Evidence that the RHD(VI) deletion genotype does not exist

A clinical and neurophysiological motor signature of Unverricht-Lundborg disease.

Revue neurologique·2017

Reference values for T, B and NK human lymphocyte subpopulations in adults.

Data in brief·2017

Influence of age, sex and HCMV-serostatus on blood lymphocyte subpopulations in healthy adults.

Cellular immunology·2017

Allelic and Epitopic Characterization of Intra-Kidney Allograft Anti-HLA Antibodies at Allograft Nephrectomy.

American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons·2016

Bone marrow tryptase as a possible diagnostic criterion for adult systemic mastocytosis.

Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology·2016

[Cryofibrinogenemia: a single-center study at the University Hospital of Toulouse, France].

La Revue de medecine interne·2015

Anti-αvβ3 antibodies in FNAIT are associated with disturbed angiogenesis and intracranial hemorrhage in men and mice.

Blood·2026

Factor VIII Aurora: A Naturally Occurring Gain of Function FVIII Variant with Enhanced FIXa Affinity.

Blood·2026

Gut Microbiota Drives Aging-related Erythropoiesis Impairment via Phenylacetic Acid-induced Histone Phenylacetylation.

Blood·2026

Neutrophils as chameleons of tissue inflammation and host-pathogen interactions.

Blood·2026

The CYB5R3 T117S Missense Variant is Associated with Attenuated Riociguat Efficacy in Sickle Cell Disease.

Blood·2026

Rapid Peak Cilta-cel Expansion is Associated with Delayed Neurotoxicity in Multiple Myeloma.

Blood·2026

Confirmation of the HLA-B*35:642 Allele in a Brazilian Individual.

HLA·2026

Identification of the Novel HLA-G*01:71 Allele Using PolyseqOne Nanopore Sequencing Technology.

HLA·2026

Non-Coding c.*6C>T Variant in RBM8A Associated With Thrombocytopenia-Absent Radius (TAR) Syndrome in Three Indian Patients.

Clinical genetics·2026

Identification of a Novel HLA-B Allele, HLA-B*35:640, Discovered by Next-Generation Sequencing.

HLA·2026

Clinical and Genetic Spectrum of Filippi Syndrome: A Systematic Review of Published Case Reports and Case Series.

Health science reports·2026

Data mining revealed no other trinucleotide repeat expansion associated with the Huntington's disease biomarker (CAG).

Clinical parkinsonism & related disorders·2026

Related Experiment Videos

Evidence that the RHD(VI) deletion genotype does not exist

Related Concept Videos

A clinical and neurophysiological motor signature of Unverricht-Lundborg disease.

Reference values for T, B and NK human lymphocyte subpopulations in adults.

Influence of age, sex and HCMV-serostatus on blood lymphocyte subpopulations in healthy adults.

Allelic and Epitopic Characterization of Intra-Kidney Allograft Anti-HLA Antibodies at Allograft Nephrectomy.

Bone marrow tryptase as a possible diagnostic criterion for adult systemic mastocytosis.

[Cryofibrinogenemia: a single-center study at the University Hospital of Toulouse, France].

Anti-αvβ3 antibodies in FNAIT are associated with disturbed angiogenesis and intracranial hemorrhage in men and mice.

Factor VIII Aurora: A Naturally Occurring Gain of Function FVIII Variant with Enhanced FIXa Affinity.

Gut Microbiota Drives Aging-related Erythropoiesis Impairment via Phenylacetic Acid-induced Histone Phenylacetylation.

Neutrophils as chameleons of tissue inflammation and host-pathogen interactions.

The CYB5R3 T117S Missense Variant is Associated with Attenuated Riociguat Efficacy in Sickle Cell Disease.

Rapid Peak Cilta-cel Expansion is Associated with Delayed Neurotoxicity in Multiple Myeloma.

Confirmation of the HLA-B*35:642 Allele in a Brazilian Individual.

Identification of the Novel HLA-G*01:71 Allele Using PolyseqOne Nanopore Sequencing Technology.

Non-Coding c.*6C>T Variant in RBM8A Associated With Thrombocytopenia-Absent Radius (TAR) Syndrome in Three Indian Patients.

Identification of a Novel HLA-B Allele, HLA-B*35:640, Discovered by Next-Generation Sequencing.

Clinical and Genetic Spectrum of Filippi Syndrome: A Systematic Review of Published Case Reports and Case Series.

Data mining revealed no other trinucleotide repeat expansion associated with the Huntington's disease biomarker (CAG).

Related Experiment Videos

Evidence that the RHD(VI) deletion genotype does not exist

Related Concept Videos

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