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Journal of Experimental & Clinical Assisted Reproduction
|
August 30, 2007
Regional clinical practice patterns in reproductive endocrinology: a collaborative transnational pilot survey of in vitro fertilization programs in the Middle East
Eric Scott Sills, Hussein S Qublan, Zeev Blumenfeld, et al.
Plos Neglected Tropical Diseases
|
July 28, 2025
Field evaluation of Standard Q Filariasis Antigen Test for Lymphatic Filariasis (LF) during a pre-transmission assessment survey in Sierra Leone, 2022
Benoit Dembele, Mohamed Salieu Bah, Abdulai Conteh, et al.
Human Molecular Genetics
|
December 26, 2016
Uner Tan syndrome caused by a homozygous TUBB2B mutation affecting microtubule stability
Martin W Breuss, Thai Nguyen, Anjana Srivatsan, et al.
Biology
|
September 23, 2022
Evolution of the Family Equidae, Subfamily Equinae, in North, Central and South America, Eurasia and Africa during the Plio-Pleistocene
Omar Cirilli, Helena Machado, Joaquin Arroyo-Cabrales, et al.
Frontiers in Immunology
|
April 26, 2024
O-GlcNAc transferase regulates collagen deposition and fibrosis resolution in idiopathic pulmonary fibrosis
Shia Vang, Eric Scott Helton, Yiming Guo, et al.
Journal of Oncology Practice
|
November 2, 2011
Creating a process to standardize regimen order sets within an electronic health record
Leslie T Busby, Sheetal Sheth, Jody Garey, et al.
Scientific Reports
|
July 3, 2015
Pros and cons of methylation-based enrichment methods for ancient DNA
Andaine Seguin-Orlando, Cristina Gamba, Clio Der Sarkissian, et al.
American Journal of Human Genetics
|
March 5, 2013
Whole-exome sequencing identifies mutated c12orf57 in recessive corpus callosum hypoplasia
Naiara Akizu, Nuri M Shembesh, Tawfeg Ben-Omran, 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 disability
Rosalind Law, Tracy Dixon-Salazar, Julie Jerber, et al.
Nature
|
August 13, 2025
New discoveries of Australopithecus and Homo from Ledi-Geraru, Ethiopia
Brian Villmoare, Lucas K Delezene, Amy L Rector, et al.
Page
of 12
Search research articles
Search
Showing results (91-100 of 113) with videos related to
Sort By:
Page
of 12
Journal of Experimental & Clinical Assisted Reproduction
|
August 30, 2007
Regional clinical practice patterns in reproductive endocrinology: a collaborative transnational pilot survey of in vitro fertilization programs in the Middle East
Eric Scott Sills, Hussein S Qublan, Zeev Blumenfeld, et al.
Plos Neglected Tropical Diseases
|
July 28, 2025
Field evaluation of Standard Q Filariasis Antigen Test for Lymphatic Filariasis (LF) during a pre-transmission assessment survey in Sierra Leone, 2022
Benoit Dembele, Mohamed Salieu Bah, Abdulai Conteh, et al.
Human Molecular Genetics
|
December 26, 2016
Uner Tan syndrome caused by a homozygous TUBB2B mutation affecting microtubule stability
Martin W Breuss, Thai Nguyen, Anjana Srivatsan, et al.
Biology
|
September 23, 2022
Evolution of the Family Equidae, Subfamily Equinae, in North, Central and South America, Eurasia and Africa during the Plio-Pleistocene
Omar Cirilli, Helena Machado, Joaquin Arroyo-Cabrales, et al.
Frontiers in Immunology
|
April 26, 2024
O-GlcNAc transferase regulates collagen deposition and fibrosis resolution in idiopathic pulmonary fibrosis
Shia Vang, Eric Scott Helton, Yiming Guo, et al.
Journal of Oncology Practice
|
November 2, 2011
Creating a process to standardize regimen order sets within an electronic health record
Leslie T Busby, Sheetal Sheth, Jody Garey, et al.
Scientific Reports
|
July 3, 2015
Pros and cons of methylation-based enrichment methods for ancient DNA
Andaine Seguin-Orlando, Cristina Gamba, Clio Der Sarkissian, et al.
American Journal of Human Genetics
|
March 5, 2013
Whole-exome sequencing identifies mutated c12orf57 in recessive corpus callosum hypoplasia
Naiara Akizu, Nuri M Shembesh, Tawfeg Ben-Omran, 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 disability
Rosalind Law, Tracy Dixon-Salazar, Julie Jerber, et al.
Nature
|
August 13, 2025
New discoveries of Australopithecus and Homo from Ledi-Geraru, Ethiopia
Brian Villmoare, Lucas K Delezene, Amy L Rector, et al.
Page
of 12