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Human Molecular Genetics
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May 13, 2016
Restoration of SMN in Schwann cells reverses myelination defects and improves neuromuscular function in spinal muscular atrophy
Gillian Hunter, Rachael A Powis, Ross A Jones, et al.
Journal of Down Syndrome & Chromosome Abnormalities
|
July 14, 2017
Variation in the Zinc Finger of PRDM9 is Associated with the Absence of Recombination along Nondisjoined Chromosomes 21 of Maternal Origin
Tiffany Renee Oliver, Candace Middlebrooks, Ariel Harden, et al.
The Journal of Cell Biology
|
May 20, 2009
Integrin-mediated axoglial interactions initiate myelination in the central nervous system
Joana Câmara, Zhen Wang, Cristina Nunes-Fonseca, et al.
Neuron
|
December 13, 2005
Neurofascins are required to establish axonal domains for saltatory conduction
Diane L Sherman, Steven Tait, Shona Melrose, et al.
Human Genetics
|
January 1, 1985
Further segregation analysis of the fragile X syndrome with special reference to transmitting males
S L Sherman, P A Jacobs, N E Morton, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
April 30, 2021
Refining the risk for fragile X-associated primary ovarian insufficiency (FXPOI) by FMR1 CGG repeat size
Emily Graves Allen, Krista Charen, Heather S Hipp, et al.
Blood
|
November 5, 1997
Effects of single-dose interleukin-12 exposure on interleukin-12-associated toxicity and interferon-gamma production
J P Leonard, M L Sherman, G L Fisher, et al.
Research in Nursing & Health
|
December 18, 2001
Improving cognitive development of low-birth-weight premature infants with the COPE program: a pilot study of the benefit of early NICU intervention with mothers
B M Melnyk, L Alpert-Gillis, N F Feinstein, et al.
American Journal of Medical Genetics
|
April 1, 1992
Characterization of a highly polymorphic dinucleotide repeat 150 KB proximal to the fragile X site
G J Riggins, S L Sherman, B A Oostra, et al.
American Journal of Medical Genetics
|
February 1, 1991
Improved prenatal detection of fra(X)(q27.3): methods for prevention of false negatives in chorionic villus and amniotic fluid cell cultures
E C Jenkins, M S Krawczun, S L Stark-Houck, et al.
Page
of 94
Search research articles
Search
Showing results (781-790 of 935) with videos related to
Sort By:
Page
of 94
Human Molecular Genetics
|
May 13, 2016
Restoration of SMN in Schwann cells reverses myelination defects and improves neuromuscular function in spinal muscular atrophy
Gillian Hunter, Rachael A Powis, Ross A Jones, et al.
Journal of Down Syndrome & Chromosome Abnormalities
|
July 14, 2017
Variation in the Zinc Finger of PRDM9 is Associated with the Absence of Recombination along Nondisjoined Chromosomes 21 of Maternal Origin
Tiffany Renee Oliver, Candace Middlebrooks, Ariel Harden, et al.
The Journal of Cell Biology
|
May 20, 2009
Integrin-mediated axoglial interactions initiate myelination in the central nervous system
Joana Câmara, Zhen Wang, Cristina Nunes-Fonseca, et al.
Neuron
|
December 13, 2005
Neurofascins are required to establish axonal domains for saltatory conduction
Diane L Sherman, Steven Tait, Shona Melrose, et al.
Human Genetics
|
January 1, 1985
Further segregation analysis of the fragile X syndrome with special reference to transmitting males
S L Sherman, P A Jacobs, N E Morton, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
April 30, 2021
Refining the risk for fragile X-associated primary ovarian insufficiency (FXPOI) by FMR1 CGG repeat size
Emily Graves Allen, Krista Charen, Heather S Hipp, et al.
Blood
|
November 5, 1997
Effects of single-dose interleukin-12 exposure on interleukin-12-associated toxicity and interferon-gamma production
J P Leonard, M L Sherman, G L Fisher, et al.
Research in Nursing & Health
|
December 18, 2001
Improving cognitive development of low-birth-weight premature infants with the COPE program: a pilot study of the benefit of early NICU intervention with mothers
B M Melnyk, L Alpert-Gillis, N F Feinstein, et al.
American Journal of Medical Genetics
|
April 1, 1992
Characterization of a highly polymorphic dinucleotide repeat 150 KB proximal to the fragile X site
G J Riggins, S L Sherman, B A Oostra, et al.
American Journal of Medical Genetics
|
February 1, 1991
Improved prenatal detection of fra(X)(q27.3): methods for prevention of false negatives in chorionic villus and amniotic fluid cell cultures
E C Jenkins, M S Krawczun, S L Stark-Houck, et al.
Page
of 94