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Nature Communications
|
December 4, 2018
Tumour-elicited neutrophils engage mitochondrial metabolism to circumvent nutrient limitations and maintain immune suppression
Christopher M Rice, Luke C Davies, Jeff J Subleski, et al.
American Journal of Human Genetics
|
July 10, 2012
HOXB1 founder mutation in humans recapitulates the phenotype of Hoxb1-/- mice
Bryn D Webb, Sherin Shaaban, Harald Gaspar, et al.
Human Reproduction (Oxford, England)
|
December 17, 2020
Harmonizing research outcomes for polycystic ovary syndrome (HARP), a marathon not a sprint: current challenges and future research need
Bassel H Al Wattar, Aurora Bueno, Miguel Garcia Martin, et al.
BMC Genetics
|
May 22, 2007
Three novel mutations in KIF21A highlight the importance of the third coiled-coil stalk domain in the etiology of CFEOM1
Wai-Man Chan, Caroline Andrews, Laryssa Dragan, et al.
Brain : a Journal of Neurology
|
February 5, 2013
A novel syndrome caused by the E410K amino acid substitution in the neuronal β-tubulin isotype 3
Sheena Chew, Ravikumar Balasubramanian, Wai-Man Chan, et al.
Investigative Ophthalmology & Visual Science
|
August 12, 2018
Genome-Wide Association Study Identifies a Susceptibility Locus for Comitant Esotropia and Suggests a Parent-of-Origin Effect
Sherin Shaaban, Sarah MacKinnon, Caroline Andrews, et al.
Topics in Cognitive Science
|
May 27, 2026
Exploring Amazonian Cognitive Diversity at Chana Research Station
Mariana Poblete, Caroline Andrews, Balthasar Bickel, et al.
NPJ Genomic Medicine
|
November 24, 2024
Germline sequence variation in cancer genes in Rwandan breast and prostate cancer cases
Achille Vc Manirakiza, Shakuntala Baichoo, Annette Uwineza, et al.
Science (New York, N.Y.)
|
July 26, 2008
Human CHN1 mutations hyperactivate alpha2-chimaerin and cause Duane's retraction syndrome
Noriko Miyake, John Chilton, Maria Psatha, et al.
HGG Advances
|
March 26, 2025
Uncovering the genetic architecture and evolutionary roots of androgenetic alopecia in African men
Rohini Janivara, Ujani Hazra, Aaron Pfennig, et al.
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of 9
Search research articles
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Showing results (51-60 of 83) with videos related to
Sort By:
Page
of 9
Nature Communications
|
December 4, 2018
Tumour-elicited neutrophils engage mitochondrial metabolism to circumvent nutrient limitations and maintain immune suppression
Christopher M Rice, Luke C Davies, Jeff J Subleski, et al.
American Journal of Human Genetics
|
July 10, 2012
HOXB1 founder mutation in humans recapitulates the phenotype of Hoxb1-/- mice
Bryn D Webb, Sherin Shaaban, Harald Gaspar, et al.
Human Reproduction (Oxford, England)
|
December 17, 2020
Harmonizing research outcomes for polycystic ovary syndrome (HARP), a marathon not a sprint: current challenges and future research need
Bassel H Al Wattar, Aurora Bueno, Miguel Garcia Martin, et al.
BMC Genetics
|
May 22, 2007
Three novel mutations in KIF21A highlight the importance of the third coiled-coil stalk domain in the etiology of CFEOM1
Wai-Man Chan, Caroline Andrews, Laryssa Dragan, et al.
Brain : a Journal of Neurology
|
February 5, 2013
A novel syndrome caused by the E410K amino acid substitution in the neuronal β-tubulin isotype 3
Sheena Chew, Ravikumar Balasubramanian, Wai-Man Chan, et al.
Investigative Ophthalmology & Visual Science
|
August 12, 2018
Genome-Wide Association Study Identifies a Susceptibility Locus for Comitant Esotropia and Suggests a Parent-of-Origin Effect
Sherin Shaaban, Sarah MacKinnon, Caroline Andrews, et al.
Topics in Cognitive Science
|
May 27, 2026
Exploring Amazonian Cognitive Diversity at Chana Research Station
Mariana Poblete, Caroline Andrews, Balthasar Bickel, et al.
NPJ Genomic Medicine
|
November 24, 2024
Germline sequence variation in cancer genes in Rwandan breast and prostate cancer cases
Achille Vc Manirakiza, Shakuntala Baichoo, Annette Uwineza, et al.
Science (New York, N.Y.)
|
July 26, 2008
Human CHN1 mutations hyperactivate alpha2-chimaerin and cause Duane's retraction syndrome
Noriko Miyake, John Chilton, Maria Psatha, et al.
HGG Advances
|
March 26, 2025
Uncovering the genetic architecture and evolutionary roots of androgenetic alopecia in African men
Rohini Janivara, Ujani Hazra, Aaron Pfennig, et al.
Page
of 9