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

Bald areas have lower cell growth, more DNA damage, and increased cell death.

Certain genetic variants increase the risk of resistance to hormone therapy in prostate cancer patients.

p63 controls Satb1 to help skin develop properly.

Mutations in the PADI3 gene may cause central centrifugal cicatricial alopecia in women of African ancestry.

The document adds two cases of Gomez-Lopez-Hernandez syndrome and suggests including trigeminal anesthesia and scalp alopecia as key diagnostic criteria.

Agaricus bisporus derived β-Glucan could be an effective cervical cancer treatment with antimicrobial and antioxidant properties.

TGM3 is important for skin and hair structure and may help diagnose cancer.

Genetic screening is crucial for accurately diagnosing APS-1 due to its varied symptoms.

Hair loss in androgenetic alopecia is caused by genetic factors and androgen excess, and can be treated with combined therapies.

GLI2 activates GLI1, promoting skin tumor growth and hair development.

Blocking certain proteins in mouse skin can reduce and shrink skin tumors.

A new gene, JMJD1C, may affect testosterone levels in men.

A new genetic mutation causes severe Leydig cell hypoplasia, affecting sexual development.

Effective management of side effects is crucial for safe use of sacituzumab govitecan in advanced breast cancer treatment.

A gene called BMAL1 plays a role in controlling hair growth.

CDP is crucial for lung and hair follicle cell development.

BCG injection helps reduce long COVID symptoms and affects hair loss differently in men and women.

Canagliflozin helps overcome progestin resistance in certain endometrial cancer cells.

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

Enzymatic synthesis improved the water solubility of the flavonoid baicalin, which may help treat hair loss conditions.

Impaired LEF1 activation speeds up skin cell development in Hutchinson-Gilford Progeria Syndrome.

Four antibodies were developed to help study hair follicle cell differentiation.

Human prostate cells produce more WISP1/CCN4 when there's not enough oxygen.

Women with non-classical congenital adrenal hyperplasia have higher levels of certain steroids, which can be reduced by treatment.

Baicalin may help reduce excessive male hormone levels in PCOS.

Understanding the APCDD1 gene can lead to new hair loss treatments.

NCSTN gene mutation causes abnormal skin cell differentiation and more inflammation, contributing to Hidradenitis Suppurativa.

Upadacitinib effectively treats pyoderma gangrenosum.

YAP and TAZ proteins are necessary for the development of two types of skin cancer.