Search

everythinglearnresearchcommunity

for

Search:↓

A new mutation in the DCAF17 gene was found in a Chinese family, causing Woodhouse-Sakati syndrome and diabetes.

Gamma rays did not change hair follicle density but increased white and hypopigmented hairs in mice.

Hair follicles in the back of the rosette fancy mouse have reversed orientations due to a gene mutation.

Stem cells help remove dead cells to keep tissues healthy by balancing cell replacement and clearance.

The PTGER2 gene is highly active in Cashmere goat skin and its activity changes with the hair growth cycle.

NF-κB signaling is crucial in many diseases and can be targeted for new treatments.

Red light exposure can slow aging in mice by improving fat metabolism.

Key genes and pathways affect wool fiber thickness, improving wool quality.

Hair growth is maintained by specific cell signals.

PLA2R1 overexpression harms kidney cells by stopping their growth cycle.

Black wolfberry ferment may help regrow hair in cases of androgenetic alopecia.

Blocking the Mitochondrial Pyruvate Carrier causes stress in hair follicles, which can be reduced by an ISR inhibitor.

New insights into cell communication in psoriasis suggest innovative drug treatments.

Cupric citrate improves growth, nutrient use, and gut health in broilers.

MicroRNA-205 helps hair grow by changing the stiffness and contraction of hair follicle cells.

Turkish Van cats' genotypes don't affect traits like eye color or hair length.

Semecarpus anacardium leaf extracts may offer safe, effective cancer treatment alternatives.

Targeted therapy with Ustekinumab significantly improved a skin condition called ILVEN, which is caused by mutations in the CARD14 gene.

Specialized ribosomes affect aging in human skin cells.

People with pattern hair loss have higher polyamine levels in the top of their head compared to the back.

Dormant melanoma cells in mice interact minimally with memory T cells due to a suppressive tumor environment.

MendelVar is a tool that helps identify important genes by combining GWAS data with Mendelian disease information.

The AUTS2 gene is linked to neurological disorders and may affect human brain development and cognition.

The 190-kbp domain contains all human type I hair keratin genes, showing their organization and evolution.

A family got a fungal infection from a boy who had contact with rabbits, but they all recovered with treatment.

A genetic mutation in the SGK3 gene causes hairlessness in Scottish Deerhounds and may relate to human hair loss.

Certain gene variations in AKT2 are more common in women with PCOS and are linked to higher levels of specific hormones and symptoms.

Genes related to pigmentation, body rhythms, and behavior change during hares' seasonal coat color transition, with a common genetic mechanism in two hare species.

Human skin can make serotonin and melatonin.

Using 17-hydroxyprogesterone levels to diagnose nonclassic congenital adrenal hyperplasia can result in many incorrect diagnoses.