走在汽車革命的路上論文書籍站
Expression ability的問題，透過圖書和論文來找解法和答案更準確安心。 我們找到下列包括價格和評價等資訊懶人包
Expression ability的問題，我們搜遍了碩博士論文和台灣出版的書籍，推薦Shipway, Jilly寫的 Chakras for Creativity: Meditations & Yoga-Based Practices to Awaken Your Creative Potential 和的 Environmental, Physiological and Chemical Controls of Adventitious Rooting in Cuttings都 可以從中找到所需的評價。
另外網站ability of expression | English examples in context - Ludwig.guru也說明：The studies presented here were designed to test the ability of expression analysis on GeneChip Human Exon 1.0 ST arrays to detect 5′-TMPRSS2-ERG-3′ hybrid ...
這兩本書分別來自 和所出版 。
國立臺灣海洋大學 海洋生物研究所 邵奕達所指導 黃辰宏的 海洋酸化對點帶石斑仔稚魚鈣離子運輸以及骨骼鈣化作用的影響 （2021），提出Expression ability關鍵因素是什麼，來自於海洋酸化、點帶石斑、離子調節、鈣離子、骨骼鈣化。
而第二篇論文高雄醫學大學 醫藥暨應用化學系博士班 王志光 教授所指導 Swathi Nedunchezian的 運用仿生支架進行骨軟骨修復組織工程的生物設計策略 （2021），提出因為有 透明質酸、明膠、混合水凝膠、3D 生物陶瓷腳手架、軟骨組織工程的重點而找出了 Expression ability的解答。
最後網站Expressing Ability in English則補充：Expressing Ability in English ; Can you lift this table? ; Can you speak English? ; Can you help me? ; Can you play the piano? ; Will you able to come to my birthday ...
Chakras for Creativity: Meditations & Yoga-Based Practices to Awaken Your Creative Potential
為了解決Expression ability 的問題，作者Shipway, Jilly 這樣論述：
Become Your Most Creative Self through Yoga, Meditation, and VisualizationHarness the power of the chakras and bring more success to all areas of your life, including art projects, business endeavors, and scientific pursuits. Jilly Shipway leads you through all seven energy centers with correspon
ding yoga practices and mindfulness techniques. She teaches you to access a deep source of inner wisdom that is the wellspring of all creativity and optimize your ability to create unique masterpieces. Your improved self-expression can even help heal trauma.Mountain Pose can ground your creative foc
us and therapeutic writing about the sun builds confidence. Visualizing light unblocks stagnant energy and walking meditations can send love to yourself and others. These simple activities, and many more like them, make it easy for you to create beauty and share your gifts with the world.
Expression ability進入發燒排行的影片
A stunning fourth-quarter comeback led by Allen Iverson. A thrilling final-minute shootout between Stephon Marbury and Kobe Bryant.
The ball in Bryant's hands for the last shot. A pass that no one expected. A last-second miss. A postgame celebration worthy of June.
Yes, it was quite an All-Star Game.
Iverson, Marbury and his Eastern Conference teammates transformed what looked like a blowout loss into an improbable 111-110 victory Sunday in a performance fitting of the 50th anniversary of the game.
"It was like a championship game out there," Dikembe Mutombo said. "I've been in the All-Star Game the last seven years, and I've never seen anything like this."
It was the kind of game that might stop people dismissing the East as far weaker than the West, the kind of game that might make the casual fan appreciate the heart and determination of some of the younger stars trying to seize the spotlight in the post-Jordan era.
Mostly, it was kind of game that any fan of any sport would prefer to see — a riveting one.
Iverson scored 15 of his 25 points in the final nine minutes, and Marbury hit two three-pointers in the final 53 seconds as the East came back from a 21-point deficit.
Bryant, the NBA's leading scorer, could have taken the last shot. Instead, in a shock to everyone sitting in the building and watching on television, he threw a pass that resulted in a last-second miss by Tim Duncan.
"Everybody was saying we couldn't win because of our size. It's not about size. It's about the size of your heart," Iverson said. "Coming into the fourth quarter, we were all sitting on the sidelines saying 'Why not us? Why can't we be the ones to come back from a 19-point deficit (after three quarters) in an All-Star Game?"
Turns out they could.
While presenting the MVP award to Iverson, NBA Commissioner David Stern, with a sly grin on his face, told Iverson that great basketball "can be wrapped — if you pardon the expression — in very small packages."
