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High throughput DNA sequence variant detection by conformation sensitive capillary electrophoresis and automated peak comparisonDAVIES, Helen; DICKS, Ed; STEVENS, Claire et al.Genomics (San Diego, Calif.). 2006, Vol 87, Num 3, pp 427-432, issn 0888-7543, 6 p.Article

Glia: Initiators and Progressors of Pathology in Parkinson's DiseaseHALLIDAY, Glenda M; STEVENS, Claire H.Movement disorders. 2011, Vol 26, Num 1, pp 6-17, issn 0885-3185, 12 p.Article

Regeneration for all? : Measuring and enhancing levels of Black and other racial minorities' economic activity = Régénération pour tous ? Mesurer et élever le niveau d'activité économique des Noirs et autres minorités racialesPEMBERTON, Simon; ALTY, Carys; BOYLAN, Rose et al.International journal of sociology and social policy. 2006, Vol 26, Num 5-6, pp 229-244, issn 0144-333X, 16 p.Article

Somatic mutations of the protein kinase gene family in human lung cancerDAVIES, Helen; HUNTER, Chris; PARKER, Adrian et al.Cancer research (Baltimore). 2005, Vol 65, Num 17, pp 7591-7595, issn 0008-5472, 5 p.Article

Mutations in the BRWD3 gene cause X-linked mental retardation associated with macrocephalyFIELD, Michael; TARPEY, Patrick S; BARTHORPE, Syd et al.American journal of human genetics. 2007, Vol 81, Num 2, pp 367-374, issn 0002-9297, 8 p.Article

Abacavir hypersensitivity reaction in primary HIV infectionSTEKLER, Joanne; MAENZA, Janine; STEVENS, Claire et al.AIDS (London). 2006, Vol 20, Num 9, pp 1269-1274, issn 0269-9370, 6 p.Article

Chromosomally unstable mouse tumours have genomic alterations similar to diverse human cancersMASER, Richard S; CHOUDHURY, Bhudipa; LIN, Eric et al.Nature (London). 2007, Vol 447, Num 7147, pp 966-971, issn 0028-0836, 6 p.Article

Mutations in ZDHHC9, which encodes a palmitoyltransferase of NRAS and HRAS, cause X-linked mental retardation associated with a marfanoid habitusRAYMOND, F. Lucy; TARPEY, Patrick S; COLE, Jennifer et al.American journal of human genetics. 2007, Vol 80, Num 5, pp 982-987, issn 0002-9297, 6 p.Article

A hypermutation phenotype and somatic MSH6 mutations in recurrent human malignant gliomas after alkylator chemotherapyHUNTER, Chris; SMITH, Raffaella; O'MEARA, Sarah et al.Cancer research (Baltimore). 2006, Vol 66, Num 8, pp 3987-3991, issn 0008-5472, 5 p.Article

Patterns of somatic mutation in human cancer genomesGREENMAN, Christopher; STEPHENS, Philip; EDKINS, Sarah et al.Nature (London). 2007, Vol 446, Num 7132, pp 153-158, issn 0028-0836, 6 p.Article

Mutations in the gene encoding the sigma 2 subunit of the adaptor protein 1 complex, AP1S2, cause X-linked mental retardationTARPEY, Patrick S; STEVENS, Claire; DICKS, Ed et al.American journal of human genetics. 2006, Vol 79, Num 6, pp 1119-1124, issn 0002-9297, 6 p.Article

Mutations in the DLG3 gene cause nonsyndromic X-linked mental retardationTARPEY, Patrick; PARNAU, Josep; KORNY, Angelique et al.American journal of human genetics. 2004, Vol 75, Num 2, pp 318-324, issn 0002-9297, 7 p.Article

X-linked protocadherin 19 mutations cause female-limited epilepsy and cognitive impairmentDIBBENS, Leanne M; TARPEY, Patrick S; EDKINS, Sarah et al.Nature genetics. 2008, Vol 40, Num 6, pp 776-781, issn 1061-4036, 6 p.Article

Mutations in CUL4b, which encodes a ubiquitin E3 ligase subunit, cause an X-linked mental retardation syndrome associated with aggressive outbursts, seizures, relative macrocephaly, central obesity, hypogonadism, pes cavus, and tremorTARPEY, Patrick S; RAYMOND, F. Lucy; BARTHORPE, Syd et al.American journal of human genetics. 2007, Vol 80, Num 2, pp 345-352, issn 0002-9297, 8 p.Article

Mutations in UPF3B, a member of the nonsense-mediated mRNA decay complex, cause syndromic and nonsyndromic mental retardationTARPEY, Patrick S; RAYMOND, F. Lucy; O'MEARA, Sarah et al.Nature genetics. 2007, Vol 39, Num 9, pp 1127-1133, issn 1061-4036, 7 p.Article

Mutations in FRMD7, a newly identified member of the FERM family, cause X-linked idiopathic congenital nystagmusTARPEY, Patrick; THOMAS, Shery; REINECKE, Robert D et al.Nature genetics. 2006, Vol 38, Num 11, pp 1242-1244, issn 1061-4036, 3 p.Article

Mutations of the BRAF gene in human cancerDAVIES, Helen; BIGNELL, Graham R; DAVIS, Hell et al.Nature (London). 2002, Vol 417, Num 6892, pp 949-954, issn 0028-0836Article

HIV Dynamics in Seminal Plasma during Primary HIV InfectionSTEKLER, Joanne; SYCKS, Brian J; HOLTE, Sarah et al.AIDS research and human retroviruses. 2008, Vol 24, Num 10, pp 1269-1274, issn 0889-2229, 6 p.Article

Screening for Acute HIV Infection : Lessons LearnedSTEKLER, Joanne; MAENZA, Janine; STEVENS, Claire E et al.Clinical infectious diseases. 2007, Vol 44, Num 3, pp 459-461, issn 1058-4838, 3 p.Article

Evaluation of a low-dose nonoxynol-9 gel for the prevention of sexually transmitted diseases: A randomized clinical trialRICHARDSON, Barbra A; LAVREYS, Ludo; MARTIN, Harold L et al.Sexually transmitted diseases. 2001, Vol 28, Num 7, pp 394-400, issn 0148-5717Article

Conserved HIV-1 Epitopes Continuously Elicit Subdominant Cytotoxic T-Lymphocyte ResponsesYI LIU; MCNEVIN, John; ROLLAND, Morgane et al.The Journal of infectious diseases. 2009, Vol 200, Num 12, pp 1825-1833, issn 0022-1899, 9 p.Article

Mucopurulent cervicitis and Mycoplasma genitaliumMANHART, Lisa E; CRITCHLOW, Cathy W; HOLMES, King K et al.The Journal of infectious diseases. 2003, Vol 187, Num 4, pp 650-657, issn 0022-1899, 8 p.Article

Virus-Specific CD8+ T-Cell Responses Better Define HIV Disease Progression than HLA GenotypeDINGES, Warren L; RICHARDT, Julia; MOODIE, Zoe et al.Journal of virology. 2010, Vol 84, Num 9, pp 4461-4468, issn 0022-538X, 8 p.Article

Selection on the human immunodeficiency virus type 1 proteome following primary infectionYI LIU; MCNEVIN, John; MAENZA, Janine et al.Journal of virology. 2006, Vol 80, Num 19, pp 9519-9529, issn 0022-538X, 11 p.Article

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