Medicine
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14 august 2019 01:02:39 |
| A novel CLCNKB mutation in a Chinese girl with classic Bartter syndrome: a case report (BMC Medical Genetics) |
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Tweet Bartter syndrome (BS) is a rare autosomal recessive disorder of salt reabsorption at the thick ascending limb of the Henle loop, characterized by hypokalemia, salt loss, metabolic alkalosis, hyperreninemic hyp... |
| 179 viewsCategory: Genetics, Medicine |
 Novel reference genes in colorectal cancer identify a distinct subset of high stage tumors and their associated histologically normal colonic tissues (BMC Medical Genetics)Bicistronic transfer of CDKN2A and p53 culminates in collaborative killing of human lung cancer cells in vitro and in vivo (Gene Therapy) 
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