Search

everythinglearnresearchcommunity

for

Search:↓

New ABCA12 gene mutations were linked to a skin condition with scaling and hair loss, and a treatment helped with hair loss in a related case.

Platelet lysate is better than fetal bovine serum for growing stem cells and healing wounds.

A mother and daughter had severe skin, hair, and eye issues linked to IFAP.

The RHD4 gene is crucial for consistent root hair growth in Arabidopsis thaliana.

FGF signaling is a promising target for developing treatments for wounds, metabolic diseases, and cancer.

Plerixafor may help treat pigmentation disorders by promoting skin repigmentation.

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

Truncating mutations in the C2orf37 gene cause Woodhouse–Sakati syndrome.

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

High glucocorticoids cause pancreatic malfunction and malabsorption, reversible with enzyme supplements.

The fibroin-based formulation strengthens and repairs chemically damaged hair.

Changing the diet of mice lacking the enzyme CBS can affect symptoms related to the genetic condition.

IPM enhances skin penetration of hydrophilic drugs.

EBF1 controls hair type and length.

The study found that variations in hair protein genes are likely due to evolutionary deletions or duplications.

Thiopurines help treat IBD but require genetic testing to avoid side effects.

A boronic acid copolymer quickly forms cell clusters, useful for tissue and tumor modeling.

Interferon β from hair cells stops the growth of other hair cells.

Mutations in the Vitamin D receptor gene can cause hair loss similar to mutations in the Hairless gene.

A unique gene mutation causes vitamin D-resistant rickets without causing hair loss.

Combining fat grafts with botulinum toxin helps improve Raynaud's symptoms.

Calanthoside may help hair growth by boosting cell proliferation.

Hair follicle sampling is a feasible method to measure FMRP and FMR1 mRNA levels in children.

A new mutation linked to partial Androgen Insensitivity Syndrome and prostate cancer was found in a patient unhappy with their female gender assignment.

Reduced matriptase activity causes skin and hair issues in both humans and mice.