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A different gene near the hairless gene on chromosome 8p21 causes a rare hair loss condition in a German family.

The document concludes that the development of certain tumors is influenced by genetic background and that a specific gene modification can lead to tumor regression and reduced growth.

A person with Turner Syndrome showed severe schizophrenia that didn't respond to treatment and had brain shrinkage.

Men have worse COVID-19 outcomes than women due to genetic and hormonal differences.

Female cuckoo color differences are linked to their unique genes and help avoid male harassment.

Cancer cells often have more copies of TERT and TERC genes, which helps them grow and could affect patient outcomes.

Pallister-Killian Syndrome is a complex genetic disorder requiring coordinated care and genetic counseling.

Autism's genetics are linked with early age of puberty and less hair loss, but not with hormone levels or polycystic ovary syndrome.

A gene called HDAC9 might be a new factor in male-pattern baldness.

The document concludes that the human keratin gene cluster is complex, with a need for updated naming to reflect over 50 functional genes important for hair and skin biology.

An Australian with rare hair loss and eye conditions had a gene linked to both, not seen together before.

Hair microscopy is useful for diagnosing hair disorders, but clear definitions are needed for accurate genetic analysis.

Androgen receptors are key for development and health, affecting conditions like prostate cancer and male pattern baldness.

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

Dermatologists give better information on pathology forms, hypersensitivity vasculitis is a common skin issue, misdiagnoses can occur, and various skin conditions are linked to loss of elastin or genetic factors.

The research found that genetic factors for male pattern baldness in African men differ significantly from those in Europeans.

A mutation in mice causes hair loss and skin issues due to a defect in a gene affecting cell adhesion.

A child with skin and heart issues had rare genetic mutations affecting skin and heart cell cohesion.

Porphyra-334 may help reduce wrinkles and promote hair growth.

A man with Klinefelter syndrome had a leg ulcer that didn't heal well, even with treatment.

Researchers found a new area on chromosome 2 linked to a genetic hair loss condition.

Scientists found a gene in mice that causes early hearing loss.

A second domain of high sulfur KAP genes on chromosome 21q23 is crucial for hair structure.

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

A genetic duplication on chromosome 5 was linked to a woman's unique combination of medical conditions.

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.

Over half of the children had abnormal hair under a microscope, with many having genetic hair conditions.

The document concludes that careful diagnosis is crucial for chromosome 13q deletion syndrome, tamoxifen can cause reversible eye damage, finasteride may be linked to cataracts, and OCT is useful for diagnosing macular diseases.

Researchers mapped and categorized specific keratin-associated protein genes on human chromosome 21q22.1.

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