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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).
320873 Ensembl ENSG00000040731 ENSMUSG00000022321 UniProt Q9Y6N8 P70408 RefSeq (mRNA) NM_001190450 NM_006727 NM_001317222 NM_001317224 NM_001362460 NM_009865 NM_001316758 RefSeq (protein) NP_001304151 NP_001304153 NP_006718 NP_001349389 NP_001304153.1 NP_001303687 NP_033995 Location (UCSC) Chr 5: 24.49 – 24.64 Mb Chr 15: 18.82 – 19.01 Mb PubMed search Wikidata View/Edit Human View/Edit ...
The compound, Cs 3 CdH 5, prepared by the reaction of caesium hydride, CsH, and cadmium metal powder at high temperature contains the CdH 2− 4 ion, along with caesium cations, Cs +, and hydride anions, H −. The tetrahedral anion is an example of an ionic complex of CdH 2. The average Cd-H bond length in CdH 2− 4 is 182pm.
The chances of needing another surgery are about 1%. It usually takes 3–6 weeks to return to work and 6 weeks before you can eat normally again. Gastrointestinal side effects like bloating might ...
An acquired diaphragmatic hernia (ADH) is usually the result of a blunt or penetrating injury. Traffic accidents and falls cause the majority of blunt injuries. Penetrating injuries are usually ...
Bochdalek hernia is one of two forms of a congenital diaphragmatic hernia, the other form being Morgagni hernia. A Bochdalek hernia is a congenital abnormality in which an opening exists in the infant's diaphragm, allowing normally intra-abdominal organs (particularly the stomach and intestines) to enter into the thoracic cavity.
1 in 1,000 (term babies) [3] Hip dysplasia is an abnormality of the hip joint where the socket portion does not fully cover the ball portion, resulting in an increased risk for joint dislocation. [1] Hip dysplasia may occur at birth or develop in early life. [1] Regardless, it does not typically produce symptoms in babies less than a year old. [3]
Function. This gene encodes a type II classical cadherin from the cadherin superfamily, integral membrane proteins that mediate calcium-dependent cell-cell adhesion. Mature cadherin proteins are composed of a large N-terminal extracellular domain, a single membrane-spanning domain, and a small, highly conserved C-terminal cytoplasmic domain.