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A G Roberts

Showing results (71-80 of 82) with videos related to

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Nature Genetics|May 1, 1996
A R59W mutation in human protoporphyrinogen oxidase results in decreased enzyme activity and is prevalent in South Africans with variegate porphyriaP N Meissner, T A Dailey, R J Hift, et al.
Human Molecular Genetics|November 13, 1998
Molecular characterization of homozygous variegate porphyriaA G Roberts, H Puy, T A Dailey, et al.
Clinical Immunology (Orlando, Fla.)|June 25, 2017
High resolution IgH repertoire analysis reveals fetal liver as the likely origin of life-long, innate B lymphopoiesis in humansAnindita Roy, Vojtech Bystry, Georg Bohn, et al.
Brain : a Journal of Neurology|December 28, 2020
Abnormal dorsal attention network activation in memory impairment after traumatic brain injuryEmma-Jane Mallas, Sara De Simoni, Gregory Scott, et al.
Journal of Immunology (Baltimore, Md. : 1950)|February 1, 2011
Activated invariant NKT cells regulate osteoclast development and functionMing Hu, J H Duncan Bassett, Lynett Danks, et al.
The Journal of Investigative Dermatology|November 9, 2000
Co-inheritance of mutations in the uroporphyrinogen decarboxylase and hemochromatosis genes accelerates the onset of porphyria cutanea tardaJ J Brady, H A Jackson, A G Roberts, et al.
Blood|April 26, 2003
Stem cell transplantation for chronic myeloid leukemia in childrenKate Cwynarski, Irene A G Roberts, Simona Iacobelli, et al.
Nature Communications|September 15, 2021
Chromatin-based, in cis and in trans regulatory rewiring underpins distinct oncogenic transcriptomes in multiple myelomaJaime Alvarez-Benayas, Nikolaos Trasanidis, Alexia Katsarou, et al.
Journal of Medical Genetics|January 20, 2004
The 16189 variant of mitochondrial DNA occurs more frequently in C282Y homozygotes with haemochromatosis than those without iron loadingK J Livesey, V L C Wimhurst, K Carter, et al.
Blood|January 11, 2022
Systems medicine dissection of chr1q-amp reveals a novel PBX1-FOXM1 axis for targeted therapy in multiple myelomaNikolaos Trasanidis, Alexia Katsarou, Kanagaraju Ponnusamy, et al.
Pageof 9

Showing results (71-80 of 82) with videos related to

Sort By:
Pageof 9
Nature Genetics|May 1, 1996
A R59W mutation in human protoporphyrinogen oxidase results in decreased enzyme activity and is prevalent in South Africans with variegate porphyriaP N Meissner, T A Dailey, R J Hift, et al.
Human Molecular Genetics|November 13, 1998
Molecular characterization of homozygous variegate porphyriaA G Roberts, H Puy, T A Dailey, et al.
Clinical Immunology (Orlando, Fla.)|June 25, 2017
High resolution IgH repertoire analysis reveals fetal liver as the likely origin of life-long, innate B lymphopoiesis in humansAnindita Roy, Vojtech Bystry, Georg Bohn, et al.
Brain : a Journal of Neurology|December 28, 2020
Abnormal dorsal attention network activation in memory impairment after traumatic brain injuryEmma-Jane Mallas, Sara De Simoni, Gregory Scott, et al.
Journal of Immunology (Baltimore, Md. : 1950)|February 1, 2011
Activated invariant NKT cells regulate osteoclast development and functionMing Hu, J H Duncan Bassett, Lynett Danks, et al.
The Journal of Investigative Dermatology|November 9, 2000
Co-inheritance of mutations in the uroporphyrinogen decarboxylase and hemochromatosis genes accelerates the onset of porphyria cutanea tardaJ J Brady, H A Jackson, A G Roberts, et al.
Blood|April 26, 2003
Stem cell transplantation for chronic myeloid leukemia in childrenKate Cwynarski, Irene A G Roberts, Simona Iacobelli, et al.
Nature Communications|September 15, 2021
Chromatin-based, in cis and in trans regulatory rewiring underpins distinct oncogenic transcriptomes in multiple myelomaJaime Alvarez-Benayas, Nikolaos Trasanidis, Alexia Katsarou, et al.
Journal of Medical Genetics|January 20, 2004
The 16189 variant of mitochondrial DNA occurs more frequently in C282Y homozygotes with haemochromatosis than those without iron loadingK J Livesey, V L C Wimhurst, K Carter, et al.
Blood|January 11, 2022
Systems medicine dissection of chr1q-amp reveals a novel PBX1-FOXM1 axis for targeted therapy in multiple myelomaNikolaos Trasanidis, Alexia Katsarou, Kanagaraju Ponnusamy, et al.
Pageof 9