The candidate spermatogenesis gene RBMY has a homologue on the human X chromosome

Orientation-dependent Dxz4 contacts shape the 3D structure of the inactive X chromosome.

Nature communications·2018

Conservation of a chromosome arm in two distantly related marsupial species.

Cytogenetic and genome research·2009

ISCN standard idiograms.

Current protocols in human genetics·2008

Chromosome banding techniques.

Current protocols in human genetics·2008

Sex determination in platypus and echidna: autosomal location of SOX3 confirms the absence of SRY from monotremes.

Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology·2008

Reproduction of Blue-black Grassquits in central Brazil.

Brazilian journal of biology = Revista brasleira de biologia·2007

CCNB1IP1 regulatory evolution underlies gradual increases in cortical size and folding in primates.

Nature genetics·2026

A human single-cell atlas identifies OLR1+ scar-associated macrophages as a potential therapeutic target for chronic liver disease.

Nature genetics·2026

Germline homologous recombination deficiency influences TP53-mutant clonal hematopoiesis fitness during platinum and PARP inhibitor treatment.

Nature genetics·2026

Single-cell analysis of chromatin accessibility in the human intestine identifies regulatory programs and clarifies genetic associations in Crohn's disease.

Nature genetics·2026

Euchromatin forms condensed domains with short active regions on the surface.

Nature genetics·2026

Genome-wide mapping of common and rare variant effects on adiposity across childhood.

Nature genetics·2026

Identification of Potential Therapeutic Target Genes for Bipolar Disorder through Systematic Druggable Genome-wide Mendelian Randomization.

Current drug targets·2026

Facilitated Cascade Genetic Testing for Relatives of Individuals With BRCA1/2 Pathogenic Variants: A Randomized Controlled Trial.

Journal of clinical oncology : official journal of the American Society of Clinical Oncology·2026

Müllerian Duct Aplasia in a Girl With SMARCB1-Related Coffin-Siris Syndrome: A Rare Co-Occurring Anomaly.

Clinical genetics·2026

An IRAT109 NAM population: Genetic characterization and mapping utility for trait dissection in japonica rice (Oryza sativa L.).

The plant genome·2026

[Serological and Genotypic Analysis of a Family with B(A) Subtype].

Zhongguo shi yan xue ye xue za zhi·2026

STOML1 as an Exploratory Candidate Gene for Autosomal Dominant Iris and Chorioretinal Coloboma in a British Family.

Genes·2026

Related Experiment Videos

The candidate spermatogenesis gene RBMY has a homologue on the human X chromosome

Related Concept Videos

Orientation-dependent Dxz4 contacts shape the 3D structure of the inactive X chromosome.

Conservation of a chromosome arm in two distantly related marsupial species.

ISCN standard idiograms.

Chromosome banding techniques.

Sex determination in platypus and echidna: autosomal location of SOX3 confirms the absence of SRY from monotremes.

Reproduction of Blue-black Grassquits in central Brazil.

CCNB1IP1 regulatory evolution underlies gradual increases in cortical size and folding in primates.

A human single-cell atlas identifies OLR1+ scar-associated macrophages as a potential therapeutic target for chronic liver disease.

Germline homologous recombination deficiency influences TP53-mutant clonal hematopoiesis fitness during platinum and PARP inhibitor treatment.

Single-cell analysis of chromatin accessibility in the human intestine identifies regulatory programs and clarifies genetic associations in Crohn's disease.

Euchromatin forms condensed domains with short active regions on the surface.

Genome-wide mapping of common and rare variant effects on adiposity across childhood.

Identification of Potential Therapeutic Target Genes for Bipolar Disorder through Systematic Druggable Genome-wide Mendelian Randomization.

Facilitated Cascade Genetic Testing for Relatives of Individuals With BRCA1/2 Pathogenic Variants: A Randomized Controlled Trial.

Müllerian Duct Aplasia in a Girl With SMARCB1-Related Coffin-Siris Syndrome: A Rare Co-Occurring Anomaly.

An IRAT109 NAM population: Genetic characterization and mapping utility for trait dissection in japonica rice (Oryza sativa L.).

[Serological and Genotypic Analysis of a Family with B(A) Subtype].

STOML1 as an Exploratory Candidate Gene for Autosomal Dominant Iris and Chorioretinal Coloboma in a British Family.

Related Experiment Videos

The candidate spermatogenesis gene RBMY has a homologue on the human X chromosome

Related Concept Videos

Related Articles