Search

everythinglearnresearchcommunity

for

Search:↓

Lymphoid-specific helicase (Lsh) is crucial for skin growth, change, and healing after injury.

Epidermolysis bullosa is a genetic disease causing fragile skin and blisters in both animals and humans.

The review highlights the importance of stem cells in hair health and suggests new treatment strategies for hair loss conditions.

Faulty Notch signalling may cause hair follicle changes and inflammation in hidradenitis suppurativa.

The document concludes that understanding sulfation biology is crucial for creating treatments due to its importance in biological functions and disease.

Corneous beta-proteins evolved uniquely in reptiles and birds, forming scales, claws, beaks, and feathers.

Different types of cells in the eye express specific keratins at various stages of development.

Nellore cattle have genetic variations linked to their adaptation to tropical environments.

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

Mannosylerythritol lipids are good for skin and hair care products.

A litter of cats had a hair condition similar to a mouse mutation, leading to hair loss and abnormal hair and skin.

Lef1 is essential for normal skin, hair growth, and healing wounds in mice.

Hidradenitis Suppurativa has genetic links, with certain gene mutations more common in patients and a third of cases having a family history.

The article concludes that better understanding gene regulation related to seasonal changes can offer insights into the mechanisms of seasonal timing in mammals.

The KRTAP7-1 gene is very similar across different cattle and yak breeds and likely plays a role in hair strength and shape.

Scientists found cells in hair that are key for growth and color.

Hair growth is controlled by specific gene clusters and proteins, and cysteine affects hair gene expression in sheep.

Multi-omics techniques help understand the molecular causes of androgenetic alopecia.

A cluster of sulfur-rich hair protein genes was found on chromosome 17.

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

Inhibiting AP1 in mice skin causes structural changes and weakens the skin barrier.

Jumonji genes are important for development and their mutations can cause abnormalities, especially in the heart and brain.

Key genes regulate hair follicle phase changes in Inner Mongolia cashmere goats.

The research explains how a human enzyme binds and processes its substrate, which could relate to its role in biological functions and hair loss.

Night shift work disrupts the body's natural clock genes.

Eating collagen peptides may help with skin and hair growth.

Modified pep7, named EPM peptide, effectively promotes hair growth at low concentrations and works well with minoxidil.

Chemical hair straightening improves smoothness and shine but may cause side effects, suggesting a need for safer methods.

Specific genes influence hair and cashmere growth in Laiwu black goats.

MendelVar is a tool that helps identify important genes by combining GWAS data with Mendelian disease information.