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P Lichtner

Showing results (11-20 of 27) with videos related to

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Journal of Molecular Medicine (Berlin, Germany)|July 12, 2002
Expression and mutation analysis of BRUNOL3, a candidate gene for heart and thymus developmental defects associated with partial monosomy 10pP Lichtner, T Attié-Bitach, S Schuffenhauer, et al.
Neurobiology of Aging|April 26, 2008
Polymorphisms in the receptor for GDNF (RET) are not associated with Parkinson's disease in Southern GermanyC B Lücking, P Lichtner, E R Kramer, et al.
European Journal of Human Genetics : EJHG|October 22, 1998
Cloning and gene structure of the rod cGMP phosphodiesterase delta subunit gene (PDED) in man and mouseB Lorenz, C Migliaccio, P Lichtner, et al.
American Journal of Medical Genetics|May 3, 1996
Craniosynostosis suggestive of Saethre-Chotzen syndrome: clinical description of a large kindred and exclusion of candidate regions on 7pS von Gernet, S Schuffenhauer, A Golla, et al.
Journal of Molecular Biology|May 26, 1999
Genetic and structural characterization of the human mitochondrial inner membrane translocaseM F Bauer, K Gempel, A S Reichert, et al.
Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Metabolisme|November 10, 2007
No association of sequence variants in the neuropeptide Y2 receptor (NPY2R) gene with early onset obesity in GermansH-J Wang, A-K Wermter, T T Nguyen, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|February 9, 2021
Investigation of gamma secretase gene complex mutations in German population with Hidradenitis suppurativa designate a complex polygenic heritageS Vural, M Baumgartner, P Lichtner, et al.
Neurology|December 13, 2006
Idiopathic generalized epilepsy phenotypes associated with different EFHC1 mutationsE Stogmann, P Lichtner, C Baumgartner, et al.
International Journal of Molecular Medicine|February 15, 2001
Complete form of X-linked congenital stationary night blindness: refined mapping and evidence of genetic homogeneityC M Pusch, J Maurer, J Ramser, et al.
Human Molecular Genetics|June 19, 2001
Cloning of the human MCCA and MCCB genes and mutations therein reveal the molecular cause of 3-methylcrotonyl-CoA: carboxylase deficiencyA Holzinger, W Röschinger, F Lagler, et al.
Pageof 3

Showing results (11-20 of 27) with videos related to

Sort By:
Pageof 3
Journal of Molecular Medicine (Berlin, Germany)|July 12, 2002
Expression and mutation analysis of BRUNOL3, a candidate gene for heart and thymus developmental defects associated with partial monosomy 10pP Lichtner, T Attié-Bitach, S Schuffenhauer, et al.
Neurobiology of Aging|April 26, 2008
Polymorphisms in the receptor for GDNF (RET) are not associated with Parkinson's disease in Southern GermanyC B Lücking, P Lichtner, E R Kramer, et al.
European Journal of Human Genetics : EJHG|October 22, 1998
Cloning and gene structure of the rod cGMP phosphodiesterase delta subunit gene (PDED) in man and mouseB Lorenz, C Migliaccio, P Lichtner, et al.
American Journal of Medical Genetics|May 3, 1996
Craniosynostosis suggestive of Saethre-Chotzen syndrome: clinical description of a large kindred and exclusion of candidate regions on 7pS von Gernet, S Schuffenhauer, A Golla, et al.
Journal of Molecular Biology|May 26, 1999
Genetic and structural characterization of the human mitochondrial inner membrane translocaseM F Bauer, K Gempel, A S Reichert, et al.
Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Metabolisme|November 10, 2007
No association of sequence variants in the neuropeptide Y2 receptor (NPY2R) gene with early onset obesity in GermansH-J Wang, A-K Wermter, T T Nguyen, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|February 9, 2021
Investigation of gamma secretase gene complex mutations in German population with Hidradenitis suppurativa designate a complex polygenic heritageS Vural, M Baumgartner, P Lichtner, et al.
Neurology|December 13, 2006
Idiopathic generalized epilepsy phenotypes associated with different EFHC1 mutationsE Stogmann, P Lichtner, C Baumgartner, et al.
International Journal of Molecular Medicine|February 15, 2001
Complete form of X-linked congenital stationary night blindness: refined mapping and evidence of genetic homogeneityC M Pusch, J Maurer, J Ramser, et al.
Human Molecular Genetics|June 19, 2001
Cloning of the human MCCA and MCCB genes and mutations therein reveal the molecular cause of 3-methylcrotonyl-CoA: carboxylase deficiencyA Holzinger, W Röschinger, F Lagler, et al.
Pageof 3