Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Adi, Meiri"'
Autor:
Grace Swickley, Yehoshua Bloch, Lidor Malka, Adi Meiri, Sharon Noy-Lotan, Amiel Yanai, Hannah Tamary, Benny Motro
Publikováno v:
BMC Molecular and Cell Biology, Vol 21, Iss 1, Pp 1-12 (2020)
Abstract Background Congenital dyserythropoietic anemia type I (CDA I), is an autosomal recessive disease with macrocytic anemia in which erythroid precursors in the bone marrow exhibit pathognomonic abnormalities including spongy heterochromatin and
Externí odkaz:
https://doaj.org/article/6e117771ef5c441294be37568e85ff4e
Autor:
Rivka Margalit, Carmel Armon, Sharon Wolfson, Adi Meiri, Liraz Avraham, Yael Bugen, Ran Shorer, Amir Cohen
Publikováno v:
Journal of Neurology. 269:2479-2485
Parental lineage has been shown to increase the risk of Alzheimer’s disease (AD) in the offspring, with greater risk attributed to maternal lineage. While 40 genes/loci have been linked to the risk of developing AD, none has been found on the X chr
Autor:
Benny Motro, Lidor Malka, Adi Meiri, Yehoshua Bloch, Hannah Tamary, Amiel Yanai, Grace Swickley, Sharon Noy-Lotan
Publikováno v:
BMC Molecular and Cell Biology, Vol 21, Iss 1, Pp 1-12 (2020)
BMC Molecular and Cell Biology
BMC Molecular and Cell Biology
Background Congenital dyserythropoietic anemia type I (CDA I), is an autosomal recessive disease with macrocytic anemia in which erythroid precursors in the bone marrow exhibit pathognomonic abnormalities including spongy heterochromatin and chromati
Autor:
Carmel, Armon, Sharon, Wolfson, Rivka, Margalit, Liraz, Avraham, Yael, Bugen, Amir, Cohen, Adi, Meiri, Ran, Shorer
Publikováno v:
Journal of neurology. 269(5)
Parental lineage has been shown to increase the risk of Alzheimer's disease (AD) in the offspring, with greater risk attributed to maternal lineage. While 40 genes/loci have been linked to the risk of developing AD, none has been found on the X chrom