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Overexpressing thrombospondin-1 in mice skin prevents UVB-induced skin damage.

Bleaching hair damages protein structure, especially keratin, leading to weakened hair.

The ITGB6 gene is important for tissue repair and hair growth, and mutations can lead to enamel defects and other health issues.

Fluorescence can effectively measure acne treatment progress.

The Rotterdam Study found risk factors for elderly diseases, links between lifestyle and genetics with health conditions, and aimed to explore new areas like DNA methylation and sensory input effects on brain function.

Rhodococcus equi causes severe pneumonia in young foals, and effective vaccines are needed due to foals' weak immune responses.

UVB is good for a skin condition in Asian kids, a lotion works for head lice, a drug helps with a skin blistering disorder, a foam reduces itchiness in skin inflammation, birthmarks can be more widespread, and criteria for a neurocutaneous disorder were agreed upon.

The document concludes that certain genetic mutations and dietary factors are involved in acne development, and treatments like isotretinoin and diet changes can help manage it.

The rhg mutation in mice affects the Oat gene, causing hair growth issues and other symptoms.

Understanding the genetics of rare inherited ichthyosis syndromes is key for better treatments and genetic counseling.

Patients with Shwachman-Diamond syndrome often get misdiagnosed due to a wide range of symptoms, including immune system problems and bone abnormalities.

A new MBTPS2 gene variant disrupts fat metabolism and collagen production, causing Osteogenesis imperfecta.

Skin lesions in Carney Complex are caused by a gene change in some skin cells that leads to increased pigmentation and may lead to tumors.

Cri-du-chat syndrome can cause skin and oral lesions affecting nutrition and quality of life.

A Brazilian male with IFAP syndrome has a unique genetic variant causing his condition.

Researchers created a mouse model of a type of rickets that does not cause hair loss.

Not having enough or having too much of the protein Grainyhead-like 3 leads to various developmental problems.

A girl with Denys-Drash syndrome was misdiagnosed due to biotin affecting her hormone test results.

Mutations in specific keratin genes cause improper hair structure in mice due to faulty keratin protein assembly.

Knocking out certain genes in mice helps understand skin and hair growth problems.

A new gene variant in the DSP gene is linked to a unique type of hair loss.

Key genes linked to hair growth and cancer were identified in hairless mice.

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

The review highlights the importance of stem cells in hair health and suggests new treatment strategies for hair loss conditions.

Progerin affects cell shape but not hair or skin in mice.

Enhancers and super-enhancers are key in controlling specific gene activity and can play a role in cancer development.

A new MTX2 gene mutation caused a severe genetic disorder in a young Chinese girl.

The document concludes that various childhood hair and nail disorders exist, some may improve on their own, and advances in genetics and immunology could enhance treatment and counseling.

Eating a Mediterranean diet and taking certain supplements may improve symptoms of PCOS.

The conclusion is that genetic testing is important for diagnosing and treating various genetic hair disorders.