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Results 1 to 25 of 93

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Absence of association of androgen receptor trinucleotide expansion and poor semen qualityERASMUSON, Tanya; SIN, Iris L; SIN, Frank Y. T et al.International journal of andrology (Print). 2003, Vol 26, Num 1, pp 46-51, issn 0105-6263, 6 p.Article

Molecular analysis of the androgen receptor in ten prostate cancer specimens obtained before and after androgen ablationLAMB, Dolores J; PUXEDDU, Efisio; MALIK, Nusrat et al.Journal of andrology. 2003, Vol 24, Num 2, pp 215-225, issn 0196-3635, 11 p.Article

A novel haplotype of spinocerebellar ataxia type 6 contributes to the highest prevalence in Western JapanTERASAWA, Hideo; ODA, Masaya; MORINO, Hiroyuki et al.Neuroscience letters. 2004, Vol 358, Num 2, pp 107-110, issn 0304-3940, 4 p.Article

Analysis of SCA8 and SCA12 loci in 134 Italian ataxic patients negative for SCAT-3, 6 and 7 CAG expansionsBRUSCO, Alfredo; CAGNOLI, Claudia; FRANCO, Alessandra et al.Journal of neurology. 2002, Vol 249, Num 7, pp 923-929, issn 0340-5354, 7 p.Article

Relationship between the CAG Repeat Polymorphism in the Androgen Receptor Gene and Acne in the Han Ethnic GroupZHI YANG; HAIJING YU; BAOWEN CHENG et al.Dermatology (Basel). 2009, Vol 218, Num 4, pp 302-306, issn 1018-8665, 5 p.Article

CAG repeat size correlates to electrophysiological motor and sensory phenotypes in SBMASUZUKI, Keisuke; KATSUNO, Masahisa; HIRAYAMA, Masaaki et al.Brain. 2008, Vol 131, pp 229-239, issn 0006-8950, 11 p., 1Article

Molecular characterization of the commonly used human androgen receptor expression vector, pSG5-ARLITVINOV, Ivan V; CHAWNSHANG CHANG; ISAACS, John T et al.The Prostate. 2004, Vol 58, Num 4, pp 319-324, issn 0270-4137, 6 p.Article

Importance of CAG repeat length in childhood-onset dentatorubral―pallidoluysian atrophyMARUYAMA, Shinsuke; SAITO, Yoshiaki; MINAMI, Narihiro et al.Journal of neurology. 2012, Vol 259, Num 11, pp 2329-2334, issn 0340-5354, 6 p.Article

Long-Term Disability and Prognosis in DentatorubralPallidoluysian Atrophy: a Correlation with CAG Repeat LengthHASEGAWA, Arika; IKEUCHI, Takeshi; KOIKE, Ryoko et al.Movement disorders. 2010, Vol 25, Num 11, pp 1694-1700, issn 0885-3185, 7 p.Article

Detection of CAG repeats in pre-eclampsia/eclampsia using the repeat expansion detection methodFREED, K. A; COOPER, D. W; BRENNECKE, S. P et al.Molecular human reproduction. 2005, Vol 11, Num 7-8, pp 481-487, issn 1360-9947, 7 p.Article

Molecular epidemiology of spinocerebellar ataxias in Cuba : Insights into SCA2 founder effect in HolguinVELAZQUEZ PEREZ, Luis; SANCHEZ CRUZ, Gilberto; GONZALEZ ZALDIVAR, Yanetza et al.Neuroscience letters. 2009, Vol 454, Num 2, pp 157-160, issn 0304-3940, 4 p.Article

Longitudinal changes of outcome measures in spinal and bulbar muscular atrophyHASHIZUME, Atsushi; KATSUNO, Masahisa; SOBUE, Gen et al.Brain. 2012, Vol 135, pp 2838-2848, issn 0006-8950, 11 p., 9Article

Possible association between the androgen receptor gene and autism spectrum disorderHENNINGSSON, Susanne; JONSSON, Lina; BETANCUR, Catalina et al.Psychoneuroendocrinology. 2009, Vol 34, Num 5, pp 752-761, issn 0306-4530, 10 p.Article

