The relative DNA contents of the eutherian and marsupial X chromosomes

High-resolution mapping of the S and Z loci of Phalaris coerulescens.

Genome·2004

Sequence-specific identification of 18 pathogenic microorganisms using microarray technology.

Molecular and cellular probes·2002

Molecular cloning, physical mapping, and expression analysis of a novel gene, BCL2L12, encoding a proline-rich protein with a highly conserved BH2 domain of the Bcl-2 family.

Genomics·2001

Absence of PPP2R1A mutations in Wilms tumor.

Oncogene·2001

Identification and characterization of KLK14, a novel kallikrein serine protease gene located on human chromosome 19q13.4 and expressed in prostate and skeletal muscle.

Genomics·2001

A physical and transcript map of the MCOLN1 gene region on human chromosome 19p13.3-p13.2.

Genomics·2001

Gene mapping in marsupials and monotremes. II. Assignments to the X chromosome of dasyurid marsupials.

Cytogenetics and cell genetics·2012

Trisomy 17 in a bonobo (Pan paniscus) and deletion of 3q in a lowland gorilla (Gorilla gorilla gorilla): comparison with human trisomy 18 and human deletion 4q syndrome.

Cytogenetics and cell genetics·2002

A case of azoospermia in a bull carrying a Y-autosome reciprocal translocation.

Cytogenetics and cell genetics·2002

The pattern of phylogenomic evolution of the Canidae.

Cytogenetics and cell genetics·2002

Analysis of chromosomal aberrations involving chromosome 1q31-->q53 in a DMBA-induced rat fibrosarcoma cell line: amplification and overexpression of Jak2.

Cytogenetics and cell genetics·2002

The mouse Arhgef6 gene: cDNA sequence, expression analysis, and chromosome assignment.

Cytogenetics and cell genetics·2002

Overcoming a diagnostic blindspot: Identifying balanced translocations in Mendelian rare disease cohorts.

medRxiv : the preprint server for health sciences·2026

Organelle Volume Facilitates Spindle Positioning During C . elegans Female Meiosis.

bioRxiv : the preprint server for biology·2026

Somatic instability of the C9orf72 repeat expansion in blood differs between patients with amyotrophic lateral sclerosis or frontotemporal dementia.

medRxiv : the preprint server for health sciences·2026

FAT1 generates a nuclear fragment that impairs DNA damage repair in gastric cancer.

The Journal of biological chemistry·2026

Results from the VANISH study: A prospective multicenter study validating a single-nucleotide polymorphism-based noninvasive prenatal test to assess aneuploidy risk in surviving twins of vanishing twin pregnancies.

Pregnancy (Hoboken, N.J.)·2026

Loss-of-function variants in CFAP57, SEPTIN4, SPEM2, and CFAP46 cause asthenoteratozoospermia.

Human reproduction (Oxford, England)·2026

Related Experiment Videos

The relative DNA contents of the eutherian and marsupial X chromosomes

Related Concept Videos

High-resolution mapping of the S and Z loci of Phalaris coerulescens.

Sequence-specific identification of 18 pathogenic microorganisms using microarray technology.

Molecular cloning, physical mapping, and expression analysis of a novel gene, BCL2L12, encoding a proline-rich protein with a highly conserved BH2 domain of the Bcl-2 family.

Absence of PPP2R1A mutations in Wilms tumor.

Identification and characterization of KLK14, a novel kallikrein serine protease gene located on human chromosome 19q13.4 and expressed in prostate and skeletal muscle.

A physical and transcript map of the MCOLN1 gene region on human chromosome 19p13.3-p13.2.

Gene mapping in marsupials and monotremes. II. Assignments to the X chromosome of dasyurid marsupials.

Trisomy 17 in a bonobo (Pan paniscus) and deletion of 3q in a lowland gorilla (Gorilla gorilla gorilla): comparison with human trisomy 18 and human deletion 4q syndrome.

A case of azoospermia in a bull carrying a Y-autosome reciprocal translocation.

The pattern of phylogenomic evolution of the Canidae.

Analysis of chromosomal aberrations involving chromosome 1q31-->q53 in a DMBA-induced rat fibrosarcoma cell line: amplification and overexpression of Jak2.

The mouse Arhgef6 gene: cDNA sequence, expression analysis, and chromosome assignment.

Overcoming a diagnostic blindspot: Identifying balanced translocations in Mendelian rare disease cohorts.

Organelle Volume Facilitates Spindle Positioning During C . elegans Female Meiosis.

Somatic instability of the C9orf72 repeat expansion in blood differs between patients with amyotrophic lateral sclerosis or frontotemporal dementia.

FAT1 generates a nuclear fragment that impairs DNA damage repair in gastric cancer.

Results from the VANISH study: A prospective multicenter study validating a single-nucleotide polymorphism-based noninvasive prenatal test to assess aneuploidy risk in surviving twins of vanishing twin pregnancies.

Loss-of-function variants in CFAP57, SEPTIN4, SPEM2, and CFAP46 cause asthenoteratozoospermia.

Related Experiment Videos

The relative DNA contents of the eutherian and marsupial X chromosomes

Abstract:

Related Concept Videos

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