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  • 1
    In: Stem Cell Research, Elsevier BV, Vol. 33 ( 2018-12), p. 51-55
    Type of Medium: Online Resource
    ISSN: 1873-5061
    Language: English
    Publisher: Elsevier BV
    Publication Date: 2018
    detail.hit.zdb_id: 2393143-7
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  • 2
    In: Applied Physics Letters, AIP Publishing, Vol. 90, No. 19 ( 2007-05-07)
    Abstract: The authors demonstrate the temperature-dependent behavior of the surface plasmon (SP) coupling with two InGaN∕GaN quantum-well (QW) structures of different internal quantum efficiencies. The SP modes are generated at the interface between the QW structures and Ag thin films coated on their tops. It is observed that the SP-QW coupling rate increases with temperature. Such a trend may rely on several factors, including the availability of carriers with sufficient momenta for transferring the energy and momentum into the SP modes and possibly the variation of the SP density of state with temperature. Although the required momentum matching condition only needs the thermal energy corresponding to a few tens of Kelvins, the carrier delocalization process results in a significantly higher probability of SP-carrier momentum matching and hence SP-QW coupling.
    Type of Medium: Online Resource
    ISSN: 0003-6951 , 1077-3118
    RVK:
    Language: English
    Publisher: AIP Publishing
    Publication Date: 2007
    detail.hit.zdb_id: 211245-0
    detail.hit.zdb_id: 1469436-0
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  • 3
    In: Applied Physics Letters, AIP Publishing, Vol. 91, No. 6 ( 2007-08-06)
    Abstract: The authors demonstrate the leakage of surface plasmon (SP) through the Ohmic contact of either p-type or n-type GaN layer in the coupling process between SP and an InGaN∕GaN quantum well (QW). It is shown that the photoluminescence (PL) intensity is significantly reduced when an Ohmic contact is formed, in contrast to the case of significant PL enhancement when an insulating thin layer is applied between the doped semiconductor and metal. The observation implies that, in using the SP-QW coupling for enhancing emission in a light-emitting diode, the metals for Ohmic contact and SP generation must be isolated from each other. A thin dielectric interlayer in the region for SP-QW coupling is useful for avoiding the leakage of SP energy.
    Type of Medium: Online Resource
    ISSN: 0003-6951 , 1077-3118
    RVK:
    Language: English
    Publisher: AIP Publishing
    Publication Date: 2007
    detail.hit.zdb_id: 211245-0
    detail.hit.zdb_id: 1469436-0
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  • 4
    In: Applied Physics Letters, AIP Publishing, Vol. 89, No. 9 ( 2006-08-28)
    Abstract: The authors fabricate blue/green two-wavelength, InGaN∕GaN quantum-well (QW), flip-chip micro-light-emitting diodes (μ-LEDs) of different mesa sizes by stacking QWs of different indium contents. It is found that the blue/green contrast ratio of such a μ-LED increases with the mesa size. The relatively stronger blue intensity in a device of a larger mesa area is due to its higher operation junction temperature such that hole migration can be enhanced through thermally exciting holes to escape from the QW (green emitting) closest to the p-type layer and to be captured by the neighboring QWs (blue emitting). The higher junction temperature in such a μ-LED of a larger mesa area is due to its smaller ratio of the sidewall surface area over the active volume, leading to the less effective sidewall heat radiation and light extraction.
    Type of Medium: Online Resource
    ISSN: 0003-6951 , 1077-3118
    RVK:
    Language: English
    Publisher: AIP Publishing
    Publication Date: 2006
    detail.hit.zdb_id: 211245-0
    detail.hit.zdb_id: 1469436-0
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  • 5
    In: Journal of Clinical Oncology, American Society of Clinical Oncology (ASCO), Vol. 33, No. 20 ( 2015-07-10), p. 2303-2310
    Abstract: Adenocarcinoma is the most dominant type of lung cancer in never-smoker patients. The risk alleles from genome-wide association studies have small odds ratios and unclear biologic roles. Here we have taken an approach featuring suitable medical actionability to identify alleles with low population frequency but high disease-causing potential. Patients and Methods Whole-genome sequencing was performed for a family with an unusually high density of lung adenocarcinoma with available DNA from the affected mother, four affected daughters, and one nonaffected son. Candidate risk alleles were confirmed by matrix-assisted laser desorption ionization time of flight mass spectroscopy. Validation was conducted in an external cohort of 1,135 participants without cancer and 1,312 patients with lung adenocarcinoma. Family follow-ups were performed by genotyping the relatives of the original proband and the relatives of the identified risk-allele carriers. Low-dose computed tomography scans of the chest were evaluated for lung abnormalities. Results YAP1 R331W missense mutation from the original family was identified and validated in the external controls and the cohort with lung adenocarcinoma. The YAP1 mutant-allele carrier frequency was 1.1% in patients with lung adenocarcinoma compared with 0.18% in controls (P = .0095), yielding an odds ratio (adjusted for age, sex, and smoking status) of 5.9. Among the relatives, YAP1-mutant carriers have overwhelmingly higher frequencies of developing lung adenocarcinoma or ground-glass opacity lung lesions than those who do not carry the mutation (10:0 v 1:7; P 〈 .001). YAP1 mutation was shown to increase the colony formation ability and invasion potential of lung cancer cells. Conclusion These results implicated YAP1 R331W as an allele predisposed for lung adenocarcinoma with high familial penetrance. Low-dose computed tomography scans may be recommended to this subpopulation, which is at high risk for lung cancer, for personalized prevention and health management.
