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J Justice

Showing results (121-130 of 299) with videos related to

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Disease Models & Mechanisms|December 15, 2019
From blood development to disease: a paradigm for clinical translationMonica J Justice, Julija Hmeljak, Vijay G Sankaran, et al.
Disease Models & Mechanisms|July 10, 2024
Translating multiscale research in rare diseaseKirsty M Hooper, Monica J Justice, Monkol Lek, et al.
American Journal of Ophthalmology|April 1, 1980
Variable expressivity in autosomal dominant aniridia by clinical, electrophysiologic, and angiographic criteriaH M Hittner, V M Riccardi, R E Ferrell, et al.
Genesis (New York, N.Y. : 2000)|February 14, 2006
Visceral endoderm function is regulated by quaking and required for vascular developmentBrenda L Bohnsack, Lihua Lai, Jennifer L Northrop, et al.
Blood|September 11, 2008
hem6: an ENU-induced recessive hypochromic microcytic anemia mutation in the mouseMeng Tian, Dean R Campagna, Lanette S Woodward, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|December 1, 1975
Dominant cone-rod dystrophyH M Hittner, A L Murphree, C A Garcia, et al.
Molecular and Cellular Endocrinology|February 15, 2012
Cell-type specific modulation of pituitary cells by activin, inhibin and follistatinLouise M Bilezikjian, Nicholas J Justice, Alissa N Blackler, et al.
Biology Open|April 24, 2016
PRDM14 promotes RAG-dependent Notch1 driver mutations in mouse T-ALLBrandi L Carofino, Bernard Ayanga, Lauren J Tracey, et al.
Genomics|September 19, 1998
Keratocan (Kera), a corneal keratan sulfate proteoglycan, maps to the distal end of mouse chromosome 10J L Funderburgh, A L Perchellet, J Swiergiel, et al.
Genomics|January 15, 1997
Comparative mapping in the beige-satin region of mouse chromosome 13C M Perou, A Perchellet, T Jago, et al.
Pageof 30

Showing results (121-130 of 299) with videos related to

Sort By:
Pageof 30
Disease Models & Mechanisms|December 15, 2019
From blood development to disease: a paradigm for clinical translationMonica J Justice, Julija Hmeljak, Vijay G Sankaran, et al.
Disease Models & Mechanisms|July 10, 2024
Translating multiscale research in rare diseaseKirsty M Hooper, Monica J Justice, Monkol Lek, et al.
American Journal of Ophthalmology|April 1, 1980
Variable expressivity in autosomal dominant aniridia by clinical, electrophysiologic, and angiographic criteriaH M Hittner, V M Riccardi, R E Ferrell, et al.
Genesis (New York, N.Y. : 2000)|February 14, 2006
Visceral endoderm function is regulated by quaking and required for vascular developmentBrenda L Bohnsack, Lihua Lai, Jennifer L Northrop, et al.
Blood|September 11, 2008
hem6: an ENU-induced recessive hypochromic microcytic anemia mutation in the mouseMeng Tian, Dean R Campagna, Lanette S Woodward, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|December 1, 1975
Dominant cone-rod dystrophyH M Hittner, A L Murphree, C A Garcia, et al.
Molecular and Cellular Endocrinology|February 15, 2012
Cell-type specific modulation of pituitary cells by activin, inhibin and follistatinLouise M Bilezikjian, Nicholas J Justice, Alissa N Blackler, et al.
Biology Open|April 24, 2016
PRDM14 promotes RAG-dependent Notch1 driver mutations in mouse T-ALLBrandi L Carofino, Bernard Ayanga, Lauren J Tracey, et al.
Genomics|September 19, 1998
Keratocan (Kera), a corneal keratan sulfate proteoglycan, maps to the distal end of mouse chromosome 10J L Funderburgh, A L Perchellet, J Swiergiel, et al.
Genomics|January 15, 1997
Comparative mapping in the beige-satin region of mouse chromosome 13C M Perou, A Perchellet, T Jago, et al.
Pageof 30