Meiotic CAG repeat instability in spinocerebellar ataxia type 6 : Maternally transmitted elongation in a presumed sporadic caseLINDQUIST, Suzanne Granhøj; NØRREMOLLE, Anne; HJERMIND, Lena Elisabeth et al.Journal of the neurological sciences. 2006, Vol 241, Num 1-2, pp 95-98, issn 0022-510X, 4 p.Article

Early Symptoms in Spinocerebellar Ataxia Type 1, 2, 3, and 6GLOBAS, Christoph; DU MONTCEL, Sophie Tezenas; MELEGH, Bela et al.Movement disorders. 2008, Vol 23, Num 15, pp 2232-2238, issn 0885-3185, 7 p.Article

The role of the polyglutamine tract in androgen receptorPALAZZOLO, Isabella; GLIOZZI, Alessandra; RUSMINI, Paola et al.Journal of steroid biochemistry and molecular biology. 2008, Vol 108, Num 3-5, pp 245-253, issn 0960-0760, 9 p.Conference Paper

Early onset, non fluctuating spinocerebellar ataxia and a novel missense mutation in CACNA1A geneTONELLI, Alessandra; D'ANGELO, Maria Grazia; SALATI, Roberto et al.Journal of the neurological sciences. 2006, Vol 241, Num 1-2, pp 13-17, issn 0022-510X, 5 p.Article

Association of androgen receptor CAG repeat polymorphism with VO2max response to hypoxic training in North China Han menWANG, H. Y; HU, Y; WANG, S. H et al.International journal of andrology (Print). 2010, Vol 33, Num 6, pp 794-799, issn 0105-6263, 6 p.Article

Late onset Huntington Disease : Clinical and genetic characteristics of 34 casesLIPE, Hillary; BIRD, Thomas.Journal of the neurological sciences. 2009, Vol 276, Num 1-2, pp 159-162, issn 0022-510X, 4 p.Article

Spinocerebellar ataxias types 1, 2 and 3 : Age adjusted clinical severity of disease at presentation correlates with size of CAG repeat lengthsNETRAVATHI, M; PRAMOD KUMAR PAL; PURUSHOTTAM, Meera et al.Journal of the neurological sciences. 2009, Vol 277, Num 1-2, pp 83-86, issn 0022-510X, 4 p.Article

Spinocerebellar ataxia type 17 (SCA17) : Oculomotor phenotype and clinical characterization of 15 Italian patientsMARIOTTI, Caterina; ALPINI, Dario; TARONI, Franco et al.Journal of neurology. 2007, Vol 254, Num 11, pp 1538-1546, issn 0340-5354, 9 p.Article

Case of maternally transmitted juvenile Huntington's disease with a very large trinucleotide repeatPAPAPETROPOULOS, Spiridon; LOPEZ-ALBEROLA, Roberto; BAUMBACH, Lisa et al.Movement disorders. 2005, Vol 20, Num 10, pp 1380-1383, issn 0885-3185, 4 p.Article

Association between CAG repeat length in the PPP2R2B gene and Alzheimer disease in the Japanese populationKIMURA, Ryo; MORIHARA, Takashi; KUDO, Takashi et al.Neuroscience letters. 2011, Vol 487, Num 3, pp 354-357, issn 0304-3940, 4 p.Article

Spinocerebellar Ataxia Type 12 Identified in Two Italian Families May Mimic Sporadic AtaxiaBRUSSINO, Alessandro; GRAZIANO, Claudio; MICCOLI, Sara et al.Movement disorders. 2010, Vol 25, Num 9, pp 1269-1273, issn 0885-3185, 5 p.Article

Effects of SCA1, MJD, and DPRLA triplet repeat polymorphisms on cognitive phenotypes in a normal population of adolescent twinsLUCIANO, M; HINE, E; WRIGHT, M. J et al.American journal of medical genetics. Part B, Neuropsychiatric genetics. 2007, Vol 144, Num 1, pp 95-100, issn 1552-4841, 6 p.Article

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