    Type of Medium: Online Resource
    ISSN: 0732-183X , 1527-7755
    RVK:
    RVK:
    Language: English
    Publisher: American Society of Clinical Oncology (ASCO)
    Publication Date: 2015
    detail.hit.zdb_id: 2005181-5
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  • 6
    In: Journal of Applied Physics, AIP Publishing, Vol. 101, No. 11 ( 2007-06-01)
    Abstract: We compare the x-ray diffraction (XRD) results of two InGaN∕GaN quantum-well (QW) structures to observe the effects of prestrained growth by depositing a low-indium QW before the growth of five high-indium QWs. From the results of reciprocal space mapping, we observe the fully strained condition in the QWs of the control sample. However, in the sample of prestrained growth, the average strain is partially relaxed. By using an XRD fitting algorithm for calibrating QW parameters, we obtain reasonable values for the compositions and thicknesses of the QWs in both samples. In particular, by assuming a nonuniform strain relaxation distribution among the five high-indium QWs in the prestrained sample, we obtain reasonable composition variations among the QWs. The high-indium QW closest to the low-indium one is most strain-relaxed and has the highest indium incorporation, leading to the longest-wavelength emission. The observed red shift with increasing electron penetration depth in the cathodo-luminescence spectra of the prestrained sample is consistent with the distributions of calibrated strain relaxation and indium composition. The results of high-resolution transmission electron microscopy and effective band gap calculation also agree with the above conclusions.
    Type of Medium: Online Resource
    ISSN: 0021-8979 , 1089-7550
    Language: English
    Publisher: AIP Publishing
    Publication Date: 2007
    detail.hit.zdb_id: 220641-9
    detail.hit.zdb_id: 3112-4
    detail.hit.zdb_id: 1476463-5
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  • 7
    In: Obesity Surgery, Springer Science and Business Media LLC, Vol. 29, No. 2 ( 2019-2), p. 387-393
    Type of Medium: Online Resource
    ISSN: 0960-8923 , 1708-0428
    Language: English
    Publisher: Springer Science and Business Media LLC
    Publication Date: 2019
    detail.hit.zdb_id: 2087903-9
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  • 8
    Online Resource
    Online Resource
    The Electrochemical Society ; 2019
    In:  ECS Meeting Abstracts Vol. MA2019-01, No. 26 ( 2019-05-01), p. 1286-1286
    In: ECS Meeting Abstracts, The Electrochemical Society, Vol. MA2019-01, No. 26 ( 2019-05-01), p. 1286-1286
    Abstract: INTRODUCTION Recently, the interest in high quality GaN films has in-creased, GaN and its alloys show good performance at high-power, high-frequency transistors. Because of large mismatches of lattice constant and thermal expansion between GaN epitaxial film and sapphire substrate, however, the high-density dislocation ranging from 108-1010cm -2 does degrade the diode performance profoundly. Thus, growth of GaN with low threading dislocation(TD) has been more and more important. The single-step growth on pattern sapphire substrate(PSS) has been widely used for fabrication of reliable high quality GaN films. To improve the Schottky diode’s performance, high TD density must be considered. Using the PSS technique, we can significantly reduce the TD density. For an ideal Schottky diode the I-V characteristic[1] is given by I=I 0 exp(qV/nkT) . [1-exp(-qV/kT)] and I 0 =SAT 2 exp(-Фb/kT), In this work, the PSS method developed by ourselves[2] is used to improve the GaN epitaxial film quality, which is then applied to the fabrication of Schottky diode on the GaN film. At last, different pattern dimensions are compared to find an optimum GaN Schottky diode. DEVICE FABRICATION The PSS pattern was defined by Electron-Beam lithography system. The arrayed nanostructure was designed to be arranged on the commercial c-plane(001) sapphire substrate. The dimensions of the arrayed nanostructure are related to the quality of GaN and can be defined as dimension: 600nm, means spacing: 600nm, diameter: 600nm of the fabricated PSS hole array. Next, the reactive ion etching system(RIE) was used to transfer