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Neurobiology of Aging
|
October 27, 2006
Citicoline is not protective in experimental models of Huntington's disease
Stéphane Mievis, Marc Levivier, Gilbert Vassart, et al.
The Journal of Biological Chemistry
|
January 1, 2004
The C-terminal nonapeptide of mature chemerin activates the chemerin receptor with low nanomolar potency
Valérie Wittamer, Françoise Grégoire, Patrick Robberecht, et al.
Molecular Endocrinology (Baltimore, Md.)
|
February 19, 2005
Thyroid transcription factor 1 rescues PAX8/p300 synergism impaired by a natural PAX8 paired domain mutation with dominant negative activity
Helmut Grasberger, Usanee Ringkananont, Paule Lefrancois, et al.
European Journal of Clinical Investigation
|
August 13, 2011
Lack of responsiveness to 1-desamino-D arginin vasopressin (desmopressin) in male patients with nephrogenic syndrome of inappropriate antidiuresis: from bench to bedside
Frederic Vandergheynst, Olivier Pradier, Ingrid Beukinga, et al.
Developmental Biology
|
January 13, 2006
Defective postnatal development of the male reproductive tract in LGR4 knockout mice
Fernando Mendive, Patrick Laurent, Grégory Van Schoore, et al.
Developmental Biology
|
April 28, 2009
LGR5 deficiency deregulates Wnt signaling and leads to precocious Paneth cell differentiation in the fetal intestine
Marie Isabelle Garcia, Mariangela Ghiani, Anne Lefort, et al.
The Journal of Biological Chemistry
|
February 22, 2005
An activation switch in the rhodopsin family of G protein-coupled receptors: the thyrotropin receptor
Eneko Urizar, Sylvie Claeysen, Xavier Deupí, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
June 16, 2005
Premature ovarian aging in mice deficient for Gpr3
Catherine Ledent, Isabelle Demeestere, David Blum, et al.
Neuromolecular Medicine
|
November 23, 2006
Lack of minocycline efficiency in genetic models of Huntington's disease
Stéphane Mievis, Marc Levivier, David Communi, et al.
The Journal of Clinical Endocrinology and Metabolism
|
March 6, 2004
A mutation in the follicle-stimulating hormone receptor as a cause of familial spontaneous ovarian hyperstimulation syndrome
Lucia Montanelli, Anne Delbaere, Costantino Di Carlo, et al.
Page
of 9
Search research articles
Search
Showing results (21-30 of 82) with videos related to
Sort By:
Page
of 9
Neurobiology of Aging
|
October 27, 2006
Citicoline is not protective in experimental models of Huntington's disease
Stéphane Mievis, Marc Levivier, Gilbert Vassart, et al.
The Journal of Biological Chemistry
|
January 1, 2004
The C-terminal nonapeptide of mature chemerin activates the chemerin receptor with low nanomolar potency
Valérie Wittamer, Françoise Grégoire, Patrick Robberecht, et al.
Molecular Endocrinology (Baltimore, Md.)
|
February 19, 2005
Thyroid transcription factor 1 rescues PAX8/p300 synergism impaired by a natural PAX8 paired domain mutation with dominant negative activity
Helmut Grasberger, Usanee Ringkananont, Paule Lefrancois, et al.
European Journal of Clinical Investigation
|
August 13, 2011
Lack of responsiveness to 1-desamino-D arginin vasopressin (desmopressin) in male patients with nephrogenic syndrome of inappropriate antidiuresis: from bench to bedside
Frederic Vandergheynst, Olivier Pradier, Ingrid Beukinga, et al.
Developmental Biology
|
January 13, 2006
Defective postnatal development of the male reproductive tract in LGR4 knockout mice
Fernando Mendive, Patrick Laurent, Grégory Van Schoore, et al.
Developmental Biology
|
April 28, 2009
LGR5 deficiency deregulates Wnt signaling and leads to precocious Paneth cell differentiation in the fetal intestine
Marie Isabelle Garcia, Mariangela Ghiani, Anne Lefort, et al.
The Journal of Biological Chemistry
|
February 22, 2005
An activation switch in the rhodopsin family of G protein-coupled receptors: the thyrotropin receptor
Eneko Urizar, Sylvie Claeysen, Xavier Deupí, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
June 16, 2005
Premature ovarian aging in mice deficient for Gpr3
Catherine Ledent, Isabelle Demeestere, David Blum, et al.
Neuromolecular Medicine
|
November 23, 2006
Lack of minocycline efficiency in genetic models of Huntington's disease
Stéphane Mievis, Marc Levivier, David Communi, et al.
The Journal of Clinical Endocrinology and Metabolism
|
March 6, 2004
A mutation in the follicle-stimulating hormone receptor as a cause of familial spontaneous ovarian hyperstimulation syndrome
Lucia Montanelli, Anne Delbaere, Costantino Di Carlo, et al.
Page
of 9