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Medicine
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February 10, 2025
Salivary duct carcinoma presenting with unilateral multiple cranial nerve lesions and concurrent intracranial metastasis: A case report
Bo Zhu, Qing-Zi Zhang, Kun Guo, et al.
The Journal of Investigative Dermatology
|
November 10, 2019
Allele-Specific Small Interfering RNA Corrects Aberrant Cellular Phenotype in Keratitis-Ichthyosis-Deafness Syndrome Keratinocytes
Ming Yang Lee, Hong-Zhan Wang, Thomas W White, et al.
Annals of Neurology
|
November 24, 2025
Effects of Thymectomy in Late-Onset Myasthenia Gravis: A Multi-Center Longitudinal Retrospective Study
Jiaxin Chen, Chunhua Su, Li Feng, et al.
Bioorganic & Medicinal Chemistry Letters
|
August 17, 2011
Pyrrolidin-3-yl-N-methylbenzamides as potent histamine 3 receptor antagonists
Dahui Zhou, Jonathan L Gross, Jean Y Sze, et al.
Drug Discovery Today
|
April 18, 2012
Evidence-based approach to assess passive diffusion and carrier-mediated drug transport
Li Di, Per Artursson, Alex Avdeef, et al.
Molecular Pharmaceutics
|
April 12, 2012
pH-Dependent solubility and permeability criteria for provisional biopharmaceutics classification (BCS and BDDCS) in early drug discovery
Manthena V Varma, Iain Gardner, Stefanus J Steyn, et al.
Therapeutic Advances in Neurological Disorders
|
January 13, 2025
Short-term and long-term prognoses in AChR-Ab positive very-late-onset myasthenia gravis patients
Nairong Xie, Qing Liu, Qi Wen, et al.
Physiology & Behavior
|
March 20, 2016
Exendin-4, a glucagon-like peptide 1 receptor agonist, protects against amyloid-β peptide-induced impairment of spatial learning and memory in rats
Xiao-Tao Jia, Ye-Tian, Yuan-Li, et al.
Human Gene Therapy. Clinical Development
|
October 22, 2013
Phase I study protocol for ex-vivo lentiviral gene therapy for the inherited skin disease, Netherton Syndrome
Wei-Li Di, Jemima E Mellerio, Catina Bernadis, et al.
Frontiers in Genetics
|
December 6, 2021
Missense Mutations of Codon 116 in the <i>SOD1</i> Gene Cause Rapid Progressive Familial ALS and Predict Short Viability With PMA Phenotype
Xinmei Wen, Wenjia Zhu, Nan L Xia, et al.
Page
of 30
Search research articles
Search
Showing results (211-220 of 293) with videos related to
Sort By:
Page
of 30
Medicine
|
February 10, 2025
Salivary duct carcinoma presenting with unilateral multiple cranial nerve lesions and concurrent intracranial metastasis: A case report
Bo Zhu, Qing-Zi Zhang, Kun Guo, et al.
The Journal of Investigative Dermatology
|
November 10, 2019
Allele-Specific Small Interfering RNA Corrects Aberrant Cellular Phenotype in Keratitis-Ichthyosis-Deafness Syndrome Keratinocytes
Ming Yang Lee, Hong-Zhan Wang, Thomas W White, et al.
Annals of Neurology
|
November 24, 2025
Effects of Thymectomy in Late-Onset Myasthenia Gravis: A Multi-Center Longitudinal Retrospective Study
Jiaxin Chen, Chunhua Su, Li Feng, et al.
Bioorganic & Medicinal Chemistry Letters
|
August 17, 2011
Pyrrolidin-3-yl-N-methylbenzamides as potent histamine 3 receptor antagonists
Dahui Zhou, Jonathan L Gross, Jean Y Sze, et al.
Drug Discovery Today
|
April 18, 2012
Evidence-based approach to assess passive diffusion and carrier-mediated drug transport
Li Di, Per Artursson, Alex Avdeef, et al.
Molecular Pharmaceutics
|
April 12, 2012
pH-Dependent solubility and permeability criteria for provisional biopharmaceutics classification (BCS and BDDCS) in early drug discovery
Manthena V Varma, Iain Gardner, Stefanus J Steyn, et al.
Therapeutic Advances in Neurological Disorders
|
January 13, 2025
Short-term and long-term prognoses in AChR-Ab positive very-late-onset myasthenia gravis patients
Nairong Xie, Qing Liu, Qi Wen, et al.
Physiology & Behavior
|
March 20, 2016
Exendin-4, a glucagon-like peptide 1 receptor agonist, protects against amyloid-β peptide-induced impairment of spatial learning and memory in rats
Xiao-Tao Jia, Ye-Tian, Yuan-Li, et al.
Human Gene Therapy. Clinical Development
|
October 22, 2013
Phase I study protocol for ex-vivo lentiviral gene therapy for the inherited skin disease, Netherton Syndrome
Wei-Li Di, Jemima E Mellerio, Catina Bernadis, et al.
Frontiers in Genetics
|
December 6, 2021
Missense Mutations of Codon 116 in the <i>SOD1</i> Gene Cause Rapid Progressive Familial ALS and Predict Short Viability With PMA Phenotype
Xinmei Wen, Wenjia Zhu, Nan L Xia, et al.
Page
of 30