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The document reports unique growth lines in a child after Stevens-Johnson syndrome, skin reaction from parsnips and sun in a girl, and itchy skin with xanthomas in a boy with Alagille syndrome.

Hair loss can be linked to hormonal changes, and physical conditions like heart defects can cause depression.

The transgene likely activated an oncogene or interrupted a tumor suppressor gene, causing melanoma in mice.

Puberty involves complex hormonal changes, varies by gender and ethnicity, and requires careful monitoring for abnormalities.

Introducing the rat OTC gene partially corrected OTC deficiency in mice.

Growth factors greatly affect hair loss, with different levels seen in men, women, younger patients, and at the start of the condition.

Cri-du-chat syndrome can cause skin and oral lesions affecting nutrition and quality of life.

Wharton’s Jelly stem cells from the umbilical cord improve skin healing and hair growth without scarring.

Runx1 affects hair growth, cancer development, and autoimmune diseases in epithelial tissues.

FGF13 gene changes cause excessive hair growth in a rare condition.

Neuroactive steroids and the enzyme 5α-reductase might be involved in the development of Tourette's syndrome.

A woman with a unique syndrome similar to TRPS has a genetic change near the TRPS1 gene, affecting its regulation.

Non-surgical procedures can help reduce wrinkles and stimulate skin repair by understanding skin aging at the molecular level.

Certain DNA regions in alpacas are linked to fiber diameter.

Genomic profiling for myeloid cancers can find important inherited mutations, but it's challenging when these mutations aren't related to the patient's symptoms.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

Dihydrotestosterone makes arteries stiffer in female mice by reducing estrogen receptor expression.

New liposome treatment successfully delivers CRISPR to deactivate a key enzyme in androgen-related disorders.

Taking L-cystine and vitamin B6 can prevent hair loss caused by smoke in mice.

A woman with acromegaloidism and normal growth hormone levels had a rare X-Tetrasomy, suggesting a need to study X-chromosome genes for their role in growth and facial development.

High androgen levels and genetic factors likely cause Becker's nevus and related symptoms.

N-acetyl-L-cysteine (NAC) can prevent DNA damage and protect cells from harm.

Acute leukemias with the Philadelphia chromosome may be biphenotypic, and identifying this is important for proper treatment.

The TCL1 transgenic mouse model is useful for understanding human B-cell leukemia and testing new treatments.

BAY 43-9006 helps control kidney cancer growth but doesn't significantly increase overall survival.

A position effect on the TRPS1 gene causes excessive hair growth in humans and mice.

A woman had both Graham Little-Piccardi-Lassueur syndrome, causing hair loss, and complete androgen insensitivity syndrome, making her genetically male but physically female. This suggests androgens don't affect the hair loss condition.

Minoxidil in breast milk may harm nursing infants.

Untreated congenital adrenal hyperplasia can lead to complications like stroke and needs glucocorticoid treatment.

A 19-year-old male had two rare skin conditions causing scarring and permanent hair loss.