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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 thrombocytopenia
S 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 IgG
Jennifer 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 subjects
H 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 phylogeny
Hameed 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 gingivalis
N 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 Scotland
I 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 paraparesis
F 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 haplotypes
A Curtis, L Strain, M Mennie, et al.
Page
of 106
Search research articles
Search
Showing results (691-700 of 1,051) with videos related to
Sort By:
Page
of 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 thrombocytopenia
S 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 IgG
Jennifer 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 subjects
H 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 phylogeny
Hameed 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 gingivalis
N 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 Scotland
I 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 paraparesis
F 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 haplotypes
A Curtis, L Strain, M Mennie, et al.
Page
of 106