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This gene is located in a six-cadherin cluster in a region on the long arm of chromosome 16 that is involved in loss of heterozygosity events in breast and prostate cancer. In addition, aberrant expression of this protein is observed in cervical adenocarcinomas.
Hypotrichosis with juvenile macular dystrophy is an autosomal recessive hereditary disease. [2] It is caused by a combination of mutations ( compound heterozygosity) in the CDH3 gene, which codes for Cadherin-3 (also known as P-Cadherin), a calcium-binding protein that is responsible for cellular adhesion in various tissues. [citation needed]
Cadherin related family member 3 (CDHR3), also known as CDH28 or its abbreviation CDHR3, is a protein that in humans is encoded by the CDHR3 gene. The protein is predominately expressed in respiratory epithelium and the first notion of its clinical implications was from the discovery that genetic variation of CDHR3 is strongly associated to early severe asthma exacerbations in children.
VE-cadherin is a classical cadherin from the cadherin superfamily and the gene is located in a six-cadherin cluster in a region on the long arm of chromosome 16 that is involved in loss of heterozygosity events in breast and prostate cancer. The encoded protein is a calcium-dependent cell–cell adhesion glycoprotein composed of five ...
Cadherin-1 or Epithelial cadherin (E-cadherin), (not to be confused with the APC/C activator protein CDH1) is a protein that in humans is encoded by the CDH1 gene. [5] Mutations are correlated with gastric, breast, colorectal, thyroid, and ovarian cancers. CDH1 has also been designated as CD324 ( cluster of differentiation 324).
EEM syndrome. EEM syndrome has an autosomal recessive pattern of inheritance. EEM syndrome (or E ctodermal dysplasia, E ctrodactyly and M acular dystrophy syndrome) [1] is an autosomal recessive [2] congenital malformation disorder affecting tissues associated with the ectoderm ( skin, hair, nails, teeth ), and also the hands, feet and eyes.
Hereditary diffuse gastric cancer (HDGC) is an inherited cancer syndrome that increases your risk of stomach cancer and lobular breast cancer. Learn about symptoms, causes, diagnosis, treatment ...
CDH3. CDH3 may refer to: Cadherin 3, a human gene. Finlay Air Park. Category: Letter–number combination disambiguation pages.
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