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British Journal of Haematology
|
October 30, 2009
WASP plays a novel role in regulating platelet responses dependent on alphaIIbbeta3 integrin outside-in signalling
Anna Shcherbina, Jessica Cooley, Maxim I Lutskiy, et al.
Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing
|
February 27, 2026
PertSpectra: Interpretable Matrix Factorization for Predicting Functional Impact of Genetic Perturbation Experiments
Seowon Chang, Anna Shcherbina, Tal Ashuach, et al.
Genes
|
January 25, 2025
Novel <i>LYST</i> Variants Lead to Aberrant Splicing in a Patient with Chediak-Higashi Syndrome
Maxim Aleksenko, Elena Vlasova, Amina Kieva, et al.
The Journal of Allergy and Clinical Immunology. Global
|
May 6, 2024
Combined therapy with IL-1 and JAK inhibitors in a patient with the <i>NLRP1</i> gene mutation and a complex inflammatory phenotype
Vasily Burlakov, Anna Kozlova, Dmitry Pershin, et al.
The Journal of Applied Laboratory Medicine
|
April 21, 2026
Development, Validation, and Clinical Application of an HPLC-Based Method for Determining Adenosine Deaminase Activity in Adenosine Deaminase Deficiency-Severe Combined Immunodeficiency
Maria Petrik, Evgeny Litvin, Andrey Osipyants, et al.
British Journal of Haematology
|
January 20, 2021
Nicotinamide (vitamin B3) treatment improves response to G-CSF in severe congenital neutropenia patients
Ekaterina Deordieva, Oksana Shvets, Kirill Voronin, et al.
Orphanet Journal of Rare Diseases
|
May 5, 2019
Hematopoietic stem cell transplantation in a patient with type 1 mosaic variegated aneuploidy syndrome
Alexandra Laberko, Dmitry Balashov, Elena Deripapa, et al.
British Journal of Haematology
|
May 22, 2025
Efficacy and safety of romiplostim and eltrombopag in management of thrombocytopenia in Wiskott-Aldrich syndrome patients
Anna Ogneva, Yulia Rodina, Dmitry Pershin, et al.
Human Genomics
|
October 7, 2025
Recurrent acute liver failure and neutropenia caused by a novel homozygous RINT1 variant: a brief report of phenotypic expansion and population-specific findings
Еkaterina Nuzhnaya, Andrey Marakhonov, Nikolai Prokhorov, et al.
Pediatric Blood & Cancer
|
March 23, 2011
Four novel ELANE mutations in patients with congenital neutropenia
Maria Kurnikova, Michael Maschan, Evgeniya Dinova, et al.
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Search research articles
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Showing results (11-20 of 149) with videos related to
Sort By:
Page
of 15
British Journal of Haematology
|
October 30, 2009
WASP plays a novel role in regulating platelet responses dependent on alphaIIbbeta3 integrin outside-in signalling
Anna Shcherbina, Jessica Cooley, Maxim I Lutskiy, et al.
Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing
|
February 27, 2026
PertSpectra: Interpretable Matrix Factorization for Predicting Functional Impact of Genetic Perturbation Experiments
Seowon Chang, Anna Shcherbina, Tal Ashuach, et al.
Genes
|
January 25, 2025
Novel <i>LYST</i> Variants Lead to Aberrant Splicing in a Patient with Chediak-Higashi Syndrome
Maxim Aleksenko, Elena Vlasova, Amina Kieva, et al.
The Journal of Allergy and Clinical Immunology. Global
|
May 6, 2024
Combined therapy with IL-1 and JAK inhibitors in a patient with the <i>NLRP1</i> gene mutation and a complex inflammatory phenotype
Vasily Burlakov, Anna Kozlova, Dmitry Pershin, et al.
The Journal of Applied Laboratory Medicine
|
April 21, 2026
Development, Validation, and Clinical Application of an HPLC-Based Method for Determining Adenosine Deaminase Activity in Adenosine Deaminase Deficiency-Severe Combined Immunodeficiency
Maria Petrik, Evgeny Litvin, Andrey Osipyants, et al.
British Journal of Haematology
|
January 20, 2021
Nicotinamide (vitamin B3) treatment improves response to G-CSF in severe congenital neutropenia patients
Ekaterina Deordieva, Oksana Shvets, Kirill Voronin, et al.
Orphanet Journal of Rare Diseases
|
May 5, 2019
Hematopoietic stem cell transplantation in a patient with type 1 mosaic variegated aneuploidy syndrome
Alexandra Laberko, Dmitry Balashov, Elena Deripapa, et al.
British Journal of Haematology
|
May 22, 2025
Efficacy and safety of romiplostim and eltrombopag in management of thrombocytopenia in Wiskott-Aldrich syndrome patients
Anna Ogneva, Yulia Rodina, Dmitry Pershin, et al.
Human Genomics
|
October 7, 2025
Recurrent acute liver failure and neutropenia caused by a novel homozygous RINT1 variant: a brief report of phenotypic expansion and population-specific findings
Еkaterina Nuzhnaya, Andrey Marakhonov, Nikolai Prokhorov, et al.
Pediatric Blood & Cancer
|
March 23, 2011
Four novel ELANE mutations in patients with congenital neutropenia
Maria Kurnikova, Michael Maschan, Evgeniya Dinova, et al.
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of 15