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A Simple and Efficient Method for Simulating the Electronic Absorption Spectra of Criegee Intermediates: Benchmarking on CH 2 OO and CH 3 CHOO.

Autor: McCoy JC; University of Louisiana at Lafayette, Lafayette, Louisiana 70503, United States., Marchetti B; University of Louisiana at Lafayette, Lafayette, Louisiana 70503, United States., Thodika M; Temple University, Philadelphia, Pennsylvania 19122, United States., Karsili TNV; University of Louisiana at Lafayette, Lafayette, Louisiana 70503, United States.

Publikováno v: The journal of physical chemistry. A [J Phys Chem A] 2021 May 20; Vol. 125 (19), pp. 4089-4097. Date of Electronic Publication: 2021 May 10.

Structural perspective of BMP ligands and signaling.

Autor: Gipson GR; Department of Molecular Genetics, Biochemistry, and Microbiology, University of Cincinnati, Medical Sciences Building, Cincinnati, OH 45267, USA., Goebel EJ; Department of Molecular Genetics, Biochemistry, and Microbiology, University of Cincinnati, Medical Sciences Building, Cincinnati, OH 45267, USA., Hart KN; Department of Pharmacology and Systems Physiology, University of Cincinnati, Medical Sciences Building, Cincinnati, OH 45267, USA., Kappes EC; Department of Molecular Genetics, Biochemistry, and Microbiology, University of Cincinnati, Medical Sciences Building, Cincinnati, OH 45267, USA., Kattamuri C; Department of Molecular Genetics, Biochemistry, and Microbiology, University of Cincinnati, Medical Sciences Building, Cincinnati, OH 45267, USA., McCoy JC; Department of Molecular Genetics, Biochemistry, and Microbiology, University of Cincinnati, Medical Sciences Building, Cincinnati, OH 45267, USA., Thompson TB; Department of Molecular Genetics, Biochemistry, and Microbiology, University of Cincinnati, Medical Sciences Building, Cincinnati, OH 45267, USA. Electronic address: Tom.Thompson@uc.edu.

Publikováno v: Bone [Bone] 2020 Nov; Vol. 140, pp. 115549. Date of Electronic Publication: 2020 Jul 27.

Mutations in GDF11 and the extracellular antagonist, Follistatin, as a likely cause of Mendelian forms of orofacial clefting in humans.

