Identification of individual chromosomes in the human karyotype by their banding pattern after proteolytic digestion

Aniridia, male pseudohermaphroditism, gonadoblastoma, mental retardation, and del 11p13.

Human genetics·2016

Cloning and sequencing of SOB3, a human gene coding for a sperm protein homologous to an antimicrobial protein and potentially involved in zona pellucida binding.

Molecular human reproduction·2001

Adhesion proteins expressed on human gamete surfaces and egg activation.

Biology of the cell·2000

Cloning and characterization of SOB1, a new testis-specific cDNA encoding a human sperm protein probably involved in oocyte recognition.

Biochemical and biophysical research communications·1999

Flow cytometric method to isolate round spermatids from mouse testis.

Human reproduction (Oxford, England)·1999

Flow cytometry isolation and reverse transcriptase-polymerase chain reaction characterization of human round spermatids in infertile patients.

Human reproduction (Oxford, England)·1999

Cytological and cytogenetical studies on brain tumors. VI. No evidence for a translocation in 22-monosomic meningiomas.

Humangenetik·1975

Climate associated variations in the human serum albumin level.

Humangenetik·1975

A technique for in situ karyotyping of primary amniotic fluid cell cultures.

Humangenetik·1975

Sister chromatid exchanges and chromatid interchanges in bloom's syndrome.

Humangenetik·1975

Trisomy 9p due to paternal translocation, t(9;13) (q13;q12).

Humangenetik·1975

The Bf locus in the HLA region of chromosome 6: linkage and association studies.

Humangenetik·1975

Wavelet-based whole genome doubling aware single-cell copy number calling.

Nucleic acids research·2026

Ki-67 regulates heterochromatin organization in neurons and forms condensates with heterochromatic components.

Nature communications·2026

Cell cycle-dependent chromatin motion: a role for DNA content doubling over cohesion.

Nucleic acids research·2026

Division Specific Biologically Effective Dose Predicts Gamma Knife Radiosurgery Outcomes in Multiple Sclerosis-Associated Trigeminal Neuralgia.

Neurosurgery practice·2026

X;7 Translocation at p21.1 and q31.31 Disrupting DMD: A Multiomics Study of a Male Dystrophinopathy Case.

Human mutation·2026

Renal proteomic landscape of a patient with Fanconi renotubular syndrome carrying a novel GATM variant.

Frontiers in physiology·2026

Related Experiment Videos

Identification of individual chromosomes in the human karyotype by their banding pattern after proteolytic digestion

Related Concept Videos

Aniridia, male pseudohermaphroditism, gonadoblastoma, mental retardation, and del 11p13.

Cloning and sequencing of SOB3, a human gene coding for a sperm protein homologous to an antimicrobial protein and potentially involved in zona pellucida binding.

Adhesion proteins expressed on human gamete surfaces and egg activation.

Cloning and characterization of SOB1, a new testis-specific cDNA encoding a human sperm protein probably involved in oocyte recognition.

Flow cytometric method to isolate round spermatids from mouse testis.

Flow cytometry isolation and reverse transcriptase-polymerase chain reaction characterization of human round spermatids in infertile patients.

Cytological and cytogenetical studies on brain tumors. VI. No evidence for a translocation in 22-monosomic meningiomas.

Climate associated variations in the human serum albumin level.

A technique for in situ karyotyping of primary amniotic fluid cell cultures.

Sister chromatid exchanges and chromatid interchanges in bloom's syndrome.

Trisomy 9p due to paternal translocation, t(9;13) (q13;q12).

The Bf locus in the HLA region of chromosome 6: linkage and association studies.

Wavelet-based whole genome doubling aware single-cell copy number calling.

Ki-67 regulates heterochromatin organization in neurons and forms condensates with heterochromatic components.

Cell cycle-dependent chromatin motion: a role for DNA content doubling over cohesion.

Division Specific Biologically Effective Dose Predicts Gamma Knife Radiosurgery Outcomes in Multiple Sclerosis-Associated Trigeminal Neuralgia.

X;7 Translocation at p21.1 and q31.31 Disrupting DMD: A Multiomics Study of a Male Dystrophinopathy Case.

Renal proteomic landscape of a patient with Fanconi renotubular syndrome carrying a novel GATM variant.

Related Experiment Videos

Identification of individual chromosomes in the human karyotype by their banding pattern after proteolytic digestion

Related Concept Videos

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