[Biochemical study of continuous human blood cell lines. Comparative study with fresh cells]

Persistent Müllerian duct syndrome due to anti-Müllerian hormone receptor 2 microdeletions: a diagnostic challenge.

Human reproduction (Oxford, England)·2020

A novel mutation of anti-Mullerian hormone gene in Persistent Mullerian Duct Syndrome presented with bilateral cryptorchidism: a case report.

Journal of pediatric urology·2013

A visual pitfall: persistent Müllerian duct syndrome (PMDS).

Acta paediatrica (Oslo, Norway : 1992)·2007

Autosomal recessive segregation of a truncating mutation of anti-Müllerian type II receptor in a family affected by the persistent Müllerian duct syndrome contrasts with its dominant negative activity in vitro.

The Journal of clinical endocrinology and metabolism·2001

Ovarian granulosa cell tumors express a functional membrane receptor for anti-Müllerian hormone in transgenic mice.

Endocrinology·2001

Resistance to induced apoptosis in the human neuroblastoma cell line SK-N-SH in relation to neuronal differentiation. Role of Bcl-2 protein family.

European journal of biochemistry·2001

Intranuclear arrangement of human chromosome 12 is reflected in metaphase chromosomes as non-random bending.

Annales de genetique·2004

Trisomy 4 associated with double minute chromosomes and MYC amplification in acute myeloblastic leukemia.

Annales de genetique·2004

Large duplication 4q25-q34 with mild clinical effect.

Annales de genetique·2004

A submicroscopic unbalanced subtelomeric translocation t(2p;10q) identified by fluorescence in situ hybridization: fetus with increased nuchal translucency and normal standard karyotype with later growth and developmental delay, rhombencephalosynapsis (RES).

Annales de genetique·2004

Partial trisomy 8q and partial monosomy 18p: a case report.

Annales de genetique·2004

Partial trisomy 18q11.2-->qter due to de novo unbalanced translocation of chromosomes 15 and 18 analyzed by fluorescence in situ hybridization.

Annales de genetique·2004

Metabolic regulation of stem cell plasticity.

Current opinion in genetics & development·2026

Stress-induced remodeling of membrane-bound organelles in budding yeast.

Current research in microbial sciences·2026

Nucleotide Metabolism in Health and Disease.

MedComm·2026

Glutathione in redox homeostasis: Bridging molecular mechanisms, bioavailability constraints, and translational challenges in systemic therapeutics.

Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie·2026

Lactate signaling and lactylation in retina: From physiological Warburg effect to pathological metabolic reprogramming.

Progress in retinal and eye research·2026

The quantitative amino acid economy of yeast reveals public versus private goods and guides syntrophic community design.

mSystems·2026

Related Experiment Videos

[Biochemical study of continuous human blood cell lines. Comparative study with fresh cells]

Related Concept Videos

Persistent Müllerian duct syndrome due to anti-Müllerian hormone receptor 2 microdeletions: a diagnostic challenge.

A novel mutation of anti-Mullerian hormone gene in Persistent Mullerian Duct Syndrome presented with bilateral cryptorchidism: a case report.

A visual pitfall: persistent Müllerian duct syndrome (PMDS).

Autosomal recessive segregation of a truncating mutation of anti-Müllerian type II receptor in a family affected by the persistent Müllerian duct syndrome contrasts with its dominant negative activity in vitro.

Ovarian granulosa cell tumors express a functional membrane receptor for anti-Müllerian hormone in transgenic mice.

Resistance to induced apoptosis in the human neuroblastoma cell line SK-N-SH in relation to neuronal differentiation. Role of Bcl-2 protein family.

Intranuclear arrangement of human chromosome 12 is reflected in metaphase chromosomes as non-random bending.

Trisomy 4 associated with double minute chromosomes and MYC amplification in acute myeloblastic leukemia.

Large duplication 4q25-q34 with mild clinical effect.

A submicroscopic unbalanced subtelomeric translocation t(2p;10q) identified by fluorescence in situ hybridization: fetus with increased nuchal translucency and normal standard karyotype with later growth and developmental delay, rhombencephalosynapsis (RES).

Partial trisomy 8q and partial monosomy 18p: a case report.

Partial trisomy 18q11.2-->qter due to de novo unbalanced translocation of chromosomes 15 and 18 analyzed by fluorescence in situ hybridization.

Metabolic regulation of stem cell plasticity.

Stress-induced remodeling of membrane-bound organelles in budding yeast.

Nucleotide Metabolism in Health and Disease.

Glutathione in redox homeostasis: Bridging molecular mechanisms, bioavailability constraints, and translational challenges in systemic therapeutics.

Lactate signaling and lactylation in retina: From physiological Warburg effect to pathological metabolic reprogramming.

The quantitative amino acid economy of yeast reveals public versus private goods and guides syntrophic community design.

Related Experiment Videos

[Biochemical study of continuous human blood cell lines. Comparative study with fresh cells]

Related Concept Videos

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