Found: 57
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Genetic diversity in tropical maize inbred lines: heterotic group assignment and hybrid performance determined by RFLP markers.
- Published in:
- Plant Breeding, 2000, v. 119, n. 6, p. 491, doi. 10.1046/j.1439-0523.2000.00539.x
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- Publication type:
- Article
Intratendinous ganglion in the extensor digitorum brevis tendon.
- Published in:
- 2009
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- Publication type:
- journal article
Polymorphic sequences of the tyrosinase gene: allele analysis on 16 OCA1 patients in Japan indicate that three polymorphic sequences in the tyrosinase gene promoter could be powerful markers for indirect gene diagnosis.
- Published in:
- Journal of Human Genetics, 2002, v. 47, n. 1, p. 1, doi. 10.1007/s10038-002-8648-3
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- Publication type:
- Article
Tongue-palatal contact changes in patients with skeletal mandibular prognathism after sagittal split ramus osteotomy: an electropalatography study.
- Published in:
- Journal of Oral Rehabilitation, 2017, v. 44, n. 9, p. 673, doi. 10.1111/joor.12530
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- Publication type:
- Article
The Role of Finance in the Strategic-Planning and Decision-Making Process.
- Published in:
- Graziadio Business Report, 2010, v. 13, n. 1, p. 1
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- Publication type:
- Article
Multiphase ECG-triggered 3D contrast-enhanced MR angiography: utility for evaluation of hilar and mediastinal invasion of bronchogenic carcinoma.
- Published in:
- 2001
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- Publication type:
- journal article
Relation between Gunpowder Burning‐Rate Responses to Oscillating Pressure and an Oscillating Radiant Heat Flux.
- Published in:
- Combustion, Explosion, & Shock Waves, 2003, v. 39, n. 1, p. 68, doi. 10.1023/A:1022153403728
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- Publication type:
- Article
Site-mutagenesis in hemoglobin: attempts to control the oxygen affinity with cooperativity preserved
- Published in:
- Protein Engineering, 1998, v. 11, n. 3, p. 199, doi. 10.1093/protein/11.3.199
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- Publication type:
- Article
Predicting the prognosis of non-small cell lung cancer patient treated with conservative therapy using contrast-enhanced MR imaging.
- Published in:
- 2000
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- Publication type:
- journal article
A novel NCSTN missense mutation in the signal peptide domain causes hidradenitis suppurativa, which has features characteristic of an autoinflammatory keratinization disease.
- Published in:
- British Journal of Dermatology, 2020, v. 182, n. 2, p. 491, doi. 10.1111/bjd.18445
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- Publication type:
- Article
A patient with bullous pemphigoid with mucosal involvement serologically positive for anti‐BP230 autoantibodies only.
- Published in:
- British Journal of Dermatology, 2020, v. 182, n. 1, p. 221, doi. 10.1111/bjd.18343
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- Publication type:
- Article
Acrodermatitis continua of Hallopeau with dense infiltration of IgG4‐positive cells in the lesional dermis.
- Published in:
- British Journal of Dermatology, 2019, v. 180, n. 4, p. 941, doi. 10.1111/bjd.17405
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- Publication type:
- Article
Autosomal dominant progressive hyperpigmentation and lentigines in a Japanese pedigree due to a missense mutation near the C‐terminus of KIT.
- Published in:
- British Journal of Dermatology, 2018, v. 179, n. 5, p. 1210, doi. 10.1111/bjd.16895
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- Publication type:
- Article
Sterol profiles are valuable biomarkers for phenotype expression of Conradi–Hünermann–Happle syndrome with EBP mutations.
- Published in:
- British Journal of Dermatology, 2018, v. 179, n. 5, p. 1186, doi. 10.1111/bjd.16823
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- Publication type:
- Article
Bilateral striatal necrosis and dyschromatosis symmetrica hereditaria: A–I editing efficiency of ADAR1 mutants and phenotype expression.
- Published in:
- 2018
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- Publication type:
- Letter to the Editor
Filaggrin gene mutations may influence the persistence of food allergies in Japanese primary school children.
- Published in:
- 2018
- By:
- Publication type:
- Letter to the Editor
A novel <italic>IFIH1</italic> mutation in the pincer domain underlies the clinical features of both Aicardi–Goutières and Singleton–Merten syndromes in a single patient.
- Published in:
- British Journal of Dermatology, 2018, v. 178, n. 2, p. e111, doi. 10.1111/bjd.15869
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- Publication type:
- Article
Image Gallery: Unilaterally dominant acrokeratoelastoidosis (punctate palmoplantar keratoderma type 3).
