Search research articles
Contact Us
Filters
Showing results (81-90 of 96) with videos related to
Page
of 10
Sort By:
British Journal of Cancer
|
July 13, 2021
Transcriptome profiles of stem-like cells from primary breast cancers allow identification of ITGA7 as a predictive marker of chemotherapy response
Noha Gwili, Stacey J Jones, Waleed Al Amri, et al.
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.
Plos One
|
April 8, 2017
A tubulin alpha 8 mouse knockout model indicates a likely role in spermatogenesis but not in brain development
Christine P Diggle, Isabel Martinez-Garay, Zoltan Molnar, 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
|
November 3, 2018
Biallelic Mutations in LRRC56, Encoding a Protein Associated with Intraflagellar Transport, Cause Mucociliary Clearance and Laterality Defects
Serge Bonnefoy, Christopher M Watson, Kristin D Kernohan, 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.
Nature Genetics
|
November 22, 2011
Mutations in MEGF10, a regulator of satellite cell myogenesis, cause early onset myopathy, areflexia, respiratory distress and dysphagia (EMARDD)
Clare V Logan, Barbara Lucke, Caroline Pottinger, et al.
Plos Genetics
|
September 19, 2014
HEATR2 plays a conserved role in assembly of the ciliary motile apparatus
Christine P Diggle, Daniel J Moore, Girish Mali, 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.
American Journal of Human Genetics
|
December 3, 2013
Recessive mutations in SLC38A8 cause foveal hypoplasia and optic nerve misrouting without albinism
James A Poulter, Musallam Al-Araimi, Ivan Conte, et al.
Page
of 10
Search research articles
Search
Showing results (81-90 of 96) with videos related to
Sort By:
Page
of 10
British Journal of Cancer
|
July 13, 2021
Transcriptome profiles of stem-like cells from primary breast cancers allow identification of ITGA7 as a predictive marker of chemotherapy response
Noha Gwili, Stacey J Jones, Waleed Al Amri, et al.
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.
Plos One
|
April 8, 2017
A tubulin alpha 8 mouse knockout model indicates a likely role in spermatogenesis but not in brain development
Christine P Diggle, Isabel Martinez-Garay, Zoltan Molnar, 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
|
November 3, 2018
Biallelic Mutations in LRRC56, Encoding a Protein Associated with Intraflagellar Transport, Cause Mucociliary Clearance and Laterality Defects
Serge Bonnefoy, Christopher M Watson, Kristin D Kernohan, 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.
Nature Genetics
|
November 22, 2011
Mutations in MEGF10, a regulator of satellite cell myogenesis, cause early onset myopathy, areflexia, respiratory distress and dysphagia (EMARDD)
Clare V Logan, Barbara Lucke, Caroline Pottinger, et al.
Plos Genetics
|
September 19, 2014
HEATR2 plays a conserved role in assembly of the ciliary motile apparatus
Christine P Diggle, Daniel J Moore, Girish Mali, 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.
American Journal of Human Genetics
|
December 3, 2013
Recessive mutations in SLC38A8 cause foveal hypoplasia and optic nerve misrouting without albinism
James A Poulter, Musallam Al-Araimi, Ivan Conte, et al.
Page
of 10