Human Molecular Genetics,volume 13,issue 13  (07-2013)

Period of time: 2013年13期

Publisher: Oxford University Press

Founded in: 1992

Total resources: 344

ISSN: 1460-2083

Subject: Q3 Genetics

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Human Molecular Genetics,volume 13,issue 13

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Fxr1 knockout mice show a striated muscle phenotype: implications for Fxr1p function in vivo

By Mientjes Edwin J.,Willemsen Rob,Kirkpatrick Laura L.,Nieuwenhuizen Ingeborg M.,Hoogeveen-Westerveld Marianne,Verweij Marcel,Reis Surya,Bardoni Barbara,Hoogeveen Andre T.,Oostra Ben A.,Nelson David L. in (2004)

Human Molecular Genetics,volume 13,issue 13 , Vol. 13, Iss. 13, 2004-07 , pp. 1291-1302

Oxford University Press

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Whole genome scanning identifies genotypes associated with recurrence and metastasis in prostate tumors

By Paris Pamela L.,Andaya Armann,Fridlyand Jane,Jain Ajay N.,Weinberg Vivian,Kowbel David,Brebner John H.,Simko Jeff,Watson J.E. Vivienne,Volik Stas,Albertson Donna G.,Pinkel Daniel,Alers Janneke C.,van der Kwast Theodorus H.,Vissers Kees J.,Schroder Fritz H.,Wildhagen Mark F.,Febbo Phillip G.,Chinnaiyan Arul M.,Pienta Kenneth J.,Carroll Peter R.,Rubin Mark A.,Collins Colin,van Dekken Herman in (2004)

Human Molecular Genetics,volume 13,issue 13 , Vol. 13, Iss. 13, 2004-07 , pp. 1303-1313

Oxford University Press

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GABRD encoding a protein for extra- or peri-synaptic GABA A receptors is a susceptibility locus for generalized epilepsies

By Dibbens Leanne M.,Feng Hua-Jun,Harkin Louise A.,Hodgson Bree L.,Scott Darren,Jenkins Misty,Petrou Steven,Sutherland Grant R.,Scheffer Ingrid E.,Berkovic Samuel F.,Macdonald Robert L.,Mulley John C. in (2004)

Human Molecular Genetics,volume 13,issue 13 , Vol. 13, Iss. 13, 2004-07 , pp. 1315-1319

Oxford University Press

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Partial loss of presenilins causes seborrheic keratosis and autoimmune disease in mice

By Tournoy Jos,Bossuyt Xavier,Snellinx An,Regent Marleen,Garmyn Marian,Serneels Lutgarde,Saftig Paul,Craessaerts Katleen,De Strooper Bart,Hartmann Dieter in (2004)

Human Molecular Genetics,volume 13,issue 13 , Vol. 13, Iss. 13, 2004-07 , pp. 1321-1331

Oxford University Press

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Dosage-dependent over-expression of genes in the trisomic region of Ts1Cje mouse model for Down syndrome

By Amano Kenji,Sago Haruhiko,Uchikawa Chiharu,Suzuki Taishi,Kotliarova Svetlana E.,Nukina Nobuyuki,Epstein Charles J.,Yamakawa Kazuhiro in (2004)

Human Molecular Genetics,volume 13,issue 13 , Vol. 13, Iss. 13, 2004-07 , pp. 1333-1340

Oxford University Press

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Platelet-activating factor-acetylhydrolase and PAF-receptor gene haplotypes in relation to future cardiovascular event in patients with coronary artery disease

By Ninio Ewa,Tregouet David,Carrier Jean-Luc,Stengel Dominique,Bickel Christoph,Perret Claire,Rupprecht Hans J.,Cambien François,Blankenberg Stefan, for the Athero in (2004)

Human Molecular Genetics,volume 13,issue 13 , Vol. 13, Iss. 13, 2004-07 , pp. 1341-1351

Oxford University Press

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Corticosteroid pharmacogenetics: association of sequence variants in CRHR1 with improved lung function in asthmatics treated with inhaled corticosteroids

By Tantisira Kelan G.,Lake Stephen,Silverman Eric S.,Palmer Lyle J.,Lazarus Ross,Silverman Edwin K.,Liggett Stephen B.,Gelfand Erwin W.,Rosenwasser Lanny J.,Richter Brent,Israel Elliot,Wechsler Michael,Gabriel Stacey,Altshuler David,Lander Eric,Drazen Jeffrey,Weiss Scott T. in (2004)

Human Molecular Genetics,volume 13,issue 13 , Vol. 13, Iss. 13, 2004-07 , pp. 1353-1359

Oxford University Press

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Progressive decrease in chaperone protein levels in a mouse model of Huntington's disease and induction of stress proteins as a therapeutic approach

By Hay David G.,Sathasivam Kirupa,Tobaben Sönke,Stahl Bernd,Marber Michael,Mestril Ruben,Mahal Amarbirpal,Smith Donna L.,Woodman Ben,Bates Gillian P. in (2004)

Human Molecular Genetics,volume 13,issue 13 , Vol. 13, Iss. 13, 2004-07 , pp. 1389-1405

Oxford University Press

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