Evidence for two linked loci controlling ther serologically defined leukocyte antigens of chimpanzees (ChL-A)

Genetic polymorphism of serum complement components in the chimpanzee.

Immunogenetics·2012

Multi-Locus control of MLC reactions in rhesus monkeys.

Immunogenetics·2011

Visual prognosis in immunocompetent patients with herpes zoster ophthalmicus.

Acta ophthalmologica Scandinavica·2003

Histocompatibility and corneal transplantation.

Developments in ophthalmology·2002

Longitudinal analysis of varicella-zoster virus DNA on the ocular surface associated with herpes zoster ophthalmicus.

American journal of ophthalmology·2001

Risk and prognostic factors of postherpetic neuralgia and focal sensory denervation: a prospective evaluation in acute herpes zoster ophthalmicus.

The Clinical journal of pain·2001

Four amino acid exchanges located in the alpha-2 domain specify the novel HLA-B*50:20 allele.

Tissue antigens·2015

A novel HLA-A02 variant, HLA-A02:575, detected in a Taiwanese bone marrow hematopoietic stem cell donor.

Tissue antigens·2015

Identification of a novel HLA-A*02:06:01:02 allele in a Chinese individual by sequence-based typing.

Tissue antigens·2015

Genetic variation of the MHC class II DRB genes in the Japanese weasel, Mustela itatsi, endemic to Japan, compared with the Siberian weasel, Mustela sibirica.

Tissue antigens·2015

Questionable expression of unstable DQ heterodimer containing HLA-DQA1*01:07.

Tissue antigens·2015

Characterization of bovine MHC class II DRB3 diversity in South American Holstein cattle populations.

Tissue antigens·2015

Clinical and Molecular Spectrum of KBG Syndrome in the Largest Independent Turkish Cohort: Novel ANKRD11 Variants, 16q24.3 Deletions, and Structural Insights for Robust ANKRD11 Variant Interpretation.

Balkan medical journal·2026

Autosomal recessive HOXA3 deficiency causes congenital athymia and laryngeal malformation.

The Journal of allergy and clinical immunology·2026

CRP-albumin-lymphocyte index and multisystem diseases: a phenome-wide Mendelian randomization study.

Molecular genetics and genomics : MGG·2026

Congenital Hyperinsulinism With Paternally Inherited ABCC8 Variants: A Single Center Experience Over a Decade in Singapore.

Journal of the ASEAN Federation of Endocrine Societies·2026

Gestational age modifies associations between Group B Streptococcus genomic characteristics and postnatal age at disease onset.

Nature communications·2026

Clinical, immunological, and molecular characteristics of severe combined immune deficiency in China.

Human genetics·2026

Related Experiment Videos

Evidence for two linked loci controlling ther serologically defined leukocyte antigens of chimpanzees (ChL-A)

Related Concept Videos

Genetic polymorphism of serum complement components in the chimpanzee.

Multi-Locus control of MLC reactions in rhesus monkeys.

Visual prognosis in immunocompetent patients with herpes zoster ophthalmicus.

Histocompatibility and corneal transplantation.

Longitudinal analysis of varicella-zoster virus DNA on the ocular surface associated with herpes zoster ophthalmicus.

Risk and prognostic factors of postherpetic neuralgia and focal sensory denervation: a prospective evaluation in acute herpes zoster ophthalmicus.

Four amino acid exchanges located in the alpha-2 domain specify the novel HLA-B*50:20 allele.

A novel HLA-A02 variant, HLA-A02:575, detected in a Taiwanese bone marrow hematopoietic stem cell donor.

Identification of a novel HLA-A*02:06:01:02 allele in a Chinese individual by sequence-based typing.

Genetic variation of the MHC class II DRB genes in the Japanese weasel, Mustela itatsi, endemic to Japan, compared with the Siberian weasel, Mustela sibirica.

Questionable expression of unstable DQ heterodimer containing HLA-DQA1*01:07.

Characterization of bovine MHC class II DRB3 diversity in South American Holstein cattle populations.

Clinical and Molecular Spectrum of KBG Syndrome in the Largest Independent Turkish Cohort: Novel ANKRD11 Variants, 16q24.3 Deletions, and Structural Insights for Robust ANKRD11 Variant Interpretation.

Autosomal recessive HOXA3 deficiency causes congenital athymia and laryngeal malformation.

CRP-albumin-lymphocyte index and multisystem diseases: a phenome-wide Mendelian randomization study.

Congenital Hyperinsulinism With Paternally Inherited ABCC8 Variants: A Single Center Experience Over a Decade in Singapore.

Gestational age modifies associations between Group B Streptococcus genomic characteristics and postnatal age at disease onset.

Clinical, immunological, and molecular characteristics of severe combined immune deficiency in China.

Related Experiment Videos

Evidence for two linked loci controlling ther serologically defined leukocyte antigens of chimpanzees (ChL-A)

Related Concept Videos

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