the pattern from photoresist to SiO2 mask, and then the mixed liquid of H2SO4(96%) and H3PO4(85%) was used to etch substrate at 230°C for 60 minutes to make a pyramid shape pattern. Metal-organic-chemical-vapor-deposition(MOCVD) was used to grow GaN thin films. The epitaxial growth began with a 25nm-thick GaN nucleation layer and then an insulating GaN of 4μm thickness as a device buffer layer. The buffer layer has a resistivity greater than 200MΩcm2 to prevent leakage. A 30nm unintentionally doped AlGaN layer and a 2nm GaN cap layer were then grown to complete the modulation doped structure. Schottky devices of both on the planar region and on the pattern region were fabricated on the same substrate for comparison as shown in Fig.1. The process began with mesa iso-selectively etch AlGaN/GaN to mesa etch for electrical isolation. After the dry-etch isolation, Ge/Ti/Al/Ti/Au(10/20/100/55/100nm) were evaporated and annealed at 860°C for 20sec to form source and drain ohmic contacts. THIN FLIM QUALITY ANALYSIS To analyze the quality of GaN thin films, Raman spectrum and EPD(Etching Pit Density) are jointly performed on AlGaN/GaN samples on the planar and pattern regions. The Raman shift and full-width-half-maximum(FWHM) of Raman spectrum were measured to compare the strain and quality of GaN on the planar region and the PSS region. As shown in the Fig.2-1, Raman shifts of the PSS region in different dimension is lower than the planar region and closer to freestanding GaN(567cm -1 )[3], which means that the PSS region has less stress accumulation. Fig.2-2 shows that the FWHM trend is the same as Raman shift, which means the quality is improved as the PSS dimension goes down. The narrowest Raman FWHM implies the lowest-stress of GaN and thus the optimum crystal quality, while the widest Raman FWHM of the conventional planar region implies the worst crystal quality of GaN. The EPD experiment used H3PO4 at 230°C for 5 minutes. The dislocation density on the planar region is 3.87x106(cm -2 ), higher than 1.37x106(cm -2 ) on the pattern region. This proves that the FWHM of the Raman spectrum corresponds to the reliability of the crystal quality, and that our PSS method does improve the crystal quality. CONTACT RESISTANCE ANALYSIS Schottky contact resistance was measured as shown in Fig.4. As the PSS dimension goes down, the contact resistivity goes down. That is, the proposed GaN thin film on the pattern region has a better quality than that on the planar region. Also, the Schottky contact on the proposed pattern region has a lower resistivity than that on the conventional planar region. Conclusion We have fabricated high quality GaN thin films by MOCVD on the Pattern Sapphire Substrate(PSS). Both Raman spectrum and EPD show that the PSS can magnificently improve the GaN film quality. The defect density has a tendency to correlate with the electrical properties of the component. To reduce defect density and improve electrical performance, different pattern dimensions are designed in the Schottky diodes. By using our PSS technology, the EPD can be reduced from 3.87x106(cm -2 ) to 1.37x106(cm -2 ) and the Raman spectrum FWHM can be reduced from 2.46(cm -1 ) to 2.33(cm -1 ). Also, the Schottky contact resistivity can be reduced from 0.0657(Ωcm 2 ) to 0.00266(Ωcm 2 ). Figure 1
    Type of Medium: Online Resource
    ISSN: 2151-2043
    Language: Unknown
    Publisher: The Electrochemical Society
    Publication Date: 2019
    detail.hit.zdb_id: 2438749-6
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  • 9
    Online Resource
    Online Resource
    Springer Science and Business Media LLC ; 2020
    In:  Orphanet Journal of Rare Diseases Vol. 15, No. 1 ( 2020-12)
    In: Orphanet Journal of Rare Diseases, Springer Science and Business Media LLC, Vol. 15, No. 1 ( 2020-12)
