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Bioorganic & Medicinal Chemistry Letters|May 22, 2012
Synthesis and SAR of selective small molecule neuropeptide Y Y2 receptor antagonistsGopi Kumar Mittapalli, Danielle Vellucci, Jun Yang, et al.
BMC Medical Genetics|May 27, 2018
Splicing defect in FKBP10 gene causes autosomal recessive osteogenesis imperfecta disease: a case reportFatemeh Maghami, Seyed Mohammad Bagher Tabei, Hossein Moravej, et al.
Journal of Genetics|September 2, 2021
Investigating the association between common DRD2/ANKK1 genetic polymorphisms and schizophrenia: a meta-analysisParham Habibzadeh, Azim Nemati, Hassan Dastsooz, et al.
BMC Medical Genetics|May 5, 2017
A case report of novel mutation in PRF1 gene, which causes familial autosomal recessive hemophagocytic lymphohistiocytosisMohammad Reza Bordbar, Farzaneh Modarresi, Mohammad Ali Farazi Fard, et al.
Frontiers in Genetics|January 8, 2021
Case Report: Expanding the Genetic and Phenotypic Spectrum of Autosomal Recessive Spastic Ataxia of Charlevoix-SaguenayParham Habibzadeh, Zahra Tabatabaei, Soroor Inaloo, et al.
Cancer Cell International|August 8, 2020
Molecular mechanisms of long non-coding RNAs in anaplastic thyroid cancer: a systematic reviewHilda Samimi, Sayed Mahmoud Sajjadi-Jazi, Soroush Seifirad, et al.
Psychopharmacology|August 13, 2016
The nociceptin/orphanin FQ receptor agonist SR-8993 as a candidate therapeutic for alcohol use disorders: validation in rat modelsAbdul Maruf Asif Aziz, Shaun Brothers, Gregory Sartor, et al.
Cell and Tissue Research|March 27, 2003
Activity-induced and developmental downregulation of the Nogo receptorAnna Josephson, Alexandra Trifunovski, Camilla Schéele, et al.
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