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Treatment of diabetes by xenogeneic islets without immunosuppression. Use of a vascularized bioartificial pancreas.
- Published in:
- 1996
- By:
- Publication type:
- journal article
Treatment of severely diabetic pancreatectomized dogs using a diffusion-based hybrid pancreas.
- Published in:
- 1992
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- Publication type:
- journal article
Chorea-acanthocytosis: Clinical and genetic findings in three families from the Arabian peninsula.
- Published in:
- Movement Disorders, 2003, v. 18, n. 4, p. 403, doi. 10.1002/mds.10361
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- Publication type:
- Article
McLeod syndrome and neuroacanthocytosis with a novel mutation in the XK gene.
- Published in:
- Movement Disorders, 2000, v. 15, n. 6, p. 1282, doi. 10.1002/1531-8257(200011)15:6<1282::AID-MDS1042>3.0.CO;2-2
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- Publication type:
- Article
Controversies in organ donation: the altruistic living donor.
- Published in:
- Nephrology Dialysis Transplantation, 2001, v. 16, n. 3, p. 619, doi. 10.1093/ndt/16.3.619
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- Publication type:
- Article
Talking genes--the molecular basis of language development.
- Published in:
- Biologist, 2002, v. 49, n. 6, p. 255
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- Publication type:
- Article
Molecular Genetic Investigations of Autism.
- Published in:
- Journal of Autism & Developmental Disorders, 1998, v. 28, n. 5, p. 427, doi. 10.1023/A:1026056522602
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- Publication type:
- Article
Effect of gamma-irradiation on mouse pancreatic islet-allograft survival.
- Published in:
- 1989
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- Publication type:
- journal article
Effect of γ-Irradiation on Mouse Pancreatic Islet-Allograft Survival.
- Published in:
- Diabetes, 1989, v. 38, p. 154, doi. 10.2337/diab.38.1.s154
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- Publication type:
- Article
Consortium Fine Localization of X-Linked Charcot-Marie-Tooth Disease (CMTX1): Additional Support that Connexin32 Is the Defect in CMTX1.
- Published in:
- Human Heredity, 1995, v. 45, n. 3, p. 121, doi. 10.1159/000154272
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- Publication type:
- Article
Molecular evolution of FOXP2, a gene involved in speech and language.
- Published in:
- Nature, 2002, v. 418, n. 6900, p. 869, doi. 10.1038/nature01025
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- Publication type:
- Article
Germline mutations in the EXT1 and EXT2 genes in Korean patients with hereditary multiple exostoses.
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- Journal of Human Genetics, 1999, v. 44, n. 4, p. 230, doi. 10.1007/s100380050149
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- Publication type:
- Article
Lipocalin 2 is required for BCR-ABL-induced tumorigenesis.
- Published in:
- Oncogene, 2008, v. 27, n. 47, p. 6110, doi. 10.1038/onc.2008.209
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- Publication type:
- Article
PCSK6 is associated with handedness in individuals with dyslexia.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 3, p. 608, doi. 10.1093/hmg/ddq475
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- Publication type:
- Article
The dyslexia-associated gene KIAA0319 encodes highly N- and O-glycosylated plasma membrane and secreted isoforms.
- Published in:
- Human Molecular Genetics, 2008, v. 17, n. 6, p. 859, doi. 10.1093/hmg/ddm358
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- Publication type:
- Article
The chromosome 6p22 haplotype associated with dyslexia reduces the expression of KIAA0319, a novel gene involved in neuronal migration.
- Published in:
- Human Molecular Genetics, 2006, v. 15, n. 10, p. 1659, doi. 10.1093/hmg/ddl089
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- Publication type:
- Article
Parent-of-origin effects on handedness and schizophrenia susceptibility on chromosome 2p12–q11.
- Published in:
- Human Molecular Genetics, 2003, v. 12, n. 24, p. 3225, doi. 10.1093/hmg/ddg362
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- Publication type:
- Article
A Deletion Involving CD 38 and BST 1 Results in a Fusion Transcript in a Patient With Autism and Asthma.
- Published in:
- Autism Research: Official Journal of the International Society for Autism Research, 2014, v. 7, n. 2, p. 254, doi. 10.1002/aur.1365
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- Publication type:
- Article
Dual copy number variants involving 16p11 and 6q22 in a case of childhood apraxia of speech and pervasive developmental disorder.
