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Basonuclin 2 is vital for the development of facial bones, hair follicles, and male germ cells in adult mice, and its absence can lead to dwarfism and abnormal follicles.

The same hormone can affect gene expression differently in various tissues, which could lead to new treatments for conditions like hair loss.

Chemotherapy-induced hair loss is partly due to decreased laminin-511 and increased laminin-332.

A gene mutation causes early keratinocyte maturation leading to hair loss in Olmsted syndrome.

The study identified 12 potential biomarkers for hair loss and how they affect hair growth.

The peach gene CTG134 helps control the interaction between auxin and ethylene, which could lead to new agricultural chemicals.

A woman with a unique syndrome similar to TRPS has a genetic change near the TRPS1 gene, affecting its regulation.

Transglutaminase activity is important for skin and is found in both mammals and birds.

Overexpression of HDGF in melanocytes does not cause cancer.

GLI1 might protect against the start of skin cancer and is not linked to cancer severity.

A new mRNA variant of the SCF gene in sheep skin produces a shorter, different protein.

RSPO1 mutations in certain patients lead to skin cells that don't develop properly and are more likely to become invasive, increasing the risk of skin cancer.

A specific genetic change is linked to mental disorders, intellectual disability, and possibly autoimmune disease in a family.

Eyelid cells share signaling components but differ in pathway activity.

Blocking Janus kinase 1 helps stop inflammation and regrow hair, making it a good treatment for hair loss from alopecia areata.

White blood cells and their traps can slow down the process of new hair growth after a wound.

Keratin protein production in cells is controlled by a complex system that changes with cell type, health, and conditions like injury or cancer.

A specific pathway involving AR, miR-221, and IGF-1 plays a key role in causing common hair loss.

Skin cancer often starts from Lgr5+ progenitor cells.

A pet ferret had a serious infection from Mycobacterium xenopi, which can spread to humans.

CaBP1 and CaBP2 are necessary for proper hearing and neurotransmission in the ear's inner hair cells.

Keeping β-catenin levels high in mammary cells disrupts their development and branching.

Removing Dicer from pigment cells in newborn mice causes early hair graying and changes in cell migration molecules.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

Botryococcus terribilis Ethanol Extract may reduce inflammation by changing gene expression in cells.

Acne treatment with isotretinoin increases the presence of p53, a protein, in skin and oil glands, which may help reduce acne severity.

The research found specific genes and pathways that control fur development and color in young American minks.

Prdm1 is necessary for early whisker development in mice but not for other hair, and its absence changes nerve and brain patterns related to whiskers.

MicroRNA-148a is crucial for maintaining healthy skin and hair growth by affecting stem cell functions.