An anonymous genomic probe (p lambda KP20.1) detects a multi-allelic locus on chromosome 19 (D19S25)

Microsatellite variation of ESR1, ESR2, and AR in Serbian women with primary ovarian insufficiency.

Climacteric : the journal of the International Menopause Society·2018

Lack of association between ESR1 gene polymorphisms and premature ovarian failure in Serbian women.

Climacteric : the journal of the International Menopause Society·2013

Differential activities of the RET tyrosine kinase receptor isoforms during mammalian embryogenesis.

Genes & development·2001

Homeodomain proteins Mox1 and Mox2 associate with Pax1 and Pax3 transcription factors.

FEBS letters·2001

Isolation of the avian homologue of the homeobox gene Mox2 and analysis of its expression pattern in developing somites and limbs.

Mechanisms of development·2001

Genomewide genetic linkage analysis confirms the presence of susceptibility loci for schizophrenia, on chromosomes 1q32.2, 5q33.2, and 8p21-22 and provides support for linkage to schizophrenia, on chromosomes 11q23.3-24 and 20q12.1-11.23.

American journal of human genetics·2001

AID self-assembly and multistranded DNA binding drive synapsis in class switch recombination.

Nucleic acids research·2026

Coronavirus NSP14 drives internal m7G modification to rewire host splicing and promote viral replication.

Nucleic acids research·2026

Insights into the recruitment of the H3K4me3 reader Spp1 by the meiotic double-strand break protein Mer2.

Nucleic acids research·2026

Newly synthesized histones: passive or active players in the regulation of epigenetic inheritance?

Nucleic acids research·2026

ETfinder: harnessing conserved C-terminal tails of single-stranded DNA-binding proteins for mining and engineering RecET systems in non-model microbial chassis.

Nucleic acids research·2026

MOSAIC enables selective transfer and fairness-aware generalization in cross-species DNA methylation prediction.

Nucleic acids research·2026

Molecular characterization of FAM222B as a novel disease gene for dominant cardiovascular laterality defects.

Scientific reports·2026

Genetic architecture and inheritance patterns of Leber hereditary optic neuropathy among 419 Chinese pedigrees carrying the ND4 11778G>A mutation.

Journal of genetics and genomics = Yi chuan xue bao·2026

Integrating LNA-qPCR and full-length SMN1 sequencing for precision SMA carrier screening: large-scale validation in 30,849 individuals.

Clinica chimica acta; international journal of clinical chemistry·2026

Novel splice site variants in GBA1 are associated with Gaucher disease and genotype-phenotype correlations.

Brain & development·2026

High-Resolution Physical Mapping and Chromosomal Transmission in Sugarcane Progeny.

The Journal of heredity·2026

Loci Associated With Susceptibility to Biliary Atresia-A Genome-Wide Association Study in Taiwan.

Pediatrics international : official journal of the Japan Pediatric Society·2026

Related Experiment Videos

An anonymous genomic probe (p lambda KP20.1) detects a multi-allelic locus on chromosome 19 (D19S25)

Related Concept Videos

Microsatellite variation of ESR1, ESR2, and AR in Serbian women with primary ovarian insufficiency.

Lack of association between ESR1 gene polymorphisms and premature ovarian failure in Serbian women.

Differential activities of the RET tyrosine kinase receptor isoforms during mammalian embryogenesis.

Homeodomain proteins Mox1 and Mox2 associate with Pax1 and Pax3 transcription factors.

Isolation of the avian homologue of the homeobox gene Mox2 and analysis of its expression pattern in developing somites and limbs.

Genomewide genetic linkage analysis confirms the presence of susceptibility loci for schizophrenia, on chromosomes 1q32.2, 5q33.2, and 8p21-22 and provides support for linkage to schizophrenia, on chromosomes 11q23.3-24 and 20q12.1-11.23.

AID self-assembly and multistranded DNA binding drive synapsis in class switch recombination.

Coronavirus NSP14 drives internal m7G modification to rewire host splicing and promote viral replication.

Insights into the recruitment of the H3K4me3 reader Spp1 by the meiotic double-strand break protein Mer2.

Newly synthesized histones: passive or active players in the regulation of epigenetic inheritance?

ETfinder: harnessing conserved C-terminal tails of single-stranded DNA-binding proteins for mining and engineering RecET systems in non-model microbial chassis.

MOSAIC enables selective transfer and fairness-aware generalization in cross-species DNA methylation prediction.

Molecular characterization of FAM222B as a novel disease gene for dominant cardiovascular laterality defects.

Genetic architecture and inheritance patterns of Leber hereditary optic neuropathy among 419 Chinese pedigrees carrying the ND4 11778G>A mutation.

Integrating LNA-qPCR and full-length SMN1 sequencing for precision SMA carrier screening: large-scale validation in 30,849 individuals.

Novel splice site variants in GBA1 are associated with Gaucher disease and genotype-phenotype correlations.

High-Resolution Physical Mapping and Chromosomal Transmission in Sugarcane Progeny.

Loci Associated With Susceptibility to Biliary Atresia-A Genome-Wide Association Study in Taiwan.

Related Experiment Videos

An anonymous genomic probe (p lambda KP20.1) detects a multi-allelic locus on chromosome 19 (D19S25)

Related Concept Videos

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