- Published in:
- British Journal of Dermatology, 2017, v. 177, n. 4, p. e157, doi. 10.1111/bjd.15817
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- Publication type:
- Article
Autosomal dominant familial generalized pustular psoriasis caused by a CARD14 mutation.
- Published in:
- British Journal of Dermatology, 2017, v. 177, n. 4, p. e133, doi. 10.1111/bjd.15442
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- Publication type:
- Article
Deficient stratum corneum intercellular lipid in a Japanese patient with lamellar ichthyosis with a homozygous deletion mutation in SDR9C7.
- Published in:
- British Journal of Dermatology, 2017, v. 177, n. 3, p. e62, doi. 10.1111/bjd.15315
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- Publication type:
- Article
Dowling-Degos disease with mutations in POFUT1 is clinicopathologically distinct from reticulate acropigmentation of Kitamura.
- Published in:
- British Journal of Dermatology, 2015, v. 173, n. 2, p. 584, doi. 10.1111/bjd.13702
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- Publication type:
- Article
A novel IL36RN/IL1F5 homozygous nonsense mutation, p.Arg10X, in a Japanese patient with adult-onset generalized pustular psoriasis.
- Published in:
- British Journal of Dermatology, 2012, v. 167, n. 3, p. 699, doi. 10.1111/j.1365-2133.2012.10953.x
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- Publication type:
- Article
Genotype analysis in a patient with oculocutaneous albinism 1 minimal pigment type.
- Published in:
- British Journal of Dermatology, 2012, v. 166, n. 4, p. 896, doi. 10.1111/j.1365-2133.2011.10690.x
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- Publication type:
- Article
Respiratory impedance is correlated with airway narrowing in asthma using three‐dimensional computed tomography.
- Published in:
- Clinical & Experimental Allergy, 2018, v. 48, n. 3, p. 278, doi. 10.1111/cea.13083
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- Publication type:
- Article
Human Adipose-Derived Stromal/Stem Cells Protect Against STZ-Induced Hyperglycemia: Analysis of hASC-Derived Paracrine Effectors.
- Published in:
- Stem Cells, 2014, v. 32, n. 7, p. 1831, doi. 10.1002/stem.1676
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- Publication type:
- Article
Intensity of the Geomagnetic Field during a Reversed Polarity.
- Published in:
- Nature, 1966, v. 212, n. 5059, p. 274, doi. 10.1038/212274a0
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- Publication type:
- Article
Coherent heterodyne-assisted pulsed spectroscopy: sub-Doppler two-photon spectra of krypton, characterizing a tunable nonlinear-optical ultraviolet light source.
- Published in:
- Applied Physics B: Lasers & Optics, 2010, v. 99, n. 4, p. 609, doi. 10.1007/s00340-010-3982-1
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- Publication type:
- Article
Ponderomotive force near cyclotron resonance.
- Published in:
- Journal of Plasma Physics, 1987, v. 38, n. 1, p. 43, doi. 10.1017/S0022377800012393
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- Publication type:
- Article
Spontaneous excitation of magnetic fields and collapse dynamics in a Langmuir plasma.
- Published in:
- Journal of Plasma Physics, 1981, v. 26, n. 1, p. 123, doi. 10.1017/S0022377800010588
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- Publication type:
- Article
Effect of antioxidants on histamine receptor activation and sustained postexercise vasodilatation in humans.
- Published in:
- Experimental Physiology, 2015, v. 100, n. 4, p. 435, doi. 10.1113/EP085030
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- Publication type:
- Article
Unraveling the Lining of ERISA Health Insurer Pockets--A Vote for National Federal Common Law Adoption of the Make Whole Doctrine.
- Published in:
- Brigham Young University Law Review, 2000, v. 2000, n. 1, p. 427
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- Publication type:
- Article
One Trillion Dollars? An Analysis of Y2K Employment Implications for Attorneys.
- Published in:
- Brigham Young University Law Review, 1999, v. 1999, n. 4, p. 1529
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- Publication type:
- Article
Exploratory aspirin resistance trial in healthy Japanese volunteers (J-ART) using platelet aggregation as a measure of thrombogenicity.
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- Pharmacogenomics Journal, 2007, v. 7, n. 6, p. 395, doi. 10.1038/sj.tpj.6500435
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- Publication type:
- Article
Factor Xa inhibitors for preventing recurrent thrombosis in patients with antiphospholipid syndrome: a longitudinal cohort study.
