Sci Rep
Large deletions in immunoglobulin genes are associated with a sustained absence of DNA Polymerase ?.
Lerner LK, Nguyen TV, Castro LP, Vilar JB, Munford V, Le Guillou M, Mohammad MM, Vergé V, Rosselli F, Menck CFM, Sarasin A, Aoufouchi S
Somatic hypermutation of immunoglobulin genes is a highly mutagenic process that is B cell-specific and occurs during antigen-driven responses leading ...
Read More
Source: PubMed
Int J Mol Sci
Drosophila as a Model Organism to Understand the Effects during Development of TFIIH-Related Human Diseases.
Zurita M, Murillo-Maldonado JM
Human mutations in the transcription and nucleotide excision repair (NER) factor TFIIH are linked with three human syndromes: xeroderma pigmentosum (X ...
Read More
Source: PubMed
Int. J. Biol. Macromol.
New structural insights into the recognition of undamaged splayed-arm DNA with a single pair of non-complementary nucleotides by human nucleotide excision repair protein XPA.
Lian FM, Yang X, Jiang YL, Yang F, Li C, Yang W, Qian C
XPA (Xeroderma pigmentosum complementation group A) is a core scaffold protein that plays significant roles in DNA damage verification and recruiting ...
Read More
Source: PubMed
Pediatr Dermatol 2020 Jan 19
Basosquamous carcinoma and melanoma collision tumor in a child with xeroderma pigmentosum.
Bostanci S, Akay BN, Kirmizi A, Okcu Heper A, Farabi B
Xeroderma pigmentosum (XP) is a rare autosomal recessive genodermatosis associated with hypersensitivity to ultraviolet radiation (UVR), being due to ...
Read More
Source: PubMed
Br. J. Dermatol. 2020 Jan 20
Quality of life in the photodermatoses: the hidden toll of photosensitivity.
Walburn J, Sarkany RPE
Read More
Source: PubMed
Sci Rep
Large deletions in immunoglobulin genes are associated with a sustained absence of DNA Polymerase ?.
Lerner LK, Nguyen TV, Castro LP, Vilar JB, Munford V, Le Guillou M, Mohammad MM, Vergé V, Rosselli F, Menck CFM, Sarasin A, Aoufouchi S
Somatic hypermutation of immunoglobulin genes is a highly mutagenic process that is B cell-specific and occurs during antigen-driven responses leading ...
Read More
Source: PubMed
Int J Mol Sci
Drosophila as a Model Organism to Understand the Effects during Development of TFIIH-Related Human Diseases.
Zurita M, Murillo-Maldonado JM
Human mutations in the transcription and nucleotide excision repair (NER) factor TFIIH are linked with three human syndromes: xeroderma pigmentosum (X ...
Read More
Source: PubMed
Int. J. Biol. Macromol.
New structural insights into the recognition of undamaged splayed-arm DNA with a single pair of non-complementary nucleotides by human nucleotide excision repair protein XPA.
Lian FM, Yang X, Jiang YL, Yang F, Li C, Yang W, Qian C
XPA (Xeroderma pigmentosum complementation group A) is a core scaffold protein that plays significant roles in DNA damage verification and recruiting ...
Read More
Source: PubMed
Pediatr Dermatol 2020 Jan 19
Basosquamous carcinoma and melanoma collision tumor in a child with xeroderma pigmentosum.
Bostanci S, Akay BN, Kirmizi A, Okcu Heper A, Farabi B
Xeroderma pigmentosum (XP) is a rare autosomal recessive genodermatosis associated with hypersensitivity to ultraviolet radiation (UVR), being due to ...
Read More
Source: PubMed
Br. J. Dermatol. 2020 Jan 20
Quality of life in the photodermatoses: the hidden toll of photosensitivity.
Walburn J, Sarkany RPE
Read More
Source: PubMed
Sci Rep
Large deletions in immunoglobulin genes are associated with a sustained absence of DNA Polymerase ?.
