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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.

A woman's unique dementia was misdiagnosed, a genetic mutation increases Parkinson's risk with age, and finasteride may help with Tourette syndrome.

Proper niche formation in Drosophila requires Slit-Robo signaling for cell migration.

Ancient DNA blocks are still present in human genomes, possibly due to advantages they provide.

Isotretinoin's effects and side effects, like birth defects and depression, might be due to it causing cell death in various cells.

A specific gene mutation is linked to a hereditary form of dystonia that responds well to certain medications.

A group has developed therapies that show promise for treating cancer and various other conditions.

Melanoma's complexity requires personalized treatments due to key genetic mutations and tumor-initiating cells.

A specific genetic deletion in goats affects cashmere yield and thickness.

New treatments for Alopecia Areata show promise but need to be more effective and affordable.

A specific DNA region is crucial for Foxn1 gene expression in thymus cells but not in hair follicles.

Deleting Snai2 and Snai3 causes fatal autoimmunity.

Certain genetic variants increase the risk of resistance to hormone therapy in prostate cancer patients.

CPK1 helps root hair growth in Arabidopsis by activating channels for calcium signaling.

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

A gene deletion in mice causes weak protein, immune issues, hair loss, airway problems, and wasting disease.

The conclusion is that certain genetic factors and blood types may affect COVID-19 severity, but changes in ACE2 and TMPRSS2 genes are not clearly linked to it.

The gene p53 is crucial for removing damaged cells to allow for healthy tissue renewal.

FOXN1 gene variants cause low T cells and immune issues from birth.

Maintaining DNA health in stem cells is key to preventing aging and tissue breakdown.

Asian hair is generally straight and thick, with unique disorders and properties, and more research is needed to understand it fully.

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

STK11 gene polymorphism does not predict metformin response in PCOS.

Melatonin may help with nerve pain, a hepatitis C drug is effective but has side effects, a treatment for mouth sores works but can cause blood issues, ear reconstruction with an implant is safe, HIV transmission from mother to child in Taiwan is now 0% with treatment, certain blood problems are more common in people with a tongue condition, a gene and being overweight are linked to hair loss in some women, a new technique could reduce radiation for lung nodule patients, a hepatitis treatment may lower cancer recurrence after a procedure, and adding extra screening improves tuberculosis detection in patients with lung infections.

The Rotterdam Study updated findings on elderly health, focusing on heart disease, genetics, lifestyle effects, and disease understanding.

MC4R gene variants not linked to female hair loss.

Blocking the FGF5 gene in sheep leads to more fine wool and active hair follicles due to changes in certain cell signaling pathways.

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

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

Foxp3 is crucial for regulatory T cell function, and targeting these cells may help treat immune disorders.