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A Curtis

Showing results (691-700 of 1,051) with videos related to

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Neuroreport|January 6, 1999
Novel insertion in the KSP region of the neurofilament heavy gene in amyotrophic lateral sclerosis (ALS)J Tomkins, P Usher, J Y Slade, et al.
Hematology (Amsterdam, Netherlands)|December 29, 2017
A patient with oxaliplatin immune-induced syndrome (OIIS) who also developed leucovorin and palonosetron-associated thrombocytopeniaS A Curtis, B R Curtis, A I Lee, et al.
Journal of Periodontal Research|July 13, 2002
Recognition of the carbohydrate modifications to the RgpA protease of Porphyromonas gingivalis by periodontal patient serum IgGJennifer M Slaney, Minnie Rangarajan, Joseph Aduse-Opoku, et al.
Journal of Periodontal Research|January 31, 2008
Antibodies to periodontal pathogens and coronary artery calcification in type 1 diabetic and nondiabetic subjectsH M Colhoun, J M Slaney, M B Rubens, et al.
Molecular Pharmaceutics|August 28, 2025
Aggregate Suppression of Recombinant Human Serum Albumin (HSA) by Adenosine Triphosphate (ATP)Nikita Vekaria, Shuyuan Tan, Eleonora Cerasoli, et al.
Molecular Biology and Evolution|May 25, 2007
Plastid genome sequence of the cryptophyte alga Rhodomonas salina CCMP1319: lateral transfer of putative DNA replication machinery and a test of chromist plastid phylogenyHameed Khan, Natalie Parks, Catherine Kozera, et al.
Oral Microbiology and Immunology|January 24, 2007
Interleukin-1alpha stimulation in monocytes by periodontal bacteria: antagonistic effects of Porphyromonas gingivalisN Bostanci, R Allaker, U Johansson, et al.
Human Genetics|September 1, 1990
The haplotype distribution of the delta F508 mutation in cystic fibrosis families in ScotlandI McIntosh, A Curtis, M L Lorenzo, et al.
Journal of Medical Genetics|May 1, 1996
Analysis of GLRA1 in hereditary and sporadic hyperekplexia: a novel mutation in a family cosegregating for hyperekplexia and spastic paraparesisF V Elmslie, S M Hutchings, V Spencer, et al.
Prenatal Diagnosis|October 1, 1988
First-trimester prenatal diagnosis of cystic fibrosis using fibroblasts from a deceased index child to establish haplotypesA Curtis, L Strain, M Mennie, et al.
Pageof 106

Showing results (691-700 of 1,051) with videos related to

Sort By:
Pageof 106
Neuroreport|January 6, 1999
Novel insertion in the KSP region of the neurofilament heavy gene in amyotrophic lateral sclerosis (ALS)J Tomkins, P Usher, J Y Slade, et al.
Hematology (Amsterdam, Netherlands)|December 29, 2017
A patient with oxaliplatin immune-induced syndrome (OIIS) who also developed leucovorin and palonosetron-associated thrombocytopeniaS A Curtis, B R Curtis, A I Lee, et al.
Journal of Periodontal Research|July 13, 2002
Recognition of the carbohydrate modifications to the RgpA protease of Porphyromonas gingivalis by periodontal patient serum IgGJennifer M Slaney, Minnie Rangarajan, Joseph Aduse-Opoku, et al.
Journal of Periodontal Research|January 31, 2008
Antibodies to periodontal pathogens and coronary artery calcification in type 1 diabetic and nondiabetic subjectsH M Colhoun, J M Slaney, M B Rubens, et al.
Molecular Pharmaceutics|August 28, 2025
Aggregate Suppression of Recombinant Human Serum Albumin (HSA) by Adenosine Triphosphate (ATP)Nikita Vekaria, Shuyuan Tan, Eleonora Cerasoli, et al.
Molecular Biology and Evolution|May 25, 2007
Plastid genome sequence of the cryptophyte alga Rhodomonas salina CCMP1319: lateral transfer of putative DNA replication machinery and a test of chromist plastid phylogenyHameed Khan, Natalie Parks, Catherine Kozera, et al.
Oral Microbiology and Immunology|January 24, 2007
Interleukin-1alpha stimulation in monocytes by periodontal bacteria: antagonistic effects of Porphyromonas gingivalisN Bostanci, R Allaker, U Johansson, et al.
Human Genetics|September 1, 1990
The haplotype distribution of the delta F508 mutation in cystic fibrosis families in ScotlandI McIntosh, A Curtis, M L Lorenzo, et al.
Journal of Medical Genetics|May 1, 1996
Analysis of GLRA1 in hereditary and sporadic hyperekplexia: a novel mutation in a family cosegregating for hyperekplexia and spastic paraparesisF V Elmslie, S M Hutchings, V Spencer, et al.
Prenatal Diagnosis|October 1, 1988
First-trimester prenatal diagnosis of cystic fibrosis using fibroblasts from a deceased index child to establish haplotypesA Curtis, L Strain, M Mennie, et al.
Pageof 106