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  • 1-10 ل  110 نتائج ل ""Zebrafish Proteins""

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Publication : human molecular genetics
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Academic Journal

Identification of conserved skeletal enhancers associated with craniosynostosis risk genes

Subjects: Biological Sciences; Genetics; Human Genome

  • Source: Human Molecular Genetics. 33(10)

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Academic Journal

Mitochondrial abnormalities contribute to muscle weakness in a Dnajb6 deficient zebrafish model

Subjects: 0303 health sciences; Muscle Weakness; Nerve Tissue Proteins

  • Source: Hum Mol Genet

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Academic Journal

Identification of conserved skeletal enhancers associated with craniosynostosis risk genes

Subjects: BMP signaling; Enhancer Elements; Bone Morphogenetic Protein 2

  • Source: Human Molecular Genetics, vol 33, iss 10

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Academic Journal

Functional analysis of germline VANGL2 variants using rescue assays of vangl2 knockout zebrafish

Subjects: Heart Defects, Congenital; Planar Cell Polarity; Cell Polarity

  • Source: Hum Mol Genet

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Academic Journal

Myofibrillar myopathy hallmarks associated with ZAK deficiency

Subjects: Filamins; Zebrafish Proteins; Mice

  • Source: Hum Mol GenetStonadge, A, Genzor, A V, Russell, A, Hamed, M F, Romero, N, Evans, G, Pownall, B, Bekker-Jensen, S & Blanco, G 2023, ' Myofibrillar myopathy hallmarks associated with ZAK

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Academic Journal

Clock genes rescue nphp mutations in zebrafish

Subjects: 0303 health sciences; Zebrafish Proteins; Ciliopathies

  • Source: Hum Mol Genet

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Academic Journal

IPIP27A cooperates with OCRL to support endocytic traffic in the zebrafish pronephric tubule

Subjects: Male; 0301 basic medicine; Inositol Phosphates

  • Source: Oltrabella, F, Jackson-Crawford, A, Yan, G, Rixham, S, Starborg, T & Lowe, M 2021, ' IPIP27A cooperates with OCRL to support endocytic traffic in the zebrafish

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Academic Journal

A Neurexin2aa deficiency results in axon pathfinding defects and increased anxiety in zebrafish

Subjects: Genetics & Heredity; Motor Neurons; 0301 basic medicine

  • Source: Human Molecular Genetics. 29:3765-3780

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Academic Journal

Disruption of foxc1 genes in zebrafish results in dosage-dependent phenotypes overlapping Axenfeld-Rieger syndrome

Subjects: Heart Defects, Congenital; 0301 basic medicine; Heterozygote

  • Source: Human Molecular Genetics. 29:2723-2735

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Academic Journal

TCF12 haploinsufficiency causes autosomal dominant Kallmann syndrome and reveals network-level interactions between causal loci

Subjects: Adult; Male; Neurons

  • Source: Human Molecular Genetics. 29:2435-2450

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  • 1-10 ل  110 نتائج ل ""Zebrafish Proteins""