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Showing results (121-130 of 153) with videos related to

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Journal of Cancer Research and Clinical Oncology|April 6, 1999
Differential expression of mucins and trefoil peptides in native epithelium, Barrett's metaplasia and squamous cell carcinoma of the oesophagusC Labouvie, J C Machado, F Carneiro, et al.
The Journal of Biological Chemistry|October 25, 1991
Atypical beta-adrenergic receptor in 3T3-F442A adipocytes. Pharmacological and molecular relationship with the human beta 3-adrenergic receptorB Fève, L J Emorine, F Lasnier, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology|April 22, 1999
E-cadherin gene mutations provide a genetic basis for the phenotypic divergence of mixed gastric carcinomasJ C Machado, P Soares, F Carneiro, et al.
Neurobiology of Disease|July 20, 2002
Substitutions in the conserved C2C domain of otoferlin cause DFNB9, a form of nonsyndromic autosomal recessive deafnessF Mirghomizadeh, M Pfister, F Apaydin, et al.
Human Heredity|December 22, 1998
Variable distribution of TFF2 (Spasmolysin) alleles in Europeans does not indicate predisposition to gastric cancerE dos Santos Silva, T Kayademir, F Regateiro, et al.
HNO|September 5, 2009
[Influence of exogenic factors on age-related hearing impairment]M Baur, E Fransen, A Tropitzsch, et al.
Human Molecular Genetics|November 14, 1997
cDNA cloning and chromosomal mapping of a predicted coiled-coil proline-rich protein immunogenic in meningioma patientsD Heckel, N Brass, U Fischer, et al.
Molecular Biology and Evolution|July 16, 2004
PCR-induced sequence alterations hamper the typing of prehistoric bone samples for diagnostic achondroplasia mutationsC M Pusch, M Broghammer, G J Nicholson, et al.
Arteriosclerosis (Dallas, Tex.)|May 1, 1986
Observations on leukocytes from patients with severe familial hypercholesterolemiaH A Dresel, D P Via, M Stöhr, et al.
Human Genetics|October 6, 1998
The SOX10/Sox10 gene from human and mouse: sequence, expression, and transactivation by the encoded HMG domain transcription factorC Pusch, E Hustert, D Pfeifer, et al.
Pageof 16

Showing results (121-130 of 153) with videos related to

Sort By:
Pageof 16
Journal of Cancer Research and Clinical Oncology|April 6, 1999
Differential expression of mucins and trefoil peptides in native epithelium, Barrett's metaplasia and squamous cell carcinoma of the oesophagusC Labouvie, J C Machado, F Carneiro, et al.
The Journal of Biological Chemistry|October 25, 1991
Atypical beta-adrenergic receptor in 3T3-F442A adipocytes. Pharmacological and molecular relationship with the human beta 3-adrenergic receptorB Fève, L J Emorine, F Lasnier, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology|April 22, 1999
E-cadherin gene mutations provide a genetic basis for the phenotypic divergence of mixed gastric carcinomasJ C Machado, P Soares, F Carneiro, et al.
Neurobiology of Disease|July 20, 2002
Substitutions in the conserved C2C domain of otoferlin cause DFNB9, a form of nonsyndromic autosomal recessive deafnessF Mirghomizadeh, M Pfister, F Apaydin, et al.
Human Heredity|December 22, 1998
Variable distribution of TFF2 (Spasmolysin) alleles in Europeans does not indicate predisposition to gastric cancerE dos Santos Silva, T Kayademir, F Regateiro, et al.
HNO|September 5, 2009
[Influence of exogenic factors on age-related hearing impairment]M Baur, E Fransen, A Tropitzsch, et al.
Human Molecular Genetics|November 14, 1997
cDNA cloning and chromosomal mapping of a predicted coiled-coil proline-rich protein immunogenic in meningioma patientsD Heckel, N Brass, U Fischer, et al.
Molecular Biology and Evolution|July 16, 2004
PCR-induced sequence alterations hamper the typing of prehistoric bone samples for diagnostic achondroplasia mutationsC M Pusch, M Broghammer, G J Nicholson, et al.
Arteriosclerosis (Dallas, Tex.)|May 1, 1986
Observations on leukocytes from patients with severe familial hypercholesterolemiaH A Dresel, D P Via, M Stöhr, et al.
Human Genetics|October 6, 1998
The SOX10/Sox10 gene from human and mouse: sequence, expression, and transactivation by the encoded HMG domain transcription factorC Pusch, E Hustert, D Pfeifer, et al.
Pageof 16