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Cranial anatomy of the early cynodont Galesaurus planiceps and the origin of mammalian endocranial characters

Journal of anatomy, 2019-05, Vol.234 (5), p.592-621

2019

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Graveyards — Special landfills

The Science of the total environment, 2012-03, Vol.419, p.90-97

2012

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Cranial anatomy of Bolotridon frerensis , an enigmatic cynodont from the Middle Triassic of South Africa, and its phylogenetic significance

PeerJ (San Francisco, CA), 2021-06, Vol.9, p.e11542-e11542, Article e11542

2021

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The origin and evolution of Cynodontia (Synapsida, Therapsida): Reassessment of the phylogeny and systematics of the earliest members of this clade using 3D‐imaging technologies

Anatomical record (Hoboken, N.J. : 2007), 2024-04, Vol.307 (4), p.1634-1730

2024

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Community structure and feeding ecology of mesopelagic fishes in the slope waters of King George Island (South Shetland Islands, Antarctica)

Deep-sea research. Part I, Oceanographic research papers, 2004-11, Vol.51 (11), p.1685-1708

2004

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Spiking of contemporary human template DNA with ancient DNA extracts induces mutations under PCR and generates nonauthentic mitochondrial sequences

Molecular biology and evolution, 2004-05, Vol.21 (5), p.957-964

2004

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Novel Endocranial Data on the Early Therocephalian Lycosuchus vanderrieti Underpin High Character Variability in Early Theriodont Evolution

Frontiers in ecology and evolution, 2020-01, Vol.7

2020

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A genetic perspective on myopia

Cellular and molecular life sciences : CMLS, 2005-04, Vol.62 (7-8), p.800-808

2005

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The complete form of X-linked congenital stationary night blindness is caused by mutations in a gene encoding a leucine-rich repeat protein

Nature genetics, 2000-11, Vol.26 (3), p.324-327

2000

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Comment on "The brain of LB1, Homo floresiensis"

Science (American Association for the Advancement of Science), 2005-10, Vol.310 (5746), p.236; author reply 236-236

2005

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Substitutions in the Conserved C2C Domain of Otoferlin Cause DFNB9, a Form of Nonsyndromic Autosomal Recessive Deafness

Neurobiology of disease, 2002-07, Vol.10 (2), p.157-164

2002

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Palaeopathological and variant conditions of the Homo heidelbergensis type specimen (Mauer, Germany)

Journal of human evolution, 2003-04, Vol.44 (4), p.479-495

2003

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Segregation Patterns and Heteroplasmy Prevalence in Leber's Hereditary Optic Neuropathy

Investigative ophthalmology & visual science, 2001-05, Vol.42 (6), p.1208-1214

2001

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Eleonora of Toledo (1522-1562): Evidence for tuberculosis and leishmaniasis co-infection in Renaissance Italy

International journal of paleopathology, 2012-12, Vol.2 (4), p.231-235

2012

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Down's syndrome in ancient Europe

The Lancet (British edition), 2003-09, Vol.362 (9388), p.1000-1000

2003

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Morphometric analysis of untreated adult skulls in syndromic and nonsyndromic craniosynostosis

Neurosurgical review, 2008-04, Vol.31 (2), p.179-188

2008

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The SOx10/Sox10 gene from human and mouse : sequence, expression, and transactivation by the encoded hmg domain transcription factor

Human genetics, 1998-08, Vol.103 (2), p.115-123

1998

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Repair of degraded duplex DNA from prehistoric samples using Escherichia coli DNA polymerase I and T4 DNA ligase

Nucleic acids research, 1998-02, Vol.26 (3), p.857-859

1998

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Slow and Fast Rod ERG Pathways in Patients with X-Linked Complete Stationary Night Blindness Carrying Mutations in the NYX Gene

Investigative ophthalmology & visual science, 2001-10, Vol.42 (11), p.2728-2736

2001

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A Polymerase Chain Reaction Inhibitor of Ancient Hard and Soft Tissue DNA Extracts Is Determined as Human Collagen Type I

Analytical biochemistry, 1998-06, Vol.259 (2), p.283-286

1998

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Otoferlin interacts with myosin VI: implications for maintenance of the basolateral synaptic structure of the inner hair cell

Human molecular genetics, 2009-08, Vol.18 (15), p.2779-2790

2009

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PCR-induced sequence alterations hamper the typing of prehistoric bone samples for diagnostic achondroplasia mutations

Molecular biology and evolution, 2004-11, Vol.21 (11), p.2005-2011

2004

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Refinement of the DFNA4 locus to a 1.44 Mb region in 19q13.33

Journal of molecular medicine (Berlin, Germany), 2004-06, Vol.82 (6), p.398-402

2004

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Fossil record of meningioma

The Lancet (British edition), 2003-08, Vol.362 (9381), p.408-408

2003

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Hirschsprung, RET-SOX and beyond: the challenge of examining non-mendelian traits (Review)

International journal of molecular medicine, 2002-10, Vol.10 (4), p.367

2002

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Cranial anatomy of the early cynodont Galesaurus planiceps and the origin of mammalian endocranial characters

Graveyards — Special landfills

Cranial anatomy of Bolotridon frerensis , an enigmatic cynodont from the Middle Triassic of South Africa, and its phylogenetic significance

The origin and evolution of Cynodontia (Synapsida, Therapsida): Reassessment of the phylogeny and systematics of the earliest members of this clade using 3D‐imaging technologies

Community structure and feeding ecology of mesopelagic fishes in the slope waters of King George Island (South Shetland Islands, Antarctica)

Spiking of contemporary human template DNA with ancient DNA extracts induces mutations under PCR and generates nonauthentic mitochondrial sequences

Novel Endocranial Data on the Early Therocephalian Lycosuchus vanderrieti Underpin High Character Variability in Early Theriodont Evolution

A genetic perspective on myopia

The complete form of X-linked congenital stationary night blindness is caused by mutations in a gene encoding a leucine-rich repeat protein

Comment on "The brain of LB1, Homo floresiensis"

Substitutions in the Conserved C2C Domain of Otoferlin Cause DFNB9, a Form of Nonsyndromic Autosomal Recessive Deafness

Palaeopathological and variant conditions of the Homo heidelbergensis type specimen (Mauer, Germany)

Segregation Patterns and Heteroplasmy Prevalence in Leber's Hereditary Optic Neuropathy

Eleonora of Toledo (1522-1562): Evidence for tuberculosis and leishmaniasis co-infection in Renaissance Italy

Down's syndrome in ancient Europe

Morphometric analysis of untreated adult skulls in syndromic and nonsyndromic craniosynostosis

The SOx10/Sox10 gene from human and mouse : sequence, expression, and transactivation by the encoded hmg domain transcription factor

Repair of degraded duplex DNA from prehistoric samples using Escherichia coli DNA polymerase I and T4 DNA ligase

Slow and Fast Rod ERG Pathways in Patients with X-Linked Complete Stationary Night Blindness Carrying Mutations in the NYX Gene

A Polymerase Chain Reaction Inhibitor of Ancient Hard and Soft Tissue DNA Extracts Is Determined as Human Collagen Type I

Otoferlin interacts with myosin VI: implications for maintenance of the basolateral synaptic structure of the inner hair cell

PCR-induced sequence alterations hamper the typing of prehistoric bone samples for diagnostic achondroplasia mutations

Refinement of the DFNA4 locus to a 1.44 Mb region in 19q13.33

Fossil record of meningioma

Hirschsprung, RET-SOX and beyond: the challenge of examining non-mendelian traits (Review)

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