Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Rose Veile"'
Autor:
Aron P. Bercz, Farzaan Kassam, Grace M. Niziolek, Lou Ann Friend, Amy T. Makley, Mackenzie C. Morris, Michael D. Goodman, Rose Veile, Timothy A. Pritts
Publikováno v:
Journal of Surgical Research. 244:63-68
BACKGROUND: Several serum biomarkers have been studied to diagnose incidence and severity of traumatic brain injury (TBI), but a reliable biomarker in TBI has yet to be identified. Ubiquitin carboxy-terminal hydrolase L1 (UCH-L1) has been proposed as
Autor:
Jay A. Johannigman, Amy T. Makley, Timothy A. Pritts, Rose Veile, Lou Ann Friend, Mark D. Johnson, Michael D. Goodman, Joel Elterman, Grace E. Martin
Publikováno v:
Military Medicine. 184:e460-e467
IntroductionWhile damage control surgery and resuscitation techniques have revolutionized the care of injured service members who sustain severe traumatic hemorrhage, the physiologic and inflammatory consequences of hemostatic resuscitation and stage
Autor:
Jennifer S. Stone, Michael Lovett, Mark E. Warchol, Nicolas Daudet, Matthew Barton, Jeffrey Ku, Rose Veile
Publikováno v:
Developmental Biology. 428:39-51
The loss of sensory hair cells from the inner ear is a leading cause of hearing and balance disorders. The mammalian ear has a very limited ability to replace lost hair cells, but the inner ears of non-mammalian vertebrates can spontaneously regenera
Autor:
Yuan Chieh Ku, Rose Veile, Nicole A. Renaud, Michael Lovett, Courtney C. J. Voelker, Cynthia Helms, Mark E. Warchol
Publikováno v:
The Journal of Neuroscience. 34:3523-3535
Sensory hair cell loss is the major cause of hearing and balance disorders. Mammals are incapable of sustained hair cell regeneration, but lower vertebrates can regenerate these mechano-electrical transducers. We present the first comprehensive trans
Publikováno v:
Developmental Dynamics. 238:3093-3102
Haploinsufficiency for the transcription factor GATA3 leads to hearing loss in humans. It is expressed throughout the auditory sensory epithelium (SE). In the vestibular organs, GATA3 is limited to the striola reversal zone of the utricle. Stereocili
Autor:
Rose Veile, Anne M. Bowcock, Mathew Dobbs, Missy Allen, John A. Herring, Michael Lovett, Lazlos Szappanos, Jose A. Morcuende, Stavros Bashiardes, Carol Wise
Publikováno v:
Human Genetics. 115:81-89
Idiopathic scoliosis (IS) affects approximately 2%-3% of the population and has a heritable component. The genetics of this disorder are complex. Here, we describe a family in which a pericentric inversion of chromosome 8 co-segregates with IS. We ha
Autor:
Carol Wise, Michael Lovett, Christine E. Seidman, Joseph D. Gillum, Noralane M. Lindor, Stavros Bashiardes, Rose Veile
Publikováno v:
Human Molecular Genetics. 11:961-969
PAPA syndrome (pyogenic sterile arthritis, pyoderma gangrenosum, and acne, OMIM #604416) and familial recurrent arthritis (FRA) are rare inherited disorders of early onset, primarily affecting skin and joint tissues. Recurring inflammatory episodes l
Autor:
Michael Lovett, Anne M. Bowcock, Elif Arioglu, Rebecca A. Speckman, Rose Veile, Abhimanyu Garg, Simeon I. Taylor, Lynda Bennett, Fenghe Du
Publikováno v:
The American Journal of Human Genetics. 66(4):1192-1198
Familial partial lipodystrophy (FPLD), Dunnigan variety, is an autosomal dominant disorder characterized by marked loss of subcutaneous adipose tissue from the extremities and trunk but by excess fat deposition in the head and neck. The disease is fr
Autor:
Kara E. Powder, Mark E. Warchol, Stavros Bashiardes, Yuan-Chieh Ku, David M. Alvarado, Meghan K Spriggs, Rose Veile, Michael Lovett, Judith D. Speck, R. D Hawkins
Sensory hair cells of the inner ear are the mechanoelectric transducers of sound and head motion. In mammals, damage to sensory hair cells leads to hearing or balance deficits. Nonmammalian vertebrates such as birds can regenerate hair cells after in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4934053ed637565bd8102bbd5fe05d69
https://europepmc.org/articles/PMC3086586/
https://europepmc.org/articles/PMC3086586/
Autor:
Anne M. Bowcock, Rose Veile, Lynn Blackburn, John Zempel, Christina A. Gurnett, Michael Lovett
Publikováno v:
Archives of neurology. 65(4)
Objective To determine gene(s) disrupted in a patient with partial frontal lobe epilepsy and cognitive impairment with concomitant de novo balanced chromosomal translocation t(2;13)(q24;q31). Design Fluorescence in situ hybridization and array compar