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COLQ
The First Case of Congenital Myasthenic Syndrome Caused by A
S41598-021-87168-0 1 Vol.:(0123456789)
Clinical/Scientific Notes
Variation in Protein Coding Genes Identifies Information Flow
COLQ-MUTANT CONGENITAL MYASTHENIC SYNDROME with MICROCEPHALY: a UNIQUE CASE Sulaiman Bazee Al-Mobarak1, with LITERATURE REVIEW Mohammad A
COLQ Variant Associated with Devon Rex and Sphynx Feline Hereditary Myopathy
COLQ (NM 080539) Human Untagged Clone Product Data
Gene Expression Changes in the Ventral Tegmental Area of Male Mice with Alternative Social Behavior Experience in Chronic Agonistic Interactions
A COLQ Missense Mutation in Sphynx and Devon Rex Cats with Congenital Myasthenic Syndrome
COLQ (NM 005677) Human Untagged Clone – SC303680 | Origene
COLQ Gene Collagen Like Tail Subunit of Asymmetric Acetylcholinesterase
Exploring Molecular Mechanism of Traditional Chinese Medicine
Identification of Key Genes in Atrial Fibrillation Using Bioinformatics Analysis Yueheng Liu†, Rui Tang†, Ye Zhao, Xuan Jiang, Yuchao Wang and Tianxiang Gu*
Evolutionarily Conserved Regulation of Embryonic Fast-Twitch Skeletal Muscle
Full Text (PDF)
Human Endplate Acetylcholinesterase Deficiency Caused by Mutations in the Collagen-Like Tail Subunit (Colq) of the Asymmetric Enzyme
Degenerative and Regenerative Pathways Underlying Duchenne Muscular Dystrophy Revealed by Single-Nucleus RNA Sequencing
Mutation in the Human Acetylcholinesterase-Associated
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Characteristic Arrangement of Nucleosomes Is Predictive of Chromatin
Deciphering Colq Induced Mechanisms in the Control of Achr Mrna Levels Jennifer Karmouch
Aberrant Expression of Collagen Family Genes in the Brain Regions Developing Under Agonistic Interactions in Male Mice
A COLQ Missense Mutation in Sphynx and Devon Rex
An Introduction to Protein–Ligand Binding Site Prediction Methods