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LIM domain kinase 1

The LIMK1 gene provides instructions for making a protein that is highly active in the brain, where it is thought to be involved in the growth and development of nerve cells. Studies suggest that this protein may play an important role in areas of the brain that are responsible for processing visual-spatial information (visuospatial constructive cognition). These parts of the brain are important for visualizing an object as a set of parts and performing tasks such as writing, drawing, constructing models, and assembling puzzles.

Normal function

The LIMK1 gene provides instructions for making a protein that is highly active in the brain, where it is thought to be involved in the growth and development of nerve cells. Studies suggest that this protein may play an important role in areas of the brain that are responsible for processing visual-spatial information (visuospatial constructive cognition). These parts of the brain are important for visualizing an object as a set of parts and performing tasks such as writing, drawing, constructing models, and assembling puzzles.

Within cells, the LIMK1 protein likely regulates aspects of the cytoskeleton, the structural framework that helps to determine cell shape, size, and movement. The LIMK1 protein helps control the organisation of actin filaments, which are long, thin fibers that are part of the cytoskeleton. Actin filaments are necessary for several normal cellular functions, such as cell division, cell movement (motility), maintenance of cell shape, transport of proteins and other molecules within cells, and chemical signaling between cells.

Conditions referring to this gene or chromosome

Other names

LIM kinase

LIM kinase 1

LIM motif-containing protein kinase

LIMK

LIMK-1

LIMK1_HUMAN

Related patient information and medicines

ניוון שרירים

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ניוון שרירים

Limb-girdle muscular dystrophy (LGMD) LGMDs cause weakness in the muscles around the top of the arms and legs, which is why 'limb girdle' is used in the name of this condition. Also, if a child has delayed motor milestones (as mentioned above), a doctor may... MD may be diagnosed using one or more of the following tests: A blood test for creatine.

הפרעות אגירת גליקוגן

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הפרעות אגירת גליקוגן

הפרעות אגירת גליקוגן are a group of inherited diseases. They result from a problem with one of the proteins (known as enzymes) involved in the conversion of glucose to glycogen, or the breakdown of glycogen back into glucose. They mostly tend to affect your liver and muscles. Most are diagnosed in childhood. Type VI (Hers' disease). Type VII.

צלע צווארית

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צלע צווארית

Blood vessel compression or ... In the rare case that you have blockage of one of your blood vessels by a blood clot, treatment with a medicine is needed urgently to break down the clot. This used to be in the form of an anticoagulant such as warfarin but recently 'clot busters' such as urokinase have also been used. Treatment with an.

סרטן כבד ראשוני

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סרטן כבד ראשוני

It is not likely to be curat... There are new medicines being developed for the treatment of liver cancer. For example, sorafenib is a type of medicine called a multi-targeted kinase inhibitor. It interferes with the growth of cancer cells. Research has shown that sorafenib can be beneficial for people with advanced hepatocellular carcinoma..

דושן ניוון שרירים

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דושן ניוון שרירים

It causes progressive muscle weakness and is a serious condition which starts in early childhood. The muscle weakness is mainly in the 'proximal' muscles, which are those near the trunk of the body, around the hips and the shoulders. The first step in making the diagnosis is a blood test. This tests for creatine kinase. ילדים עם DMD always.

פומפוליקס

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פומפוליקס

Its effectiveness for pompholyx is still being studied, so it is not recommended yet. Dapilumab : this medication is used for a type of eczema called atopic dermatitis. In some cases it has been shown to be helpful for the treatment of pompholyx. Janus Kinase (JAK) inhibitors : these medications, available as creams or pills, target specific.

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  • 12 אפריל 2023 | הגרסה האחרונה
  • 1 במרץ 2022 | פורסם במקור

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