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Plos One
|
November 14, 2014
Homozygosity mapping and whole exome sequencing reveal a novel homozygous COL18A1 mutation causing Knobloch syndrome
Alireza Haghighi, Amit Tiwari, Niloofar Piri, et al.
Molecular Vision
|
March 7, 2006
Sutural cataract associated with a mutation in the ferritin light chain gene (FTL) in a family of Indian origin
Vanita Vanita, James Fielding Hejtmancik, Hans Christian Hennies, et al.
Human Molecular Genetics
|
August 21, 2007
Sequence-based bioinformatic prediction and QUASEP identify genomic imprinting of the KCNK9 potassium channel gene in mouse and human
Nico Ruf, Sylvia Bähring, Danuta Galetzka, et al.
Die Naturwissenschaften
|
July 29, 2003
A longitudinal study of age-specific reproductive output and body condition among male rhesus macaques, Macaca mulatta
Fred B Bercovitch, Anja Widdig, Andrea Trefilov, et al.
Naunyn-Schmiedeberg'S Archives of Pharmacology
|
August 31, 2010
The Arg16Gly-β(2)-adrenoceptor single nucleotide polymorphism: exercise capacity and survival in patients with end-stage heart failure
Kirsten Leineweber, Ulrich H Frey, Gero Tenderich, et al.
Gynecologic Oncology
|
December 5, 2006
Polymorphism of IL-1alpha, IL-1beta and IL-10 in patients with advanced ovarian cancer: results of a prospective study with 147 patients
Elena Ioana Braicu, Alexander Mustea, Mohammad R Toliat, et al.
Circulation
|
June 3, 2004
Novel gene locus for autosomal dominant left ventricular noncompaction maps to chromosome 11p15
Sabine Sasse-Klaassen, Susanne Probst, Brenda Gerull, et al.
Human Mutation
|
April 27, 2011
U1 snRNA-mediated gene therapeutic correction of splice defects caused by an exceptionally mild BBS mutation
Fabian Schmid, Esther Glaus, Daniel Barthelmes, et al.
Plant Physiology
|
September 30, 2015
Floral Induction in Arabidopsis by FLOWERING LOCUS T Requires Direct Repression of BLADE-ON-PETIOLE Genes by the Homeodomain Protein PENNYWISE
Fernando Andrés, Maida Romera-Branchat, Rafael Martínez-Gallegos, et al.
American Journal of Medical Genetics. Part A
|
October 13, 2020
Ultra-rapid emergency genomic diagnosis of Donahue syndrome in a preterm infant within 17 hours
Daniel Bamborschke, Özkan Özdemir, Mona Kreutzer, et al.
Page
of 52
Search research articles
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Showing results (71-80 of 517) with videos related to
Sort By:
Page
of 52
Plos One
|
November 14, 2014
Homozygosity mapping and whole exome sequencing reveal a novel homozygous COL18A1 mutation causing Knobloch syndrome
Alireza Haghighi, Amit Tiwari, Niloofar Piri, et al.
Molecular Vision
|
March 7, 2006
Sutural cataract associated with a mutation in the ferritin light chain gene (FTL) in a family of Indian origin
Vanita Vanita, James Fielding Hejtmancik, Hans Christian Hennies, et al.
Human Molecular Genetics
|
August 21, 2007
Sequence-based bioinformatic prediction and QUASEP identify genomic imprinting of the KCNK9 potassium channel gene in mouse and human
Nico Ruf, Sylvia Bähring, Danuta Galetzka, et al.
Die Naturwissenschaften
|
July 29, 2003
A longitudinal study of age-specific reproductive output and body condition among male rhesus macaques, Macaca mulatta
Fred B Bercovitch, Anja Widdig, Andrea Trefilov, et al.
Naunyn-Schmiedeberg'S Archives of Pharmacology
|
August 31, 2010
The Arg16Gly-β(2)-adrenoceptor single nucleotide polymorphism: exercise capacity and survival in patients with end-stage heart failure
Kirsten Leineweber, Ulrich H Frey, Gero Tenderich, et al.
Gynecologic Oncology
|
December 5, 2006
Polymorphism of IL-1alpha, IL-1beta and IL-10 in patients with advanced ovarian cancer: results of a prospective study with 147 patients
Elena Ioana Braicu, Alexander Mustea, Mohammad R Toliat, et al.
Circulation
|
June 3, 2004
Novel gene locus for autosomal dominant left ventricular noncompaction maps to chromosome 11p15
Sabine Sasse-Klaassen, Susanne Probst, Brenda Gerull, et al.
Human Mutation
|
April 27, 2011
U1 snRNA-mediated gene therapeutic correction of splice defects caused by an exceptionally mild BBS mutation
Fabian Schmid, Esther Glaus, Daniel Barthelmes, et al.
Plant Physiology
|
September 30, 2015
Floral Induction in Arabidopsis by FLOWERING LOCUS T Requires Direct Repression of BLADE-ON-PETIOLE Genes by the Homeodomain Protein PENNYWISE
Fernando Andrés, Maida Romera-Branchat, Rafael Martínez-Gallegos, et al.
American Journal of Medical Genetics. Part A
|
October 13, 2020
Ultra-rapid emergency genomic diagnosis of Donahue syndrome in a preterm infant within 17 hours
Daniel Bamborschke, Özkan Özdemir, Mona Kreutzer, et al.
Page
of 52