How Do You Spell WILMS GENES?

Pronunciation: [wˈɪlmz d͡ʒˈiːnz] (IPA)

Wilms Genes is a term used in genetics to refer to a group of genes that are responsible for the development of kidneys during embryonic stages. The spelling of the term is based on the name of the German surgeon Max Wilms, who first discovered the connection between these genes and kidney development. The pronunciation of the term follows the IPA phonetic transcription as /wɪlmz dʒiːnz/. The first syllable, "Wilms", is pronounced as /wɪlmz/, with a short "i" sound and a silent "s" at the end. The second syllable, "Genes", is pronounced as /dʒiːnz/, with a long "e" sound and a strong "s" at the end.

WILMS GENES Meaning and Definition

1. Wilms genes refer to a group of genes that are associated with the development of Wilms tumor, a type of kidney cancer that primarily affects children. These genes play a critical role in the normal growth and development of kidney cells during embryonic development.

   The most well-known and extensively studied Wilms gene is WT1 (Wilms tumor 1), which is located on chromosome 11. This gene encodes a protein known as a transcription factor, which is involved in the regulation of gene expression. The protein produced by WT1 is important for the development and functioning of the kidneys, as it is involved in the control of cell growth, differentiation, and survival.

   In addition to WT1, other Wilms genes include WTX, CTNNB1, and TP53, which are also involved in the development and progression of Wilms tumor. These genes are thought to interact with each other and with other cellular pathways to regulate cell division and control the growth of kidney cells.

   Mutations or alterations in Wilms genes can disrupt the normal development of kidney cells, leading to the formation of Wilms tumor. Wilms tumor usually arises within the first few years of a child's life and is characterized by the presence of a mass or tumor in one or both kidneys. Treatment for Wilms tumor typically involves a combination of surgery, radiation therapy, and chemotherapy, depending on the stage and severity of the tumor.

   Understanding the function and role of Wilms genes provides insights into the molecular mechanisms underlying the development of Wilms tumor and may contribute to the development of targeted therapies for this childhood cancer.

Common Misspellings for WILMS GENES

• wjlms gene
• qilms genes
• ailms genes
• silms genes
• eilms genes
• 3ilms genes
• 2ilms genes
• wulms genes
• wjlms genes
• wklms genes
• wolms genes
• w9lms genes
• w8lms genes
• wikms genes
• wipms genes
• wioms genes
• wilns genes
• wilks genes
• wiljs genes
• wilma genes

Etymology of WILMS GENES

The term "Wilms Genes" has its etymology rooted in the history of medicine. It is derived from the name of Dr. Max Wilms, a German surgeon and pathologist who first described Wilms tumor, also known as nephroblastoma, in 1899.

Wilms tumor is a rare type of kidney cancer that primarily affects children. As medical research progressed, it was discovered that this condition can be caused by genetic abnormalities. Researchers identified certain genes that play a crucial role in the development of Wilms tumor, specifically mutations in the WT1 (Wilms tumor 1) gene.

Therefore, the term "Wilms Genes" refers to the genes involved in the development and progression of Wilms tumor, primarily WT1. The name is a tribute to Dr. Max Wilms for his pioneering work and contribution to the understanding of this specific kidney cancer.