<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>15(3)</volume><submitter>Garciaz S</submitter><pubmed_abstract>We studied a cohort of 367 healthy related donors who volunteered to donate their hematopoietic stem cells for allogeneic transplantation. All donors were homogeneously cared for at a single institution, and received rhG-CSF as a mobilization treatment prior to undergoing apheresis. Peripheral blood CD34+ cell counts were used as the main surrogate marker for rhG-CSF induced mobilization. We searched whether inter-individual variations in known genetic polymorphisms located in genes whose products are functionally important for mobilization, could affect the extent of CD34+ mobilization, either individually or in combination. We found little or no influence of individual SNPs or haplotypes for the SDF1, CXCR4, VCAM and VLA4 genes, whether using CD34+ cell counts as a continuous or a catego</pubmed_abstract><journal>PloS one</journal><pagination>e0228878</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7058310</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Analysis of a large single institution cohort of related donors fails to detect a relation between SDF1/CXCR4 or VCAM/VLA4 genetic polymorphisms and the level of hematopoietic progenitor cell mobilization in response to G-CSF.</pubmed_title><pmcid>PMC7058310</pmcid><pubmed_authors>Picard C</pubmed_authors><pubmed_authors>Fournel C</pubmed_authors><pubmed_authors>di Cristofaro J</pubmed_authors><pubmed_authors>Boher JM</pubmed_authors><pubmed_authors>Granata A</pubmed_authors><pubmed_authors>Lemarie C</pubmed_authors><pubmed_authors>Chiaroni J</pubmed_authors><pubmed_authors>Sfumato P</pubmed_authors><pubmed_authors>Calmels B</pubmed_authors><pubmed_authors>Garciaz S</pubmed_authors><pubmed_authors>Imbert AM</pubmed_authors><pubmed_authors>Chabannon C</pubmed_authors><pubmed_authors>Blaise D</pubmed_authors></additional><is_claimable>false</is_claimable><name>Analysis of a large single institution cohort of related donors fails to detect a relation between SDF1/CXCR4 or VCAM/VLA4 genetic polymorphisms and the level of hematopoietic progenitor cell mobilization in response to G-CSF.</name><description>We studied a cohort of 367 healthy related donors who volunteered to donate their hematopoietic stem cells for allogeneic transplantation. All donors were homogeneously cared for at a single institution, and received rhG-CSF as a mobilization treatment prior to undergoing apheresis. Peripheral blood CD34+ cell counts were used as the main surrogate marker for rhG-CSF induced mobilization. We searched whether inter-individual variations in known genetic polymorphisms located in genes whose products are functionally important for mobilization, could affect the extent of CD34+ mobilization, either individually or in combination. We found little or no influence of individual SNPs or haplotypes for the SDF1, CXCR4, VCAM and VLA4 genes, whether using CD34+ cell counts as a continuous or a catego</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020</publication><modification>2026-04-29T13:15:58.888Z</modification><creation>2020-05-22T13:21:57Z</creation></dates><accession>S-EPMC7058310</accession><cross_references><pubmed>32134938</pubmed><doi>10.1371/journal.pone.0228878</doi></cross_references></HashMap>