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IFN-γ and IL-2 are important for T cell activation in hair loss in mice.

Prolactin affects when mice shed and grow hair.

The STIM1 R304W mutation in mice leads to bone changes and teeth hair growth.

Certain mutations in the PADI3 gene may increase the risk of developing a type of scarring hair loss common in women of African descent.

Doxazosin mesylate and saw palmetto cause genetic changes in fruit flies.

A new technology showed that the SOX9 gene might control heart scar formation after injury, suggesting new treatment possibilities.

Certain genetic variants reduce enzyme activity, contributing to non-classic congenital adrenal hyperplasia.

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

A Jordanian family with Clouston syndrome has a common GJB6 gene mutation.

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

A baby with KID syndrome died from infections and organ failure at 18 months old.

The gene Prss53 affects hair shape and bone development in rabbits.

Screening for the NUDT15 gene variant can prevent severe side effects from thiopurine drugs in East-Asian people.

Copper treatments increase copper in all tissues, but brindled female mice accumulate much more copper in their kidneys without clinical effects, unlike brindled male mice where brain copper deficiency is clinically significant.

A patient with myotonic dystrophy had several autoimmune disorders and thyroid cancer, suggesting a possible link between these conditions.

Foxi3 expression in developing teeth and hair is controlled by the ectodysplasin pathway.

Taking riboflavin and eating less lysine can help some people with a specific genetic disorder avoid brain damage.

Blocking interferon-gamma helps prevent and treat hair loss in Alopecia Areata.

Gene variant linked to prostate cancer, hormone levels, and hair loss.

Some women with PCOS have CYP21 mutations and IRS1 variants, but these genetic factors are not major contributors to PCOS.

Hairless mice lack fur due to a genetic mutation affecting skin response, not hormone issues.

Severe insulin resistance can be managed with medication, lifestyle changes, and treatment for related conditions.

Patients with GATA2 deficiency show early skin symptoms that help diagnose the condition.

Budesonide and N-acetylcysteine reduced tumors and alopecia in mice, regardless of FHIT gene status.

Tsukushi helps control inflammation and aids in wound healing.

The severity of symptoms in nonclassical congenital adrenal hyperplasia is not determined by CYP21A2 gene variations.

Maize hybrids show better early growth due to complex gene interactions from their parent strains.

The p.P25L mutation in the KRT5 gene causes a rare skin condition that worsens over time and may lead to hair loss starting in young adulthood.

No clear link between specific gene and hair loss in Mexican brothers.

Advanced imaging techniques are crucial for accurately diagnosing Monilethrix, a rare hair disorder.