Search

everythinglearnresearchcommunity

for

Search:↓

Mutations in the LSS gene cause hair loss and may affect brain development, with varying severity.

3D-bioprinting models of pancreatic cancer could help personalize treatments but need more testing.

Hidradenitis suppurativa is linked to autoinflammation and immune system issues.

The C-allele and CC-genotype in the PTPN22 gene lower the risk of alopecia areata.

A gene variant causes a skin and hair disorder by disrupting protein balance.

CCCA affects adolescents too, with genetic and environmental links, requiring careful diagnosis.

Bone marrow stem cells and their medium help hair regrowth.

Hordenine may help hair grow by activating a specific cell growth pathway.

SCUBE3 is a potential target for cancer and alopecia treatment but is challenging to target due to its varied roles.

Certain gene variations in Jiangnan cashmere goats are linked to important traits like birth weight and fiber quality, useful for breeding.

Zinc supplements and weaning cured a breast-fed baby's zinc deficiency caused by a gene mutation.

A gene mutation causes lanceolate hair in rats by disrupting hair shaft integrity.

A new genetic mutation in the hairless gene causes a rare hair loss disorder.

A new mutation in the HR gene is linked to a rare form of hair loss with limb deformities.

A new gene mutation causes long hair in some Maine Coon cats.

A mutation in the vitamin D receptor causes severe resistance to vitamin D, affecting bone health but not hair growth.

Mutations in the hHb6 gene cause the hair disorder monilethrix.

A specific mutation in the K25 gene causes a rare genetic disorder with curly hair at birth and later hair loss, along with dental issues.

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

A new gene mutation causes a rare type of hair loss.

A genetic variant in the KRT25 gene causes tightly curled hair.

New mutations in MBTPS2 reduce its function and cause IFAP syndrome with unusual symptoms.

A specific gene mutation causes Olmsted syndrome.

A new gene mutation caused a man's rare skin condition, Schöpf-Schulz-Passarge syndrome.

A 12-year-old boy with PAIS successfully developed male characteristics using high-dose testosterone and anastrozole.

A new gene mutation causes vitamin D resistance and rickets, treatable with calcium therapy.

Keratin 17 gene mutations cause both steatocystoma multiplex and pachyonychia congenita type 2.

The FGF5 gene determines hair length in dogs.

Congenital atrichia with papular lesions is often misdiagnosed, and new diagnostic criteria can improve accuracy.

A specific gene variant (rs4833095) is linked to a higher risk of alopecia areata in Koreans.