The comment was a clever reference to Iverson's height -- he is an inch or two shy of 6 feet -- and Iverson's rap album, which was criticized for its lyrics and led to a meeting with the commissioner.
Iverson, who starred collegiately in this city at Georgetown and had a large contingent of family and friends in the arena, presented his MVP trophy to his mother.
"My family, my friends, everybody that's been with me through my struggles and pain knows it's a tribute," Iverson said. "I think it's going to be beautiful for years to come because every year it seems like we get somebody else with a different kind of God-given ability to add to this league."
The East trailed 95-74 with nine minutes left after the West dominated the first 39 minutes behind its superior size. It appeared the game would come out looking like a mismatch that would back up all the Western Conference superiority theories that have been thrown around so frequently this season.
But the East started pecking away, and Iverson walked over to the scorer's table during a timeout and asked if anyone wanted to wager whether the East would make a comeback.
That's exactly what the East proceeded to do, with Jerry Stackhouse and Vince Carter making three-point shots that were followed by a three-point play by Iverson to cut the West's lead to 100-96.
Iverson scored the East's next two points from the line, and Tracy McGrady tied it on a putback with 3:10 left.
"We had every reason to make this like a regular All-Star Game and lay down and stop playing, and it didn't happen," East coach Larry Brown said. "I had no idea we could come from behind. It was a wonderful ending for us."
Iverson scored the East's next five points, and a chant of "M-V-P! M-V-P!" was heard after his two foul shots gave the East a 105-104 lead.
But that chant might have revved up someone else, instead.
Someone named Bryant.
In a down-the-stretch performance reminiscent of his play in the Lakers' Game 4 overtime victory over Indiana in last year's NBA Finals, Bryant kept getting the ball and putting it in the basket.
海洋酸化對點帶石斑仔稚魚鈣離子運輸以及骨骼鈣化作用的影響
為了解決Expression ability 的問題，作者黃辰宏 這樣論述：
根據政府間氣候變化專門委員會（IPCC）的預測，在本世紀末，二氧化碳濃度將提升至500~900 µatm，海水的酸鹼值則下降至7.9~7.7。海洋酸化會造成海水中碳酸鈣（CaCO3）飽和濃度升高，不利碳酸鈣在海水當中產生固態沉澱，並影響貝類以及珊瑚外骨骼的形成。此外，水體酸化可能會影響硬骨魚類的離子調節與發育生長，但並不清楚水體酸化是如何影響海洋硬骨魚類鈣離子的調節恆定性。本實驗比較飼養於正常的海水（pH 8.1）及不同酸化程度的海水（pH 7.8 與 pH 7.4）中40日齡點帶石斑仔稚魚，鈣離子運輸蛋白以及骨骼鈣質代謝相關基因在發育過程中的表現量變化。整體而言，實驗發現在酸化的環境之下仔
稚魚的成長與骨骼鈣離子累積並不會受到影響。然而，根據仔稚魚的離子調節、骨骼形成與鈣離子累積等數據的主成分分析卻顯示，水體酸化會影響整體的離子調節能力發展，以及可能輕微地影響對骨骼鈣離子沉積與再吸收。但是，若是以單一因子或以線性回歸進行分析與比較，則難以界定酸化對任何一組離子調控相關基因，例如細胞基底膜的鈣離子幫浦（pmca）、上皮鈣離子通道（ecac）以及運輸能量來源的鈉鉀離子幫浦基因的直接影響。此外，與骨骼鈣質沉積相關的成骨細胞（bglap）及破骨細胞（ctsk and trap）在海水酸化得情況下也並無獨立的顯著差異。實驗雖然表明在高二氧化碳的水體中，pH下降可能造成仔稚魚離子調節、骨骼形
成與鈣離子累積等因子的相互作用，而導致整體的生理差異。本研究亦顯示，點帶石斑魚仔稚魚的生長對高度酸化條件並不敏感，但此研究不能排除未來海洋酸化對沿海海水中的水產養殖業和野生種群影響的可能性。以目前而言，在海洋酸化的情況之下，硬骨魚的離子調節與鈣離子平衡的調節機制尚不明朗，須待更多研究證明。
Environmental, Physiological and Chemical Controls of Adventitious Rooting in Cuttings
為了解決Expression ability 的問題，作者 這樣論述：
The goal of this book is to provide a review, as thorough and up-to-date as possible, of the state-of-the-art of the environmental, physiological and chemical controls of adventitious rooting in cuttings obtained from plants. In plants, adventitious roots, which are highly useful for vegetative prop
agation (or clonal propagation) are produced mainly from leaves, hypocotyls, stems or shoots. Vegetative propagation may occur naturally by making use of propagules such as roots, underground and aerial stems, leaves, buds and bulbils. It may also be done artificially through regenerative organs (rh
izomes, bulbs, and corms) and by utilizing specialized methods, like cutting, grafting and layering. The technique of stem cuttings has long been used as an effective and economical method/measure of clonal propagation of uniform and pathogen-free plants of elite genotypes/germplasms. This is partic
