Search

everythinglearnresearchcommunity

for

Search:↓

The methylation of the HOXC8 gene's exon 1 affects cashmere fiber length in goats.

A new mouse mutation causes skin and hair defects due to a gene change.

A new mRNA variant of the SCF gene in sheep skin produces a shorter, different protein.

Researchers found two new genetic variants linked to Alzheimer's disease.

Certain genetic variants in ERN1, TACR3, and SPPL2C are linked to when Alzheimer's disease starts.

Mutations in the POC1A gene can cause a unique form of extreme insulin resistance and short stature.

A baby from an Indian family had a rare genetic disorder causing no scalp or body hair due to a specific gene deletion.

Genetic variation in the androgen receptor gene mainly causes early-onset hair loss, with maternal inheritance playing a key role.

Mice that can regenerate tissue have cells that pause in the cell cycle, which is important for healing, similar to axolotls.

Researchers found a new mutation in the FERMT1 gene in a Spanish family with Kindler syndrome.

Certain genetic variations in the A2M gene are linked to better milk quality in Murrah buffaloes.

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

New genetic mutations causing hair loss were found in a Chinese family.

The research showed that CRISPR/Cas9 can fix mutations causing a skin disease in stem cells, which then improved skin grafts in mice, but more work on safety and efficiency is needed.

A specific gene change in APCDD1 increases the risk of hair loss.

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

A defective gene causes hair loss and taste insensitivity in BTBR mice.

Certain genes and X chromosome patterns may significantly contribute to the development of hair loss.

Certain gene variations are linked to a higher risk of severe acne, suggesting a genetic influence on the condition.

A new HRAS gene variant may cause a range of symptoms including intellectual disability and psychiatric issues.

Astrotactin2 affects hair follicle orientation and skin cell polarity.

Disrupting the FGF5 gene in rabbits leads to longer hair by extending the hair growth phase.

The human type II 5α-reductase gene, linked to certain male health conditions, has a specific structure and low similarity to other related genes.

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

A gene deletion causes the "hairless" trait in Iffa Credo rats.

Hair keratins evolved from ancient proteins, diversifying through gene changes, crucial for forming claws and later hair in mammals.

DHT affects bone growth by altering gene activity in osteoblasts, potentially complicating steroid use.

Researchers identified a new variant of the FGF5 gene in sheep that affects hair length.

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

An 8-year-old girl has a rare genetic disorder causing complete, irreversible hair loss and skin bumps.