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1.
Arthrosc Tech ; 13(5): 102959, 2024 May.
Article in English | MEDLINE | ID: mdl-38835477

ABSTRACT

Shoulder joint instability can lead to bone loss on both the glenoid side and the posterior part of the humeral head, known as bipolar bone loss. To restore glenoid defects, bone procedures like the Latarjet operation or free bone block transfer from the iliac crest are the primary options, restoring defects of up to 25% to 30%. However, in some cases, the glenoid defect may exceed 40%. This article discusses a unique technique for restoring glenoid bone defects up to 50%, using 2 bone grafts-a free graft from the iliac crest and the coracoid process with conjoint tendon complex. This technique is called "double block sandwich technique."

2.
J Nanosci Nanotechnol ; 7(1): 306-15, 2007 Jan.
Article in English | MEDLINE | ID: mdl-17455496

ABSTRACT

Most important aspect of nanotechnology applications in the information ultrahigh storage is the miniaturization of data carrier elements of the storage media with emphasis on the long-term stability. Proposed two-dimensional ultrahigh-density X-ray optical memory, named X-ROM, with long-term stability is an information carrier basically destined for digital data archiving. X-ROM is a semiconductor wafer, in which the high-reflectivity nanosized X-ray mirrors are embedded. Data are encoded due to certain positions of the mirrors. Ultrahigh-density data recording procedure can e.g., be performed via mask-less zone-plate-array lithography (ZPAL), spatial-phase-locked electron-beam lithography (SPLEBL), or focused ion-beam lithography (FIB). X-ROM manufactured by nanolithography technique is a write-once memory useful for terabit-scale memory applications, if the surface area of the smallest recording pits is less than 100 nm2. In this case the X-ROM surface-storage capacity of a square centimetre becomes by two orders of magnitude higher than the volumetric data density really achieved for three-dimensional optical data storage medium. Digital data read-out procedure from proposed X-ROM can e.g., be performed via glancing-angle incident X-ray micro beam (GIX) using the well-developed X-ray reflectometry technique. In presented theoretical paper the crystal-analyser operating like an image magnifier is added to the set-up of X-ROM data handling system for the purpose analogous to case of application the higher numerical aperture objective in optical data read-out system. We also propose the set-up of the X-ROM readout system based on more the one incident X-ray micro beam. Presented scheme of two-beam data handling system, which operates on two mutually perpendicular well-collimated monochromatic incident X-ray micro beams, essentially increases the reliability of the digital information read-out procedure. According the graphs of characteristic functions presented in paper, one may choose optimally the incident radiation wavelength, as well as the angle of incidence of X-ray micro beams, appropriate for proposed digital data read-out procedure.


Subject(s)
Computer Storage Devices , Information Storage and Retrieval , Nanotechnology/methods , Computers , Electrochemistry/methods , Electrons , Models, Theoretical , Semiconductors , Signal Processing, Computer-Assisted , Software , X-Ray Diffraction , X-Rays
3.
Proc Natl Acad Sci U S A ; 96(8): 4455-60, 1999 Apr 13.
Article in English | MEDLINE | ID: mdl-10200283

ABSTRACT

Achondroplasia, the most common form of dwarfism in man, is a dominant genetic disorder caused by a point mutation (G380R) in the transmembrane region of fibroblast growth factor receptor 3 (FGFR3). We used gene targeting to introduce the human achondroplasia mutation into the murine FGFR3 gene. Heterozygotes for this point mutation that carried the neo cassette were normal whereas neo+ homozygotes had a phenotype similar to FGFR3-deficient mice, exhibiting bone overgrowth. This was because of interference with mRNA processing in the presence of the neo cassette. Removal of the neo selection marker by Cre/loxP recombination yielded a dominant dwarf phenotype. These mice are distinguished by their small size, shortened craniofacial area, hypoplasia of the midface with protruding incisors, distorted brain case with anteriorly shifted foramen magnum, kyphosis, and narrowed and distorted growth plates in the long bones, vertebrae, and ribs. These experiments demonstrate that achondroplasia results from a gain-of-FGFR3-function leading to inhibition of chondrocyte proliferation. These achondroplastic dwarf mice represent a reliable and useful model for developing drugs for potential treatment of the human disease.


Subject(s)
Achondroplasia/genetics , Growth Plate/growth & development , Protein-Tyrosine Kinases , Receptors, Fibroblast Growth Factor/genetics , Receptors, Fibroblast Growth Factor/physiology , Achondroplasia/pathology , Achondroplasia/physiopathology , Amino Acid Substitution , Animals , Bone Development , Disease Models, Animal , Growth Plate/pathology , Heterozygote , Humans , Mice , Mice, Inbred Strains , Mice, Knockout , Point Mutation , Receptor, Fibroblast Growth Factor, Type 3 , Receptors, Fibroblast Growth Factor/deficiency , Restriction Mapping
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