[Probable linkage between the locus PGM1 and peptidase C in man]

Guidelines for presymptomatic testing for Huntington's disease: past, present and future in France.

Revue neurologique·2015

The involvement of the trans-generational effect in the high incidence of the hydatidiform mole in Africa.

Placenta·2014

The presymptomatic phase of Huntington disease.

Revue neurologique·2012

[Critical approach to clinical trials: difficulties of such research in Lebanon].

Revue neurologique·2012

A one year prevalence study of schizophrenia on Reunion Island.

European psychiatry : the journal of the Association of European Psychiatrists·2009

Homozygous mutation of the PHOX2B gene in congenital central hypoventilation syndrome (Ondine's Curse).

Human mutation·2008

[Effects of cyclic AMP treatment on the migration of primordial germ cells in the embryo of Xenopus laevis].

Comptes rendus hebdomadaires des seances de l'Academie des sciences. Serie D: Sciences naturelles·1978

[Cloning of the hepatitis B virus genome in Escherichia coli].

Comptes rendus hebdomadaires des seances de l'Academie des sciences. Serie D: Sciences naturelles·1978

[Modulation of humoral immunity in the mouse by means of grafts carrying reticulated polysaccharides].

Comptes rendus hebdomadaires des seances de l'Academie des sciences. Serie D: Sciences naturelles·1978

[Isolation in east Senegal of a yellow fever virus strain from a pool of Aedes belonging to the subgenus Diceromyia].

Comptes rendus hebdomadaires des seances de l'Academie des sciences. Serie D: Sciences naturelles·1978

[delta-9-Tetrahydrocannabinol (THC) inhibition of the membrane transport system for thymidine].

Comptes rendus hebdomadaires des seances de l'Academie des sciences. Serie D: Sciences naturelles·1978

[Study on the distribution of methyl-mercury (203Hg) by whole body autoradiography of macaque monkeys (Macaca irus)].

Comptes rendus hebdomadaires des seances de l'Academie des sciences. Serie D: Sciences naturelles·1978

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

The first 25 years of the NICHD Structural Birth Defects Initiative.

Developmental biology·2026

Related Experiment Videos

[Probable linkage between the locus PGM1 and peptidase C in man]

Related Concept Videos

Guidelines for presymptomatic testing for Huntington's disease: past, present and future in France.

The involvement of the trans-generational effect in the high incidence of the hydatidiform mole in Africa.

The presymptomatic phase of Huntington disease.

[Critical approach to clinical trials: difficulties of such research in Lebanon].

A one year prevalence study of schizophrenia on Reunion Island.

Homozygous mutation of the PHOX2B gene in congenital central hypoventilation syndrome (Ondine's Curse).

[Effects of cyclic AMP treatment on the migration of primordial germ cells in the embryo of Xenopus laevis].

[Cloning of the hepatitis B virus genome in Escherichia coli].

[Modulation of humoral immunity in the mouse by means of grafts carrying reticulated polysaccharides].

[Isolation in east Senegal of a yellow fever virus strain from a pool of Aedes belonging to the subgenus Diceromyia].

[delta-9-Tetrahydrocannabinol (THC) inhibition of the membrane transport system for thymidine].

[Study on the distribution of methyl-mercury (203Hg) by whole body autoradiography of macaque monkeys (Macaca irus)].

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.

The first 25 years of the NICHD Structural Birth Defects Initiative.

Related Experiment Videos

[Probable linkage between the locus PGM1 and peptidase C in man]

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