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The British Journal of Dermatology
|
January 26, 2010
Immunohistochemical localization of cellular NFATc1 does not predict clinical responses to ciclosporin in subcutaneous panniculitis-like T-cell non-Hodgkin lymphoma
S Tauro, S Maccallum, M J Groves, et al.
Human Molecular Genetics
|
July 23, 2003
Hereditary sensory neuropathy is caused by a mutation in the delta subunit of the cytosolic chaperonin-containing t-complex peptide-1 (Cct4 ) gene
Ming-Jen Lee, Dennis A Stephenson, Michael J Groves, et al.
European Journal of Human Genetics : EJHG
|
March 8, 2007
Relationship between E23K (an established type II diabetes-susceptibility variant within KCNJ11), polycystic ovary syndrome and androgen levels
Thomas M Barber, Amanda J Bennett, Anna L Gloyn, et al.
Cancer Research
|
June 19, 2013
LIN28 Expression in malignant germ cell tumors downregulates let-7 and increases oncogene levels
Matthew J Murray, Harpreet K Saini, Charlotte A Siegler, et al.
The Journal of Clinical Endocrinology and Metabolism
|
February 12, 2005
Analysis of multiple data sets reveals no association between the insulin gene variable number tandem repeat element and polycystic ovary syndrome or related traits
Brenda L Powell, Lema Haddad, Amanda Bennett, et al.
The Journal of Clinical Endocrinology and Metabolism
|
May 6, 2004
Large-scale analysis of the relationship between CYP11A promoter variation, polycystic ovarian syndrome, and serum testosterone
Michelle Gaasenbeek, Brenda L Powell, Ulla Sovio, et al.
Orphanet Journal of Rare Diseases
|
February 13, 2013
Barth syndrome
Sarah L N Clarke, Ann Bowron, Iris L Gonzalez, et al.
Diabetes Care
|
November 21, 2018
Plasma Fucosylated Glycans and C-Reactive Protein as Biomarkers of HNF1A-MODY in Young Adult-Onset Nonautoimmune Diabetes
Agata Juszczak, Tamara Pavić, Frano Vučković, et al.
Diabetes
|
March 1, 2007
Common variation in the LMNA gene (encoding lamin A/C) and type 2 diabetes: association analyses in 9,518 subjects
Katharine R Owen, Christopher J Groves, Robert L Hanson, et al.
Diabetologia
|
May 15, 2008
Association of variants in the fat mass and obesity associated (FTO) gene with polycystic ovary syndrome
T M Barber, A J Bennett, C J Groves, et al.
Page
of 43
Search research articles
Search
Showing results (361-370 of 425) with videos related to
Sort By:
Page
of 43
The British Journal of Dermatology
|
January 26, 2010
Immunohistochemical localization of cellular NFATc1 does not predict clinical responses to ciclosporin in subcutaneous panniculitis-like T-cell non-Hodgkin lymphoma
S Tauro, S Maccallum, M J Groves, et al.
Human Molecular Genetics
|
July 23, 2003
Hereditary sensory neuropathy is caused by a mutation in the delta subunit of the cytosolic chaperonin-containing t-complex peptide-1 (Cct4 ) gene
Ming-Jen Lee, Dennis A Stephenson, Michael J Groves, et al.
European Journal of Human Genetics : EJHG
|
March 8, 2007
Relationship between E23K (an established type II diabetes-susceptibility variant within KCNJ11), polycystic ovary syndrome and androgen levels
Thomas M Barber, Amanda J Bennett, Anna L Gloyn, et al.
Cancer Research
|
June 19, 2013
LIN28 Expression in malignant germ cell tumors downregulates let-7 and increases oncogene levels
Matthew J Murray, Harpreet K Saini, Charlotte A Siegler, et al.
The Journal of Clinical Endocrinology and Metabolism
|
February 12, 2005
Analysis of multiple data sets reveals no association between the insulin gene variable number tandem repeat element and polycystic ovary syndrome or related traits
Brenda L Powell, Lema Haddad, Amanda Bennett, et al.
The Journal of Clinical Endocrinology and Metabolism
|
May 6, 2004
Large-scale analysis of the relationship between CYP11A promoter variation, polycystic ovarian syndrome, and serum testosterone
Michelle Gaasenbeek, Brenda L Powell, Ulla Sovio, et al.
Orphanet Journal of Rare Diseases
|
February 13, 2013
Barth syndrome
Sarah L N Clarke, Ann Bowron, Iris L Gonzalez, et al.
Diabetes Care
|
November 21, 2018
Plasma Fucosylated Glycans and C-Reactive Protein as Biomarkers of HNF1A-MODY in Young Adult-Onset Nonautoimmune Diabetes
Agata Juszczak, Tamara Pavić, Frano Vučković, et al.
Diabetes
|
March 1, 2007
Common variation in the LMNA gene (encoding lamin A/C) and type 2 diabetes: association analyses in 9,518 subjects
Katharine R Owen, Christopher J Groves, Robert L Hanson, et al.
Diabetologia
|
May 15, 2008
Association of variants in the fat mass and obesity associated (FTO) gene with polycystic ovary syndrome
T M Barber, A J Bennett, C J Groves, et al.
Page
of 43