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ZmSPL10, ZmSPL14, and ZmSPL26 genes are essential for forming maize structures needed for pollen capture and kernel production.

Mohs micrographic surgery is effective for treating basal cell carcinoma on the eyelid, while radiotherapy has higher recurrence rates, and topical vitamin D3 may reduce and delay BCC formation in mice.

Dermoscopy helped diagnose a rare hair disorder in a 2-year-old boy.

WWOX deficiency in mice causes skin and fat tissue problems due to disrupted cell survival signals.

External factors can cause skin cancer cells that usually don't spread to grow and form tumors in mice.

Two genes, ERBB4 and ROR1, may cause the unique pigmentation in Lanping black-boned sheep.

Pets in Egypt can pass skin fungus, especially Microsporum canis, to humans, with outdoor and young pets being more at risk.

Anti-Desmocollin 3 antibodies can cause atypical pemphigus symptoms.

The report expanded knowledge of MBTPS1-related disorders by identifying new symptoms.

The Oat mouse model shows mild retinal degeneration, useful for testing treatments.

A mouse gene mutation increases the risk of skin cancer.

Mutations in the LSS gene cause a rare type of hereditary hair loss.

The patient's symptoms improved with treatment but recurred when the steroid dose was reduced, requiring ongoing therapy.

Both genetic and hormonal factors are crucial for bird sex differentiation, and disturbances can cause sex reversal.

The Msi2 protein helps keep hair follicle stem cells inactive, controlling hair growth and regeneration.

A new syndrome was linked to two new genetic changes in the MBTPS1 gene in a 14-year-old girl.

Cat color patterns are determined early in development by gene expression and epidermal changes, with the Dickkopf 4 gene playing a crucial role.

Mouse models help understand alopecia areata and find treatments.

A patient in Portugal with chronic pulmonary histoplasmosis had a complex medical history and environmental exposures.

miRNA-24 affects goat coat color by controlling proteins involved in pigment production.

A new gene mutation causes a rare type of hair loss.

A specific gene mutation (Y449H in K10) was found in a patient with severe skin disorder.

A new mutation in the PLEC gene causes a rare condition with skin blistering, muscle weakness, and hair loss.

A mutation in the hHb3 gene is linked to the hair disorder monilethrix.

A specific gene mutation in KRT86 is linked to hair disorder in a Chinese Han family.

Monilethrix causes different levels of hair loss in family members.

Mouse Scube3 affects teeth, tongue, vibrissae, and eye development, but not facial structure or limb growth.

A rare genetic mutation caused severe symptoms in a 6-year-old girl with mandibuloacral dysplasia type A.