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Brain : a Journal of Neurology
|
June 26, 2018
Intronic pentanucleotide TTTCA repeat insertion in the SAMD12 gene causes familial cortical myoclonic tremor with epilepsy type 1
Zhidong Cen, Zhengwen Jiang, You Chen, et al.
Science China. Life Sciences
|
February 3, 2026
Deficiency of primate-specific TFDP3 causes male infertility with oligoasthenoteratozoospermia in humans and cynomolgus monkeys
Chunyu Liu, Chaofeng Tu, Peng Li, et al.
Frontiers in Genetics
|
November 3, 2017
Exome-Wide Meta-Analysis Identifies Rare 3'-UTR Variant in ERCC1/CD3EAP Associated with Symptoms of Sleep Apnea
Ashley van der Spek, Annemarie I Luik, Desana Kocevska, et al.
Environmental Pollution (Barking, Essex : 1987)
|
July 13, 2023
Smoking, blood DNA methylation sites and lung cancer risk
Arce Domingo-Relloso, Roby Joehanes, Zulema Rodriguez-Hernandez, et al.
Kidney International Reports
|
December 19, 2024
CFAP47 is Implicated in X-Linked Polycystic Kidney Disease
Takayasu Mori, Takuya Fujimaru, Chunyu Liu, et al.
The Open Medicinal Chemistry Journal
|
September 25, 2014
Synthesis and Biological Evaluation of Macrocyclized Betulin Derivatives as a Novel Class of Anti-HIV-1 Maturation Inhibitors
Jun Tang, Stacey A Jones, Jerry L Jeffery, et al.
International Journal of Biological Sciences
|
January 12, 2023
Novel <i>FSIP2</i> Variants Induce Super-Length Mitochondrial Sheath and Asthenoteratozoospermia in Humans
Mingrong Lv, Dongdong Tang, Hui Yu, et al.
Science Bulletin
|
April 18, 2024
Diagnostic and prognostic performance of artificial intelligence-based fully-automated on-site CT-FFR in patients with CAD
Bangjun Guo, Mengchun Jiang, Xiang Guo, et al.
Molecular Genetics and Genomics : MGG
|
August 24, 2022
NGS-driven molecular diagnosis of heterogeneous hereditary neurological disorders reveals novel and known variants in disease-causing genes
Ayaz Khan, Shixiong Tian, Muhammad Tariq, et al.
American Journal of Medical Genetics. Part A
|
October 26, 2021
A recurrent rare intronic variant in CAPN3 alters mRNA splicing and causes autosomal recessive limb-girdle muscular dystrophy-1 in three Pakistani pedigrees
Kamal Khan, Sarmad Mehmood, Chunyu Liu, et al.
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Search research articles
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Showing results (621-630 of 749) with videos related to
Sort By:
Page
of 75
Brain : a Journal of Neurology
|
June 26, 2018
Intronic pentanucleotide TTTCA repeat insertion in the SAMD12 gene causes familial cortical myoclonic tremor with epilepsy type 1
Zhidong Cen, Zhengwen Jiang, You Chen, et al.
Science China. Life Sciences
|
February 3, 2026
Deficiency of primate-specific TFDP3 causes male infertility with oligoasthenoteratozoospermia in humans and cynomolgus monkeys
Chunyu Liu, Chaofeng Tu, Peng Li, et al.
Frontiers in Genetics
|
November 3, 2017
Exome-Wide Meta-Analysis Identifies Rare 3'-UTR Variant in ERCC1/CD3EAP Associated with Symptoms of Sleep Apnea
Ashley van der Spek, Annemarie I Luik, Desana Kocevska, et al.
Environmental Pollution (Barking, Essex : 1987)
|
July 13, 2023
Smoking, blood DNA methylation sites and lung cancer risk
Arce Domingo-Relloso, Roby Joehanes, Zulema Rodriguez-Hernandez, et al.
Kidney International Reports
|
December 19, 2024
CFAP47 is Implicated in X-Linked Polycystic Kidney Disease
Takayasu Mori, Takuya Fujimaru, Chunyu Liu, et al.
The Open Medicinal Chemistry Journal
|
September 25, 2014
Synthesis and Biological Evaluation of Macrocyclized Betulin Derivatives as a Novel Class of Anti-HIV-1 Maturation Inhibitors
Jun Tang, Stacey A Jones, Jerry L Jeffery, et al.
International Journal of Biological Sciences
|
January 12, 2023
Novel <i>FSIP2</i> Variants Induce Super-Length Mitochondrial Sheath and Asthenoteratozoospermia in Humans
Mingrong Lv, Dongdong Tang, Hui Yu, et al.
Science Bulletin
|
April 18, 2024
Diagnostic and prognostic performance of artificial intelligence-based fully-automated on-site CT-FFR in patients with CAD
Bangjun Guo, Mengchun Jiang, Xiang Guo, et al.
Molecular Genetics and Genomics : MGG
|
August 24, 2022
NGS-driven molecular diagnosis of heterogeneous hereditary neurological disorders reveals novel and known variants in disease-causing genes
Ayaz Khan, Shixiong Tian, Muhammad Tariq, et al.
American Journal of Medical Genetics. Part A
|
October 26, 2021
A recurrent rare intronic variant in CAPN3 alters mRNA splicing and causes autosomal recessive limb-girdle muscular dystrophy-1 in three Pakistani pedigrees
Kamal Khan, Sarmad Mehmood, Chunyu Liu, et al.
Page
of 75