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Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

New CRISPR/Cas9 variants and nanotechnology-based delivery methods are improving cancer treatment, but choosing the best variant and overcoming certain limitations remain challenges.

A woman with a rare hormone resistance condition also had missing teeth and hair loss, which might be new symptoms of her genetic disorder.

Prdm1 is necessary for early whisker development in mice but not for other hair, and its absence changes nerve and brain patterns related to whiskers.

Basement membrane changes are crucial for hair follicle development.

Genetic variants can affect valproic acid's effectiveness, side effects, and levels in epilepsy treatment.

Afro-textured hair needs personalized care due to its unique genetic traits.

Topical ceramide treatment partially improves the skin condition in Jack Russell Terriers with a genetic skin disorder.

Editing the FGF5 gene in sheep increases fine wool growth.

Bimatoprost helps with hair growth and eye conditions but can be costly and have side effects.

Enzymes involved in Vitamin A metabolism affect hair growth and type in mice.

Genetic analysis of rabbits identified key genes for traits like coat color, body size, and fertility.

The Shen Bai Hair Growing Decoction may help treat hair loss by promoting hair growth and reducing inflammation.

The TRPV3 gene variant may cause the long-haired suri alpaca coat.

STK11 gene polymorphism does not predict metformin response in PCOS.

Cells lacking the Bax protein can outcompete others, leading to better tissue repair and hair growth.

A special gene region controls the re-emergence of a primitive wool type in Merino sheep, improving their wool yield and adaptability.

Androgen treatment with dihydrotestosterone may help maintain height in patients with 5-α-reductase type 2 deficiency, especially before puberty.

Men and women respond differently to drugs for COVID-19, high cholesterol, and diabetes, which suggests a need for personalized treatments.

The document concludes that inflammation markers can be used in diabetes, vitamin D3 affects immune pathways, hyperthyroidism changes hormone levels, androgen levels help diagnose Adrenocortical Carcinoma, erectile dysfunction is linked to diabetes, hypogonadism is common in HIV-infected males, and hormones can be biomarkers for various conditions.

New tools show that in fish, NPY increases feeding and somatostatin decreases it.

Certain gene variations are linked to the thickness of cashmere goat hair.

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.

Androgenetic alopecia, or hair loss, is caused by a mix of genetics, hormones, and environment, where testosterone affects hair growth and causes hair to become smaller and grow for a shorter time.

CCC1 is essential for pH balance and normal cell function in plants.

CCC1 is essential for ion balance and proper plant cell function.

CCC1 is crucial for pH balance in plant cells, affecting growth and stress tolerance.

A man with both Klinefelter syndrome and primary hyperparathyroidism showed a rare combination of symptoms and genetic patterns.

Certain immune molecules and stress affect hair loss, and while genes play a role, more research is needed to fully understand and treat it.