Pascal and Francis Bibliographic Databases

Help

Search results

Your search

au.\*:("ZHENGLIN YANG")

Publication Year[py]

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Discipline (document) [di]

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Author Country

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Results 1 to 25 of 36

  • Page / 2
Export

Selection :

  • and

A 0.5-V 35-μW 85-dB DR Double-Sampled ΔΣ Modulator for Audio ApplicationsZHENGLIN YANG; LIBIN YAO; YONG LIAN et al.IEEE journal of solid-state circuits. 2012, Vol 47, Num 3, pp 722-735, issn 0018-9200, 14 p.Article

Process-induced stress analysis of composite laminates using semi-analytical Hamiltonian methodHAORAN CHEN; ZHENGLIN YANG; JEMAH, A. K et al.Composite structures. 1998, Vol 41, Num 1, pp 49-55, issn 0263-8223Article

Transgenic indica rice expressing a bitter melon (Momordica charantia) class I chitinase gene (McCHIT1) confers enhanced resistance to Magnaporthe grisea and Rhizoctonia solaniPING LI; YAN PEI; XIANCHUN SANG et al.European journal of plant pathology. 2009, Vol 125, Num 4, pp 530-540, issn 0929-1873, 11 p.Article

A Reappraisal of the Clinical Spectrum of North Carolina Macular DystrophyKHURANA, Rahul N; XUFANG SUN; PEARSON, Eric et al.Ophthalmology (Rochester, MN). 2009, Vol 116, Num 10, pp 1976-1983, issn 0161-6420, 8 p.Article

The R345W mutation in EFEMP1 is pathogenic and causes AMD-like deposits in miceLI FU; GARLAND, Donita; ZHENGLIN YANG et al.Human molecular genetics (Print). 2007, Vol 16, Num 20, pp 2411-2422, issn 0964-6906, 12 p.Article

Mutations in the RPGR gene cause X-linked cone dystrophyZHENGLIN YANG; PEACHEY, Neal S; MOSHFEGHI, Darius M et al.Human molecular genetics (Print). 2002, Vol 11, Num 5, pp 605-611, issn 0964-6906Article

Rolling-leaf14 is a 20G-Fe (II) oxygenase family protein that modulates rice leaf rolling by affecting secondary cell wall formation in leavesLIKUI FANG; FANGMING ZHAO; YUNFEI CONG et al.Plant biotechnology journal (Print). 2012, Vol 10, Num 5, pp 524-532, issn 1467-7644, 9 p.Article

MUTATION IN CONNEXIN 32 CAUSES CHARCOT-MARIE-TOOTH DISEASE IN A LARGE CHINESE FAMILYFUQIANG GUO; YI SHI; YING LIN et al.Muscle & nerve. 2010, Vol 42, Num 5, pp 715-721, issn 0148-639X, 7 p.Article

Assessment of purity of rice CMS lines using cpDNA markerXIANCHUN SANG; ZHENGLIN YANG; BINGQIANG ZHONG et al.Euphytica. 2006, Vol 152, Num 2, pp 177-183, issn 0014-2336, 7 p.Article

A novel mutation in LMX1B gene causes nail-patella syndrome in a large Chinese familyYING LIN; JUAN ZHAO; SHIPEI CHEN et al.Bone (New York, NY). 2008, Vol 43, Num 3, pp 591-595, issn 8756-3282, 5 p.Article

A family with X-linked optic atrophy linked to the OPA2 locus Xp11.4-Xp11.2KATZ, Bradley J; YU ZHAO; WARNER, Judith E. A et al.American journal of medical genetics. Part A. 2006, Vol 140, Num 20, pp 2207-2211, issn 1552-4825, 5 p.Article

Clinical characterization and genetic mapping of North Carolina macular dystrophyZHENGLIN YANG; ZONGZHONG TONG; CHORICH, Louis J et al.Vision research (Oxford). 2008, Vol 48, Num 3, pp 470-477, issn 0042-6989, 8 p.Article

