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Sigmar Stricker

Showing results (31-40 of 79) with videos related to

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Journal of Medical Genetics|May 28, 2013
Whole exome sequencing identifies FGF16 nonsense mutations as the cause of X-linked recessive metacarpal 4/5 fusionAleksander Jamsheer, Tomasz Zemojtel, Mateusz Kolanczyk, et al.
Development (Cambridge, England)|March 8, 2018
Genome-wide strategies identify downstream target genes of chick connective tissue-associated transcription factorsMickael Orgeur, Marvin Martens, Georgeta Leonte, et al.
Journal of Medical Genetics|June 22, 2012
Microduplications upstream of MSX2 are associated with a phenocopy of cleidocranial dysplasiaClaus Eric Ott, Hendrikje Hein, Silke Lohan, et al.
Stem Cell Research|August 28, 2018
Odd skipped-related 1 (Osr1) identifies muscle-interstitial fibro-adipogenic progenitors (FAPs) activated by acute injuryJürgen Stumm, Pedro Vallecillo-García, Sophie Vom Hofe-Schneider, et al.
Scientific Reports|August 20, 2017
IRS4, a novel modulator of BMP/Smad and Akt signalling during early muscle differentiationGina Dörpholz, Arunima Murgai, Jerome Jatzlau, et al.
FEBS Letters|December 29, 2005
Mammalian mitochondrial nitric oxide synthase: characterization of a novel candidateTomasz Zemojtel, Mateusz Kolanczyk, Nadine Kossler, et al.
Human Molecular Genetics|August 31, 2004
A molecular pathogenesis for transcription factor associated poly-alanine tract expansionsAndrea N Albrecht, Uwe Kornak, Annett Böddrich, et al.
Human Molecular Genetics|December 18, 2009
A cis-regulatory site downregulates PTHLH in translocation t(8;12)(q13;p11.2) and leads to Brachydactyly Type EPhilipp G Maass, Jutta Wirth, Atakan Aydin, et al.
The Journal of Clinical Investigation|October 25, 2012
A misplaced lncRNA causes brachydactyly in humansPhilipp G Maass, Andreas Rump, Herbert Schulz, et al.
Development (Cambridge, England)|September 2, 2024
Mesenchymal Osr1+ cells regulate embryonic lymphatic vessel formationPedro Vallecillo-García, Mira Nicola Kühnlein, Mickael Orgeur, et al.
Pageof 8

Showing results (31-40 of 79) with videos related to

Sort By:
Pageof 8
Journal of Medical Genetics|May 28, 2013
Whole exome sequencing identifies FGF16 nonsense mutations as the cause of X-linked recessive metacarpal 4/5 fusionAleksander Jamsheer, Tomasz Zemojtel, Mateusz Kolanczyk, et al.
Development (Cambridge, England)|March 8, 2018
Genome-wide strategies identify downstream target genes of chick connective tissue-associated transcription factorsMickael Orgeur, Marvin Martens, Georgeta Leonte, et al.
Journal of Medical Genetics|June 22, 2012
Microduplications upstream of MSX2 are associated with a phenocopy of cleidocranial dysplasiaClaus Eric Ott, Hendrikje Hein, Silke Lohan, et al.
Stem Cell Research|August 28, 2018
Odd skipped-related 1 (Osr1) identifies muscle-interstitial fibro-adipogenic progenitors (FAPs) activated by acute injuryJürgen Stumm, Pedro Vallecillo-García, Sophie Vom Hofe-Schneider, et al.
Scientific Reports|August 20, 2017
IRS4, a novel modulator of BMP/Smad and Akt signalling during early muscle differentiationGina Dörpholz, Arunima Murgai, Jerome Jatzlau, et al.
FEBS Letters|December 29, 2005
Mammalian mitochondrial nitric oxide synthase: characterization of a novel candidateTomasz Zemojtel, Mateusz Kolanczyk, Nadine Kossler, et al.
Human Molecular Genetics|August 31, 2004
A molecular pathogenesis for transcription factor associated poly-alanine tract expansionsAndrea N Albrecht, Uwe Kornak, Annett Böddrich, et al.
Human Molecular Genetics|December 18, 2009
A cis-regulatory site downregulates PTHLH in translocation t(8;12)(q13;p11.2) and leads to Brachydactyly Type EPhilipp G Maass, Jutta Wirth, Atakan Aydin, et al.
The Journal of Clinical Investigation|October 25, 2012
A misplaced lncRNA causes brachydactyly in humansPhilipp G Maass, Andreas Rump, Herbert Schulz, et al.
Development (Cambridge, England)|September 2, 2024
Mesenchymal Osr1+ cells regulate embryonic lymphatic vessel formationPedro Vallecillo-García, Mira Nicola Kühnlein, Mickael Orgeur, et al.
Pageof 8