- Published in:
- European Journal of Human Genetics, 2013, v. 21, n. 4, p. 361, doi. 10.1038/ejhg.2012.166
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- Publication type:
- Article
Identification of a VPS13A founder mutation in French Canadian families with chorea-acanthocytosis.
- Published in:
- Neurogenetics, 2005, v. 6, n. 3, p. 151, doi. 10.1007/s10048-005-0220-9
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- Publication type:
- Article
Identification of a yeast artificial chromosome (YAC) spanning the synovial sarcoma-specific t(X;18)(p11.2;q11.2) breakpoint.
- Published in:
- Genes, Chromosomes & Cancer, 1993, v. 6, n. 3, p. 182, doi. 10.1002/gcc.2870060309
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- Publication type:
- Article
Phytotoxicity of Low-Molecular-Weight Phenols from Olive Mill Waste Waters.
- Published in:
- Bulletin of Environmental Contamination & Toxicology, 2001, v. 67, n. 3, p. 0352, doi. 10.1007/s001280132
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- Publication type:
- Article
Rabbit Antithymocyte Globulin (Thymoglobulin): 25 Years and New Frontiers in Solid Organ Transplantation and Haematology.
- Published in:
- Drugs, 2010, v. 70, n. 6, p. 691, doi. 10.2165/11315940-000000000-00000
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- Publication type:
- Article
CNVs leading to fusion transcripts in individuals with autism spectrum disorder.
- Published in:
- European Journal of Human Genetics, 2012, v. 20, n. 11, p. 1141, doi. 10.1038/ejhg.2012.73
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- Publication type:
- Article
Genome-wide analysis of genetic susceptibility to language impairment in an isolated Chilean population.
- Published in:
- European Journal of Human Genetics, 2011, v. 19, n. 6, p. 687, doi. 10.1038/ejhg.2010.251
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- Publication type:
- Article
Linkage and candidate gene studies of autism spectrum disorders in European populations.
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- European Journal of Human Genetics, 2010, v. 18, n. 9, p. 1013, doi. 10.1038/ejhg.2010.69
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- Publication type:
- Article
Corrigendum to: Linkage and candidate gene studies of autism spectrum disorders in European populations.
- Published in:
- 2010
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- Publication type:
- Correction notice
Assessing the impact of FOXP1 mutations on developmental verbal dyspraxia.
- Published in:
- European Journal of Human Genetics, 2009, v. 17, n. 10, p. 1354, doi. 10.1038/ejhg.2009.43
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- Publication type:
- Article
Copy number variation and association analysis of SHANK3 as a candidate gene for autism in the IMGSAC collection.
- Published in:
- European Journal of Human Genetics, 2009, v. 17, n. 10, p. 1347, doi. 10.1038/ejhg.2009.47
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- Publication type:
- Article
MET and autism susceptibility: family and case–control studies.
- Published in:
- European Journal of Human Genetics, 2009, v. 17, n. 6, p. 749, doi. 10.1038/ejhg.2008.215
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- Publication type:
- Article
A 15q13.3 microdeletion segregating with autism.
- Published in:
- European Journal of Human Genetics, 2009, v. 17, n. 5, p. 687, doi. 10.1038/ejhg.2008.228
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- Publication type:
- Article
Focus on behavioural genetics.
- Published in:
- European Journal of Human Genetics, 2006, v. 14, n. 6, p. 647, doi. 10.1038/sj.ejhg.5201599
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- Publication type:
- Article
SLC25A12 and CMYA3 gene variants are not associated with autism in the IMGSAC multiplex family sample.
- Published in:
- European Journal of Human Genetics, 2006, v. 14, n. 1, p. 123, doi. 10.1038/sj.ejhg.5201444
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- Publication type:
- Article
Comparison of fluorescent single-strand conformation polymorphism analysis and denaturing high-performance liquid chromatography for detection of EXT1 and EXT2 mutations in hereditary multiple exostoses.
- Published in:
- European Journal of Human Genetics, 2000, v. 8, n. 1, p. 24, doi. 10.1038/sj.ejhg.5200409
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- Publication type:
- Article
Integrated physical and transcript map of 5q31.3-qter.
