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Graphene oxide and indole-3-acetic acid together inhibit root growth in Brassica napus L. by affecting multiple plant hormone pathways.

Minoxidil improves blood flow and vessel flexibility, potentially helping with vascular stiffness.

Hydrogen peroxide and monoethanolamine in hair dye can cause dermatitis and hair loss.

ΔNp63α helps control a protein that stops cancer cells from spreading.

Skin problems like itching, dry skin, and hair loss are more common in hepatitis C patients after interferon treatment, but lichen planus is not linked to the infection.

Mice can correct hair follicle orientation without certain genes, but proper overall alignment needs those genes.

PTHrP and its receptor can control blood vessel growth and hair development in mouse skin.

Women with polycystic ovary syndrome tend to have a longer anogenital distance.

FOXN1 gene mutations cause a rare, severe immune disease treatable with cell or tissue transplants.

STAT5 activation is crucial for starting the hair growth phase.

Loss of keratin K2 causes skin problems and inflammation.

Mice lacking fibromodulin have disrupted healing patterns, leading to abnormal skin repair and scarring.

Dutasteride makes alcohol less sedating and may lead to less drinking in men.

Mice without the Sp6 gene have problems developing several body parts, including hair, teeth, limbs, and lungs.

Severe insulin resistance can be managed with medication, lifestyle changes, and treatment for related conditions.

Peginterferon alfa-2b and ribavirin therapy for hepatitis C can cause serious side effects, some different from those reported in clinical trials.

APS-1 in Italy shows diverse AIRE mutations and various autoimmune issues.

Psychotropic medications can cause skin reactions, including severe conditions like SJS and TEN, and it's important for psychiatrists to recognize and manage these side effects.

Smad1 and Smad5 are essential for hair follicle development and stem cell sleepiness.

The document describes a woman with familial Parkinson's disease due to a genetic mutation, showing severe symptoms and poor response to treatment, and suggests finasteride may help reduce symptoms in Tourette syndrome.

The research concluded that selection significantly shaped the genetic variation of the X chromosome, with certain regions affected by past selective events.

New treatments for PCOS focus on insulin resistance and reducing testosterone levels, along with traditional hormone therapies.

The study concluded that PKP1 is essential for skin integrity and hair growth, and its dysfunction causes the symptoms of ectodermal dysplasia/skin fragility syndrome.

Certain defective glucocorticoid receptor mutants move faster inside cell nuclei and work less effectively.

Steroidogenic isoenzymes may help improve treatments for common hair loss.

People who carry the 21-Hydroxylase Deficiency gene are not more likely to have excessive male hormone levels.

Hedychium spicatum has medicinal properties but needs more research for scientific validation and use.

Researchers found genetic mutations causing hypohidrotic ectodermal dysplasia in 88% of studied patients and identified new mutations and genetic variations affecting the disease.

BAF200 is essential for proper heart and coronary artery formation.

Future research on ectodysplasin should explore its role in diseases, stem cells, and evolution, and continue developing treatments for genetic disorders like hypohidrotic ectodermal dysplasia.