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D Schlessinger

Showing results (241-250 of 263) with videos related to

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American Journal of Human Genetics|August 1, 1997
A submicroscopic deletion in Xq26 associated with familial situs ambiguusG B Ferrero, M Gebbia, G Pilia, et al.
Genome Research|July 19, 2000
Eleven densely clustered genes, six of them novel, in 176 kb of mouse t-complex DNAG J Kargul, R Nagaraja, T Shimada, et al.
Nutrition, Metabolism, and Cardiovascular Diseases : NMCD|March 27, 2009
Age- and gender-specific awareness, treatment, and control of cardiovascular risk factors and subclinical vascular lesions in a founder population: the SardiNIA StudyA Scuteri, S S Najjar, M Orru', et al.
Human Molecular Genetics|April 1, 1995
Three genes that escape X chromosome inactivation are clustered within a 6 Mb YAC contig and STS map in Xp11.21-p11.22A P Miller, K Gustashaw, D J Wolff, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 16, 1997
The Tabby phenotype is caused by mutation in a mouse homologue of the EDA gene that reveals novel mouse and human exons and encodes a protein (ectodysplasin-A) with collagenous domainsA K Srivastava, J Pispa, A J Hartung, et al.
Nature Genetics|November 14, 1997
X-linked situs abnormalities result from mutations in ZIC3M Gebbia, G B Ferrero, G Pilia, et al.
Nutrition, Metabolism, and Cardiovascular Diseases : NMCD|November 30, 2015
No evidence of association between subclinical thyroid disorders and common carotid intima medial thickness or atherosclerotic plaqueA P Delitala, F Filigheddu, M Orrù, et al.
Human Molecular Genetics|September 25, 1997
Differential expression pattern of XqPAR-linked genes SYBL1 and IL9R correlates with the structure and evolution of the regionM D'Esposito, M R Matarazzo, A Ciccodicola, et al.
Human Molecular Genetics|October 1, 1995
An integrated physical and genetic map of a 35 Mb region on chromosome Xp22.3-Xp21.3G B Ferrero, B Franco, E J Roth, et al.
The Journal of Clinical Endocrinology and Metabolism|October 13, 1998
Mutational analysis of PHEX gene in X-linked hypophosphatemiaP H Dixon, P T Christie, C Wooding, et al.
Pageof 27

Showing results (241-250 of 263) with videos related to

Sort By:
Pageof 27
American Journal of Human Genetics|August 1, 1997
A submicroscopic deletion in Xq26 associated with familial situs ambiguusG B Ferrero, M Gebbia, G Pilia, et al.
Genome Research|July 19, 2000
Eleven densely clustered genes, six of them novel, in 176 kb of mouse t-complex DNAG J Kargul, R Nagaraja, T Shimada, et al.
Nutrition, Metabolism, and Cardiovascular Diseases : NMCD|March 27, 2009
Age- and gender-specific awareness, treatment, and control of cardiovascular risk factors and subclinical vascular lesions in a founder population: the SardiNIA StudyA Scuteri, S S Najjar, M Orru', et al.
Human Molecular Genetics|April 1, 1995
Three genes that escape X chromosome inactivation are clustered within a 6 Mb YAC contig and STS map in Xp11.21-p11.22A P Miller, K Gustashaw, D J Wolff, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 16, 1997
The Tabby phenotype is caused by mutation in a mouse homologue of the EDA gene that reveals novel mouse and human exons and encodes a protein (ectodysplasin-A) with collagenous domainsA K Srivastava, J Pispa, A J Hartung, et al.
Nature Genetics|November 14, 1997
X-linked situs abnormalities result from mutations in ZIC3M Gebbia, G B Ferrero, G Pilia, et al.
Nutrition, Metabolism, and Cardiovascular Diseases : NMCD|November 30, 2015
No evidence of association between subclinical thyroid disorders and common carotid intima medial thickness or atherosclerotic plaqueA P Delitala, F Filigheddu, M Orrù, et al.
Human Molecular Genetics|September 25, 1997
Differential expression pattern of XqPAR-linked genes SYBL1 and IL9R correlates with the structure and evolution of the regionM D'Esposito, M R Matarazzo, A Ciccodicola, et al.
Human Molecular Genetics|October 1, 1995
An integrated physical and genetic map of a 35 Mb region on chromosome Xp22.3-Xp21.3G B Ferrero, B Franco, E J Roth, et al.
The Journal of Clinical Endocrinology and Metabolism|October 13, 1998
Mutational analysis of PHEX gene in X-linked hypophosphatemiaP H Dixon, P T Christie, C Wooding, et al.
Pageof 27