Search research articles
Contact Us
Filters
Showing results (31-40 of 77) with videos related to
Page
of 8
Sort By:
European Journal of Human Genetics : EJHG
|
November 27, 2008
Interstitial deletion of 6q25.2-q25.3: a novel microdeletion syndrome associated with microcephaly, developmental delay, dysmorphic features and hearing loss
Sandesh Chakravarthy Sreenath Nagamani, Ayelet Erez, Christine Eng, et al.
European Journal of Human Genetics : EJHG
|
August 9, 2012
Detection of copy-number variation in AUTS2 gene by targeted exonic array CGH in patients with developmental delay and autistic spectrum disorders
Sandesh C S Nagamani, Ayelet Erez, Bruria Ben-Zeev, et al.
Molecular Genetics and Metabolism
|
October 9, 2012
A randomized controlled trial to evaluate the effects of high-dose versus low-dose of arginine therapy on hepatic function tests in argininosuccinic aciduria
Sandesh C S Nagamani, Oleg A Shchelochkov, Mary A Mullins, et al.
Nature Communications
|
December 5, 2018
MTCH2-mediated mitochondrial fusion drives exit from naïve pluripotency in embryonic stem cells
Amir Bahat, Andres Goldman, Yehudit Zaltsman, et al.
Neurogenetics
|
May 28, 2009
Alu-specific microhomology-mediated deletions in CDKL5 in females with early-onset seizure disorder
Ayelet Erez, Amina J Patel, Xueqing Wang, et al.
Neurogenetics
|
August 15, 2012
Small genomic rearrangements involving FMR1 support the importance of its gene dosage for normal neurocognitive function
Sandesh C S Nagamani, Ayelet Erez, Frank J Probst, et al.
Oncogene
|
April 27, 2004
Sil overexpression in lung cancer characterizes tumors with increased mitotic activity
Ayelet Erez, Marina Perelman, Stephen M Hewitt, et al.
Oncogene
|
August 30, 2019
The mitochondrial carrier Citrin plays a role in regulating cellular energy during carcinogenesis
Shiran Rabinovich, Alon Silberman, Lital Adler, et al.
Cell Reports
|
November 21, 2019
ASL Metabolically Regulates Tyrosine Hydroxylase in the Nucleus Locus Coeruleus
Shaul Lerner, Elmira Anderzhanova, Sima Verbitsky, et al.
Human Molecular Genetics
|
November 25, 2010
Phenylbutyrate therapy for maple syrup urine disease
Nicola Brunetti-Pierri, Brendan Lanpher, Ayelet Erez, et al.
Page
of 8
Search research articles
Search
Showing results (31-40 of 77) with videos related to
Sort By:
Page
of 8
European Journal of Human Genetics : EJHG
|
November 27, 2008
Interstitial deletion of 6q25.2-q25.3: a novel microdeletion syndrome associated with microcephaly, developmental delay, dysmorphic features and hearing loss
Sandesh Chakravarthy Sreenath Nagamani, Ayelet Erez, Christine Eng, et al.
European Journal of Human Genetics : EJHG
|
August 9, 2012
Detection of copy-number variation in AUTS2 gene by targeted exonic array CGH in patients with developmental delay and autistic spectrum disorders
Sandesh C S Nagamani, Ayelet Erez, Bruria Ben-Zeev, et al.
Molecular Genetics and Metabolism
|
October 9, 2012
A randomized controlled trial to evaluate the effects of high-dose versus low-dose of arginine therapy on hepatic function tests in argininosuccinic aciduria
Sandesh C S Nagamani, Oleg A Shchelochkov, Mary A Mullins, et al.
Nature Communications
|
December 5, 2018
MTCH2-mediated mitochondrial fusion drives exit from naïve pluripotency in embryonic stem cells
Amir Bahat, Andres Goldman, Yehudit Zaltsman, et al.
Neurogenetics
|
May 28, 2009
Alu-specific microhomology-mediated deletions in CDKL5 in females with early-onset seizure disorder
Ayelet Erez, Amina J Patel, Xueqing Wang, et al.
Neurogenetics
|
August 15, 2012
Small genomic rearrangements involving FMR1 support the importance of its gene dosage for normal neurocognitive function
Sandesh C S Nagamani, Ayelet Erez, Frank J Probst, et al.
Oncogene
|
April 27, 2004
Sil overexpression in lung cancer characterizes tumors with increased mitotic activity
Ayelet Erez, Marina Perelman, Stephen M Hewitt, et al.
Oncogene
|
August 30, 2019
The mitochondrial carrier Citrin plays a role in regulating cellular energy during carcinogenesis
Shiran Rabinovich, Alon Silberman, Lital Adler, et al.
Cell Reports
|
November 21, 2019
ASL Metabolically Regulates Tyrosine Hydroxylase in the Nucleus Locus Coeruleus
Shaul Lerner, Elmira Anderzhanova, Sima Verbitsky, et al.
Human Molecular Genetics
|
November 25, 2010
Phenylbutyrate therapy for maple syrup urine disease
Nicola Brunetti-Pierri, Brendan Lanpher, Ayelet Erez, et al.
Page
of 8