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Results 1 to 25 of 339

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Peace propaganda and biomedical experimentation : Influential uses of radioisotopes in endocrinology and molecular genetics in Spain (1947-1971)SANTESMASES, Maria Jesus.Journal of the history of biology. 2006, Vol 39, Num 4, pp 765-794, issn 0022-5010, 30 p.Article

Boosting the Power of Schizophrenia Genetics by Leveraging New Statistical ToolsANDREASSEN, Ole A; THOMPSON, Wesley K; DALE, Anders M et al.Schizophrenia bulletin. 2014, Vol 40, Num 1, pp 13-17, issn 0586-7614, 5 p.Article

The genetics of autistic disorders and its clinical relevance : a review of the literatureFREITAG, C. M.Molecular psychiatry. 2007, Vol 12, Num 1, pp 2-22, issn 1359-4184, 21 p.Article

A novel mutation of the glomulin gene in an Italian family with autosomal dominant cutaneous glomuvenous malformationsBORRONI, Riccardo G; NARULA, Nupoor; DIEGOLI, Marta et al.Experimental dermatology. 2011, Vol 20, Num 12, pp 1032-1034, issn 0906-6705, 3 p.Article

A standardized framework for the validation and verification of clinical molecular genetic testsMATTOCKS, Christopher J; MORRIS, Michael A; MATTHIJS, Gert et al.European journal of human genetics. 2010, Vol 18, Num 12, pp 1276-1288, issn 1018-4813, 13 p.Article

ARNT2 mutation causes hypopituitarism, post-natal microcephaly, visual and renal anomaliesWEBB, Emma A; ALMUTAIR, Angham; ALAHMESH, Mohammed A et al.Brain. 2013, Vol 136, pp 3096-3105, issn 0006-8950, 10 p., 10Article

Molecular pathology of endometrial carcinomaMATIAS-GUIU, Xavier; PRAT, Jaime.Histopathology. 2013, Vol 62, Num 1, pp 111-123, issn 0309-0167, 13 p.Article

PAX2 gene mutations in pediatric and young adult transplant recipients: kidney and urinary tract malformations without ocular anomaliesNEGRISOLO, S; BENETTI, E; CENTI, S et al.Clinical genetics. 2011, Vol 80, Num 6, pp 581-585, issn 0009-9163, 5 p.Article

Renin-angiotensin system in kidney development: renal tubular dysgenesisGUBLER, Marie Claire; ANTIGNAC, Corinne.Kidney international. 2010, Vol 77, Num 5, pp 400-406, issn 0085-2538, 7 p.Article

The Impact of Cytomorphology, Cytogenetics, Molecular Genetics, and Immunophenotyping in a Comprehensive Diagnostic Workup of Myelodysplastic SyndromesBACHER, Ulrike; HAFERLACH, Torsten; KERN, Wolfgang et al.Cancer. 2009, Vol 115, Num 19, pp 4524-4532, issn 0008-543X, 9 p.Article

(A)sexual reproduction : a review of life cycles of grape phylloxera, Daktulosphaira vitifoliaeFORNECK, Astrid; HUBER, Lars.Entomologia experimentalis et applicata. 2009, Vol 131, Num 1, pp 1-10, issn 0013-8703, 10 p.Article

Genetic aspects of pathological gambling: a complex disorder with shared genetic vulnerabilitiesLOBO, Daniela S. S; KENNEDY, James L.Addiction (Abingdon. Print). 2009, Vol 104, Num 9, pp 1454-1465, issn 0965-2140, 12 p.Article

Genomic analysis of the HER2/TOP2A amplicon in breast cancer and breast cancer cell linesARRIOLA, Edurne; MARCHIO, Caterina; JONES, Chris et al.Laboratory investigation. 2008, Vol 88, Num 5, pp 491-503, issn 0023-6837, 13 p.Article

Molecular profiling pleomorphic lobular carcinomas of the breast : evidence for a common molecular genetic pathway with classic lobular carcinomasSIMPSON, P. T; REIS-FILHO, J. S; REID, L et al.Journal of pathology. 2008, Vol 215, Num 3, pp 231-244, issn 0022-3417, 14 p.Article

Fraser and ablepharon macrostomia phenotypes : Concurrence in one family and association with mutated FRAS1PONTES CAVALCANTI, Denise; MATEJAS, Verena; LUQUETTI, Daniela et al.American journal of medical genetics. Part A. 2007, Vol 143, Num 3, pp 241-247, issn 1552-4825, 7 p.Article

Molecular genetics of bipolar disorder and depressionKATO, Tadafumi.Psychiatry and clinical neurosciences (Carlton. Print). 2007, Vol 61, Num 1, pp 3-19, issn 1323-1316, 17 p.Article

A de novo PABPN1 germline mutation in a patient with oculopharyngeal muscular dystrophyGÜRTLER, Nicolas; PLASILOVA, Martina; PODVINEC, Mihael et al.The Laryngoscope. 2006, Vol 116, Num 1, pp 111-114, issn 0023-852X, 4 p.Article

Sudden cardiac death not related to coronary atherosclerosisLADICH, Elena; VIRMANI, Renu; BURKE, Allen et al.Toxicologic pathology. 2006, Vol 34, Num 1, pp 52-57, issn 0192-6233, 6 p.Conference Paper

Genomewide linkage study in the Irish affected sib pair study of alcohol dependence : evidence for a susceptibility region for symptoms of alcohol dependence on chromosome 4PRESCOTT, C. A; SULLIVAN, P. F; ROBINSON, V. P et al.Molecular psychiatry. 2006, Vol 11, Num 6, pp 603-611, issn 1359-4184, 9 p.Article

Pleomorphic lobular carcinoma of the breast : role of comprehensive molecular pathology in characterization of an entityREIS-FILHO, Jorge S; SIMPSON, Pete T; PALACIOS, Jose et al.Journal of pathology. 2005, Vol 207, Num 1, pp 1-13, issn 0022-3417, 13 p.Article

Molecular pathogenesis of oligodendroglial tumorsJEUKEN, Judith W. M; VON DEIMLING, Andreas; WESSELING, Pieter et al.Journal of neuro-oncology. 2004, Vol 70, Num 2, pp 161-181, issn 0167-594X, 21 p.Article

Rapid detection of Phytophthora cinnamomi using PCR with primers derived from the Lpv putative storage protein genesKONG, P; HONG, C. X; RICHARDSON, P. A et al.Plant pathology. 2003, Vol 52, Num 6, pp 681-693, issn 0032-0862, 13 p.Article

Eighteen Years of Experience With Acinetobacter baumannii in a Tertiary Care HospitalSILVIA MUNOZ-PRICE, L; ARHEART, Kristopher; NORDMANN, Patrice et al.Critical care medicine. 2013, Vol 41, Num 12, pp 2733-2742, issn 0090-3493, 10 p.Article

Inverted formin 2 mutations with variable expression in patients with sporadic and hereditary focal and segmental glomerulosclerosisGBADEGESIN, Rasheed A; LAVIN, Peter J; OTTATI, Carolina et al.Kidney international. 2012, Vol 81, Num 1, pp 94-99, issn 0085-2538, 6 p.Article

Common variants in the sex hormone-binding globulin gene (SHBG) and polycystic ovary syndrome (PCOS) in Mediterranean womenMARTINEZ-GARCIA, M. Angeles; GAMBINERI, Alessandra; ALPANES, Macarena et al.Human reproduction (Oxford. Print). 2012, Vol 27, Num 12, pp 3569-3576, issn 0268-1161, 8 p.Article

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