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Xinyang Tablet improves heart function in sepsis by reducing inflammation.

Multitarget drugs are needed to better treat complex diseases.

ATP-sensitive K+ channel subunits, particularly Sur2A, play a significant role in various cancers.

Hawthorn-probiotic postbiotic may relieve constipation in elderly.

Endoplasmic reticulum stress plays a key role in developing atherosclerosis.

Young adults who had liver disease as children often experience significant health problems and frequently need transplants.

Gefitinib and Sasam-Kyeongokgo together significantly reduce cancer growth and improve immune response in mice.

Adipose-derived stem cells can help repair and improve eye tissues and appearance.

Bone growth is controlled by both internal and external signals, involving stem cells and tissue interactions.

New ABCA12 gene mutations were linked to a skin condition with scaling and hair loss, and a treatment helped with hair loss in a related case.

The ABI1 gene contributes to prostate cancer progression and treatment resistance.

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

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

848 genes related to fat and metabolism are less active in people with Central Centrifugal Cicatricial Alopecia.

BAF200 is essential for proper heart and coronary artery formation.

Cantú syndrome is caused by mutations in the ABCC9 gene.

A girl with excessive hair growth had a genetic change on chromosome 17 that reduced the activity of two genes linked to hair growth.

ABCG2 protein marks stem-like skin cells in human epidermis.

Certain gene variations may increase the risk and severity of alopecia areata.

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

A new mutation in the CYP11B1 gene was found in a woman with mild hyperandrogenemia, a rare cause of non-classic congenital adrenal hyperplasia.

Hair follicles can be used to study gene mutations in Stargardt disease.

The AR gene is linked to male-pattern baldness, TNFSF4 to heart disease, SLC19A3 to BBGD, MCT8 to a syndrome, and segmental duplications to genetic variation.

A certain gene variation can affect protein production and is linked to male pattern baldness.

The Apc gene is crucial for normal skin and thymus development.

CCCA in women of African ancestry may be caused by PADI3 gene mutations and intense hair grooming.

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

MCHR2 gene duplications may be linked to alopecia areata.

A girl with Becker naevus syndrome has a genetic variant in the ACTB gene related to her symptoms.

New mutations in the SLC39A4 gene found in twins help understand the genetic cause of acrodermatitis enteropathica.