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European Journal of Human Genetics : EJHG
|
February 4, 2016
A maternal deletion upstream of the imprint control region 2 in 11p15 causes loss of methylation and familial Beckwith-Wiedemann syndrome
Jasmin Beygo, Ivana Joksic, Tim M Strom, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
January 11, 2000
Identification of brain-specific and imprinted small nucleolar RNA genes exhibiting an unusual genomic organization
J Cavaillé, K Buiting, M Kiefmann, et al.
The Journal of Biological Chemistry
|
April 11, 2021
Complement receptor 3 mediates both sinking phagocytosis and phagocytic cup formation via distinct mechanisms
Stefan Walbaum, Benjamin Ambrosy, Paula Schütz, et al.
Plos One
|
October 17, 2013
Deep bisulfite sequencing of aberrantly methylated loci in a patient with multiple methylation defects
Jasmin Beygo, Ole Ammerpohl, Daniela Gritzan, et al.
The Journal of Biological Chemistry
|
January 5, 2021
Complement receptor 3 mediates both sinking phagocytosis and phagocytic cup formation via distinct mechanisms
Stefan Walbaum, Benjamin Ambrosy, Paula Schütz, et al.
Nature Genetics
|
October 1, 1995
Cloning of the putative tumour suppressor gene for hereditary multiple exostoses (EXT1)
J Ahn, H J Lüdecke, S Lindow, et al.
Clinical Genetics
|
February 1, 1990
Use of the RB1 cDNA as a diagnostic probe in retinoblastoma families
A D Goddard, R A Phillips, V Greger, et al.
American Journal of Medical Genetics
|
December 2, 1996
Validation studies of SNRPN methylation as a diagnostic test for Prader-Willi syndrome
T Kubota, J S Sutcliffe, S Aradhya, et al.
Human Genetics
|
March 12, 2004
SNURF-SNRPN and UBE3A transcript levels in patients with Angelman syndrome
Maren Runte, Peter M Kroisel, Gabriele Gillessen-Kaesbach, et al.
European Journal of Human Genetics : EJHG
|
December 27, 2007
IGF2/H19 hypomethylation in Silver-Russell syndrome and isolated hemihypoplasia
Michael Zeschnigk, Beate Albrecht, Karin Buiting, et al.
Page
of 37
Search research articles
Search
Showing results (271-280 of 368) with videos related to
Sort By:
Page
of 37
European Journal of Human Genetics : EJHG
|
February 4, 2016
A maternal deletion upstream of the imprint control region 2 in 11p15 causes loss of methylation and familial Beckwith-Wiedemann syndrome
Jasmin Beygo, Ivana Joksic, Tim M Strom, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
January 11, 2000
Identification of brain-specific and imprinted small nucleolar RNA genes exhibiting an unusual genomic organization
J Cavaillé, K Buiting, M Kiefmann, et al.
The Journal of Biological Chemistry
|
April 11, 2021
Complement receptor 3 mediates both sinking phagocytosis and phagocytic cup formation via distinct mechanisms
Stefan Walbaum, Benjamin Ambrosy, Paula Schütz, et al.
Plos One
|
October 17, 2013
Deep bisulfite sequencing of aberrantly methylated loci in a patient with multiple methylation defects
Jasmin Beygo, Ole Ammerpohl, Daniela Gritzan, et al.
The Journal of Biological Chemistry
|
January 5, 2021
Complement receptor 3 mediates both sinking phagocytosis and phagocytic cup formation via distinct mechanisms
Stefan Walbaum, Benjamin Ambrosy, Paula Schütz, et al.
Nature Genetics
|
October 1, 1995
Cloning of the putative tumour suppressor gene for hereditary multiple exostoses (EXT1)
J Ahn, H J Lüdecke, S Lindow, et al.
Clinical Genetics
|
February 1, 1990
Use of the RB1 cDNA as a diagnostic probe in retinoblastoma families
A D Goddard, R A Phillips, V Greger, et al.
American Journal of Medical Genetics
|
December 2, 1996
Validation studies of SNRPN methylation as a diagnostic test for Prader-Willi syndrome
T Kubota, J S Sutcliffe, S Aradhya, et al.
Human Genetics
|
March 12, 2004
SNURF-SNRPN and UBE3A transcript levels in patients with Angelman syndrome
Maren Runte, Peter M Kroisel, Gabriele Gillessen-Kaesbach, et al.
European Journal of Human Genetics : EJHG
|
December 27, 2007
IGF2/H19 hypomethylation in Silver-Russell syndrome and isolated hemihypoplasia
Michael Zeschnigk, Beate Albrecht, Karin Buiting, et al.
Page
of 37