ularly true for various species of horticultural and forestry value. The technique is of special importance for plants producing seeds that are highly recalcitrant and have a very low germination percentage. Quite often, both in vitro and in vivo clonal propagations are carried out using different t
ypes of explants. For in vitro clonal propagation usually axillary buds in the nodal segments are used, while various types of stem cuttings are chosen for in vivo propagation. Adventitious root formation in cuttings is a crucial physiological process for clonal propagation of many plant species. Ov
erall, a plethora of factors affect the adventitious rooting of cuttings, adding to the complexity of the phenomenon. The main factors which control adventitious root formation are types of cuttings, presence of leaf area on cuttings, types of hormones and their concentration, duration of hormonal t
reatment (quick dip, long soak, dry dip, spray dip, or total immerse method), maturation (juvenile or mature), genotype, explant position (basal, middle or apical cuttings), irradiance, temperature, water availability, season, mineral nutrition, rooting conditions, and/or proliferation medium. The i
dentification and the use of correct combination and/or hormonal or auxin treatments have improved the rooting potential even in hard-to-root species. It has been noticed that in spite of a thorough control of environmental factors in the modern propagation industry, high economic losses still occur
because of insufficient rooting. Therefore, understanding of each aspect associated with the adventitious root formation in cuttings is important and remains a fertile discipline for research. Pretreatment of cuttings with auxins such as indole-3-acetic acid, indole-3-butyric acid and a-naphthalene
acetic acid causes metabolic changes during the adventitious root formation, which consists of three successive but independent phases, namely induction, initiation, and expression. The induction phase comprises of molecular and biochemical events without visible changes, the initiation phase is ch
aracterized by cell divisions and root primordia organization, and the expression phase denotes the intra-stem growth of root primordia and the emergence of roots. Since rooting is a high-energy-demanding process, rooting ability of cuttings has been frequently discussed in relation to soluble and s
torage carbohydrate contents. Availability of energy sources as well as supply of nitrogen and amino-acid affects the pace and intensity of adventitious root formation. Furthermore, significant alterations in enzyme activities and metabolite accumulation observed in plant cuttings suggest that the a
ctivity of specific enzymes and metabolites governs the adventitious root formation. For instance, oxidative enzymes, widely distributed in higher plants, have special significance during the rooting. In many studies, changes in the pattern of oxidative enzymes such as peroxidase, indole acetic acid
oxidase, etc, have been taken as the biochemical markers for the successive rooting phases. Further, cutting-edge tools of genome and proteome analysis have been used to understand molecular regulations, gene actions, and cellular processes involved in adventitious root formation. Several candidate
genes have been identified to provoke the induction, initiation, and maintenance of adventitious root primordia-associated signaling cascading network. Considering these crucial points, it becomes essential to understand the underlying factors and their interactions during the formation of adventit
ious roots in cuttings. Given the above, effort has been made in the present book to cover a wide range of topics, as mentioned above, and discuss the environmental, physiological, and chemical controls of adventitious rooting in cuttings. The authors have crafted each chapter with immense clarity,
reviewing up-to-date literature and presenting lucid illustrations.
