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Showing results (81-90 of 89) with videos related to

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Human Genetics|April 26, 2007
Complex chromosome 17p rearrangements associated with low-copy repeats in two patients with congenital anomaliesL E L M Vissers, P Stankiewicz, S A Yatsenko, et al.
Chemico-Biological Interactions|February 25, 2010
PRiMA directs a restricted localization of tetrameric AChE at synapsesHeidi Q Xie, K Wing Leung, Vicky P Chen, et al.
Orphanet Journal of Rare Diseases|June 14, 2015
De novo deletions and duplications of 17q25.3 cause susceptibility to cardiovascular malformationsF J Probst, R A James, L C Burrage, et al.
Leukemia|October 17, 2003
Standardization and quality control studies of 'real-time' quantitative reverse transcriptase polymerase chain reaction of fusion gene transcripts for residual disease detection in leukemia - a Europe Against Cancer programJ Gabert, E Beillard, V H J van der Velden, et al.
Zhonghua Wai Ke Za Zhi [Chinese Journal of Surgery]|December 8, 2022
[Endovascular abdominal aortic aneurysm repair with a new stent graft:early results from a multicenter study]H P Zhang, X W Zhang, X C Dai, et al.
Journal of Medical Genetics|July 9, 2009
Microdeletions including YWHAE in the Miller-Dieker syndrome region on chromosome 17p13.3 result in facial dysmorphisms, growth restriction, and cognitive impairmentS C Sreenath Nagamani, F Zhang, O A Shchelochkov, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|December 1, 1996
The glutathione S-transferase M1 (GSTM1) null genotype and benzidine-associated bladder cancer, urine mutagenicity, and exfoliated urothelial cell DNA adductsN Rothman, R B Hayes, T V Zenser, et al.
Journal of Medical Genetics|September 25, 2008
20p12.3 microdeletion predisposes to Wolff-Parkinson-White syndrome with variable neurocognitive deficitsS R Lalani, J V Thakuria, G F Cox, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology|May 16, 2026
Preclinical characterization and phase 1 results of TQB2102, a first-in-class HER2 biparatopic antibody-drug conjugate, in patients with advanced solid tumorsD Y Ruan, S Y Lin, J J Huang, et al.
Pageof 9

Showing results (81-90 of 89) with videos related to

Sort By:
Pageof 9
You have reached the last page of results.This site can display upto 89 results.
Human Genetics|April 26, 2007
Complex chromosome 17p rearrangements associated with low-copy repeats in two patients with congenital anomaliesL E L M Vissers, P Stankiewicz, S A Yatsenko, et al.
Chemico-Biological Interactions|February 25, 2010
PRiMA directs a restricted localization of tetrameric AChE at synapsesHeidi Q Xie, K Wing Leung, Vicky P Chen, et al.
Orphanet Journal of Rare Diseases|June 14, 2015
De novo deletions and duplications of 17q25.3 cause susceptibility to cardiovascular malformationsF J Probst, R A James, L C Burrage, et al.
Leukemia|October 17, 2003
Standardization and quality control studies of 'real-time' quantitative reverse transcriptase polymerase chain reaction of fusion gene transcripts for residual disease detection in leukemia - a Europe Against Cancer programJ Gabert, E Beillard, V H J van der Velden, et al.
Zhonghua Wai Ke Za Zhi [Chinese Journal of Surgery]|December 8, 2022
[Endovascular abdominal aortic aneurysm repair with a new stent graft:early results from a multicenter study]H P Zhang, X W Zhang, X C Dai, et al.
Journal of Medical Genetics|July 9, 2009
Microdeletions including YWHAE in the Miller-Dieker syndrome region on chromosome 17p13.3 result in facial dysmorphisms, growth restriction, and cognitive impairmentS C Sreenath Nagamani, F Zhang, O A Shchelochkov, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|December 1, 1996
The glutathione S-transferase M1 (GSTM1) null genotype and benzidine-associated bladder cancer, urine mutagenicity, and exfoliated urothelial cell DNA adductsN Rothman, R B Hayes, T V Zenser, et al.
Journal of Medical Genetics|September 25, 2008
20p12.3 microdeletion predisposes to Wolff-Parkinson-White syndrome with variable neurocognitive deficitsS R Lalani, J V Thakuria, G F Cox, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology|May 16, 2026
Preclinical characterization and phase 1 results of TQB2102, a first-in-class HER2 biparatopic antibody-drug conjugate, in patients with advanced solid tumorsD Y Ruan, S Y Lin, J J Huang, et al.
Pageof 9