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Cantú syndrome may be linked to pituitary adenomas.

We need better ways to test and understand SARMs to make safer and more effective treatments.

People with Myotonic Dystrophy type 1 are more likely to have certain skin conditions, but not more likely to get skin cancer.

A specific thyroid hormone resistance mutation may be linked to different types of hair loss.

Disruptions in sleep-wake cycles can cause health problems like mental, metabolic, and heart diseases, and cancer.

Bald thigh syndrome in sighthounds is caused by structural defects in hair shafts due to downregulated genes and proteins.

Ficus carica extract improved fertility in rats and may help with certain health conditions.

Crossbreeding improves goat fiber quality, and specific genes affect hair traits and color.

Mechanical forces are crucial for shaping cells and forming tissues during development.

The research found a way to identify and study skin cells with stem cell traits, revealing they behave differently in culture and questioning current stemness assessment methods.

KRT85 gene variations can help improve wool traits in sheep through selective breeding.

A specific gene variant is linked to heart disease, increased heart muscle, curly hair, and thick skin on palms and soles.

Low-coverage sequencing is a cost-effective way to identify genes related to wool traits in rabbits.

Treatment with moisturizers improved the skin condition of a girl with a rare genetic skin disorder.

The trial aims to understand how obesity and lifestyle affect circadian rhythms in people with schizophrenia and bipolar disorder.

A Chinese male with a new genetic mutation has a skin condition and severe urinary issues, with treatments having mixed success.

Red clover extract-based scalp treatments significantly improved hair volume and reduced hair loss and damage.

A 37-year-old male with severe skin and internal issues has a rare inherited skin condition called dystrophic epidermolysis bullosa.

Not having enough cystatin M/E protein causes less hair growth and dry skin.

The document concludes that patient outcomes for Congenital Adrenal Hyperplasia are often not ideal because of poor management and a need for better diagnosis and treatment methods.

New treatments for skin and hair repair show promise, but further improvements are needed.

Researchers discovered potential origins and new treatments for skin cancer, including biomarkers for melanoma and therapies that reduce tumor growth.

The environment around the time of conception can change the VTRNA2-1 gene in a way that lasts for years and may affect disease risk.

Kennedy's disease leads to muscle weakness and sensory issues, has no cure but manageable symptoms, and future treatments look promising.

The document concludes that more research is needed to understand excessive hair growth in women with normal hormone levels and regular ovulation.

Researchers developed a 3D model of human hair follicle cells that can help understand hair growth and test new hair loss treatments.

The conclusion suggests that prostate cancer should be classified by castration status and that new therapies targeting androgen receptor signaling show promise.

A patient with a larger than usual genetic mutation had a broader range of symptoms for a muscle disease.

Changes in the SREBF1 gene cause a rare genetic skin and hair disorder.

Male hormones cause different growth in identical human hair follicles due to their unique epigenetic characteristics.