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The ocular albinism type 1 protein, an intracellular G protein-coupled receptor, regulates melanosome transport in pigment cells

Human molecular genetics, 2008-11, Vol.17 (22), p.3487-3501

2008

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Identification and Characterization of YME1L1, a Novel Paraplegin-Related Gene

Genomics (San Diego, Calif.), 2000-05, Vol.66 (1), p.48-54

2000

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The ocular albinism type 1 protein, an intracellular G protein-coupled receptor, regulates melanosome transport in pigment cells

Human molecular genetics, 2017-08, Vol.26 (15), p.3028-3029

2017

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Cloning of the Human Interferon-Related Developmental Regulator (IFRD1) Gene Coding for the PC4 Protein, a Member of a Novel Family of Developmentally Regulated Genes

Genomics (San Diego, Calif.), 1998-07, Vol.51 (2), p.233-242

1998

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The Gene Encoding a Cationic Amino Acid Transporter (SLC7A4) Maps to the Region Deleted in the Velocardiofacial Syndrome

Genomics (San Diego, Calif.), 1998-04, Vol.49 (2), p.230-236

1998

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SLC7A7 , encoding a putative permease-related protein, is mutated in patients with lysinuric protein intolerance

Nature genetics, 1999-03, Vol.21 (3), p.297-301

1999

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Oa1 knock-out: new insights on the pathogenesis of ocular albinism type 1

Human molecular genetics, 2000-11, Vol.9 (19), p.2781-2788

2000

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A gene deleted in Kallmann's syndrome shares homology with neural cell adhesion and axonal path-finding molecules

Nature (London), 1991-10, Vol.353 (6344), p.529-536

1991

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Defective intracellular transport and processing of OA1 is a major cause of ocular albinism type 1

Human molecular genetics, 2000-12, Vol.9 (20), p.3011-3018

2000

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Structure of the SLC7A7 Gene and Mutational Analysis of Patients Affected by Lysinuric Protein Intolerance

American journal of human genetics, 2000-01, Vol.66 (1), p.92-99

2000

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Intragenic Deletion of the KALIG-1 Gene in Kallmann's Syndrome

The New England journal of medicine, 1992-06, Vol.326 (26), p.1752-1755

1992

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Lysinuric protein intolerance characterized by bone marrow abnormalities and severe clinical course

The Journal of pediatrics, 1995-02, Vol.126 (2), p.246-251

1995

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SLC7A8, a Gene Mapping within the Lysinuric Protein Intolerance Critical Region, Encodes a New Member of the Glycoprotein-Associated Amino Acid Transporter Family

Genomics (San Diego, Calif.), 1999-12, Vol.62 (2), p.297-303

1999

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Structure of the mouse growth/differentiation factor 9 gene

Biochimica et biophysica acta, 1994-05, Vol.1222 (1), p.125-128

1994

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The delta F508 mutation in cystic fibrosis patients of southern Italy

Human genetics, 1990-09, Vol.85 (4), p.430-431

1990

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Brief report: intragenic deletion of the KALIG-1 gene in Kallmann's syndrome

The New England journal of medicine, 1992-06, Vol.326 (26), p.1752-1755

1992

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Brief Report: Intragenic Deletion of the Kalig-I Gene in Kallmannʼs Syndrome

Obstetrical & gynecological survey, 1992-11, Vol.47 (11), p.795-796

1992

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Variable penetrance of hypogonadism in a sibship with Kallmann syndrome due to a deletion of the KAL gene

American journal of medical genetics, 1995-07, Vol.57 (3), p.476-478

1995

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Dual-Task Performance in Multiple Sclerosis' Patients: Cerebellum Matters?

Archives of clinical neuropsychology, 2021-05, Vol.36 (4), p.517-526

2021

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Dose point kernels in liquid water: An intra-comparison between GEANT4-DNA and a variety of Monte Carlo codes

Applied radiation and isotopes, 2014-01, Vol.83 (Part B), p.137-141

2014

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Relapsing–remitting and secondary‐progressive multiple sclerosis patients differ in decoding others' emotions by their eyes

European journal of neurology, 2022-02, Vol.29 (2), p.505-514

2022

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FRCM Strengthened Masonry Panels: The Role of Mechanical Anchorages and Symmetric Layouts

Key engineering materials, 2017-07, Vol.747, p.334-341

2017

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Molecular scale track structure simulations in liquid water using the Geant4-DNA Monte-Carlo processes

Applied radiation and isotopes, 2011, Vol.69 (1), p.220-226

2011

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Oligorecurrent prostate cancer limited to lymph nodes: getting our ducks in a row: Nodal oligorecurrent prostate cancer

World journal of urology, 2019-12, Vol.37 (12), p.2607-2613

2019

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Oligorecurrent prostate cancer limited to lymph nodes: getting our ducks in a row

World journal of urology, 2019-12, Vol.37 (12), p.2607-2613

2019

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The ocular albinism type 1 protein, an intracellular G protein-coupled receptor, regulates melanosome transport in pigment cells

Identification and Characterization of YME1L1, a Novel Paraplegin-Related Gene

The ocular albinism type 1 protein, an intracellular G protein-coupled receptor, regulates melanosome transport in pigment cells

Cloning of the Human Interferon-Related Developmental Regulator (IFRD1) Gene Coding for the PC4 Protein, a Member of a Novel Family of Developmentally Regulated Genes

The Gene Encoding a Cationic Amino Acid Transporter (SLC7A4) Maps to the Region Deleted in the Velocardiofacial Syndrome

SLC7A7 , encoding a putative permease-related protein, is mutated in patients with lysinuric protein intolerance

Oa1 knock-out: new insights on the pathogenesis of ocular albinism type 1

A gene deleted in Kallmann's syndrome shares homology with neural cell adhesion and axonal path-finding molecules

Defective intracellular transport and processing of OA1 is a major cause of ocular albinism type 1

Structure of the SLC7A7 Gene and Mutational Analysis of Patients Affected by Lysinuric Protein Intolerance

Intragenic Deletion of the KALIG-1 Gene in Kallmann's Syndrome

Lysinuric protein intolerance characterized by bone marrow abnormalities and severe clinical course

SLC7A8, a Gene Mapping within the Lysinuric Protein Intolerance Critical Region, Encodes a New Member of the Glycoprotein-Associated Amino Acid Transporter Family

Structure of the mouse growth/differentiation factor 9 gene

The delta F508 mutation in cystic fibrosis patients of southern Italy

Brief report: intragenic deletion of the KALIG-1 gene in Kallmann's syndrome

Brief Report: Intragenic Deletion of the Kalig-I Gene in Kallmannʼs Syndrome

Variable penetrance of hypogonadism in a sibship with Kallmann syndrome due to a deletion of the KAL gene

Dual-Task Performance in Multiple Sclerosis' Patients: Cerebellum Matters?

Dose point kernels in liquid water: An intra-comparison between GEANT4-DNA and a variety of Monte Carlo codes

Relapsing–remitting and secondary‐progressive multiple sclerosis patients differ in decoding others' emotions by their eyes

FRCM Strengthened Masonry Panels: The Role of Mechanical Anchorages and Symmetric Layouts

Molecular scale track structure simulations in liquid water using the Geant4-DNA Monte-Carlo processes

Oligorecurrent prostate cancer limited to lymph nodes: getting our ducks in a row: Nodal oligorecurrent prostate cancer

Oligorecurrent prostate cancer limited to lymph nodes: getting our ducks in a row

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