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Progesterone and its metabolites affect myelin protein expression differently in male and female rat Schwann cells.

TTNPB helps turn stem cells into neural stem cells, improving depression-like behaviors in rats.

Mice can regenerate ear tissue without the p53 protein.

Specific gene variants affect wool traits in Chinese Tan sheep.

Researchers created a new mouse model, G4, that mimics human PCOS symptoms and links the condition to a specific gene.

Blocking miR-27a increases sheep hair follicle stem cell growth and decreases cell death, which could help improve wool quality and treat hair loss.

Mutations in the P2RY5 gene cause autosomal recessive woolly hair.

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

Researchers found two genes that may explain why some Casertana pigs don't have hair.

OCIAD2 and DCN genes affect hair growth in goats by having opposite effects on a growth signaling pathway and inhibiting each other.

The research found changes in gene expression related to cell death in mouse skin that help understand hair follicle development and skin health.

MCPIP1 in myeloid cells is important for skin cancer development and healthy hair growth.

Targeted siRNA therapy may be a promising treatment for KID syndrome by reducing mutant gene expression and improving cell communication.

PRDX5 enzyme may contribute to alopecia areata by affecting oxidative stress and autoimmunity.

A child with ectodermal dysplasia-syndactyly syndrome has a new mutation in the NECTIN4 gene.

PDGFC gene may help select goats with desirable curly wool traits.

AL136131.3 slows hair growth by affecting energy processes in hair loss.

A mutation in the HR gene causes a rare form of irreversible hair loss in two Kashmiri families. Whole exome sequencing is effective for finding such mutations.

PDI helps restore over-bleached hair's strength and structure by attaching special peptides.

GLABRA2 represses root hair formation by inhibiting a specific gene.

A new mutation in the CYP11B1 gene was found in a woman with mild hyperandrogenemia, a rare cause of non-classic congenital adrenal hyperplasia.

A rare gene mutation causes skin fragility and itching without affecting hair or nails.

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

DPP4-positive fibroblasts play a major role in producing proteins that lead to skin fibrosis.

The research identified genes and non-coding RNAs in cells that could be affected by testosterone, which may help understand hair loss and prostate cancer.

A specific gene segment can make mouse skin cells glow, helping study hair growth and gene effects.

Tanning ability is linked to specific DNA changes in skin genes.

A new gene mutation may cause cyclic thrombocytopenia by affecting platelet production.

Polycomb Repressive Complex 1 is crucial for keeping stem cells stable and maintaining healthy adult tissues.