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Investigative Ophthalmology & Visual Science
|
March 20, 2012
Recessive mutations in TSPAN12 cause retinal dysplasia and severe familial exudative vitreoretinopathy (FEVR)
James A Poulter, Alice E Davidson, Manir Ali, et al.
Bioorganic & Medicinal Chemistry Letters
|
December 17, 2013
Modulating the interaction between CDK2 and cyclin A with a quinoline-based inhibitor
Yongqi Deng, Gerald W Shipps, Lianyun Zhao, et al.
American Journal of Human Genetics
|
February 10, 2009
Mutations in CNNM4 cause Jalili syndrome, consisting of autosomal-recessive cone-rod dystrophy and amelogenesis imperfecta
David A Parry, Alan J Mighell, Walid El-Sayed, et al.
American Journal of Human Genetics
|
October 4, 2016
Mutations in the pH-Sensing G-protein-Coupled Receptor GPR68 Cause Amelogenesis Imperfecta
David A Parry, Claire E L Smith, Walid El-Sayed, et al.
Nature Genetics
|
November 28, 2018
Gain-of-function DNMT3A mutations cause microcephalic dwarfism and hypermethylation of Polycomb-regulated regions
Patricia Heyn, Clare V Logan, Adeline Fluteau, et al.
American Journal of Human Genetics
|
April 14, 2009
Null mutations in LTBP2 cause primary congenital glaucoma
Manir Ali, Martin McKibbin, Adam Booth, et al.
Nature Genetics
|
March 12, 2014
Mutations in TJP2 cause progressive cholestatic liver disease
Melissa Sambrotta, Sandra Strautnieks, Efterpi Papouli, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
October 25, 2012
Phase I and pharmacologic trial of cytosine arabinoside with the selective checkpoint 1 inhibitor Sch 900776 in refractory acute leukemias
Judith E Karp, Brian M Thomas, Jacqueline M Greer, et al.
Human Molecular Genetics
|
November 10, 2011
Next generation sequencing identifies mutations in Atonal homolog 7 (ATOH7) in families with global eye developmental defects
Kamron Khan, Clare V Logan, Martin McKibbin, et al.
American Journal of Human Genetics
|
August 21, 2012
Mutations in C4orf26, encoding a peptide with in vitro hydroxyapatite crystal nucleation and growth activity, cause amelogenesis imperfecta
David A Parry, Steven J Brookes, Clare V Logan, et al.
Page
of 7
Search research articles
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Showing results (31-40 of 63) with videos related to
Sort By:
Page
of 7
Investigative Ophthalmology & Visual Science
|
March 20, 2012
Recessive mutations in TSPAN12 cause retinal dysplasia and severe familial exudative vitreoretinopathy (FEVR)
James A Poulter, Alice E Davidson, Manir Ali, et al.
Bioorganic & Medicinal Chemistry Letters
|
December 17, 2013
Modulating the interaction between CDK2 and cyclin A with a quinoline-based inhibitor
Yongqi Deng, Gerald W Shipps, Lianyun Zhao, et al.
American Journal of Human Genetics
|
February 10, 2009
Mutations in CNNM4 cause Jalili syndrome, consisting of autosomal-recessive cone-rod dystrophy and amelogenesis imperfecta
David A Parry, Alan J Mighell, Walid El-Sayed, et al.
American Journal of Human Genetics
|
October 4, 2016
Mutations in the pH-Sensing G-protein-Coupled Receptor GPR68 Cause Amelogenesis Imperfecta
David A Parry, Claire E L Smith, Walid El-Sayed, et al.
Nature Genetics
|
November 28, 2018
Gain-of-function DNMT3A mutations cause microcephalic dwarfism and hypermethylation of Polycomb-regulated regions
Patricia Heyn, Clare V Logan, Adeline Fluteau, et al.
American Journal of Human Genetics
|
April 14, 2009
Null mutations in LTBP2 cause primary congenital glaucoma
Manir Ali, Martin McKibbin, Adam Booth, et al.
Nature Genetics
|
March 12, 2014
Mutations in TJP2 cause progressive cholestatic liver disease
Melissa Sambrotta, Sandra Strautnieks, Efterpi Papouli, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
October 25, 2012
Phase I and pharmacologic trial of cytosine arabinoside with the selective checkpoint 1 inhibitor Sch 900776 in refractory acute leukemias
Judith E Karp, Brian M Thomas, Jacqueline M Greer, et al.
Human Molecular Genetics
|
November 10, 2011
Next generation sequencing identifies mutations in Atonal homolog 7 (ATOH7) in families with global eye developmental defects
Kamron Khan, Clare V Logan, Martin McKibbin, et al.
American Journal of Human Genetics
|
August 21, 2012
Mutations in C4orf26, encoding a peptide with in vitro hydroxyapatite crystal nucleation and growth activity, cause amelogenesis imperfecta
David A Parry, Steven J Brookes, Clare V Logan, et al.
Page
of 7