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首页  >  多肽  >  Human PMS2 Peptide
PMS2 (基因名), Mismatch repair endonuclease PMS2 (蛋白名), PMS2_HUMAN.
产品名称:

Human PMS2/ Mismatch repair endonuclease PMS2 Peptide

货号:

SR3164h

监管等级:
商标:
EIAab®
种属:
Human
形态:
Lyophilized powder
表征:
The peptide is characterized by mass spectroscopy
溶液澄清度:
In DMSO clear solution
Human PMS2 Peptide
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Human PMS2 Peptide
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R&D 技术数据
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该产品尚未在任何出版物中被引用。

[1].
"Four novel germline mutations in the MLH1 and PMS2 mismatch repair genes in patients with hereditary nonpolyposis colorectal cancer."

[2].
"Screening for germline mutations of MLH1, MSH2, MSH6 and PMS2 genes in Slovenian colorectal cancer patients: implications for a population specific detection strategy of Lynch syndrome."

[3].
"Prediction of Lynch syndrome in consecutive patients with colorectal cancer."

[4].
"Mismatch repair gene polymorphisms and survival in invasive ovarian cancer patients."

[5].
"The clinical phenotype of Lynch syndrome due to germ-line PMS2 mutations."

[6].
"Novel biallelic mutations in MSH6 and PMS2 genes: gene conversion as a likely cause of PMS2 gene inactivation."

[7].
"Common variants in mismatch repair genes and risk of invasive ovarian cancer."

[8].
"Heterozygous mutations in PMS2 cause hereditary nonpolyposis colorectal carcinoma (Lynch syndrome)."

[9].
"Familial mutations in PMS2 can cause autosomal dominant hereditary nonpolyposis colorectal cancer."

[10].
"Polymorphisms and HNPCC: PMS2-MLH1 protein interactions diminished by single nucleotide polymorphisms."
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