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

Different types of cell death affect skin health and inflammation, and understanding them could improve treatments for skin diseases.

Bmpr2 and Acvr2a receptors are crucial for hair retention and color.

A specific gene mutation causes long hair in Angora rabbits.

The document concludes that various signaling pathways and genetic factors are crucial for chicken feather development, affecting poultry quality.

Different methods, including stress management, healthy diet, supplements, and treatments like minoxidil, can help hair grow back after COVID-19 related hair loss.

Nrf-2-modified stem cells from hair follicles significantly improve ulcerative colitis in rats.

A certain mutation in the fetal alpha 5-reductase gene is linked to a higher risk of late miscarriage.

Human hair loss may have evolved to help increase brain size.

FGF10 and non-coding RNAs are important for cashmere goat hair follicle development.

The SOSTDC1 gene is crucial for determining sheep wool type.

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.

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

The KRT84 gene is linked to better wool quality in Gansu Alpine Fine-wool sheep.

A gene mutation in Lama3 is linked to a common type of hair loss.

Genes linked to wool fineness in sheep have been identified.

Different types of sun exposure damage skin cells and immune cells, with chronic exposure leading to more severe and lasting damage.

Dermal cells are key in controlling hair growth and could potentially be used in hair loss treatments, but more research is needed to improve hair regeneration methods.

PCOS is a complex condition in women that can lead to health issues, and lifestyle changes are the best management approach.

Human hair is made up of different keratins, some strong and some weak, with specific types appearing at various stages of hair growth.

Colorectal cancer development involves both genetic changes and epigenetic alterations like DNA methylation and microRNA changes.

Overexpressing follistatin in mice delays wound healing and reduces scar size.

Hair growth and development are controlled by specific signaling pathways.

FGF5 gene mutations cause unusually long eyelashes by affecting hair growth regulation.

Altering SSAT affects fat metabolism and body fat in mice.

Wharton’s Jelly stem cells from the umbilical cord improve skin healing and hair growth without scarring.

Mutations in TBX3 cause horses to have more even hair color instead of Dun camouflage.

Hair growth can be stimulated by combining certain skin cells, which can rejuvenate old cells and cause them to specialize in hair follicle creation.

SDF-1/CXCL12 and its receptor CXCR4 are crucial for melanocyte movement in mouse hair follicles.

Certain mouse strains develop a skin condition similar to a human hair loss disease due to genetic defects.