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

STK11 gene polymorphism does not predict metformin response in PCOS.

Hoxc13 gene affects wool length in Gansu alpine fine-wool sheep.

Three specific mutations in the LIPH gene can cause hair loss by damaging the protein's structure and function.

Researchers found a genetic link for hereditary hair loss but need more analysis to identify the exact gene.

Targeted therapy with Ustekinumab significantly improved a skin condition called ILVEN, which is caused by mutations in the CARD14 gene.

A gene variant causes patched hair loss in mice, similar to alopecia areata in humans.

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.

The BMP/Smads pathway and Id2 gene control hair follicle stem cells, affecting their rest and growth phases.

A new mutation in the CYP11B1 gene was found in a woman with mild hyperandrogenemia, a rare cause of non-classic congenital adrenal hyperplasia.

The meeting highlighted the genetic basis of female pattern hair loss and various skin health insights.

The document concludes that PCOS has a strong genetic component, but more research is needed to fully understand the specific genes involved.

Certain changes in the VEGF gene can increase or decrease the risk of polycystic ovary syndrome.

The KRTAP36-1 gene affects wool quality in Chinese Tan lambs.

The FA2H gene improves cashmere fineness by enhancing hair growth in goats.

848 genes related to fat and metabolism are less active in people with Central Centrifugal Cicatricial Alopecia.

Genetic factors influence hair traits like shape, color, and greying in Latin Americans.

Lactate production is important for activating hair growth stem cells.

Congenital Adrenal Hyperplasia is a genetic disorder with two forms, causing symptoms like early puberty and severe acne, but can be identified through screening and treated with glucocorticoids.

Obesity worsens PCOS symptoms, and PCOS may lead to more weight gain; managing both requires a holistic approach that includes mental health.

People with PCOS, especially if obese, often have NAFLD, linked to obesity, insulin resistance, and high androgen levels.

A genetic change in the EDAR gene causes the unique hair traits found in East Asians.

Deleting the CDSN gene causes severe skin and hair problems, leading to death.

A specific gene mutation causes woolly hair and hair loss.

CGRP may help protect hair follicles from immune system attacks, potentially slowing hair loss.

People with atopic dermatitis are more likely to develop other skin conditions due to shared genetics and immune pathways.

Most Hairless gene mutations reduce its ability to work with the Vitamin D Receptor, which might explain a certain type of hair loss.

A gene variant in KRT71 causes the curly fur in Selkirk Rex cats.

No consistent link between genotype and phenotype in 5-α-Reductase type 2 deficiency.

A male with aromatase deficiency improved bone health with estradiol treatment.