerating tissues, and improving conditions like psoriasis and alopecia.

Sweat glands and hair follicles are determined by opposing signals, with BMPs promoting sweat glands and blocking BMPs leading to hair follicles.

The keratin 5 mutation in a family with epidermolysis bullosa simplex was due to mosaicism, not a new mutation.

SLICK cattle have better heat tolerance due to specific gene expression and pathway differences.

Removing the ROBO4 gene in mice reduces skin inflammation and hair loss by affecting certain inflammation pathways and gene expression.

SCUBE3 is a potential target for cancer and alopecia treatment but is challenging to target due to its varied roles.

Overexpression of PKCepsilon leads to increased TNFalpha, promoting metastatic squamous cell carcinoma in mice.