Isolation and characterization of a hypervariable region [D4S163] on chromosome 4

ICSH guidelines for the verification and performance of automated cell counters for body fluids.

International journal of laboratory hematology·2014

Apoptosis repressor with caspase recruitment domain is regulated by MAPK/PI3K and confers drug resistance and survival advantage to AML.

Apoptosis : an international journal on programmed cell death·2013

Roles of the Ras/Raf/MEK/ERK pathway in leukemia therapy.

Leukemia·2011

Targeting the translational apparatus to improve leukemia therapy: roles of the PI3K/PTEN/Akt/mTOR pathway.

Leukemia·2011

CHILD syndrome: the NSDHL gene and its role in CHILD syndrome, a rare hereditary disorder.

Journal of the European Academy of Dermatology and Venereology : JEADV·2009

[Oncoplastic surgery for the treatment of breast cancer].

Minerva ginecologica·2009

CRISPR RNA architecture steers Cas9 catalysis and fidelity via a guide repeat clasp motif.

Nucleic acids research·2026

Seedless 3' pairing enables miR-17 family miRNAs to seize let-7 target sites.

Nucleic acids research·2026

OmrA sRNA inhibits translation of phosphoenolpyruvate carboxylase to impair TCA-cycle flux.

Nucleic acids research·2026

Modeling the spatial organization of replicated chromosomes in yeast reveals a loose asymmetric cohesion between sister chromatids.

Nucleic acids research·2026

Sequential-GAM constructs the single-cell geometric 3D genome structure.

Nucleic acids research·2026

The pseudouridine synthase PUSL1 modifies U39 of mitochondrial tRNAs and is linked to human neurological phenotypes.

Nucleic acids research·2026

Newborn screening and biobanking for preventable genetic disorders in Mongolia: A developing country perspective.

Regenerative therapy·2026

Whole-genome resequencing with multidimensional annotation revealed pathogenic networks in sirenomelia.

Italian journal of pediatrics·2026

Human Loss-of-Function ZNRF3 Mutation Impairs Adipose Thermogenesis and Drives Subcutaneous Fat Expansion.

Diabetes·2026

Integrated genetic identification and molecular dynamics simulations in a novel LOXL3 genetic mutation associated with Stickler syndrome.

Frontiers in genetics·2026

The ZBTB16/CUL3/ROC1 ubiquitin ligase drives the degradation of pathogenic pendrin (SLC26A4) protein variants.

Journal of biomedical science·2026

Identification and functional characterization of a SUZ12 frameshift variant in a Chinese family with Imagawa-Matsumoto syndrome.

BMC medical genomics·2026

Related Experiment Videos

Isolation and characterization of a hypervariable region [D4S163] on chromosome 4

Related Concept Videos

ICSH guidelines for the verification and performance of automated cell counters for body fluids.

Apoptosis repressor with caspase recruitment domain is regulated by MAPK/PI3K and confers drug resistance and survival advantage to AML.

Roles of the Ras/Raf/MEK/ERK pathway in leukemia therapy.

Targeting the translational apparatus to improve leukemia therapy: roles of the PI3K/PTEN/Akt/mTOR pathway.

CHILD syndrome: the NSDHL gene and its role in CHILD syndrome, a rare hereditary disorder.

[Oncoplastic surgery for the treatment of breast cancer].

CRISPR RNA architecture steers Cas9 catalysis and fidelity via a guide repeat clasp motif.

Seedless 3' pairing enables miR-17 family miRNAs to seize let-7 target sites.

OmrA sRNA inhibits translation of phosphoenolpyruvate carboxylase to impair TCA-cycle flux.

Modeling the spatial organization of replicated chromosomes in yeast reveals a loose asymmetric cohesion between sister chromatids.

Sequential-GAM constructs the single-cell geometric 3D genome structure.

The pseudouridine synthase PUSL1 modifies U39 of mitochondrial tRNAs and is linked to human neurological phenotypes.

Newborn screening and biobanking for preventable genetic disorders in Mongolia: A developing country perspective.

Whole-genome resequencing with multidimensional annotation revealed pathogenic networks in sirenomelia.

Human Loss-of-Function ZNRF3 Mutation Impairs Adipose Thermogenesis and Drives Subcutaneous Fat Expansion.

Integrated genetic identification and molecular dynamics simulations in a novel LOXL3 genetic mutation associated with Stickler syndrome.

The ZBTB16/CUL3/ROC1 ubiquitin ligase drives the degradation of pathogenic pendrin (SLC26A4) protein variants.

Identification and functional characterization of a SUZ12 frameshift variant in a Chinese family with Imagawa-Matsumoto syndrome.

Related Experiment Videos

Isolation and characterization of a hypervariable region [D4S163] on chromosome 4

Related Concept Videos

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