Search

everythinglearnresearchcommunity

for

Search:↓

A boy with chromosome 13q deletion syndrome developed eye cancer, a woman with breast cancer lost vision due to a rare side-effect of her treatment, a man's vision worsened after using a hair loss drug, and two rare disorders were discussed. Optical Coherence Tomography is useful for diagnosing and monitoring these conditions.

Key genes crucial for sheep hair follicle development were identified, aiding fine wool breeding and human hair loss research.

Inherited color dilution in rabbits is linked to DNA methylation changes.

Sex and sex hormones can affect brain inflammation in Parkinson's disease, with male mice being more affected and female mice showing a protective effect.

Loss of the Y chromosome and UTY gene activity increases cancer risk in men.

Chromosomal differences affect how muscle cells respond to testosterone.

Rare genetic variants in five specific genes are linked to male-pattern hair loss but only account for a small part of the risk.

A mother's iron levels early in pregnancy can influence the DNA makeup of her child, potentially affecting the child's health.

New single-cell analysis techniques are improving our understanding of stem cells and could help in treating diseases.

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

Researchers found genes and microRNAs that control curly fleece in Chinese Tan sheep.

The study found key factors in the cause of hidradenitis suppurativa, its link to other diseases, and identified existing drugs that could potentially treat it.

Genetic factors could lead to personalized treatments for hair loss.

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

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

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

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

The study found that a specific genetic variation in the TNFα gene is significantly linked to Alopecia Areata in the Jordanian Arab population.

Higher miR-34a levels and the A variant of the MIR-34A gene are linked to increased risk and severity of alopecia areata.

IFN-γ and IL-2 are important for T cell activation in hair loss in mice.

The 190-kbp domain contains all human type I hair keratin genes, showing their organization and evolution.

The analysis of a large pilomatricoma revealed five distinct areas with different gene activity related to hair growth and tumor development.

Blond hair in Solomon Islanders is due to a unique genetic variant, not European ancestry.

Certain genetic markers on chromosome 20 are linked to hair loss in the Han Chinese from Yunnan.

A position effect on the TRPS1 gene causes excessive hair growth in humans and mice.

Genetic data can predict male-pattern baldness with moderate accuracy, especially for early-onset cases in some European men.

The study found that variations in hair protein genes are likely due to evolutionary deletions or duplications.

Researchers found a genetic region that influences the number of coat layers in dogs.

Found different long non-coding RNAs in balding Chinese men, which may help create new treatments.

A mutation in the HR gene causes a rare form of irreversible hair loss in two Kashmiri families. Whole exome sequencing is effective for finding such mutations.