- Published in:
- European Journal of Human Genetics, 1998, v. 6, n. 3, p. 266, doi. 10.1038/sj.ejhg.5200188
- By:
- Publication type:
- Article
Hailey-Hailey Disease: Molecular and Clinical Characterization of Novel Mutations in the ATP2C1 Gene.
- Published in:
- Journal of Investigative Dermatology, 2002, v. 118, n. 2, p. 338, doi. 10.1046/j.0022-202x.2001.01675.x
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- Publication type:
- Article
Common Variants in Left/Right Asymmetry Genes and Pathways Are Associated with Relative Hand Skill.
- Published in:
- PLoS Genetics, 2013, v. 9, n. 9, p. 1, doi. 10.1371/journal.pgen.1003751
- By:
- Publication type:
- Article
A Common Variant Associated with Dyslexia Reduces Expression of the KIAA0319 Gene.
- Published in:
- PLoS Genetics, 2009, v. 5, n. 3, p. 1, doi. 10.1371/journal.pgen.1000436
- By:
- Publication type:
- Article
STUDIES ON HETEROLOGOUS ANTI-LYMPHOCYTE SERUM IN MICE. III. IMMUNOLOGIC TOLERANCE AND CHIMERISM PRODUCED ACROSS THE H-2 LOCUS WITH ADULT THYMECTOMY AND ANTI-LYMPHOCYTE SERUM*.
- Published in:
- Annals of the New York Academy of Sciences, 1966, v. 129, n. 1, p. 190, doi. 10.1111/j.1749-6632.1966.tb12851.x
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- Publication type:
- Article
Activation of c-type viruses during skin graft rejection in the mouse. Interrelationships between immunostimulation and immunosuppression.
- Published in:
- International Journal of Cancer, 1975, v. 15, n. 3, p. 493, doi. 10.1002/ijc.2910150315
- By:
- Publication type:
- Article
Reading and Language Disorders: The Importance of Both Quantity and Quality.
- Published in:
- Genes, 2014, v. 5, n. 2, p. 285, doi. 10.3390/genes5020285
- By:
- Publication type:
- Article
Multivariate Linkage Analysis of Specific Language Impairment (SLI).
- Published in:
- Annals of Human Genetics, 2007, v. 71, n. 5, p. 660, doi. 10.1111/j.1469-1809.2007.00361.x
- By:
- Publication type:
- Article
NEUROCHEMICAL STUDIES WITH l-CYCLOSERINE, A CENTRAL DEPRESSANT AGENT.
- Published in:
- Journal of Neurochemistry, 1963, v. 10, n. 11, p. 831, doi. 10.1111/j.1471-4159.1963.tb11908.x
- By:
- Publication type:
- Article
Detection of deletions spanning the Duchenne muscular dystrophy locus using a tightly linked DNA segment.
- Published in:
- Nature, 1985, v. 316, n. 6031, p. 842, doi. 10.1038/316842a0
- By:
- Publication type:
- Article
A Study on the Relationship between Electroretinogram and Optic Nerve Discharge.
- Published in:
- Ophthalmologica, 1964, v. 147, n. 1, p. 57, doi. 10.1159/000304564
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- Publication type:
- Article
Is ASMT a susceptibility gene for autism spectrum disorders? A replication study in European populations.
- Published in:
- 2007
- By:
- Publication type:
- Letter
Further evidence that the KIAA0319 gene confers susceptibility to developmental dyslexia.
- Published in:
- Molecular Psychiatry, 2006, v. 11, n. 12, p. 1085, doi. 10.1038/sj.mp.4001904
- By:
- Publication type:
- Article
Linkage disequilibrium structure of KIAA0319 and DCDC2, two candidate susceptibility genes for developmental dyslexia.
- Published in:
- Molecular Psychiatry, 2006, v. 11, n. 12, p. 1061, doi. 10.1038/sj.mp.4001930
- By:
- Publication type:
- Article
Response to paper by Molloy et al.: Linkage on 21q and 7q in autism subset with regression.
- Published in:
- 2006
- By:
- Publication type:
- Letter
Genome-wide scan of reading ability in affected sibling pairs with attention-deficit/hyperactivity disorder: unique and shared genetic effects.
- Published in:
- Molecular Psychiatry, 2004, v. 9, n. 5, p. 485, doi. 10.1038/sj.mp.4001450
- By:
- Publication type:
- Article