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The Journal of Clinical Endocrinology and Metabolism
|
November 11, 2014
Exome sequencing for the diagnosis of 46,XY disorders of sex development
Ruth M Baxter, Valerie A Arboleda, Hane Lee, et al.
Human Molecular Genetics
|
June 2, 2022
RABENOSYN separation-of-function mutations uncouple endosomal recycling from lysosomal degradation, causing a distinct Mendelian disorder
Franziska Paul, Calista Ng, Umar Bin Mohamad Sahari, et al.
Geroscience
|
May 16, 2024
Lifespan effects in male UM-HET3 mice treated with sodium thiosulfate, 16-hydroxyestriol, and late-start canagliflozin
Richard A Miller, David E Harrison, Gino A Cortopassi, et al.
Neurology. Genetics
|
August 6, 2020
Congenital myasthenic syndrome caused by a frameshift insertion mutation in <i>GFPT1</i>
Szabolcs Szelinger, Jonida Krate, Keri Ramsey, et al.
Science Advances
|
January 19, 2022
Loss of IRF2BPL impairs neuronal maintenance through excess Wnt signaling
Paul C Marcogliese, Debdeep Dutta, Shrestha Sinha Ray, et al.
Cilia
|
April 13, 2016
A novel ICK mutation causes ciliary disruption and lethal endocrine-cerebro-osteodysplasia syndrome
Machteld M Oud, Carine Bonnard, Dorus A Mans, et al.
The Journal of Trauma and Acute Care Surgery
|
October 22, 2015
The found down patient: A Western Trauma Association multicenter study
Benjamin M Howard, Lucy Z Kornblith, Amanda S Conroy, et al.
Cell Metabolism
|
May 28, 2013
EGFR mutation-induced alternative splicing of Max contributes to growth of glycolytic tumors in brain cancer
Ivan Babic, Erik S Anderson, Kazuhiro Tanaka, et al.
Journal of Neuroscience Research
|
August 28, 2007
Maternal embryonic leucine zipper kinase is a key regulator of the proliferation of malignant brain tumors, including brain tumor stem cells
Ichiro Nakano, Michael Masterman-Smith, Kuniyasu Saigusa, et al.
JAMA
|
October 19, 2014
Clinical exome sequencing for genetic identification of rare Mendelian disorders
Hane Lee, Joshua L Deignan, Naghmeh Dorrani, et al.
Page
of 84
Search research articles
Search
Showing results (761-770 of 835) with videos related to
Sort By:
Page
of 84
The Journal of Clinical Endocrinology and Metabolism
|
November 11, 2014
Exome sequencing for the diagnosis of 46,XY disorders of sex development
Ruth M Baxter, Valerie A Arboleda, Hane Lee, et al.
Human Molecular Genetics
|
June 2, 2022
RABENOSYN separation-of-function mutations uncouple endosomal recycling from lysosomal degradation, causing a distinct Mendelian disorder
Franziska Paul, Calista Ng, Umar Bin Mohamad Sahari, et al.
Geroscience
|
May 16, 2024
Lifespan effects in male UM-HET3 mice treated with sodium thiosulfate, 16-hydroxyestriol, and late-start canagliflozin
Richard A Miller, David E Harrison, Gino A Cortopassi, et al.
Neurology. Genetics
|
August 6, 2020
Congenital myasthenic syndrome caused by a frameshift insertion mutation in <i>GFPT1</i>
Szabolcs Szelinger, Jonida Krate, Keri Ramsey, et al.
Science Advances
|
January 19, 2022
Loss of IRF2BPL impairs neuronal maintenance through excess Wnt signaling
Paul C Marcogliese, Debdeep Dutta, Shrestha Sinha Ray, et al.
Cilia
|
April 13, 2016
A novel ICK mutation causes ciliary disruption and lethal endocrine-cerebro-osteodysplasia syndrome
Machteld M Oud, Carine Bonnard, Dorus A Mans, et al.
The Journal of Trauma and Acute Care Surgery
|
October 22, 2015
The found down patient: A Western Trauma Association multicenter study
Benjamin M Howard, Lucy Z Kornblith, Amanda S Conroy, et al.
Cell Metabolism
|
May 28, 2013
EGFR mutation-induced alternative splicing of Max contributes to growth of glycolytic tumors in brain cancer
Ivan Babic, Erik S Anderson, Kazuhiro Tanaka, et al.
Journal of Neuroscience Research
|
August 28, 2007
Maternal embryonic leucine zipper kinase is a key regulator of the proliferation of malignant brain tumors, including brain tumor stem cells
Ichiro Nakano, Michael Masterman-Smith, Kuniyasu Saigusa, et al.
JAMA
|
October 19, 2014
Clinical exome sequencing for genetic identification of rare Mendelian disorders
Hane Lee, Joshua L Deignan, Naghmeh Dorrani, et al.
Page
of 84