Autor: Cox TC; Division of Craniofacial Medicine, Department of Pediatrics, University of Washington, Seattle, Washington.; Center for Developmental Biology & Regenerative Medicine, Seattle Children's Research Institute, Seattle, Washington.; Department of Oral & Craniofacial Science, School of Dentistry, University of Missouri-Kansas City, Kansas City, Missouri., Lidral AC; Lidral Orthodontics, Rockford, Michigan., McCoy JC; Department of Molecular Genetics, Biochemistry, and Microbiology, University of Cincinnati, Cincinnati, Ohio., Liu H; Department of Anatomy and Cell Biology and Anatomy, University of Iowa, Iowa City, Iowa., Cox LL; Division of Craniofacial Medicine, Department of Pediatrics, University of Washington, Seattle, Washington.; Center for Developmental Biology & Regenerative Medicine, Seattle Children's Research Institute, Seattle, Washington.; Department of Oral & Craniofacial Science, School of Dentistry, University of Missouri-Kansas City, Kansas City, Missouri.; Division of Basic Sciences, Fred Hutchinson Cancer Research Center, Seattle, Washington., Zhu Y; New South Wales Health Pathology, Prince of Wales Hospital, Randwick, New South Wales, Australia.; Genetics of Learning Disability Service, Hunter Genetics, Waratah, New South Wales, Australia., Anderson RD; Department of Oral & Craniofacial Science, School of Dentistry, University of Missouri-Kansas City, Kansas City, Missouri., Moreno Uribe LM; Department of Orthodontics & the Iowa Institute for Oral Health Research, University of Iowa, Iowa City, Iowa., Anand D; Department of Biological Sciences, University of Delaware, Newark, Delaware., Deng M; Birth Defects Research Laboratory, University of Washington, Seattle, Washington., Richter CT; Department of Orthodontics & the Iowa Institute for Oral Health Research, University of Iowa, Iowa City, Iowa., Nidey NL; Department of Pediatrics, University of Iowa, Iowa City, Iowa., Standley JM; Department of Pediatrics, University of Iowa, Iowa City, Iowa., Blue EE; Division of Medical Genetics, Department of Medicine, University of Washington, Seattle, Washington., Chong JX; Division of Genetic Medicine, Department of Pediatrics, University of Washington, Seattle, Washington., Smith JD; Department of Genome Sciences, University of Washington, Seattle, Washington., Kirk EP; New South Wales Health Pathology, Prince of Wales Hospital, Randwick, New South Wales, Australia.; Centre for Clinical Genetics, Sydney Children's Hospital, New South Wales, Australia., Venselaar H; Centre for Molecular and Biomolecular Informatics, Radboud University Medical Centre, Nijmegen, The Netherlands., Krahn KN; UVA Center for Advanced Medical Analytics, School of Medicine, University of Virginia, Charlottesville, Virginia., van Bokhoven H; Department of Human Genetics, Radboud University Medical Centre, Nijmegen, The Netherlands.; Department of Cognitive Neurosciences, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, Nijmegen, The Netherlands., Zhou H; Department of Human Genetics, Radboud University Medical Centre, Nijmegen, The Netherlands.; Department of Molecular Developmental Biology, Radboud Institute for Molecular Life Sciences, Radboud University, Nijmegen, The Netherlands., Cornell RA; Department of Anatomy and Cell Biology and Anatomy, University of Iowa, Iowa City, Iowa., Glass IA; Birth Defects Research Laboratory, University of Washington, Seattle, Washington.; Division of Genetic Medicine, Department of Pediatrics, University of Washington, Seattle, Washington., Bamshad MJ; Division of Genetic Medicine, Department of Pediatrics, University of Washington, Seattle, Washington.; Department of Genome Sciences, University of Washington, Seattle, Washington., Nickerson DA; Department of Genome Sciences, University of Washington, Seattle, Washington., Murray JC; Department of Pediatrics, University of Iowa, Iowa City, Iowa., Lachke SA; Department of Biological Sciences, University of Delaware, Newark, Delaware., Thompson TB; Department of Molecular Genetics, Biochemistry, and Microbiology, University of Cincinnati, Cincinnati, Ohio., Buckley MF; New South Wales Health Pathology, Prince of Wales Hospital, Randwick, New South Wales, Australia., Roscioli T; New South Wales Health Pathology, Prince of Wales Hospital, Randwick, New South Wales, Australia.; Centre for Clinical Genetics, Sydney Children's Hospital, New South Wales, Australia.; Prince of Wales Clinical School, University of New South Wales, Randwick, New South Wales, Australia.; Neuroscience Research Australia (NeuRA), University of New South Wales, Sydney, New South Wales, Australia.

Publikováno v: Human mutation [Hum Mutat] 2019 Oct; Vol. 40 (10), pp. 1813-1825. Date of Electronic Publication: 2019 Jun 18.

Structure of the human myostatin precursor and determinants of growth factor latency.

Autor: Cotton TR; Department of Biochemistry, University of Cambridge, Cambridge, UK., Fischer G; Department of Biochemistry, University of Cambridge, Cambridge, UK., Wang X; Department of Biochemistry, University of Cambridge, Cambridge, UK., McCoy JC; Department of Molecular Genetics, Biochemistry, and Microbiology, University of Cincinnati, Cincinnati, OH, USA., Czepnik M; Department of Molecular Genetics, Biochemistry, and Microbiology, University of Cincinnati, Cincinnati, OH, USA., Thompson TB; Department of Molecular Genetics, Biochemistry, and Microbiology, University of Cincinnati, Cincinnati, OH, USA., Hyvönen M; Department of Biochemistry, University of Cambridge, Cambridge, UK mh256@cam.ac.uk.

Publikováno v: The EMBO journal [EMBO J] 2018 Feb 01; Vol. 37 (3), pp. 367-383. Date of Electronic Publication: 2018 Jan 12.