    Abstract: Glutaric aciduria type 1 (GA-1) is a rare disease connected with speech delay and neurological deficits. However, the audiological and otologic profiles of GA-1 have not yet been fully characterized. To our knowledge, this is the largest study of comprehensive audiological and otologic evaluation in patients with GA-1 to date. Methods Thirteen patients diagnosed with GA-1 between January 1994 and December 2019 with audiological, radiological and genetic manifestations were retrospectively analyzed. Hearing tests were performed in all patients. MRI was performed for radiological evaluation. Results Hearing loss was found in 76.9% (10/13) of GA-1 patients, including slight hearing loss in 46.1% (6/13) of patients, mild hearing loss in 15.4% (2/13) of patients, and moderate hearing loss in 7.7% (1/13) of patients. Normal hearing thresholds were seen in 23% (3/13) of patients. Patients with intensive care unit (ICU) admission history showed significantly worse hearing than those without (29.17 ± 12.47 vs 13.56 ± 3.93 dB HL, 95% CI 2.92–24.70, p  = 0.0176). One patient had moderate sensorineural hearing loss and a past history of acute encephalopathic crisis. No usual causative gene mutations associated with hearing loss were found in these patients. MRI showed a normal vestibulocochlear apparatus and cochlear nerve. One patient with extensive injury of the basal ganglia on MRI after acute encephalopathic crisis was found to have moderate sensorineural hearing loss. Two patients with disability scores above 5 were found to have mild to moderate hearing impairment. No obvious correlation between macrocephaly and hearing loss was found. Conclusion A high prevalence of hearing impairment is found in GA-1 patients. Adequate audiological evaluation is essential for these patients, especially for those after encephalopathic crises or with ICU admission history.
    Type of Medium: Online Resource
    ISSN: 1750-1172
    Language: English
    Publisher: Springer Science and Business Media LLC
    Publication Date: 2020
    detail.hit.zdb_id: 2225857-7
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  • 10
    In: Brain, Oxford University Press (OUP), Vol. 143, No. 11 ( 2020-11-01), p. 3352-3373
    Abstract: Parkinson’s disease is a neurodegenerative disorder with a multifactorial aetiology. Nevertheless, the genetic predisposition in many families with multi-incidence disease remains unknown. This study aimed to identify novel genes that cause familial Parkinson’s disease. Whole exome sequencing was performed in three affected members of the index family with a late-onset autosomal-dominant parkinsonism and polyneuropathy. We identified a novel heterozygous substitution c.941A & gt;C (p.Tyr314Ser) in the mitochondrial ubiquinol-cytochrome c reductase core protein 1 (UQCRC1) gene, which co-segregates with disease within the family. Additional analysis of 699 unrelated Parkinson’s disease probands with autosomal-dominant Parkinson’s disease and 1934 patients with sporadic Parkinson’s disease revealed another two variants in UQCRC1 in the probands with familial Parkinson’s disease, c.931A & gt;C (p.Ile311Leu) and an allele with concomitant splicing mutation (c.70-1G & gt;A) and a frameshift insertion (c.73_74insG, p.Ala25Glyfs*27). All substitutions were absent in 1077 controls and the Taiwan Biobank exome database from healthy participants (n = 1517 exomes). We then assayed the pathogenicity of the identified rare variants using CRISPR/Cas9-based knock-in human dopaminergic SH-SY5Y cell lines, Drosophila and mouse models. Mutant UQCRC1 expression leads to neurite degeneration and mitochondrial respiratory chain dysfunction in SH-SY5Y cells. UQCRC1 p.Tyr314Ser knock-in Drosophila and mouse models exhibit age-dependent locomotor defects, dopaminergic neuronal loss, peripheral neuropathy, impaired respiratory chain complex III activity and aberrant mitochondrial ultrastructures in nigral neurons. Furthermore, intraperitoneal injection of levodopa could significantly improve the motor dysfunction in UQCRC1 p.Tyr314Ser mutant knock-in mice. Taken together, our in vitro and in vivo studies support the functional pathogenicity of rare UQCRC1 variants in familial parkinsonism. Our findings expand an additional link of mitochondrial complex III dysfunction in Parkinson’s disease.
    Type of Medium: Online Resource
    ISSN: 0006-8950 , 1460-2156
    RVK:
    Language: English
    Publisher: Oxford University Press (OUP)
    Publication Date: 2020
    detail.hit.zdb_id: 1474117-9
    SSG: 12
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