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Yonsei Medical Journal
|
January 1, 1988
Histopathologic and immunocytochemical study of Hodgkin's disease
S I Choi, K R Kim, H J Jeong, et al.
Medical Hypotheses
|
November 26, 2002
A hypothesis of synergism: the interrelationship of T3 and insulin to disturbances in metabolic homeostasis
S R Kim, E S Tull, E O Talbott, et al.
Archives of Insect Biochemistry and Physiology
|
April 17, 1998
Purification and characterization of a male-specific protein in the hemolymph of the wax moth, Galleria mellonella L
H Y Lee, Y H Lee, S H Kang, et al.
Neurochemical Research
|
November 14, 1997
Interaction of divalent metal ions with Zn(2+)-glycerophosphocholine cholinephosphodiesterase from ox brain
K J Lee, M R Kim, Y B Kim, et al.
Journal of Korean Medical Science
|
November 19, 1997
Decreased gastric proliferation of foveolar epithelial cells after the eradication of Helicobacter pylori
T J Jang, J I Lee, J R Kim, et al.
Water Science and Technology : a Journal of the International Association on Water Pollution Research
|
May 31, 2001
Biofilm structure and mass transfer in a gas phase trickle-bed biofilter
X Zhu, M T Suidan, C Alonso, et al.
International Journal of Oral and Maxillofacial Surgery
|
March 19, 2008
Co-expression of nerve growth factor and p75NGFR in the inferior alveolar nerve after mandibular distraction osteogenesis
J-H Byun, J-H Lee, Y-J Choi, et al.
Journal of Leukocyte Biology
|
December 1, 1994
Glycosylphosphatidylinositol-anchored NAD glycohydrolase is released from peritoneal macrophages activated by interferon-gamma and lipopolysaccharide
M K Han, C Y Yim, N H An, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV
|
July 24, 2008
Compound heterozygosity for a premature termination codon and missense mutation in the exon 10 of the uroporphyrinogen III cosynthase gene causes a severe phenotype of congenital erythropoietic porphyria
T-W Kang, S-W Oh, M-R Kim, et al.
Archives of Disease in Childhood
|
July 18, 2009
Prolonged neutropenia after irinotecan-based chemotherapy in a child with polymorphisms of UGT1A1 and SLCO1B1
S Sakaguchi, F Garcia-Bournissen, R Kim, et al.
Page
of 193
Search research articles
Search
Showing results (851-860 of 1,930) with videos related to
Sort By:
Page
of 193
Yonsei Medical Journal
|
January 1, 1988
Histopathologic and immunocytochemical study of Hodgkin's disease
S I Choi, K R Kim, H J Jeong, et al.
Medical Hypotheses
|
November 26, 2002
A hypothesis of synergism: the interrelationship of T3 and insulin to disturbances in metabolic homeostasis
S R Kim, E S Tull, E O Talbott, et al.
Archives of Insect Biochemistry and Physiology
|
April 17, 1998
Purification and characterization of a male-specific protein in the hemolymph of the wax moth, Galleria mellonella L
H Y Lee, Y H Lee, S H Kang, et al.
Neurochemical Research
|
November 14, 1997
Interaction of divalent metal ions with Zn(2+)-glycerophosphocholine cholinephosphodiesterase from ox brain
K J Lee, M R Kim, Y B Kim, et al.
Journal of Korean Medical Science
|
November 19, 1997
Decreased gastric proliferation of foveolar epithelial cells after the eradication of Helicobacter pylori
T J Jang, J I Lee, J R Kim, et al.
Water Science and Technology : a Journal of the International Association on Water Pollution Research
|
May 31, 2001
Biofilm structure and mass transfer in a gas phase trickle-bed biofilter
X Zhu, M T Suidan, C Alonso, et al.
International Journal of Oral and Maxillofacial Surgery
|
March 19, 2008
Co-expression of nerve growth factor and p75NGFR in the inferior alveolar nerve after mandibular distraction osteogenesis
J-H Byun, J-H Lee, Y-J Choi, et al.
Journal of Leukocyte Biology
|
December 1, 1994
Glycosylphosphatidylinositol-anchored NAD glycohydrolase is released from peritoneal macrophages activated by interferon-gamma and lipopolysaccharide
M K Han, C Y Yim, N H An, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV
|
July 24, 2008
Compound heterozygosity for a premature termination codon and missense mutation in the exon 10 of the uroporphyrinogen III cosynthase gene causes a severe phenotype of congenital erythropoietic porphyria
T-W Kang, S-W Oh, M-R Kim, et al.
Archives of Disease in Childhood
|
July 18, 2009
Prolonged neutropenia after irinotecan-based chemotherapy in a child with polymorphisms of UGT1A1 and SLCO1B1
S Sakaguchi, F Garcia-Bournissen, R Kim, et al.
Page
of 193