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The study concludes that mutations in the AEBP1 gene can cause a form of Ehlers-Danlos syndrome and should be considered in diagnosis.

Researchers found WNT10A to be a key gene in developing goat hair follicles.

The study suggests certain ACE gene variations are more common in women with PCOS and may be linked to increased insulin resistance.

Finasteride exposure affects gene expression and anogenital distance in male rat fetuses.

A woman with a unique syndrome similar to TRPS has a genetic change near the TRPS1 gene, affecting its regulation.

Cantu syndrome, which causes excessive hair growth and skin issues, is due to a mutation in the ABCC9 gene, and understanding this could help develop new treatments for hair diseases.

A new mutation in the FLCN gene linked to Birt-Hogg-Dube syndrome was found, suggesting people with certain lung collapse should be tested for this mutation and screened for kidney and colon cancer.

Nanoparticles can be used to deliver drugs to hair follicles, potentially improving treatments for conditions like acne and alopecia, and could also be used for vaccine delivery and gene therapy.

The research found that the gene activity in mouse skin stem cells changes significantly as they age.

The research provides a gene-based framework for hair biology, highlighting the Hippo pathway's importance and suggesting links between hair disorders, cancer pathways, and the immune system.

The congress highlighted new gene therapy techniques and cell transplantation methods for treating diseases.

Nuclear shape and chromatin changes affect gene expression in skin cell differentiation.

A new mutation in the TMEM173 gene and a risk allele in IFIH1 cause a unique set of immune-related symptoms.

Loss of the Y chromosome and UTY gene activity increases cancer risk in men.

Mutations in the WNT10A gene cause Short Anagen Hair syndrome and increase the risk of male pattern hair loss.

New tools show that in fish, NPY increases feeding and somatostatin decreases it.

A new mutation in the Hairless gene causes hair loss in two Pakistani families.

The conclusion is that the nuclear lamina and LINC complex in skin cells respond to mechanical signals, affecting gene expression and cell differentiation, which is important for skin health and can impact skin diseases.

New treatments for hair growth and psoriasis may be possible, and gene differences could affect baldness and the severity of skin conditions.

Mutations in the androgen receptor gene cause different levels of androgen insensitivity, making it hard to create simple tests for the condition.

Certain mutations in a hair growth-related gene cause a type of genetic hair loss.

K_ATP channel gene mutations are linked to heart diseases, but more research is needed to understand the connection and treatment potential.

Mutations in the Vitamin D receptor gene can cause hair loss similar to mutations in the Hairless gene.

Involucrin gene expression is controlled by specific proteins and signaling pathways.

GABRA2 gene variations impact alcohol response, and hair loss medication finasteride reduces some effects.

The Foxn1 gene mutation causes hairlessness and immune system issues, and understanding it could lead to hair growth disorder treatments.

Mice without the vitamin D receptor gene lose hair due to disrupted hair follicle cycles.

A deficiency in the TTC7A gene causes immune problems, gut issues, and hair loss.

Mutations in the LSS gene cause a rare type of hereditary hair loss.

The length of the CAG repeat in the androgen receptor gene affects the risk and progression of prostate cancer, BPH, infertility, and undermasculinized genitalia.