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

Blocking CXXC5 speeds up diabetic wound healing by improving blood vessel growth and skin repair.

Basonuclin 2 is vital for the development of facial bones, hair follicles, and male germ cells in adult mice, and its absence can lead to dwarfism and abnormal follicles.

Targeting ornithine decarboxylase can help prevent skin cancer.

A new genetic variant in the LIPH gene causes hair growth issues in a Chinese patient.

CCC1 is crucial for pH balance in plant cells, affecting growth and stress tolerance.

CCL 27 levels are similar in people with and without alopecia areata.

Lipin-1 is important for skin cell differentiation and skin barrier function.

Syndecan-1 is essential for maintaining skin fat and preventing cold stress.

PRC1 is essential for proper skin development and stem cell formation by controlling gene activity.

LncRNA MTC boosts growth of goat skin cells, improving cashmere quality.

Reversible hair loss in a ring pattern on the scalp may be linked to changes in leptin levels in fat tissue.

Folliculotropic mycosis fungoides has unique molecular features and cell interactions that could guide targeted therapy.

ICL is a condition with low CD4+ T cells like AIDS but not caused by HIV, and normal CD4+ T cell counts may vary between men and women.

Albumin and prednisone improved symptoms in a woman with Cronkhite-Canada syndrome, revealing potential genetic causes.

A PKP1 gene mutation causes skin fragility and hair loss in Chesapeake Bay retriever puppies.

The boy's severe skin disorder is caused by two new mutations in his TGM1 gene.

Claudin-1 is crucial for maintaining skin barrier and preventing inflammation.

A new mutation in the human glucocorticoid receptor reduces its function and causes resistance to glucocorticoids.

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

ILC1-like cells can cause alopecia areata by affecting hair follicles.

Deleting the CD271 gene in mouse skin cells leads to disorganized skin and increased hair growth, suggesting CD271 is important for skin health.

Mice with LSS deficiency showed hair loss and cataracts, similar to humans, and can help in understanding and treating this condition.

CHI3L1 and CXCL5 proteins help promote hair growth.

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

A KLK5 inhibitor effectively improved skin symptoms in a mouse model of Netherton Syndrome.

Removing PLCg1 from skin cells caused thicker oil glands and less hair in mice.

Nonclassic congenital adrenal hyperplasia is a common genetic disorder that can cause a range of symptoms and requires personalized treatment.

Long non-coding RNAs affect feather growth in chickens in ways that don't follow traditional genetic rules.

ALRN-6924 can protect hair follicles from chemotherapy damage by temporarily stopping cell division.