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A genetic duplication on chromosome 5 was linked to a woman's unique combination of medical conditions.

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

Four circRNAs were found to be significantly different in cashmere goat skin, affecting cashmere fineness.

Certain genetic changes in the KAP22-1 gene are linked to better wool quality in Egyptian sheep.

The C-terminal tail of AHF/trichohyalin is essential for organizing keratin filaments in keratinocytes.

CCCA in women of African ancestry may be caused by PADI3 gene mutations and intense hair grooming.

Krox20 is important for maintaining stem cells in the skin and affects hair growth and color.

The protein called small nuclear ribonucleoprotein polypeptide E is identified as a cause of a type of hair loss without other symptoms.

Overexpressing COX-2 in mice skin reduces skin tumor development.

Researchers created a genetic library from a cashmere goat's skin and found new genes linked to hair growth.

Removing HIF-P4H-2 from certain skin cells in mice causes hair loss on the body but not the head.

Certain mutations in the hairless protein disrupt its ability to regulate the hair cycle.

A circular RNA helps cashmere goat hair cells become hair follicles by blocking a molecule to boost a gene important for hair growth.

Cyclooxygenase-2 overexpression in mice skin causes hair loss like human androgenetic alopecia.

Trichohyalin is a versatile protein involved in hair and skin structure.

LRIG1 protein affects hair growth by regulating skin receptors, leading to hair loss when overexpressed.

K6/ODC transgenic mice are effective for quickly identifying cancer-causing chemicals.

Lack of cystatin M/E causes thin hair and dry skin.

Vitamin C derivative may promote hair growth by activating specific genes.

The study improved understanding of gene roles in cashmere goat hair growth, aiding future cashmere production.

mrp/plf-mRNA can indicate tumor-promoting effects in skin.

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

The improved genome of the African spiny mouse will help understand its tissue regeneration abilities.

A rare genetic deletion in the KRT1 gene causes unique skin symptoms in a family.

PDF2 senses specific lipids and regulates root growth and gene expression in Arabidopsis.

Id2 gene helps keep hair follicle stem cells inactive.

TMPRSS6 is crucial for controlling hepcidin and normal iron absorption.

The study found nine new hair protein genes in human hair follicles.

Mutations in the HEPHL1 gene cause abnormal hair and cognitive issues.