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The questionnaire is valid and reliable but needs more testing for future predictions.

Cholesterol sulfate buildup due to a genetic mutation disrupts the skin barrier, leading to the scaling skin seen in X-linked ichthyosis.

Countries with stricter cultures had fewer COVID-19 cases and deaths, paranoia is linked to false memories, psychosocial intervention works as well with or without antipsychotic drugs for young people with psychosis, smartphones can detect changes in behavior indicating illness relapse, and recruitment agents show regional and gender biases.

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.

Women with Polycystic Ovary Syndrome (PCOS) have a lower health-related quality of life, especially those with an anovulatory phenotype, and need specific interventions to improve it.

Scurvy may cause symptoms similar to Sjögren's syndrome, which disappear with vitamin C.

Folliculotropic mycosis fungoides has unique molecular features and cell interactions that could guide targeted therapy.

DKK2 and SOSTDC1 together are necessary for the normal timing of the first regression phase in the hair growth cycle.

PCOS is a common hormonal disorder in women, causing symptoms like acne and irregular periods, and is managed with medication and lifestyle changes.

ETS2 drives cancer progression in squamous cell carcinoma and is linked to poor patient outcomes.

Orai1 protein is crucial for tooth development and affects enamel thickness and mineralization.

A new mutation in the TRPS1 gene caused Trichorhinophalangeal syndrome in a 17-year-old, highlighting the need for genetic testing.

Female university students in Peradeniya have low awareness of PCOS.

PCOS is common in young women, especially those aged 21-30, and often involves symptoms like irregular periods, weight gain, and acne.

Scientists created a cell model to study and find treatments for a skin disease called RDEB.

The research found genetic differences in identical twins that could explain why one twin has a disease while the other does not.

Lack of certain cells causes abnormal nipple development and nursing failure.

Forensic DNA phenotyping can help generate new leads in cold cases but faces accuracy, legal, and acceptance challenges.

Unilateral keratosis follicularis squamosa may be a new subtype, successfully treated with asiaticoside ointment.

Women with PCOS have worse physical health but similar mental health compared to those without PCOS.

The study found that a one-step antibody method is better than the LSAB method for accurately studying hair follicle structures without false positives.

Dsg1 is essential for maintaining a healthy skin barrier in mice.

Scientists used stem cells to create a model of the skin disease Epidermolysis Bullosa simplex, which helped them understand its molecular mechanisms and could aid in finding treatments.

FOXA1 and CCL2 genes are more active in women with PCOS, varying by phenotype.

Sebaceous gland organoids could improve skin regeneration and treatment.

Isoallopregnanolone may be a safe and effective treatment for reducing tics in a mouse model of Tourette syndrome.

Cow milk sugars increase fat production and inflammation in skin oil cells.