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AIRE-deficient rats developed severe autoimmune disease similar to APECED, useful for testing treatments.

A new classification system for skin cysts was proposed to improve diagnosis.

Targeting immune tolerance issues in Alopecia Areata could restore hair growth and maintain remission.

Human scalp hair follicles can be used to study how prolactin affects hair growth and cell death.

Researchers created specific antibodies that detect a protein important in development and various conditions, and can be used for research and diagnosis.

CD99 is highly present in certain skin cells and could help treat skin conditions.

A new mix of anthralin and calcipotriene might help treat severe hair loss.

Using anthralin and calcipotriene together might help treat tough cases of alopecia areata, but more research is needed to understand how it works.

Eating grape powder may reduce the severity of skin allergy symptoms.

Calcium signals and SHH guide the direction of feather growth in chicken skin.

Women with scarring alopecia are less likely to have used hormone replacement therapy or oral contraceptives compared to those with female pattern hair loss.

Myoepithelial cells can repair airways after severe injury.

Zinc levels in body fluids can help diagnose zinc deficiency in lambs, with fecal zinc as an early indicator.

Both induced and spontaneous AA lymphocytes can cause alopecia areata in mice.

Polyomavirus A2 infection in newborn mice caused hair follicle tumors.

The workshop highlighted the genetic links and psychological impacts of hair loss and skin disorders.

Certain immune cells contribute to severe hair loss in chronic alopecia areata, with Th17 cells possibly having a bigger impact than cytotoxic T cells.

Subclinical hypothyroidism in women with PCOS affects thyroid and hormone interactions but not ovary structure.

Adipocytes in atopic dermatitis skin change and worsen inflammation and fibrosis.

Genetic testing confirmed a rare disorder causing hair loss and vision problems in a Saudi family, stressing its importance for diagnosis and counseling.

A 10-year-old boy with abnormal genital development had surgery and tests to find the cause and plan treatment.

Parental support and gender-affirming care are crucial for the mental health of transgender adolescents.

An 11-year-old girl with hair thinning was diagnosed with monilethrix and early androgenetic alopecia.

A specific gene change plus an additional mutation in the same gene cause hereditary trichilemmal cysts.

Early diagnosis and treatment are crucial for complex medical conditions.

Hair follicle-derived IL-7 and IL-15 are crucial for maintaining skin-resident memory T cells and could be targeted for treating skin diseases and lymphoma.

A 4-year-old girl with hair loss was diagnosed with early-onset trichotillomania and improved with behavioral interventions.

A 15-year-old girl with no menstrual period was diagnosed with a genetic condition that makes her body unable to respond to male hormones, leading to female characteristics despite having male genetic makeup.

Mutations in the POC1A gene can cause a unique form of extreme insulin resistance and short stature.

Congenital Adrenal Hyperplasia is a genetic disorder with two forms, causing symptoms like early puberty and severe acne, but can be identified through screening and treated with glucocorticoids.