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Journal of Experimental & Clinical Cancer Research : CR
|
April 1, 2004
Metastatic-associated biological properties and differential gene expression profiles in established highly liver and peritoneal metastatic cell lines of human pancreatic cancer
K Ohno, F Hata, H Nishimori, et al.
Journal of Veterinary Internal Medicine
|
October 13, 2001
Hematologic abnormalities and outcome of 16 cats with myelodysplastic syndromes
M Hisasue, H Okayama, T Okayama, et al.
American Journal of Veterinary Research
|
July 17, 2001
Results of hyperamplification of centrosomes in naturally developing tumors of dogs
A Setoguchi, M Okuda, E Nishida, et al.
Annals of Neurology
|
February 9, 2000
The spectrum of mutations causing end-plate acetylcholinesterase deficiency
K Ohno, A G Engel, J M Brengman, et al.
Veterinary Pathology
|
May 13, 2017
Endoscopic Cytology for the Diagnosis of Chronic Enteritis and Intestinal Lymphoma in Dogs
S Maeda, M Tsuboi, K Sakai, et al.
Dementia and Geriatric Cognitive Disorders
|
August 15, 2000
The expression of presenilin 1 mRNA in skin fibroblasts and brains from sporadic Alzheimer's disease
K Ikeda, K Urakami, H Arai, et al.
The Journal of Laryngology and Otology
|
September 18, 2014
Does HMGB1 predict occult neck lymph node metastasis in early tongue carcinoma? A case-control study of 26 patients
H Hanakawa, Y Orita, Y Sato, et al.
Journal of Experimental & Clinical Cancer Research : CR
|
July 18, 2003
Differential gene expression screening between parental and highly metastatic pancreatic cancer variants using a DNA microarray
H Tanaka, F Hata, H Nishimori, et al.
Research in Veterinary Science
|
June 28, 2019
Development of canine X-chromosome inactivation pattern analysis for the detection of cell clonality by incorporating the examination of the SLIT and NTRK-like family member 4 (SLITRK4) gene
A Tomita, H Mochizuki, M Tsuboi, et al.
Human Molecular Genetics
|
September 1, 1996
New mutations in acetylcholine receptor subunit genes reveal heterogeneity in the slow-channel congenital myasthenic syndrome
A G Engel, K Ohno, M Milone, et al.
Page
of 74
Search research articles
Search
Showing results (711-720 of 737) with videos related to
Sort By:
Page
of 74
Journal of Experimental & Clinical Cancer Research : CR
|
April 1, 2004
Metastatic-associated biological properties and differential gene expression profiles in established highly liver and peritoneal metastatic cell lines of human pancreatic cancer
K Ohno, F Hata, H Nishimori, et al.
Journal of Veterinary Internal Medicine
|
October 13, 2001
Hematologic abnormalities and outcome of 16 cats with myelodysplastic syndromes
M Hisasue, H Okayama, T Okayama, et al.
American Journal of Veterinary Research
|
July 17, 2001
Results of hyperamplification of centrosomes in naturally developing tumors of dogs
A Setoguchi, M Okuda, E Nishida, et al.
Annals of Neurology
|
February 9, 2000
The spectrum of mutations causing end-plate acetylcholinesterase deficiency
K Ohno, A G Engel, J M Brengman, et al.
Veterinary Pathology
|
May 13, 2017
Endoscopic Cytology for the Diagnosis of Chronic Enteritis and Intestinal Lymphoma in Dogs
S Maeda, M Tsuboi, K Sakai, et al.
Dementia and Geriatric Cognitive Disorders
|
August 15, 2000
The expression of presenilin 1 mRNA in skin fibroblasts and brains from sporadic Alzheimer's disease
K Ikeda, K Urakami, H Arai, et al.
The Journal of Laryngology and Otology
|
September 18, 2014
Does HMGB1 predict occult neck lymph node metastasis in early tongue carcinoma? A case-control study of 26 patients
H Hanakawa, Y Orita, Y Sato, et al.
Journal of Experimental & Clinical Cancer Research : CR
|
July 18, 2003
Differential gene expression screening between parental and highly metastatic pancreatic cancer variants using a DNA microarray
H Tanaka, F Hata, H Nishimori, et al.
Research in Veterinary Science
|
June 28, 2019
Development of canine X-chromosome inactivation pattern analysis for the detection of cell clonality by incorporating the examination of the SLIT and NTRK-like family member 4 (SLITRK4) gene
A Tomita, H Mochizuki, M Tsuboi, et al.
Human Molecular Genetics
|
September 1, 1996
New mutations in acetylcholine receptor subunit genes reveal heterogeneity in the slow-channel congenital myasthenic syndrome
A G Engel, K Ohno, M Milone, et al.
Page
of 74