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S Mundlos

Showing results (61-70 of 94) with videos related to

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Human Molecular Genetics|January 1, 1995
Genetic mapping of cleidocranial dysplasia and evidence of a microdeletion in one familyS Mundlos, J B Mulliken, D L Abramson, et al.
Journal of Medical Genetics|July 15, 2005
A mutation in the receptor binding site of GDF5 causes Mohr-Wriedt brachydactyly type A2K W Kjaer, H Eiberg, L Hansen, et al.
Translational Stroke Research|September 16, 2021
The Genetic Basis of Moyamoya DiseaseR Mertens, M Graupera, H Gerhardt, et al.
Journal of Structural Biology|August 23, 2011
Fetal and postnatal mouse bone tissue contains more calcium than is present in hydroxyapatiteC Lange, C Li, I Manjubala, et al.
Journal of Medical Genetics|April 5, 2005
A homozygous BMPR1B mutation causes a new subtype of acromesomelic chondrodysplasia with genital anomaliesO Demirhan, S Türkmen, G C Schwabe, et al.
Developmental and Comparative Immunology|June 12, 2003
A single amphioxus and sea urchin runt-gene suggests that runt-gene duplications occurred in early chordate evolutionS Stricker, A J Poustka, U Wiecha, et al.
The British Journal of Dermatology|December 6, 2012
Whole-exome sequencing identifies a novel missense mutation in EDAR causing autosomal recessive hypohidrotic ectodermal dysplasia with bilateral amastia and palmoplantar hyperkeratosisA Haghighi, P Nikuei, H Haghighi-Kakhki, et al.
Bone|August 8, 2012
Deterioration of fracture healing in the mouse model of NF1 long bone dysplasiaT El Khassawna, D Toben, M Kolanczyk, et al.
Aging Cell|September 5, 2024
Targeting TGF-β signaling, oxidative stress, and cellular senescence rescues osteoporosis in gerodermia osteodysplasticaW L Chan, C H Bucher, J Goldes, et al.
Kidney International|August 17, 2006
A complex phenotype with cystic renal diseaseD Müller, E Klopocki, L M Neumann, et al.
Pageof 10

Showing results (61-70 of 94) with videos related to

Sort By:
Pageof 10
Human Molecular Genetics|January 1, 1995
Genetic mapping of cleidocranial dysplasia and evidence of a microdeletion in one familyS Mundlos, J B Mulliken, D L Abramson, et al.
Journal of Medical Genetics|July 15, 2005
A mutation in the receptor binding site of GDF5 causes Mohr-Wriedt brachydactyly type A2K W Kjaer, H Eiberg, L Hansen, et al.
Translational Stroke Research|September 16, 2021
The Genetic Basis of Moyamoya DiseaseR Mertens, M Graupera, H Gerhardt, et al.
Journal of Structural Biology|August 23, 2011
Fetal and postnatal mouse bone tissue contains more calcium than is present in hydroxyapatiteC Lange, C Li, I Manjubala, et al.
Journal of Medical Genetics|April 5, 2005
A homozygous BMPR1B mutation causes a new subtype of acromesomelic chondrodysplasia with genital anomaliesO Demirhan, S Türkmen, G C Schwabe, et al.
Developmental and Comparative Immunology|June 12, 2003
A single amphioxus and sea urchin runt-gene suggests that runt-gene duplications occurred in early chordate evolutionS Stricker, A J Poustka, U Wiecha, et al.
The British Journal of Dermatology|December 6, 2012
Whole-exome sequencing identifies a novel missense mutation in EDAR causing autosomal recessive hypohidrotic ectodermal dysplasia with bilateral amastia and palmoplantar hyperkeratosisA Haghighi, P Nikuei, H Haghighi-Kakhki, et al.
Bone|August 8, 2012
Deterioration of fracture healing in the mouse model of NF1 long bone dysplasiaT El Khassawna, D Toben, M Kolanczyk, et al.
Aging Cell|September 5, 2024
Targeting TGF-β signaling, oxidative stress, and cellular senescence rescues osteoporosis in gerodermia osteodysplasticaW L Chan, C H Bucher, J Goldes, et al.
Kidney International|August 17, 2006
A complex phenotype with cystic renal diseaseD Müller, E Klopocki, L M Neumann, et al.
Pageof 10