- Published in:
- Lupus, 2019, v. 28, n. 13, p. 1577, doi. 10.1177/0961203319881200
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- Publication type:
- Article
Long-term outcome in Japanese patients with lupus nephritis.
- Published in:
- Lupus, 2014, v. 23, n. 11, p. 1124, doi. 10.1177/0961203314536246
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- Publication type:
- Article
Trivalent inactivated influenza vaccine effective against influenza A(H3N2) variant viruses in children during the 2014/15 season, Japan.
- Published in:
- Eurosurveillance (15607917), 2016, v. 21, n. 42, p. 2, doi. 10.2807/1560-7917.ES.2016.21.42.30377
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- Publication type:
- Article
Comprehensive screening for a complete set of Japanese-population-specific filaggrin gene mutations.
- Published in:
- Allergy, 2014, v. 69, n. 4, p. 537, doi. 10.1111/all.12369
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- Publication type:
- Article
A case of pustular psoriasis possibly precipitated by periodic oestrogen/gestagen therapy for Turner syndrome.
- Published in:
- Clinical & Experimental Dermatology, 2019, v. 44, n. 7, p. e240, doi. 10.1111/ced.13979
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- Publication type:
- Article
Hyper-IgE syndrome with a novel mutation of the STAT3 gene.
- Published in:
- Clinical & Experimental Dermatology, 2016, v. 41, n. 6, p. 687, doi. 10.1111/ced.12865
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- Publication type:
- Article
Psoriasis treated with ursodeoxycholic acid: three case reports.
- Published in:
- Clinical & Experimental Dermatology, 2007, v. 32, n. 4, p. 398, doi. 10.1111/j.1365-2230.2007.02401.x
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- Publication type:
- Article
Remodelling of calcinosis cutis in a patient with scleroderma overlap syndrome.
- Published in:
- Journal of the European Academy of Dermatology & Venereology, 2020, v. 34, n. 1, p. e20, doi. 10.1111/jdv.15864
- By:
- Publication type:
- Article
Mild Hailey–Hailey disease cases with aberrant splicing variants of ATP2C1 successfully controlled with excimer light.
- Published in:
- 2018
- By:
- Publication type:
- Letter to the Editor
Dyschromatosis symmetrica hereditaria with chilblains due to a novel two‐amino‐acid deletion in the double‐stranded RNA‐binding domain of ADAR1.
- Published in:
- Journal of the European Academy of Dermatology & Venereology, 2018, v. 32, n. 10, p. e394, doi. 10.1111/jdv.15076
- By:
- Publication type:
- Article
Author's response to the comment to ‘Compound heterozygotes for filaggrin gene mutations do not always show severe atopic dermatitis’.
- Published in:
- 2018
- By:
- Publication type:
- Letter to the Editor
Trichothiodystrophy, complementation group A complicated with squamous cell carcinoma.
- Published in:
- 2018
- By:
- Publication type:
- Letter to the Editor
Hailey‐Hailey disease due to <italic>ATP2C1</italic> splice site mutation, successfully treated with minocycline hydrochloride.
- Published in:
- 2018
- By:
- Publication type:
- Case Study
Punctate palmoplantar keratoderma type 1 with a novel AAGAB frameshift mutation: intrafamilial phenotype variation due to ageing.
- Published in:
- Journal of the European Academy of Dermatology & Venereology, 2017, v. 31, n. 3, p. e175, doi. 10.1111/jdv.13906
- By:
- Publication type:
- Article
A case of epidermolytic ichthyosis showing a very mild phenotype due to a novel tail extension mutation in KRT10.
- Published in:
- Journal of the European Academy of Dermatology & Venereology, 2017, v. 31, n. 2, p. e68, doi. 10.1111/jdv.13729
- By:
- Publication type:
- Article
Ripple-pattern lichen amyloidosis in a case of ichthyosis vulgaris with a novel FLG mutation.
- Published in:
- Journal of the European Academy of Dermatology & Venereology, 2017, v. 31, n. 2, p. e130, doi. 10.1111/jdv.13877
- By:
- Publication type:
- Article
Compound heterozygotes for filaggrin gene mutations do not always show severe atopic dermatitis.
- Published in:
- Journal of the European Academy of Dermatology & Venereology, 2017, v. 31, n. 1, p. 158, doi. 10.1111/jdv.13871
- By:
- Publication type:
- Article