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Nature Communications
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October 10, 2025
SETBP1 variants outside the degron disrupt DNA-binding, transcription and neuronal differentiation capacity to cause a heterogeneous neurodevelopmental disorder
Maggie M K Wong, Rosalie A Kampen, Ruth O Braden, et al.
Molecular Ecology
|
October 6, 2005
Origin and diversification of the human parasite Schistosoma mansoni
Jess A T Morgan, Randall J Dejong, Grace O Adeoye, et al.
Biorxiv : the Preprint Server for Biology
|
October 17, 2024
Direct mitochondrial import of lactate supports resilient carbohydrate oxidation
Ahmad A Cluntun, Joseph R Visker, Jesse N Velasco-Silva, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
January 24, 2026
International Clinical Evidence-based Guideline for Kleefstra Syndrome
Arianne Bouman, Charlotte M W Gaasterland, Carla Sloof-Enthoven, et al.
Journal of Speech, Language, and Hearing Research : JSLHR
|
August 22, 2024
Research Priorities for Childhood Apraxia of Speech: A Long View
Patricia McCabe, Molly Beiting, Elaine R Hitchcock, et al.
EMBO Molecular Medicine
|
December 20, 2021
In vitro and in vivo drug screens of tumor cells identify novel therapies for high-risk child cancer
Loretta M S Lau, Chelsea Mayoh, Jinhan Xie, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology
|
April 8, 2016
Significance of histologic pattern of carcinoma and sarcoma components on survival outcomes of uterine carcinosarcoma
K Matsuo, Y Takazawa, M S Ross, et al.
Clinical Pharmacology and Therapeutics
|
February 11, 2017
Collaborating to Compete: Blood Profiling Atlas in Cancer (BloodPAC) Consortium
R L Grossman, B Abel, S Angiuoli, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
December 31, 2024
Expanding the phenotype and genotype spectrum of TAOK1 neurodevelopmental disorder and delineating TAOK2 neurodevelopmental disorder
Nour Elkhateeb, Renarta Crookes, Michael Spiller, et al.
HGG Advances
|
January 20, 2022
Novel diagnostic DNA methylation episignatures expand and refine the epigenetic landscapes of Mendelian disorders
Michael A Levy, Haley McConkey, Jennifer Kerkhof, et al.
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Showing results (1181-1190 of 1,193) with videos related to
Sort By:
Page
of 120
Nature Communications
|
October 10, 2025
SETBP1 variants outside the degron disrupt DNA-binding, transcription and neuronal differentiation capacity to cause a heterogeneous neurodevelopmental disorder
Maggie M K Wong, Rosalie A Kampen, Ruth O Braden, et al.
Molecular Ecology
|
October 6, 2005
Origin and diversification of the human parasite Schistosoma mansoni
Jess A T Morgan, Randall J Dejong, Grace O Adeoye, et al.
Biorxiv : the Preprint Server for Biology
|
October 17, 2024
Direct mitochondrial import of lactate supports resilient carbohydrate oxidation
Ahmad A Cluntun, Joseph R Visker, Jesse N Velasco-Silva, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
January 24, 2026
International Clinical Evidence-based Guideline for Kleefstra Syndrome
Arianne Bouman, Charlotte M W Gaasterland, Carla Sloof-Enthoven, et al.
Journal of Speech, Language, and Hearing Research : JSLHR
|
August 22, 2024
Research Priorities for Childhood Apraxia of Speech: A Long View
Patricia McCabe, Molly Beiting, Elaine R Hitchcock, et al.
EMBO Molecular Medicine
|
December 20, 2021
In vitro and in vivo drug screens of tumor cells identify novel therapies for high-risk child cancer
Loretta M S Lau, Chelsea Mayoh, Jinhan Xie, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology
|
April 8, 2016
Significance of histologic pattern of carcinoma and sarcoma components on survival outcomes of uterine carcinosarcoma
K Matsuo, Y Takazawa, M S Ross, et al.
Clinical Pharmacology and Therapeutics
|
February 11, 2017
Collaborating to Compete: Blood Profiling Atlas in Cancer (BloodPAC) Consortium
R L Grossman, B Abel, S Angiuoli, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
December 31, 2024
Expanding the phenotype and genotype spectrum of TAOK1 neurodevelopmental disorder and delineating TAOK2 neurodevelopmental disorder
Nour Elkhateeb, Renarta Crookes, Michael Spiller, et al.
HGG Advances
|
January 20, 2022
Novel diagnostic DNA methylation episignatures expand and refine the epigenetic landscapes of Mendelian disorders
Michael A Levy, Haley McConkey, Jennifer Kerkhof, et al.
Page
of 120