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Certain metabolites are lower in women with PCOS and could be potential markers for the condition.

Finger length ratios are not linked to the number of specific gene repeats affecting testosterone sensitivity.

Explosions don't stop hair proteins from being used to identify people.

Passiflora incarnata may help with anxiety and sleep issues but has side effects; teleconsultation for heart failure can improve quality of life; increased screen time for children during the pandemic led to more clinical complaints; older and severely affected COVID-19 patients are more likely to have long-term symptoms.

Different species and human skin models vary in their skin enzyme activities, with pig skin and some models closely matching human skin, useful for safety assessments and understanding the skin's protective roles.

Patients with advanced breast cancer and high hormone receptor levels who had surgery for ovarian/pelvic metastases lived longer, especially if they had high estrogen receptor levels.

Certain cells in the adult mouse ear come from cranial neural crest cells, but muscle and hair cells do not.

Anorexia Nervosa and Bulimia Nervosa are complex eating disorders with increasing incidence among young females, significant morbidity, and varying mortality rates, requiring more research for better treatment.

Keratin-associated proteins have ancient origins and were used for different purposes before being adapted for hair in mammals.

A gene called APCDD1, which controls hair growth, is found to be faulty in a type of hair loss called hereditary hypotrichosis simplex.

PCOS has a strong genetic basis, but more research is needed to fully understand it.

More research is needed to understand sex and racial differences in long COVID.

The gene KAP22-1 affects wool yield and fiber shape in sheep.

ALA-PDT is effective and safe for chronic X-ray dermatitis, providing complete or partial remission.

A mutation in the Soat1 gene causes hair structure defects and other health issues in AKR/J mice.

Platelet-rich plasma may help hair follicle cells grow by affecting certain genes and pathways.

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

Using SNP array testing helped quickly find the gene causing Woodhouse-Sakati syndrome in two related individuals.

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

Genetic variations affect dutasteride treatment response for male pattern hair loss.

Two specific SNPs in the TRPS1 gene cause excessive hair growth by altering the protein's structure.

Xiangdong black goats have moderate genetic diversity, minimal inbreeding, and important genes for reproduction, immunity, and other traits.

High TSPEAR levels in colorectal cancer predict worse outcomes.

High TSPEAR levels in colorectal cancer predict worse outcomes.

Two siblings had a rare immune disorder caused by a FOXN1 gene mutation.

The conclusion is that adult males with muscle weakness and hormonal imbalances should be tested for Kennedy's disease.

AXR3 and SHY2 genes control the growth and timing of root hair development in plants.

The update highlights that non-classic congenital adrenal hyperplasia is common in women with excess male hormones, requires specific hormone tests for diagnosis, and has various treatment options depending on age and symptoms.

Androgens have complex effects on hair growth, promoting it in some areas but causing hair loss in others, and our understanding of this is still evolving.

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