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The conclusion is that the variation in hair thinness in patients is mostly due to the amount of underdeveloped hairs, and treatments that thicken fine hairs might work for those with mild to severe conditions.

The document concludes that the androgen receptor's structure and function are complex, affecting how it regulates genes and is involved in diseases like prostate cancer.

The near-naked hairless mutation causes hair loss but is not due to a mutation in the hairless gene itself.

Researchers found a new genetic mutation linked to a hair condition in a Japanese boy.

A boy with a new NR5A1 gene mutation has a sex development disorder without affecting his adrenal glands.

In vivo lineage labelling is better than in vitro methods for identifying and understanding stem cells.

A gene mutation in mice causes permanent hair loss and skin issues.

Connexin-26 gene mutations may increase cancer risk in KID syndrome patients.

A new mutation in the hairless gene causes hair loss and skin wrinkling in mice.

TGFα gene mutation in mice causes abnormal skin, wavy hair, curly whiskers, and sometimes eye inflammation.

Whale genes show changes that help them live in water, like less hair and better flippers.

A Korean boy's skin and digestive symptoms were caused by a rare genetic disorder that affects zinc absorption, and he got better with zinc supplements.

A gene mutation causes woolly hair in a Syrian patient.

A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

A new mutation linked to partial Androgen Insensitivity Syndrome and prostate cancer was found in a patient unhappy with their female gender assignment.

Five different TPO gene mutations were found in PCOS patients with thyroid hormone issues.

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

A man with a rare skin condition and a new gene mutation developed high calcium levels due to his treatment.

A new gene mutation causes female pseudohermaphroditism due to glucocorticoid resistance.

The TRPV3 gene mutation affects hair growth by keeping mice in the growth phase longer, which could help treat hair loss.

The harlequin ichthyosis mouse mutation causes thick skin and early death, resembling a human skin disorder.

A specific gene mutation causes Olmsted syndrome.

Mice with the 'lanceolate hair' mutation have abnormal hair and skin similar to human Netherton's syndrome.

An 11-year-old Greek girl was diagnosed with a rare genetic disorder, highlighting the importance of genetic testing and family history.

The document concludes that mouse models are crucial for studying hair biology and that all mutant mice may have hair growth abnormalities that require detailed analysis to identify.

Boys with less severe EDA mutations in XLHED have milder symptoms and better sweat and hair production.

Mutations in the androgen receptor gene cause different levels of androgen insensitivity, making it hard to create simple tests for the condition.

Mice with a Gsdma3 gene mutation have thicker skin and longer hair follicle openings due to increased β-catenin levels.

Mutations in the P2RY5 gene cause autosomal recessive woolly hair.

Mutations in the hairless gene in mice affect its expression and lead to a range of developmental issues in multiple tissues.