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Muhammad Arshad

Showing results (721-730 of 731) with videos related to

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Human Molecular Genetics|February 22, 2015
Mutations in DCPS and EDC3 in autosomal recessive intellectual disability indicate a crucial role for mRNA decapping in neurodevelopmentIltaf Ahmed, Rebecca Buchert, Mi Zhou, et al.
American Journal of Human Genetics|December 7, 2014
Biallelic truncating mutations in FMN2, encoding the actin-regulatory protein Formin 2, cause nonsyndromic autosomal-recessive intellectual disabilityRosalind Law, Tracy Dixon-Salazar, Julie Jerber, et al.
American Journal of Human Genetics|July 19, 2011
Mutations in the alpha 1,2-mannosidase gene, MAN1B1, cause autosomal-recessive intellectual disabilityMuhammad Arshad Rafiq, Andreas W Kuss, Lucia Puettmann, et al.
Annals of Surgical Oncology|May 5, 2021
Correction to: Global Forum of Cancer Surgeons: Position Statement to Promote Cancer Surgery GloballyChandrakanth Are, David L Bartlett, Aviram Nissan, et al.
Annals of Surgical Oncology|May 27, 2020
Global Forum of Cancer Surgeons: Position Statement to Promote Cancer Surgery GloballyChandrakanth Are, David L Bartlett, Aviram Nissan, et al.
BMC Medical Genetics|June 25, 2015
Novel VPS13B Mutations in Three Large Pakistani Cohen Syndrome Families Suggests a Baloch Variant with Autistic-Like FeaturesMuhammad Arshad Rafiq, Claire S Leblond, Muhammad Arif Nadeem Saqib, et al.
Human Molecular Genetics|July 25, 2015
Mutations in the histamine N-methyltransferase gene, HNMT, are associated with nonsyndromic autosomal recessive intellectual disabilityAbolfazl Heidari, Chanakan Tongsook, Reza Najafipour, et al.
Cell|May 14, 2011
Mapping the NPHP-JBTS-MKS protein network reveals ciliopathy disease genes and pathwaysLiyun Sang, Julie J Miller, Kevin C Corbit, et al.
Annals of Surgical Oncology|January 19, 2021
Global Forum of Cancer Surgeons: Support for the Brazilian Society of Surgical Oncology Journey towards Implementation of Cytoreductive Surgery/Hyperthermic Intraperitoneal Chemotherapy in BrazilAlexandre Ferreira Oliveira, Claudio Almeida Quadros, Héber Salvador de Castro Ribeiro, et al.
The Journal of Clinical Investigation|July 3, 2019
Ankyrin-B dysfunction predisposes to arrhythmogenic cardiomyopathy and is amenable to therapyJason D Roberts, Nathaniel P Murphy, Robert M Hamilton, et al.
Pageof 74

Showing results (721-730 of 731) with videos related to

Sort By:
Pageof 74
Human Molecular Genetics|February 22, 2015
Mutations in DCPS and EDC3 in autosomal recessive intellectual disability indicate a crucial role for mRNA decapping in neurodevelopmentIltaf Ahmed, Rebecca Buchert, Mi Zhou, et al.
American Journal of Human Genetics|December 7, 2014
Biallelic truncating mutations in FMN2, encoding the actin-regulatory protein Formin 2, cause nonsyndromic autosomal-recessive intellectual disabilityRosalind Law, Tracy Dixon-Salazar, Julie Jerber, et al.
American Journal of Human Genetics|July 19, 2011
Mutations in the alpha 1,2-mannosidase gene, MAN1B1, cause autosomal-recessive intellectual disabilityMuhammad Arshad Rafiq, Andreas W Kuss, Lucia Puettmann, et al.
Annals of Surgical Oncology|May 5, 2021
Correction to: Global Forum of Cancer Surgeons: Position Statement to Promote Cancer Surgery GloballyChandrakanth Are, David L Bartlett, Aviram Nissan, et al.
Annals of Surgical Oncology|May 27, 2020
Global Forum of Cancer Surgeons: Position Statement to Promote Cancer Surgery GloballyChandrakanth Are, David L Bartlett, Aviram Nissan, et al.
BMC Medical Genetics|June 25, 2015
Novel VPS13B Mutations in Three Large Pakistani Cohen Syndrome Families Suggests a Baloch Variant with Autistic-Like FeaturesMuhammad Arshad Rafiq, Claire S Leblond, Muhammad Arif Nadeem Saqib, et al.
Human Molecular Genetics|July 25, 2015
Mutations in the histamine N-methyltransferase gene, HNMT, are associated with nonsyndromic autosomal recessive intellectual disabilityAbolfazl Heidari, Chanakan Tongsook, Reza Najafipour, et al.
Cell|May 14, 2011
Mapping the NPHP-JBTS-MKS protein network reveals ciliopathy disease genes and pathwaysLiyun Sang, Julie J Miller, Kevin C Corbit, et al.
Annals of Surgical Oncology|January 19, 2021
Global Forum of Cancer Surgeons: Support for the Brazilian Society of Surgical Oncology Journey towards Implementation of Cytoreductive Surgery/Hyperthermic Intraperitoneal Chemotherapy in BrazilAlexandre Ferreira Oliveira, Claudio Almeida Quadros, Héber Salvador de Castro Ribeiro, et al.
The Journal of Clinical Investigation|July 3, 2019
Ankyrin-B dysfunction predisposes to arrhythmogenic cardiomyopathy and is amenable to therapyJason D Roberts, Nathaniel P Murphy, Robert M Hamilton, et al.
Pageof 74