Filters: Subject: "Genetics"
101 - 125 of 159
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TitleDateTypeSetname
101 Molecular and genetic analysis of the Drosophila segmentation gene odd-paired a target of homeotic gene regulation in the embryonic midgut1996-06Textir_etd
102 Molecular genetic analysis of bithorax complex functions in Drosophila melanogaster1994-03Textir_etd
103 Molecular studies of lipoprotein lipase1991-06Textir_etd
104 Molecular variation in the angiotensinogen gene and implications for essential hypertension1999-05Textir_etd
105 MS and the Immune System2023-03Textehsl_novel_nam
106 MS and the Immune System2023-03Image/MovingImageehsl_novel_nam
107 MS and the Immune System2023-03Textehsl_novel_nam
108 Multiple Sclerosis: Epidemiology and Genetics1996-02-15Textehsl_novel_nam
109 New Concepts in CFEOM and Congenital Dysinnervation Syndromes2009-02-26Textehsl_novel_nam
110 Novel mutation in the ELOVL4 gene causes autosomal dominant Stargardt-like macular dystrophy2004Textir_uspace
111 Nuclear Magnetic resonance spectroscopy of escherichia coli tRNA (LYS) and the t RNA)LYS)-HIV RNA complex2007-05Textir_etd
112 Nuclear rotation and lineage specification in pelvetia embryos1992-12Textir_htca
113 Optic neuropathy in Wolfram's syndrome imaged with high-definition spectral domain OCT2015-02-22Textehsl_novel_nam
114 Optic neuropathy in Wolfram's syndrome imaged with high-definition spectral domain OCT2015-02-24Textehsl_novel_nam
115 Oral history interview with Bernice Williams Bowman by Bette L. Stanton1997-01-11; 1997-01-15; 1997-01-20; 1997-01-24; 1997-03-11Textdha_uhsoh
116 Oscar the grouch: A zebrafish model of heritable T cell acute lymphoblastic leukemia that displays apoptosis resistance2010Textir_etd
117 Ossification of the posterior longitudinal ligament and age-related macular degeneration: a new avenue of forensic identification2013-08Textir_etd
118 Page from Mario Capecchi NotebookImageehsl_hhs
119 Pathogenesis of Multiple Sclerosis - Opportunities for Intervention?1985-03-08Textehsl_novel_nam
120 Pathophysiology associated with a single gene (MASS1) mutation underlying the robust audiogenic seizure phenotype in Frings mice2003-05Textir_etd
121 Premalignant lesion and cancer: etiology and prospects for genetic mapping1988-12Textir_etd
122 The presence of a diagonal ear-lobe crease as an indicator of coronary artery disease.1983-08Textir_etd
123 Protection of cytoplasmic double-stranded RNA from adenosine deaminases that act on RNA in Xenopus laevis1998-08Textir_etd
124 Purification and cloning of the Xenopus laevis double-stranded RNA adenosine deaminase1997-08Textir_etd
125 Refutation of the general single locus model for the etiology of schizophrenia1982Textir_uspace
101 - 125 of 159