Search

everythinglearnresearchcommunity

for

Search:↓

Stem cell behavior varies with stimuli, and lineage changes can happen without affecting stem cell division.

miR-22, a type of microRNA, controls hair growth and its overproduction can cause hair loss, while its absence can speed up hair growth.

Deleting the PTEN gene in mice causes nerve cells to grow larger and heal better after injury, but may cause overgrowth and hair loss in older mice.

Stem cells control their future role by changing ERK signal timing, affecting tissue regeneration and cancer.

Monilethrix is linked to a gene cluster on chromosome 12.

Melanocytes are important for normal body functions and have potential uses in regenerative medicine and disease treatment.

Cells from certain embryo parts can induce head formation in another embryo, involving complex signaling pathways.

Meis1 is crucial for skin health and tumor development.

Mitochondrial problems in tooth cells lead to bad enamel and dentin development in mice.

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

Loss of Ten1 in mice causes telomere shortening and symptoms similar to human dyskeratosis congenita.

Researchers found a new genetic mutation causing a rare hair loss condition in the first Japanese child studied.

Engineered exosomes with EGF and FGF improve hair growth in mice with hair loss.

The technique allowed noninvasive tracking of hair stem cell survival and growth, showing potential for hair loss research.

Graying hair is caused by changes in gene expression affecting cell functions.

Msx2-deficient mice experience irregular hair growth and loss due to disrupted hair cycle phases.

Li2CO3 improved skin disease in a mouse model of Focal Dermal Hypoplasia without toxicity.

A 21-month-old boy has a rare genetic disorder causing sparse hair due to an LSS gene mutation.

The conclusion is that genetic testing is important for diagnosing and treating various genetic hair disorders.

Melatonin reduces BMP2 gene expression in goat hair follicles during the resting period.

Personalized sonidegib dosing can effectively treat Gorlin-Goltz syndrome with fewer side effects.

Ptch2 plays a key role in controlling stem cell function and the ability to regenerate after birth.

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

Chemicals and stem cells combined have advanced regenerative medicine with few safety concerns, focusing on improving techniques and treatment effectiveness.

Non-myeloablative stem cell transplants are a promising, less toxic option for older or weaker patients, with fewer side effects and good outcomes.

A specific gene mutation causes long hair in Angora rabbits.

Deleting part of a gene in mice causes wavy hair and high pup loss.

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

Scientists are using clumps of special stem cells to improve organ repair.

A new gene location for Keratosis follicularis squamosa was found on chromosome 7p14.3-7p12.1.