Search

everythinglearnresearchcommunity

for

Search:↓

GBP1 is a key target for treating Epstein-Barr virus-related kidney cancer, and finasteride may help.

TNF alpha in skin cells causes weight loss, hair and fat issues, and skin inflammation in mice.

Scientists created cell lines to study a genetic skin disorder using CRISPR technology.

Mice without the IL-6 gene had more hair growth after injury due to higher activity of a related protein, Stat3.

Lymphoid-specific helicase (Lsh) is crucial for skin growth, change, and healing after injury.

B-Raf and C-Raf are essential for maintaining melanocyte stem cells to prevent hair graying.

Notch signaling is crucial for specifying niche cells in Drosophila testis.

Mutant MK6a transgenes in mice cause blistering, hair loss, and potential human alopecia.

848 genes related to fat and metabolism are less active in people with Central Centrifugal Cicatricial Alopecia.

ABCG2 protein marks stem-like skin cells in human epidermis.

Merkel cell carcinoma is most likely to recur within two years of diagnosis, and factors like immune suppression, being over 75, and male sex increase this risk.

CCL5 is important for the hair growth potential of human dermal papilla cells.

Cronkhite-Canada syndrome is rare, with high mortality and cancer risk, needing more research for treatment guidelines.

The gene Tfap2b is essential for creating a type of stem cell in zebrafish that can become different pigment cells.

Folliculin deficiency causes problems with cell division and positioning due to disrupted RhoA signaling and interaction with p0071.

Targeting ACE2 and TMPRSS2 may help prevent or treat COVID-19 in cancer patients.

Interleukin-1 increases keratin K6 production in skin cells.

UTX is crucial for skin differentiation and health, especially in females.

PINCH-1 is crucial for skin cell adhesion and movement, working with EPLIN and ILK.

Early and accurate diagnosis is crucial for managing rare genetic disorders like this localized variant of junctional epidermolysis bullosa.

A specific group of immune and skin cells may cause chronic inflammation in atopic dermatitis.

Pannexin 3 is important for bone formation and the development of bone cells.

The scraggly mutation causes hair loss and skin defects in mice.

Mutations in the ABCB6 gene cause Dyschromatosis Universalis Hereditaria.

Scientists created a cell model to study and find treatments for a skin disease called RDEB.

Turning off the Lhx2 gene in mouse embryos leads to slower wound healing and scars.

High CRP levels could indicate vitamin D deficiency in people with alopecia areata.

Certain genetic markers on chromosome 20 are linked to hair loss in the Han Chinese from Yunnan.

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