Human antibody genes. Evolutionary and molecular genetic perspectives

Phenotype analysis impacts testing strategy in patients with Currarino syndrome.

Clinical genetics·2015

Further Evidence of Contrasting Phenotypes Caused by Reciprocal Deletions and Duplications: Duplication of NSD1 Causes Growth Retardation and Microcephaly.

Molecular syndromology·2013

Testing for differentially-expressed genes by maximum-likelihood analysis of microarray data.

Journal of computational biology : a journal of computational molecular cell biology·2001

Ataxia in prion protein (PrP)-deficient mice is associated with upregulation of the novel PrP-like protein doppel.

Journal of molecular biology·1999

T-cell receptor vbeta deletion and valpha polymorphism are responsible for the resistance of SWR mouse to arthritis induction.

Immunogenetics·1999

Expression of a type II collagen-specific TCR transgene accelerates the onset of arthritis in mice.

International immunology·1998

Genetic aspects of immunoglobulin A deficiency.

Advances in human genetics·1990

Structural defects in inherited and giant platelet disorders.

Advances in human genetics·1990

Mechanisms and management of IgA nephropathy progression to end-stage renal disease: From the "four-hit" theory to precision medicine.

Clinical nephrology·2026

Evaluating Selection Strategies Based on Inbreeding Load via Simulation.

Journal of animal breeding and genetics = Zeitschrift fur Tierzuchtung und Zuchtungsbiologie·2026

Molecular and clinical heterogeneity in an Iranian case series of Joubert syndrome.

Molecular genetics and metabolism reports·2026

Long-Term Follow-Up Incidence of Type 1 Diabetes and Associated Autoimmune Diseases in First-Degree Relatives.

Diabetes, obesity & metabolism·2026

Quantitative modeling of insulin signaling reveals mechanisms of insulin resistance in obese mice.

Computers in biology and medicine·2026

The K-Punch Method: An Effective Diagnostic Approach for Hirschsprung Disease in Low- and Middle-Income Countries - A Case Series.

Revista do Colegio Brasileiro de Cirurgioes·2026

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Human antibody genes. Evolutionary and molecular genetic perspectives

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Phenotype analysis impacts testing strategy in patients with Currarino syndrome.

Further Evidence of Contrasting Phenotypes Caused by Reciprocal Deletions and Duplications: Duplication of NSD1 Causes Growth Retardation and Microcephaly.

Testing for differentially-expressed genes by maximum-likelihood analysis of microarray data.

Ataxia in prion protein (PrP)-deficient mice is associated with upregulation of the novel PrP-like protein doppel.

T-cell receptor vbeta deletion and valpha polymorphism are responsible for the resistance of SWR mouse to arthritis induction.

Expression of a type II collagen-specific TCR transgene accelerates the onset of arthritis in mice.

Genetic aspects of immunoglobulin A deficiency.

Structural defects in inherited and giant platelet disorders.

Mechanisms and management of IgA nephropathy progression to end-stage renal disease: From the "four-hit" theory to precision medicine.

Evaluating Selection Strategies Based on Inbreeding Load via Simulation.

Molecular and clinical heterogeneity in an Iranian case series of Joubert syndrome.

Long-Term Follow-Up Incidence of Type 1 Diabetes and Associated Autoimmune Diseases in First-Degree Relatives.

Quantitative modeling of insulin signaling reveals mechanisms of insulin resistance in obese mice.

The K-Punch Method: An Effective Diagnostic Approach for Hirschsprung Disease in Low- and Middle-Income Countries - A Case Series.

Related Experiment Videos

Human antibody genes. Evolutionary and molecular genetic perspectives

Related Concept Videos

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