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Mast cell and nerve fiber interactions in mouse skin change with the hair cycle.

Activating β-catenin increases melanocytes and decreases Schwann cells.

The DiLiCre mouse model is an effective tool for precise genome editing using light.

Stem cell behavior varies with stimuli, and lineage changes can happen without affecting stem cell division.

Scientists created a cell model to study and find treatments for a skin disease called RDEB.

A new protein was made to detect specific skin cell growth receptors and worked in normal skin but not in skin cancer cells.

No single treatment is clearly effective for central serous chorioretinopathy.

The combination therapy significantly improved Riehl’s melanosis in patients without serious side effects.

Two patients with Cronkhite-Canada syndrome achieved remission after treatment.

Connexin 30 is usually absent in normal skin but can appear in certain skin conditions.

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

A rare genetic mutation causes resistance to vitamin D, leading to severe rickets and requires high doses of calcium and vitamin D for management.

A new mouse model helps study melanocyte cells using GFP expression.

Different types of inactive melanocyte stem cells exist with unique characteristics and potential to develop into other cells.

Trichoblastomas may mimic fetal skin development by having many Merkel cells, unlike adult skin.

P-cadherin is crucial for hair follicle pigmentation but not skin pigmentation.

Some parents have a mild form of congenital adrenal hyperplasia without symptoms, and they usually don't need treatment.

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

MOF controls key genes for skin development by regulating mitochondrial and ciliary functions.

A woman with both Cronkhite-Canada syndrome and myelodysplastic syndrome improved significantly with corticosteroid treatment.

Basal cell carcinoma shows keratin patterns similar to undifferentiated hair follicle cells.

A KRT71 mutation in Hereford cattle in Uruguay causes thin, curly hair and scaly skin.

The microenvironment affects the behavior and survival of melanocytes with the GNAQ oncogene in melanoma.

Brindled mice show abnormal catecholamine neuron development due to copper deficiency.

The compound 4c showed strong potential as an anticancer agent.

A genetic mutation caused severe rickets and alopecia in an Indian patient, but high-dose calcium and phosphate treatment improved their condition.

A girl with excessive hair growth had a genetic change on chromosome 17 that reduced the activity of two genes linked to hair growth.

A new severe form of monilethrix syndrome includes hair loss, scalp itching, cataracts, and distinct facial features.

OsPHR3 can help breed rice that efficiently uses phosphate without growth issues.