Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

B Gardiner

Showing results (41-50 of 61) with videos related to

Pageof 7
Sort By:
British Journal of Haematology|February 1, 1985
(A gamma delta beta)0-Thalassaemia in Blacks is due to a deletion of 34 kbp of DNAP S Henthorn, O Smithies, T Nakatsuji, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|January 30, 2003
Defining the autism minimum candidate gene region on chromosome 7Holli B Hutcheson, Y Bradford, S E Folstein, et al.
Hemoglobin|January 1, 1982
The percentages of Hb F and of G gamma and A gamma chains in the Hb F synthesized by reticulocytes and BFUe-derived colonies of patients with sickle cell anemiaA L Reese, C Altay, M E Headlee, et al.
Cellular Immunology|June 24, 1998
A thymic nurse cell-specific monoclonal antibodyM Pezzano, K D King, D D Philp, et al.
Physiological Genomics|July 7, 2005
Temporal and spatial transcriptional programs in murine kidney developmentG Challen, B Gardiner, G Caruana, et al.
Biochemical Genetics|February 1, 1984
Heterogeneity in the molecular basis of three types of hereditary persistence of fetal hemoglobin and the relative synthesis of the G gamma and A gamma types of gamma chainA Kutlar, M B Gardiner, M G Headlee, et al.
Circulation. Heart Failure|August 7, 2015
Deletion of capn4 Protects the Heart Against Endotoxemic Injury by Preventing ATP Synthase Disruption and Inhibiting Mitochondrial Superoxide GenerationRui Ni, Dong Zheng, Qiang Wang, et al.
Clinical Genetics|June 4, 2014
COL1A1 C-propeptide cleavage site mutation causes high bone mass, bone fragility and jaw lesions: a new cause of gnathodiaphyseal dysplasia?A M McInerney-Leo, E L Duncan, P J Leo, et al.
Diabetes|October 17, 2015
Mitochondrial Calpain-1 Disrupts ATP Synthase and Induces Superoxide Generation in Type 1 Diabetic Hearts: A Novel Mechanism Contributing to Diabetic CardiomyopathyRui Ni, Dong Zheng, Sidong Xiong, et al.
Genome Research|May 29, 2010
A global role for KLF1 in erythropoiesis revealed by ChIP-seq in primary erythroid cellsMichael R Tallack, Tom Whitington, Wai Shan Yuen, et al.
Pageof 7

Showing results (41-50 of 61) with videos related to

Sort By:
Pageof 7
British Journal of Haematology|February 1, 1985
(A gamma delta beta)0-Thalassaemia in Blacks is due to a deletion of 34 kbp of DNAP S Henthorn, O Smithies, T Nakatsuji, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|January 30, 2003
Defining the autism minimum candidate gene region on chromosome 7Holli B Hutcheson, Y Bradford, S E Folstein, et al.
Hemoglobin|January 1, 1982
The percentages of Hb F and of G gamma and A gamma chains in the Hb F synthesized by reticulocytes and BFUe-derived colonies of patients with sickle cell anemiaA L Reese, C Altay, M E Headlee, et al.
Cellular Immunology|June 24, 1998
A thymic nurse cell-specific monoclonal antibodyM Pezzano, K D King, D D Philp, et al.
Physiological Genomics|July 7, 2005
Temporal and spatial transcriptional programs in murine kidney developmentG Challen, B Gardiner, G Caruana, et al.
Biochemical Genetics|February 1, 1984
Heterogeneity in the molecular basis of three types of hereditary persistence of fetal hemoglobin and the relative synthesis of the G gamma and A gamma types of gamma chainA Kutlar, M B Gardiner, M G Headlee, et al.
Circulation. Heart Failure|August 7, 2015
Deletion of capn4 Protects the Heart Against Endotoxemic Injury by Preventing ATP Synthase Disruption and Inhibiting Mitochondrial Superoxide GenerationRui Ni, Dong Zheng, Qiang Wang, et al.
Clinical Genetics|June 4, 2014
COL1A1 C-propeptide cleavage site mutation causes high bone mass, bone fragility and jaw lesions: a new cause of gnathodiaphyseal dysplasia?A M McInerney-Leo, E L Duncan, P J Leo, et al.
Diabetes|October 17, 2015
Mitochondrial Calpain-1 Disrupts ATP Synthase and Induces Superoxide Generation in Type 1 Diabetic Hearts: A Novel Mechanism Contributing to Diabetic CardiomyopathyRui Ni, Dong Zheng, Sidong Xiong, et al.
Genome Research|May 29, 2010
A global role for KLF1 in erythropoiesis revealed by ChIP-seq in primary erythroid cellsMichael R Tallack, Tom Whitington, Wai Shan Yuen, et al.
Pageof 7