نتائج البحث

An FGF3-BMP Signaling Axis Regulates Caudal Neural Tube Closure, Neural Crest Specification and Anterior-Posterior Axis Extension.

• Authors : Anderson, Matthew J.¹; Schimmang, Thomas²; Lewandoski, Mark¹

• Source: PLoS Genetics. 5/4/2016, Vol. 12 Issue 5, p1-30. 30p.

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Genome-Wide Association Mapping in Dogs Enables Identification of the Homeobox Gene, NKX2-8, as a Genetic Component of Neural Tube Defects in Humans

• Authors : Safra, Noa; Bassuk, Alexander G; Ferguson, Polly J

Subjects: Biological Sciences; Genetics; Neurosciences

• Source: PLOS Genetics. 9(7)

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Lamin B1 Polymorphism Influences Morphology of the Nuclear Envelope, Cell Cycle Progression, and Risk of Neural Tube Defects in Mice.

• Authors : De Castro, Sandra C. P.¹; Malhas, Ashraf²; Kit-Yi Leung¹

• Source: PLoS Genetics. Nov2012, Vol. 8 Issue 11, Special section p1-14. 14p. 1 Color Photograph, 5 Graphs.

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Gpr63 is a modifier of microcephaly in Ttc21b mouse mutants.

• Authors : Snedeker J; Division of Human Genetics, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, United States of America.; Neuroscience Graduate Program, University of Cincinnati College of Medicine, Cincinnati, Ohio, United States of America.

Subjects: Adaptor Proteins, Signal Transducing/Adaptor Proteins, Signal Transducing/Adaptor Proteins, Signal Transducing/*genetics ; Embryonic Development/Embryonic Development/Embryonic Development/*genetics ; Microcephaly/Microcephaly/Microcephaly/*genetics

• Source: PLoS genetics [PLoS Genet] 2019 Nov 15; Vol. 15 (11), pp. e1008467. Date of Electronic Publication: 2019 Nov 15 (Print Publication: 2019).Publisher: Public Library of Science Country of Publication: United States NLM ID: 101239074 Publication Model: eCollection Cited Medium: Internet

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Gpr63 is a modifier of microcephaly in Ttc21b mouse mutants

• Authors : David F. Paulding; John Snedeker; Daniel R. Prows

Subjects: Cancer Research; Candidate gene; Embryology

• Source: PLoS GeneticsPLoS Genetics, Vol 15, Iss 11, p e1008467 (2019)

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Cauli: A Mouse Strain with an Ift140 Mutation That Results in a Skeletal Ciliopathy Modelling Jeune Syndrome.

• Authors : Miller, Kerry A.¹; Ah-Cann, Casey J.^1,2; Welfare, Megan F.¹

• Source: PLoS Genetics. Aug2013, Vol. 9 Issue 8, p1-15. 15p. 6 Color Photographs, 1 Chart.

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Genome-Wide Association Mapping in Dogs Enables Identification of the Homeobox Gene, NKX2-8, as a Genetic Component of Neural Tube Defects in Humans.

• Authors : Safra, Noa¹ ; Bassuk, Alexander G.²; Ferguson, Polly J.²

• Source: PLoS Genetics. Jul2013, Vol. 9 Issue 7, p1-8. 8p.

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Lamin b1 polymorphism influences morphology of the nuclear envelope, cell cycle progression, and risk of neural tube defects in mice.

• Authors : Sandra C P De Castro; Ashraf Malhas; Kit-Yi Leung

Subjects: Genetics; QH426-470

• Source: PLoS Genetics, Vol 8, Iss 11, p e1003059 (2012)

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Gpr63 is a modifier of microcephaly in Ttc21b mouse mutants.

• Authors : John Snedeker; William J Gibbons; David F Paulding

Subjects: Genetics; QH426-470

• Source: PLoS Genetics, Vol 15, Iss 11, p e1008467 (2019)

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Lamin b1 polymorphism influences morphology of the nuclear envelope, cell cycle progression, and risk of neural tube defects in mice

• Authors : Nicholas D. E. Greene; Ashraf Malhas; Peter Gustavsson

Subjects: Proteomics; Embryology; Cancer Research

• Source: PLoS Genetics, Vol 8, Iss 11, p e1003059 (2012)PLoS Genetics

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