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Neoplasma
|
June 25, 2013
Establishment of an animal model of spontaneous cervical lymph node metastasis of laryngeal squamous cell carcinoma and obtaining laryngocarcinoma cells with high metastatic potential
L W Chen, J L Wang, L Y Zhang, et al.
TAG. Theoretical and Applied Genetics. Theoretische Und Angewandte Genetik
|
February 16, 2006
QTL analysis for rice grain length and fine mapping of an identified QTL with stable and major effects
X Y Wan, J M Wan, L Jiang, et al.
Clinical Genetics
|
August 28, 2007
A distinct spectrum of SLC26A4 mutations in patients with enlarged vestibular aqueduct in China
Q-J Wang, Y-L Zhao, S-Q Rao, et al.
Translational Psychiatry
|
January 25, 2017
Early onset of inflammation during ontogeny of bipolar disorder: the NLRP2 inflammasome gene distinctly differentiates between patients and healthy controls in the transition between iPS cell and neural stem cell stages
D Vizlin-Hodzic, Q Zhai, S Illes, et al.
Genetics and Molecular Research : GMR
|
October 6, 2015
Identification of natural recombinants derived from PCV2a and PCV2b
J Hu, S L Zhai, S Y Zeng, et al.
Neurourology and Urodynamics
|
February 19, 2021
Losartan prevents bladder fibrosis and protects renal function in rat with neurogenic paralysis bladder
Yu L He, Jian G Wen, Qing S Pu, et al.
Current Molecular Medicine
|
December 19, 2013
ZIP4 is a novel diagnostic and prognostic marker in human pancreatic cancer: a systemic comparison between EUS-FNA and surgical specimens
C Xu, M B Wallace, J Yang, et al.
Journal of Medical Genetics
|
July 4, 2006
AUNX1, a novel locus responsible for X linked recessive auditory and peripheral neuropathy, maps to Xq23-27.3
Q J Wang, Q Z Li, S Q Rao, et al.
Clinical Genetics
|
March 4, 2008
Novel mutations in the vWFA2 domain of COCH in two Chinese DFNA9 families
H J Yuan, D Y Han, Q Sun, et al.
Clinical Genetics
|
September 18, 2007
A novel DFNA5 mutation, IVS8+4 A>G, in the splice donor site of intron 8 causes late-onset non-syndromic hearing loss in a Chinese family
J Cheng, D Y Han, P Dai, et al.
Page
of 8
Search research articles
Search
Showing results (61-70 of 73) with videos related to
Sort By:
Page
of 8
Neoplasma
|
June 25, 2013
Establishment of an animal model of spontaneous cervical lymph node metastasis of laryngeal squamous cell carcinoma and obtaining laryngocarcinoma cells with high metastatic potential
L W Chen, J L Wang, L Y Zhang, et al.
TAG. Theoretical and Applied Genetics. Theoretische Und Angewandte Genetik
|
February 16, 2006
QTL analysis for rice grain length and fine mapping of an identified QTL with stable and major effects
X Y Wan, J M Wan, L Jiang, et al.
Clinical Genetics
|
August 28, 2007
A distinct spectrum of SLC26A4 mutations in patients with enlarged vestibular aqueduct in China
Q-J Wang, Y-L Zhao, S-Q Rao, et al.
Translational Psychiatry
|
January 25, 2017
Early onset of inflammation during ontogeny of bipolar disorder: the NLRP2 inflammasome gene distinctly differentiates between patients and healthy controls in the transition between iPS cell and neural stem cell stages
D Vizlin-Hodzic, Q Zhai, S Illes, et al.
Genetics and Molecular Research : GMR
|
October 6, 2015
Identification of natural recombinants derived from PCV2a and PCV2b
J Hu, S L Zhai, S Y Zeng, et al.
Neurourology and Urodynamics
|
February 19, 2021
Losartan prevents bladder fibrosis and protects renal function in rat with neurogenic paralysis bladder
Yu L He, Jian G Wen, Qing S Pu, et al.
Current Molecular Medicine
|
December 19, 2013
ZIP4 is a novel diagnostic and prognostic marker in human pancreatic cancer: a systemic comparison between EUS-FNA and surgical specimens
C Xu, M B Wallace, J Yang, et al.
Journal of Medical Genetics
|
July 4, 2006
AUNX1, a novel locus responsible for X linked recessive auditory and peripheral neuropathy, maps to Xq23-27.3
Q J Wang, Q Z Li, S Q Rao, et al.
Clinical Genetics
|
March 4, 2008
Novel mutations in the vWFA2 domain of COCH in two Chinese DFNA9 families
H J Yuan, D Y Han, Q Sun, et al.
Clinical Genetics
|
September 18, 2007
A novel DFNA5 mutation, IVS8+4 A>G, in the splice donor site of intron 8 causes late-onset non-syndromic hearing loss in a Chinese family
J Cheng, D Y Han, P Dai, et al.
Page
of 8