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A new mutation in the HJV gene was found in a young woman with juvenile hemochromatosis, causing unusual symptoms like secondary hypothyroidism.

The mouse model showed defects in adult stem cell maintenance related to Hutchinson-Gilford progeria syndrome.

The hamster polyomavirus middle T antigen is linked to tumors in hamsters and associates with a specific tyrosine kinase.

HuR is essential for Treg function and preventing autoimmunity.

Researchers found a new genetic mutation linked to a hair condition in a Japanese boy.

Blocking miR-27a increases sheep hair follicle stem cell growth and decreases cell death, which could help improve wool quality and treat hair loss.

New and known mutations in the hairless gene cause a hair loss condition called Atrichia with papular lesions.

A specific gene mutation causes a rare hair loss condition in a Chinese patient.

miR-155 levels in blood could help identify alopecia areata.

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

The mutated hairless gene causes hair loss by acting as a new type of corepressor affecting thyroid hormone receptors.

A gene called APCDD1, which controls hair growth, is found to be faulty in a type of hair loss called hereditary hypotrichosis simplex.

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.

miR-218-5p helps skin and hair growth by targeting SFRP2 and activating a specific signaling pathway.

A specific microRNA, chi-miR-30b-5p, slows down the growth of hair-related cells by affecting the CaMKIIδ gene in cashmere goats.

Certain HSD3B1 gene types are linked to worse prostate cancer outcomes and affect treatment response and other health conditions.

A specific RNA increases hair stem cell growth and skin healing by affecting a protein through interaction with a microRNA.

Mutations in three genes cause Uncombable Hair Syndrome, leading to frizzy hair that can't be combed flat.

MiR-23b and miR-133 affect sheep hair growth by targeting specific genes.

Certain proteins are significantly increased in the skin of people with hidradenitis suppurativa.

Researchers found a new mutation in the HR gene causing hair loss and skin bumps in a Pakistani family.

miR-133a-3p and miR-145-5p help goat hair follicle stem cells differentiate by controlling NANOG and SOX9.

A genetic mutation in the CDH3 gene causes hair loss and vision problems in a young Saudi girl.

Mesenchymal stem cells in people with Hidradenitis Suppurativa are more inflammatory, possibly contributing to the disease.

A new mutation in the LIPH gene was found to cause a rare hair disorder in a Japanese boy.

The hr gene is crucial for skin and hair health, with mutations causing hair disorders.

The scant hair in snthr-1Bao mice is likely caused by a deletion affecting the Plcd1 gene.

A gene variant increases the risk of a type of hair loss by affecting hair protein production.

miR-486 may help prevent hair loss in alopecia areata.

A person got uncombable hair syndrome from two copies of chromosome 1 from their mother.