<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Showmaker KC</submitter><funding>NIH-NIGMS</funding><funding>NHLBI NIH HHS</funding><funding>NIGMS NIH HHS</funding><funding>NIH-NHLBI</funding><pagination>56-70</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6985787</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>52(1)</volume><pubmed_abstract>The HSRA rat is a model of congenital abnormalities of the kidney and urogenital tract (CAKUT). Our laboratory has used this model to investigate the role of nephron number (functional unit of the kidney) in susceptibility to develop kidney disease as 50-75% offspring are born with a single kidney (HSRA-S), while 25-50% are born with two kidneys (HSRA-C). HSRA-S rats develop increased kidney injury and hypertension with age compared with nephrectomized two-kidney animals (HSRA-UNX), suggesting that even slight differences in nephron number can be an important driver in decline in kidney function. The HSRA rat was selected and inbred from a family of outbred heterogeneous stock (NIH-HS) rats that exhibited a high incidence of CAKUT. The HS model was originally developed from eight inbred st</pubmed_abstract><journal>Physiological genomics</journal><pubmed_title>Whole genome sequencing and novel candidate genes for CAKUT and altered nephrogenesis in the HSRA rat.</pubmed_title><pmcid>PMC6985787</pmcid><funding_grant_id>P20GM103476</funding_grant_id><funding_grant_id>P30GM103328</funding_grant_id><funding_grant_id>P20GM104357</funding_grant_id><funding_grant_id>P20 GM121334</funding_grant_id><funding_grant_id>R01 HL137673</funding_grant_id><funding_grant_id>R01HL137673</funding_grant_id><funding_grant_id>P20 GM104357</funding_grant_id><funding_grant_id>P20 GM103476</funding_grant_id><funding_grant_id>P30 GM103328</funding_grant_id><pubmed_authors>Garrett MR</pubmed_authors><pubmed_authors>Johnson AC</pubmed_authors><pubmed_authors>Yang W</pubmed_authors><pubmed_authors>Cobb MB</pubmed_authors><pubmed_authors>Showmaker KC</pubmed_authors></additional><is_claimable>false</is_claimable><name>Whole genome sequencing and novel candidate genes for CAKUT and altered nephrogenesis in the HSRA rat.</name><description>The HSRA rat is a model of congenital abnormalities of the kidney and urogenital tract (CAKUT). Our laboratory has used this model to investigate the role of nephron number (functional unit of the kidney) in susceptibility to develop kidney disease as 50-75% offspring are born with a single kidney (HSRA-S), while 25-50% are born with two kidneys (HSRA-C). HSRA-S rats develop increased kidney injury and hypertension with age compared with nephrectomized two-kidney animals (HSRA-UNX), suggesting that even slight differences in nephron number can be an important driver in decline in kidney function. The HSRA rat was selected and inbred from a family of outbred heterogeneous stock (NIH-HS) rats that exhibited a high incidence of CAKUT. The HS model was originally developed from eight inbred st</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 Jan</publication><modification>2025-04-05T11:01:20.843Z</modification><creation>2025-04-05T11:01:20.843Z</creation></dates><accession>S-EPMC6985787</accession><cross_references><pubmed>31841396</pubmed><doi>10.1152/physiolgenomics.00112.2019</doi></cross_references></HashMap>