A variant of the HTRA1 gene increases susceptibility to age-related macular degenerationZHENGLIN YANG; CAMP, Nicola J; CHIEN, Jeremy et al.Science (Washington, D.C.). 2006, Vol 314, Num 5801, pp 992-993, issn 0036-8075, 2 p.Article

Mutations in LRP5 or FZD4 underlie the common familial exudative vitreoretinopathy locus on chromosome 11qTOOMES, Carmel; BOTTOMLEY, Helen M; WOODRUFF, Geoffrey et al.American journal of human genetics. 2004, Vol 74, Num 4, pp 721-730, issn 0002-9297, 10 p.Article

CHIMERIC FLORAL ORGANS1, Encoding a Monocot-Specific MADS Box Protein, Regulates Floral Organ Identity in RiceXIANCHUN SANG; YUNFENG LI; GUANGHUA HE et al.Plant physiology (Bethesda). 2012, Vol 160, Num 2, pp 788-807, issn 0032-0889, 20 p.Article

A 5-bp deletion in ELOVL4 is associated with two related forms of autosomal dominant macular dystrophyKANG ZHANG; KNIAZEVA, Marina; KAKUK, Laura E et al.Nature genetics. 2001, Vol 27, Num 1, pp 89-93, issn 1061-4036Article

Sequence-and target-independent angiogenesis suppression by siRNA via TLR3KLEINMAN, Mark E; YAMADA, Kiyoshi; APPUKUTTAN, Binoy et al.Nature (London). 2008, Vol 452, Num 7187, pp 591-597, issn 0028-0836, 7 p.Article

Identification and characterization of a novel mutation in the carbonic anhydrase IV gene that causes retinitis pigmentosaALVAREZ, Bernardo V; VITHANA, Eranga N; KANG ZHANG et al.Investigative ophthalmology & visual science. 2007, Vol 48, Num 8, pp 3459-3468, issn 0146-0404, 10 p.Article

Mutant carbonic anhydrase 4 impairs pH regulation and causes retinal photoreceptor degenerationZHENGLIN YANG; ALVAREZ, Bernardo V; WISSINGER, Bernd et al.Human molecular genetics (Print). 2005, Vol 14, Num 2, pp 255-265, issn 0964-6906, 11 p.Article

MULTI-FLORET SPIKELET1, Which Encodes an AP2/ERF Protein, Determines Spikelet Meristem Fate and Sterile Lemma Identity in RiceDEYONG REN; YUNFENG LI; GUANGHUA HE et al.Plant physiology (Bethesda). 2013, Vol 162, Num 2, pp 872-884, issn 0032-0889, 13 p.Article

Association of HTRA1 polymorphism and bilaterality in advanced age-related macular degenerationHAOYU CHEN; ZHENGLIN YANG; CONSTANTINE, Ryan et al.Vision research (Oxford). 2008, Vol 48, Num 5, pp 690-694, issn 0042-6989, 5 p.Article

Familial aggregation of age-related macular degeneration in the Utah populationLING LUO; HARMON, Jennifer; XIANG MA et al.Vision research (Oxford). 2008, Vol 48, Num 3, pp 494-500, issn 0042-6989, 7 p.Article

Elovl4 haploinsufficiency does not induce early onset retinal degeneration in miceWENMEI LI; YALI CHEN; HOWES, Kimberly et al.Vision research (Oxford). 2007, Vol 47, Num 5, pp 714-722, issn 0042-6989, 9 p.Article

Identification of a Susceptibility Locus in STAT4 for Behçet's Disease in Han Chinese in a Genome-Wide Association StudySHENGPINGHOU; ZHENGLIN YANG; KIJLSTRA, Aize et al.Arthritis and rheumatism. 2012, Vol 64, Num 12, pp 4104-4113, issn 0004-3591, 10 p.Article

Toll-like Receptor 3 and Geographic Atrophy in Age-Related Macular DegenerationZHENGLIN YANG; STRATTON, Charity; YUHONG CHEN et al.The New England journal of medicine. 2008, Vol 359, Num 14, pp 1456-1463, issn 0028-4793, 8 p.Article

  • Page / 2