Found: 20
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Leaf diaheliotropic movement can improve carbon gain and water use efficiency and not intensify photoinhibition in upland cotton (Gossypium hirsutum L.).
- Published in:
- Photosynthetica, 2009, v. 47, n. 4, p. 609, doi. 10.1007/s11099-009-0087-3
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- Publication type:
- Article
Keratin 17 mutation in pachyonychia congenita type 2 with early onset sebaceous cysts.
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- British Journal of Dermatology, 2003, v. 148, n. 3, p. 452, doi. 10.1046/j.1365-2133.2003.05152.x
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- Publication type:
- Article
The archaeological documentation and geochemistry of the Rua Tokitoki adze quarry and the Poike fine‐grain basalt source on Rapa Nui (Easter Island).
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- Archaeology in Oceania, 2018, v. 53, n. 1, p. 15, doi. 10.1002/arco.5132
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- Article
Eosinophilic panniculitis: Report of three cases.
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- International Journal of Dermatology, 2006, v. 45, n. 12, p. 1412, doi. 10.1111/j.1365-4632.2006.02917.x
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- Publication type:
- Article
DETERMINATION OF SURFACE VELOCITY OF A RIVER USING VIDEOS CAPTURED FROM UNMANNED AERIAL SYSTEM (UAS).
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- International Archives of the Photogrammetry, Remote Sensing & Spatial Information Sciences, 2019, v. XLII-2/W13, p. 597, doi. 10.5194/isprs-archives-XLII-2-W13-597-2019
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- Publication type:
- Article
Mutations of KRT6A are more frequent than those of KRT16 in pachyonychia congenita type 1: report of a novel and a recently reported mutation in two unrelated Chinese families.
- Published in:
- 2008
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- Publication type:
- Letter
A study of rare structural variants in schizophrenia patients and normal controls from Chinese Han population.
- Published in:
- Molecular Psychiatry, 2008, v. 13, n. 10, p. 911, doi. 10.1038/mp.2008.69
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- Publication type:
- Article
Further evidence for the association between G72/G30 genes and schizophrenia in two ethnically distinct populations.
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- Molecular Psychiatry, 2006, v. 11, n. 5, p. 479, doi. 10.1038/sj.mp.4001788
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- Publication type:
- Article
Family-based association study of Epsin 4 and Schizophrenia.
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- Molecular Psychiatry, 2006, v. 11, n. 4, p. 395, doi. 10.1038/sj.mp.4001780
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- Publication type:
- Article
No association between polymorphisms of methylenetetrahydrofolate reductase gene and schizophrenia in both Chinese and Scottish populations.
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- 2004
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- Publication type:
- Letter
Association of SNPs and haplotypes in GABA<sub>A</sub> receptor ß<sub>2</sub> gene with schizophrenia.
- Published in:
- Molecular Psychiatry, 2004, v. 9, n. 6, p. 603, doi. 10.1038/sj.mp.4001461
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- Publication type:
- Article
Polymorphisms within 5' end of the Neuregulin 1 gene are genetically associated with schizophrenia in the Chinese population.
- Published in:
- Molecular Psychiatry, 2004, v. 9, n. 1, p. 11, doi. 10.1038/sj.mp.4001436
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- Publication type:
- Article
Family-based association study of DTNBP1 in 6p22.3 and schizophrenia.
- Published in:
- 2003
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- Publication type:
- Erratum
Family-based association study of DTNBP1 in 6p22.3 and schizophrenia.
- Published in:
- Molecular Psychiatry, 2003, v. 8, n. 8, p. 717, doi. 10.1038/sj.mp.4001287
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- Publication type:
- Article
Apolipoprotein E epsilon4 allele is a risk factor for late-onset Alzheimer's disease and vascular dementia in Han Chinese.
- Published in:
- 2001
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- Publication type:
- research
Apolipoprotein E Ƹ4 allele is a risk factor for late-onset Alzheimer's disease and vascular dementia in Han Chinese.
- Published in:
- 2001
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- Publication type:
- Letter
Decreased levels of apolipoprotein A-I in plasma of schizophrenic patients.
- Published in:
- Journal of Neural Transmission, 2007, v. 114, n. 5, p. 657, doi. 10.1007/s00702-006-0607-2
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- Publication type:
- Article
MicroRNA-19a-3p suppresses invasion and metastasis of prostate cancer via inhibiting SOX4.
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- European Review for Medical & Pharmacological Sciences, 2018, v. 22, n. 19, p. 6245
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- Publication type:
- Article
Novel mutations in the vWFA2 domain of COCH in two Chinese DFNA9 families.
- Published in:
- 2008
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- Publication type:
- Letter
A novel DFNA5 mutation, IVS8+4 A>G, in the splice donor site of intron 8 causes late-onset non-syndromic hearing loss in a Chinese family.
- Published in:
- Clinical Genetics, 2007, v. 72, n. 5, p. 471, doi. 10.1111/j.1399-0004.2007.00889.x
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- Publication type:
- Article