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The HOXC13 gene affects different hair proteins in cashmere goats in varied ways and is controlled by a feedback loop and other factors.

Certain gene mutations are linked to wool quality in sheep and could help in breeding for better wool.

New markers and pathways have been found in skin tumors, helping better understand and diagnose them.

Key genes crucial for sheep hair follicle development were identified, aiding fine wool breeding and human hair loss research.

Advanced therapies like gene, cell, and tissue engineering show promise for hair regrowth in alopecia, but their safety and effectiveness need more verification.

Nanog gene boosts stem cells, helps hair growth, and may treat hair loss.

DHT affects bone growth by altering gene activity in osteoblasts, potentially complicating steroid use.

The S250C variant in a gene may cause autoimmunity and immunodeficiency by impairing protein function.

Certain genetic markers can indicate higher or lower risk for systemic lupus erythematosus.

Researchers found a new mutation in the HR gene causing hair loss and skin bumps in a Pakistani family.

ELL is crucial for gene transcription related to skin cell growth.

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 enzymes Tet2 and Tet3 are important for skin cell development and hair growth.

Newborn screening and gene therapy are expected to improve outcomes for Omenn syndrome patients.

The Msx2 gene affects feather development in Hungarian white geese and a specific gene variation could indicate feather quality.

The conclusion is that certain physical signs in the body can indicate past acute and chronic stress, which may help in child abuse investigations.

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

Hair follicles have a more inactive cell cycle than other skin cells, which may help develop targeted therapies for skin diseases and cancer.

Four genes are potential markers for hair loss condition alopecia areata, linked to a specific type of cell death.

The ABCA4 gene protects hair follicle stem cells from toxic vitamin A byproducts.

A child with ectodermal dysplasia-syndactyly syndrome has a new mutation in the NECTIN4 gene.

The gene Tfap2b is essential for creating a type of stem cell in zebrafish that can become different pigment cells.

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.

Chemotherapy and radiation therapy cause skin and hair damage by altering gene expression and signaling pathways.

Blood tests for tumor cells could improve prostate cancer diagnosis and treatment; hair loss severity linked to a gene affecting prostate conditions.

Scientists found gene mutations that affect hair loss, skin stem cells, and skin disorders, and identified drugs that may help treat blood vessel and skin conditions.

ANp63 is crucial for skin integrity, new filaggrin gene mutations link to eczema, hair can regrow from non-stem cells, sunburns are increasing, and glucocorticoids help treat skin allergies by affecting immune cells.

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

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

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