運用仿生支架進行骨軟骨修復組織工程的生物設計策略
為了解決Expression ability 的問題，作者Swathi Nedunchezian 這樣論述：
Acknowledgment iii摘要 vAbstract viiList of figures xiii1. Chapter One 1Introduction 11.1 Problem statement 11.1.1 Articular cartilage 31.1.2 Structure and composition of articular cartilage 31.1.3 Articular cartilage defect 51.2. Surgical techniques for cartilage and Osteochondral repair
currently in use 61.2.1 Bone marrow techniques 61.2.2 Mosaiplasty 81.2.3 Autologous chondrocyte implantation method 91.2.4 Matrix induced autologous chondrocyte implantation 111.3. Tissue engineering approaches to Osteochondral defect repair 121.3.1 Scaffold and hydrogel-based cell delivery 1
41.4. Cell source for tissue engineering purposes 161.4.1 Chondrocyte cells 161.4.2 Adult somatic stem cells 171.4.3 Bone marrow-derived stem cell (BMSCs) 181.4.4 Adipose-derived stem cells (ADSCs) 191.5 Scaffolds and hydrogels for tissue engineering 211.5.1 Natural hydrogels in cartilage tiss
ue engineering 251.6. Crosslinking of hydrogel for tissue engineering purpose 291.6.2 Silicon-dioxide Nanoparticle as crosslinkers in tissue engineering 341.6.3 Interaction of SiO2 nanoparticle with adipose-derived stem cells 361.7 Bio ceramics for Osteochondral tissue engineering and regenerati
on 371.7.1 Bio ceramics in Tissue engineering applications 371.7.2 Applications of bioceramics in Osteochondral tissue engineering 391.8 Research Objectives 421.8.1 The specific aims of this thesis are as follows: 43Chapter Two 44Characteristic and chondrogenic differentiation analysis of hybr
id hydrogels comprise of hyaluronic acid methacryloyl (HAMA), gelatin methacryloyl (GelMA), and the acrylate functionalized nano-silica crosslinker 442.1 Introduction 442.2 Materials and methods 522.2.1 Materials 522.2.2 Synthesis of HAMA hydrogel 522.2.4 Synthesis of acrylate functionalized nS
i crosslinker (AFnSi) 532.2.5 Identification of the synthesis HAMA and GelMA 542.2.6 Production of hybrid hydrogels 552.2.7 Identification of the synthesis AFnSi cross-linker 552.2.8 Fabrication of HG hybrid hydrogels 562.2.9.Swelling ratio evaluation 562.2.10 The microstructure morphology ana
lysis 572.2.11 Mechanical properties evaluation 572.2.12 In vitro degradation assay by hyaluronidase 582.2.13 Isolation and culturing of hADSCs 592.2.14 Cell viability assay 602.2.15 Chondrogenic marker gene expression 612.2.15 Quantification of DNA, sGAG deposition and collagen type Ⅱ synthes
is 622.2.16 Statistical analysis 632.3. Results and Discussion 632.3.1.Identification of the synthesis HAMA and GelMA 632.3.2 Identification of the AFnSi crosslinker 672.3.3 Swelling ratio of HG hybrid hydrogels 702.3.4 Morphological examination of HG hybrid hydrogels 722.3.5 Compressive stud
y of HG hybrid hydrogels 752.3.6.Viscoelastic property of HG hybrid hydrogel 782.3.7. Degradation study of HG hybrid hydrogels 812.3.8.Cell viability evaluation of hADSCs on HG hybrid hydrogels 822.3.8. Chondrogenic differentiation ability of HG hybrid hydrogels 852.4. Conclusion 90Chapter Thr
ee 92Multilayer-based scaffold for Osteochondral defect regeneration in the rabbit model 923.1 Introduction 923.2 Materials and methods 963.2.1 Preparation and Characterization of the 3D bioceramic scaffold by DLP method 963.2.2 Cell isolation and culture 973.2.3 Fabrication of the cell-laden
hydrogel/ 3D bioceramic scaffolds mimicking the Osteochondral tissue. 983.2.4 Surgery 983.2.5 Macroscopic Examination 993.2.6 Tissue Processing for paraffin block 993.2.7 Histological and Immunohistochemical Evaluation 1003.2.8 Masson’s trichrome stain 1013.3 Results and discussion 1023.3.1 C
haracterization of the 3D bioceramic scaffold by DLP method 1023.3.2 Fabrication of the hydrogel with hADSCs into the 3D bioceramic scaffold 1043.3.3 In-vivo studies using rabbit as an animal model 1053.3.5 Histological evaluation of neocartilage formation 1073.3.6 Masson’s trichrome staining an
alysis for neocartilage formation 1093.4. Conclusion 110Chapter four 1104.1 General discussion 1124.2 Future work 1134.2.1 Macroscopic Observation of neocartilage formation for 8 weeks 1145.Reference 115