A related defects

The derived temperature dependences of the peak intensities, separations and half-widths of the separate spectral peaks in the A-band phonon progressions indicate the different trends for vibration-free zero-phonon electronic transition and vibration-related lower-energy electronic transitions to high vibrational levels of the ground electronic state – lower thermal damping and more softened phonon for the zero-phonon transition, also implying the extended defect origin of the A-band photoluminescence.

9p dianmotminh02 03-05-2024 3 1   Download

Presentations "report design and manufacture of plastic injection molds" was conducted with the following contents: The thickness of the product, the relevant defects, warping, how to fix, corner boards, tendons, tendon increases hard, protruding lug, lug sticking design, holes in the product, ... Invite you to consult the documentation.

30p danhnakg 23-09-2016 54 5   Download

Sixgenes are homologs ofDrosophila sine oculisand encode transcription factors that are characterized by a conserved Six domain and homeo-domain. Of the six family members (Six1–Six6) in mice, Six1and Six4 show similar expression patterns during embryogenesis. Six1 –⁄ – mice show defective formation of various organs such as inner ear, nose, skeletal mus-cle, kidney and thymus, whereasSix4 –⁄ – mice show little anomaly in organo-genesis.

16p awards 06-04-2013 28 2   Download

Hypophosphatasia, a congenital metabolic disease related to the tissue-non-specific alkaline phosphatase gene (TNSALP), is characterized by reduced serum alkaline phosphatase levels and defective mineralization of hard tis-sues. A replacement of valine with alanine at position 406, located in the crown domain of TNSALP, was reported in a perinatal form of hypophos-phatasia.

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Tuyển tập các báo cáo nghiên cứu về lâm nghiệp được đăng trên tạp chí lâm nghiệp quốc tế đề tài:"A study on growth stresses, tension wood distribution and other related wood defects in poplar (Populus euramericana cv 1214): end splits, specific gravity and pulp yield...

13p toshiba7 08-10-2011 42 6   Download

Harrison's Internal Medicine Chapter 100. Megaloblastic Anemias Megaloblastic Anemias: Introduction The megaloblastic anemias are a group of disorders characterized by the presence of distinctive morphologic appearances of the developing red cells in the bone marrow. The cause is usually deficiency of either cobalamin (vitamin B 12) or folate, but megaloblastic anemia may arise because of genetic or acquired abnormalities affecting the metabolism of these vitamins or because of defects in DNA synthesis not related to cobalamin or folate (Table 100-1).

5p thanhongan 07-12-2010 62 4   Download

Differential Diagnosis Many of the diseases associated with splenomegaly are listed in Table 60-2. They are grouped according to the presumed basic mechanisms responsible for organ enlargement: 1.

6p konheokonmummim 03-12-2010 114 5   Download

Also lentigines. b Polyostotic fibrous dysplasia. c See also "Papulonodular Skin Lesions." d Late 1980s. A proliferation of melanocytes results in the following pigmented lesions: lentigo, melanocytic nevus, and melanoma (Chap. 83). In an adult, the majority of lentigines are related to sun exposure, which explains their distribution.

5p konheokonmummim 30-11-2010 83 6   Download

Gastric Motor Dysfunction Disturbed gastric motility is purported to cause acid reflux in some cases of indigestion. Delayed gastric emptying is also found in 25–50% of functional dyspeptics. The relation of these defects to symptom induction is uncertain; many studies show poor correlation between symptom severity and the degree of motor dysfunction. Impaired gastric fundus relaxation after eating may underlie selected dyspeptic symptoms like bloating, nausea, and early satiety.

5p ongxaemnumber1 29-11-2010 65 3   Download

Congenital Anomalies of the Lumbar Spine Spondylolysis is a bony defect in the pars interarticularis (a segment near the junction of the pedicle with the lamina) of the vertebra; the etiology may be a stress fracture in a congenitally abnormal segment. The defect (usually bilateral) is best visualized on oblique projections in plain x-rays, CT scan, or single photon emission CT (SPECT) bone scan and occurs in the setting of a single injury, repeated minor injuries, or growth.

5p ongxaemnumber1 29-11-2010 68 5   Download