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PTRF

PTRF

Protein-coding gene in the species Homo sapiens

factor, also known as Cavin1, Cavin-1 or PTRF, is a protein which in humans is encoded by the PTRF gene. PTRF (Cavin1) has been shown to be crucial for

PTRF

Congenital generalized lipodystrophy

Genetic disorder; extreme lack of fat under the skin

in the PTRF gene causes Type 4 CGL. This gene codes for a protein called polymerase I and transcript release factor. Some of the roles the PTRF product

Congenital generalized lipodystrophy

Congenital_generalized_lipodystrophy

Probability Theory and Related Fields

Academic journal

Statistics with Applications - Google Scholar Metrics". scholar.google.com. Retrieved 2022-01-04. Official website PTRF on Scimago PTRF on Mathscinet v t e

Probability Theory and Related Fields

Probability_Theory_and_Related_Fields

Caveolae

Type of lipid raft in endocytosis

caveola formation. The cavin protein family consists of Cavin1 (also known as PTRF), Cavin2 (also known as SDPR), Cavin3 (also known as SRBC) and Cavin4 (also

Caveolae

Olav Kallenberg

Swedish American mathematician

probabilists from eight different countries. Editor-in-Chief of the journal PTRF (Probability Theory and Related Fields), 1991-94. Associate Editor for Zeitschrift

Olav Kallenberg

Olav_Kallenberg

RNA polymerase I

Enzyme in eukaryotes

factor PTRF and a T-rich region, induces Pol I to terminate transcription and dissociate from the DNA and the new transcript. TTF-I and PTRF then indirectly

RNA polymerase I

RNA_polymerase_I

UQCRC1

Protein-coding gene in the species Homo sapiens

and specific fragmentation of polymerase I and transcript release factor (PTRF) at the surface of caveolae in human adipocytes". Biochem. J. 383 (Pt 2):

UQCRC1

PARVA

Protein-coding gene in the species Homo sapiens

and specific fragmentation of polymerase I and transcript release factor (PTRF) at the surface of caveolae in human adipocytes". Biochem. J. 383 (Pt 2):

PARVA

ZNF148

Gene of the species Homo sapiens

humans is encoded by the ZNF148 gene. ZNF148 has been shown to interact with PTRF and P53. Zinc finger GRCm38: Ensembl release 89: ENSMUSG00000022811 – Ensembl

ZNF148

Robert Parton

British/Australian cell biologist

M. J.; Martin, Sally; Hancock, John F.; Parton, Robert G. (2008-01-11). "PTRF-Cavin, a conserved cytoplasmic protein required for caveola formation and

Robert Parton

Robert_Parton

AOC3

Enzyme

and specific fragmentation of polymerase I and transcript release factor (PTRF) at the surface of caveolae in human adipocytes". The Biochemical Journal

AOC3

SDHA

Protein-coding gene in humans

and specific fragmentation of polymerase I and transcript release factor (PTRF) at the surface of caveolae in human adipocytes". The Biochemical Journal

SDHA

ATP5F1B

Protein-coding gene in humans

and specific fragmentation of polymerase I and transcript release factor (PTRF) at the surface of caveolae in human adipocytes". Biochem. J. 383 (Pt 2):

ATP5F1B

Barraquer–Simons syndrome

Medical condition

secreted by the adipocytes at different locations.[citation needed] Human PTRF mutations may cause secondary deficiency of caveolins, resulting in generalized

Barraquer–Simons syndrome

Barraquer–Simons_syndrome

HADHB

Protein-coding gene in the species Homo sapiens

and specific fragmentation of polymerase I and transcript release factor (PTRF) at the surface of caveolae in human adipocytes". The Biochemical Journal

HADHB

EHD2

Protein-coding gene in the species Homo sapiens

and specific fragmentation of polymerase I and transcript release factor (PTRF) at the surface of caveolae in human adipocytes". Biochem. J. 383 (Pt 2):

EHD2

ACAA2

Gene

and specific fragmentation of polymerase I and transcript release factor (PTRF) at the surface of caveolae in human adipocytes". The Biochemical Journal

ACAA2

Transcription termination factor, RNA polymerase I

Protein-coding gene in the species Homo sapiens

Hoffmann-Rohrer U, Grummt I (1998). "Cloning and functional characterization of PTRF, a novel protein which induces dissociation of paused ternary transcription

Transcription termination factor, RNA polymerase I

Transcription_termination_factor,_RNA_polymerase_I

List of OMIM disorder codes

type 3; 612526; CAV1 Lipodystrophy, congenital generalized, type 4; 613327; PTRF Lipodystrophy, familial partial; 151660; LMNA Lipodystrophy, familial partial

List of OMIM disorder codes

List_of_OMIM_disorder_codes

RSU1

Protein-coding gene in the species Homo sapiens

and specific fragmentation of polymerase I and transcript release factor (PTRF) at the surface of caveolae in human adipocytes". Biochem. J. 383 (Pt 2):

RSU1