Search

everythinglearnresearchcommunity

for

Search:↓

Congenital Adrenal Hyperplasia is a rare inherited disease causing hormone imbalances, affecting growth, fertility, and heart health, diagnosed through blood tests and treated with medication and lifestyle changes.

The review found no clear link between vitamin D receptor gene variations and polycystic ovary syndrome.

Researchers found that hair follicle stem cells can become squamous cell carcinoma due to Ras activation, which could lead to new treatments.

New method finds genetic links between Type 2 Diabetes and Prostate Cancer not seen before.

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

New treatments targeting specific genes show promise for treating keratin disorders.

Vitamin D and estrogen may help protect heart and kidney health, and maintaining sufficient vitamin D levels could be especially beneficial for African Americans, postmenopausal women, and people with chronic kidney disease.

The Wnt signaling pathway is not a major factor in the development of keratoacanthoma, a type of skin tumor.

An American Bully with a genetic skin condition improved significantly with specific topical treatments.

Studying premature aging syndromes helps understand human aging and suggests potential treatments.

The research found that PCOS has common genetic factors regardless of how it is diagnosed and is linked to metabolic and reproductive issues.

Metformin helps regulate menstrual cycles, induce ovulation, and improve pregnancy outcomes in women with PCOS.

Methotrexate is not proven to maintain remission in ulcerative colitis.

Early treatment of PCOS in teens is crucial to prevent long-term health issues like diabetes and heart disease.

The N363S gene variant does not cause higher adrenal androgen levels in women with polycystic ovary syndrome.

Siblings with signs of virilization should be tested for non-classical congenital adrenal hyperplasia, which does not affect adult height but may impact fertility and well-being if untreated.

Certain genetic markers linked to reproductive potential were identified by their impact on a protein's ability to bind to genes.

ARL15 is important for fat cell development and the release of the hormone adiponectin.

Insulin resistance is a key factor in polycystic ovary syndrome, but genetics may also contribute.

Methotrexate side effects vary by race and sex.

Nutrease powder, a high-protein, low-carb supplement, can help manage Polycystic Ovary Syndrome symptoms, regulate periods, improve ovulation, and restore fertility.

A new gene variant in the DSP gene is linked to a unique type of hair loss.

Targeted siRNA therapy may be a promising treatment for KID syndrome by reducing mutant gene expression and improving cell communication.

Genetic variants in PDE6H and LPAR6 cause vision impairment and hair loss in two Pakistani brothers.

A mother and son both had ulcerative colitis and alopecia, suggesting a genetic link in autoimmune disorders and successful treatment with cyclosporine.

Genomic profiling for myeloid cancers can find important inherited mutations, but it's challenging when these mutations aren't related to the patient's symptoms.

Choosing the right model order in brain connectivity analysis can affect the detection of differences between healthy individuals and those with seasonal affective disorder.

The NUDT15 gene variant causes severe side effects from azathioprine in some Indian patients.

Certain gene variations are not a major cause of male infertility in Nigerian men.

Common variants in the Trichohyalin gene are linked to straight hair in Europeans.