Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Dedrey, Elam"'
Autor:
Dedrey Elam, Ruth Luddy, Ferdane Kutlar, Robert E. Wenk, Erin Dainer, Abdullah Kutlar, Leslie Holley
Publikováno v:
Hemoglobin. 32:588-591
Neonatal screening for hemoglobinopathies occasionally results in the detection of novel hemoglobin (Hb) variants. Two heterozygous infants were found with different beta chain mutations, neither of which produced obvious clinical or laboratory abnor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4d17cc4fb7bc5f2eec4002f64d053483
https://doi.org/10.1080/03630260802507931
https://doi.org/10.1080/03630260802507931
Autor:
Jeanette Harbin, Ferdane Kutlar, Abdullah Kutlar, Dedrey Elam, Betsy Clair, Amy E. Vinson, Michele L. Glendenning, Aisha L. Walker
Publikováno v:
Hemoglobin. 28:317-323
beta-Globin gene cluster haplotypes were originally determined by restriction endonuclease mapping with Southern blots of polymorphic sites around the gene cluster. Over the years, haplotyping has been found to be useful, not only in population genet
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b45e16608de6d6454a0f620ebd358329
https://doi.org/10.1081/hem-200037724
https://doi.org/10.1081/hem-200037724
Publikováno v:
Hemoglobin. 27:249-252
Hb Setif results from a G→T substitution (GAC→TAC) at codon 94 of the α2‐globin gene, changing the aspartic acid to a tyrosine at residue 94 of the α chain [[1]]. The variant was first described in...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ed0b34386b33b762a1bec083c4e2fa8e
https://doi.org/10.1081/hem-120026050
https://doi.org/10.1081/hem-120026050
Autor:
Erin, Dainer, Robert E, Wenk, Ruth, Luddy, Dedrey, Elam, Leslie, Holley, Abdullah, Kutlar, Ferdane, Kutlar
Publikováno v:
Hemoglobin. 32(6)
Neonatal screening for hemoglobinopathies occasionally results in the detection of novel hemoglobin (Hb) variants. Two heterozygous infants were found with different beta chain mutations, neither of which produced obvious clinical or laboratory abnor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f3875d9ff0af77e89a24d7a907ddfebc
https://pubmed.ncbi.nlm.nih.gov/19065337
https://pubmed.ncbi.nlm.nih.gov/19065337
Publikováno v:
International Journal of Medical Sciences
Hb J Meerut is an infrequently found alpha-globin variant. It has previously been reported in various populations around the world. One particular case reported in 1994 included a Turkish family. In this report, details of a second case of Hb J Meeru
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::bb80fdae3f582a57d5089a84ea464722
https://pubmed.ncbi.nlm.nih.gov/16575421
https://pubmed.ncbi.nlm.nih.gov/16575421
Autor:
Dedrey Elam, Leslie Holley, Abdullah Kutlar, A. Addington, Ferdane Kutlar, Adekunle Adekile, Betsy Clair, K. McKie
Publikováno v:
European journal of haematology. 75(2)
PURPOSE Homozygosity for the (AT)7 allele of uridine diphosphate glucuronosyl transferase 1A (UGT1A1) gene polymorphism is associated with increased bilirubin levels in sickle cell anemia (SCA). In the present study, in addition to UGT1A1 promoter ge
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2984bdfe6575ebfd1aea036f961fbc94
https://pubmed.ncbi.nlm.nih.gov/16004608
https://pubmed.ncbi.nlm.nih.gov/16004608
Autor:
Amy E, Vinson, Aisha, Walker, Dedrey, Elam, Michele, Glendenning, Ferdane, Kutlar, Betsy, Clair, Jeanette, Harbin, Abdullah, Kutlar
Publikováno v:
Hemoglobin. 28(4)
beta-Globin gene cluster haplotypes were originally determined by restriction endonuclease mapping with Southern blots of polymorphic sites around the gene cluster. Over the years, haplotyping has been found to be useful, not only in population genet
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::84c4b44b0246486440437230d81c9cdf
https://pubmed.ncbi.nlm.nih.gov/15658187
https://pubmed.ncbi.nlm.nih.gov/15658187
Publikováno v:
Hemoglobin. 27(4)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::18c4061eb74f4af7f79e3641854437ae
https://pubmed.ncbi.nlm.nih.gov/14649316
https://pubmed.ncbi.nlm.nih.gov/14649316
Publikováno v:
International Journal of Medical Sciences. :26-27
Hb J Meerut is an infrequently found α-globin variant. It has previously been reported in various populations around the world. One particular case reported in 1994 included a Turkish family. In this report, details of a second case of Hb J Meerut i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::22eba05fa10af344f8bcb129a433c6b6
https://doi.org/10.7150/ijms.3.26
https://doi.org/10.7150/ijms.3.26
Autor:
Dedrey Elam, Kathleen McKie, Heather Yaun Hughes, Leslie Holley, Ferdane Kutlar, Abdullah Kutlar
Publikováno v:
Blood. 110:3802-3802
The occurrence of multiple globin abnormalities in one individual is not very rare, particularly in populations where hemoglobinopathies are common. In most cases, this is of genetic interest and may pose a diagnostic challenge due to the interaction
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::91568ac004b641b257fb03476ab32bf7
https://doi.org/10.1182/blood.v110.11.3802.3802
https://doi.org/10.1182/blood.v110.11.3802.3802