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A specific genetic change is linked to mental disorders, intellectual disability, and possibly autoimmune disease in a family.

The protein RSL4 is crucial for making root hairs longer by controlling genes related to cell growth.

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

Blocking a specific enzyme can reduce the negative impact of stress hormones on hair growth cells.

Genetic profiling can improve androgenetic alopecia treatment by predicting drug response and minimizing side effects.

SQSTM1 is linked to increased risk of alopecia areata.

The absence of functional sebaceous glands causes hair follicle destruction and scarring alopecia.

EDA2R gene linked to hair loss.

The DNMT3B -579G>T polymorphism may increase the risk of colorectal cancer.

Genotyping for NUDT15 p.Arg139Cys can help predict thiopurine side effects in Japanese IBD patients.

Using DNase enzymes to break down harmful NETs could be a new treatment for Stevens-Johnson syndrome and toxic epidermal necrolysis.

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

Transgenic sheep cells with spider silk gene were successfully created for future sheep hair expression.

MsPG3 protein gathers at root hair tips, aiding growth.

Csdc2 helps hair growth in cashmere goats by regulating specific genes.

Four new cases of Bachmann-Bupp syndrome suggest potential for targeted treatment.

BST2 is highly expressed in certain immune cells in alopecia areata, suggesting a role in the disease.

IVIG therapy significantly improved symptoms in a patient with APS-2 and SPS.

Targeting CXXC5 and GSK-3β may help treat male pattern baldness.

Blocking CISD1 reduces hearing loss from cisplatin in mice.

The Engrailed-1 gene plays a key role in the development of sweat glands in mice.

Higher levels of the DP2 receptor may lead to hair loss.

The report expanded knowledge of MBTPS1-related disorders by identifying new symptoms.

CCC1 is essential for ion balance and proper plant cell function.

Seven genes are highly expressed in both germ-line and hematopoietic stem cells.

Researchers created a mouse with the same mutation as humans with trichothiodystrophy, showing similar symptoms and confirming the condition is due to defects in DNA repair and gene activity.

Blocking the enzyme 11β-HSD1 might help treat obesity and metabolic issues.

Ganser syndrome may result from both organic and psychogenic factors.

GLABRA2 gene controls root-hair growth by regulating phospholipid signaling.

Somatostatin analogues effectively manage ectopic ACTH syndrome when surgery isn't possible.