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The PROCLIPI study found markers that help predict outcomes in skin lymphoma patients.

TLR3 signaling enhances the immunosuppressive properties of human periodontal ligament stem cells.

Hair growth-related cells need the enzyme SCD1 to help maintain the area that supports hair growth.

NM2 and RLC phosphorylation are essential for normal inner ear hair cell function.

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.

A CCS patient with severe complications was successfully treated using combined therapies.

The enzyme RDH12 plays a role in vision and retinal disease, with mutations leading to early onset visual loss and blindness, but the exact disease mechanism is unclear and there are no treatments yet.

CFx-δ2 from stem cells helps heal burn wounds faster.

CREB, a protein that can promote cancer traits, is controlled by β-catenin in skin cancer cells.

LSD1 is crucial for regenerating hair cells in zebrafish.

A new genetic mutation was found causing hair and eye issues in a boy.

Changing the amount of PLC5 in Arabidopsis affects root growth and drought resistance, with less PLC5 slowing root growth and more PLC5 improving drought tolerance but hindering root hair growth.

Lgr6+ cells are important for tissue repair and could be a target for treating cancer and other diseases.

A new mutation in the CDH3 gene causes hair loss and vision problems in a young girl.

HSD11b1 affects skin nerves and increases non-histaminergic itch.

lncRNA2919 slows down rabbit hair growth by stopping cell growth and causing cell death.

A new CDH3 gene mutation was found in a Spanish patient with sparse hair and eye issues.

A deletion in the CDH3 gene causes a rare disorder with short hair and vision loss.

Targeting NCoR1 can help treat heart enlargement and dysfunction.

PLDζ2 and NPC4 have different roles in lipid changes and root hair growth in Arabidopsis under low phosphate, with PLDζ2 reducing root hair growth and NPC4 promoting it.

PINCH-1 is crucial for skin cell adhesion and movement, working with EPLIN and ILK.

The patient likely has Chrousos syndrome, a rare condition causing insensitivity to glucocorticoids, requiring high-dose dexamethasone treatment.

lncRNAs are important for understanding and treating skin diseases.

Certain genetic changes in the LSS gene cause a rare skin and hair condition.

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

Discoid lupus erythematosus involves immune activation and fibrosis around hair follicles, with shared pathways across humans, dogs, and mice, suggesting potential treatments for both humans and animals.

A patient with a new PLEC gene mutation showed symptoms of both muscular dystrophy and myasthenia gravis, which improved with steroid treatment.

Certain genetic variations are linked to higher liver enzyme levels in patients treated for chronic hepatitis C with specific drugs.

Inhibiting ornithine decarboxylase may help prevent certain skin cancers.

Nonclassic congenital adrenal hyperplasia is a common genetic disorder that can cause a range of symptoms and requires personalized treatment.