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Proceedings of the National Academy of Sciences of the United States of America
|
May 10, 2001
Molecular and genealogical evidence for a founder effect in Fanconi anemia families of the Afrikaner population of South Africa
A J Tipping, T Pearson, N V Morgan, et al.
Journal of Clinical Immunology
|
September 25, 2015
Astute Clinician Report: A Novel 10 bp Frameshift Deletion in Exon 2 of ICOS Causes a Combined Immunodeficiency Associated with an Enteritis and Hepatitis
Nic Robertson, Karin R Engelhardt, Neil V Morgan, et al.
Acta Psychiatrica Scandinavica
|
May 25, 2016
Correlates of physical activity in people living with psychotic illness
S Suetani, A Waterreus, V Morgan, et al.
Blood Advances
|
January 26, 2021
Heterozygous mutation SLFN14 K208N in mice mediates species-specific differences in platelet and erythroid lineage commitment
Rachel J Stapley, Christopher W Smith, Elizabeth J Haining, et al.
Journal of Clinical Pathology
|
June 29, 2004
Molecular genetic analysis of FIH-1, FH, and SDHB candidate tumour suppressor genes in renal cell carcinoma
M R Morris, E Maina, N V Morgan, et al.
Molecular Brain
|
August 23, 2015
Insulin and IGF1 signalling pathways in human astrocytes in vitro and in vivo; characterisation, subcellular localisation and modulation of the receptors
Claire J Garwood, Laura E Ratcliffe, Sarah V Morgan, et al.
Haematologica
|
December 17, 2020
Post-translational polymodification of β1-tubulin regulates motor protein localisation in platelet production and function
Abdullah O Khan, Alexandre Slater, Annabel Maclachlan, et al.
Cell
|
August 16, 2016
The Deubiquitinase OTULIN Is an Essential Negative Regulator of Inflammation and Autoimmunity
Rune Busk Damgaard, Jennifer A Walker, Paola Marco-Casanova, et al.
Scandinavian Journal of Immunology
|
June 10, 2014
CD3G gene defects in familial autoimmune thyroiditis
B Gokturk, S Keles, M Kirac, et al.
Blood
|
January 20, 2005
A common Fanconi anemia mutation in black populations of sub-Saharan Africa
Neil V Morgan, Fahmida Essop, Ilja Demuth, et al.
Page
of 28
Search research articles
Search
Showing results (181-190 of 278) with videos related to
Sort By:
Page
of 28
Proceedings of the National Academy of Sciences of the United States of America
|
May 10, 2001
Molecular and genealogical evidence for a founder effect in Fanconi anemia families of the Afrikaner population of South Africa
A J Tipping, T Pearson, N V Morgan, et al.
Journal of Clinical Immunology
|
September 25, 2015
Astute Clinician Report: A Novel 10 bp Frameshift Deletion in Exon 2 of ICOS Causes a Combined Immunodeficiency Associated with an Enteritis and Hepatitis
Nic Robertson, Karin R Engelhardt, Neil V Morgan, et al.
Acta Psychiatrica Scandinavica
|
May 25, 2016
Correlates of physical activity in people living with psychotic illness
S Suetani, A Waterreus, V Morgan, et al.
Blood Advances
|
January 26, 2021
Heterozygous mutation SLFN14 K208N in mice mediates species-specific differences in platelet and erythroid lineage commitment
Rachel J Stapley, Christopher W Smith, Elizabeth J Haining, et al.
Journal of Clinical Pathology
|
June 29, 2004
Molecular genetic analysis of FIH-1, FH, and SDHB candidate tumour suppressor genes in renal cell carcinoma
M R Morris, E Maina, N V Morgan, et al.
Molecular Brain
|
August 23, 2015
Insulin and IGF1 signalling pathways in human astrocytes in vitro and in vivo; characterisation, subcellular localisation and modulation of the receptors
Claire J Garwood, Laura E Ratcliffe, Sarah V Morgan, et al.
Haematologica
|
December 17, 2020
Post-translational polymodification of β1-tubulin regulates motor protein localisation in platelet production and function
Abdullah O Khan, Alexandre Slater, Annabel Maclachlan, et al.
Cell
|
August 16, 2016
The Deubiquitinase OTULIN Is an Essential Negative Regulator of Inflammation and Autoimmunity
Rune Busk Damgaard, Jennifer A Walker, Paola Marco-Casanova, et al.
Scandinavian Journal of Immunology
|
June 10, 2014
CD3G gene defects in familial autoimmune thyroiditis
B Gokturk, S Keles, M Kirac, et al.
Blood
|
January 20, 2005
A common Fanconi anemia mutation in black populations of sub-Saharan Africa
Neil V Morgan, Fahmida Essop, Ilja Demuth, et al.
Page
of 28