Lerner LK, Nguyen TV, Castro LP, Vilar JB, Munford V, Le Guillou M, Mohammad MM, Vergé V, Rosselli F, Menck CFM, Sarasin A, Aoufouchi S
Somatic hypermutation of immunoglobulin genes is a highly mutagenic process that is B cell-specific and occurs during antigen-driven responses leading ...
Read More
Source: PubMed
Int J Mol Sci
Drosophila as a Model Organism to Understand the Effects during Development of TFIIH-Related Human Diseases.
Zurita M, Murillo-Maldonado JM
Human mutations in the transcription and nucleotide excision repair (NER) factor TFIIH are linked with three human syndromes: xeroderma pigmentosum (X ...
Read More
Source: PubMed
Sci Rep
Large deletions in immunoglobulin genes are associated with a sustained absence of DNA Polymerase ?.
Lerner LK, Nguyen TV, Castro LP, Vilar JB, Munford V, Le Guillou M, Mohammad MM, Vergé V, Rosselli F, Menck CFM, Sarasin A, Aoufouchi S
Somatic hypermutation of immunoglobulin genes is a highly mutagenic process that is B cell-specific and occurs during antigen-driven responses leading ...
Read More
Source: PubMed
Int. J. Biol. Macromol.
New structural insights into the recognition of undamaged splayed-arm DNA with a single pair of non-complementary nucleotides by human nucleotide excision repair protein XPA.
Lian FM, Yang X, Jiang YL, Yang F, Li C, Yang W, Qian C
XPA (Xeroderma pigmentosum complementation group A) is a core scaffold protein that plays significant roles in DNA damage verification and recruiting ...
Read More
Source: PubMed
Sci Rep
Large deletions in immunoglobulin genes are associated with a sustained absence of DNA Polymerase ?.
Lerner LK, Nguyen TV, Castro LP, Vilar JB, Munford V, Le Guillou M, Mohammad MM, Vergé V, Rosselli F, Menck CFM, Sarasin A, Aoufouchi S
Somatic hypermutation of immunoglobulin genes is a highly mutagenic process that is B cell-specific and occurs during antigen-driven responses leading ...
Read More
Source: PubMed
Pediatr Dermatol 2020 Jan 19
Basosquamous carcinoma and melanoma collision tumor in a child with xeroderma pigmentosum.
Bostanci S, Akay BN, Kirmizi A, Okcu Heper A, Farabi B
Xeroderma pigmentosum (XP) is a rare autosomal recessive genodermatosis associated with hypersensitivity to ultraviolet radiation (UVR), being due to ...
Read More
Source: PubMed
Int J Mol Sci
Drosophila as a Model Organism to Understand the Effects during Development of TFIIH-Related Human Diseases.
Zurita M, Murillo-Maldonado JM
Human mutations in the transcription and nucleotide excision repair (NER) factor TFIIH are linked with three human syndromes: xeroderma pigmentosum (X ...
Read More
Source: PubMed
Int J Mol Sci
Drosophila as a Model Organism to Understand the Effects during Development of TFIIH-Related Human Diseases.
Zurita M, Murillo-Maldonado JM
Human mutations in the transcription and nucleotide excision repair (NER) factor TFIIH are linked with three human syndromes: xeroderma pigmentosum (X ...
Read More
Source: PubMed
Br. J. Dermatol. 2020 Jan 20
Quality of life in the photodermatoses: the hidden toll of photosensitivity.
Walburn J, Sarkany RPE
Read More
Source: PubMed
Int. J. Biol. Macromol.
New structural insights into the recognition of undamaged splayed-arm DNA with a single pair of non-complementary nucleotides by human nucleotide excision repair protein XPA.
Lian FM, Yang X, Jiang YL, Yang F, Li C, Yang W, Qian C
XPA (Xeroderma pigmentosum complementation group A) is a core scaffold protein that plays significant roles in DNA damage verification and recruiting ...
Read More
Source: PubMed
Int. J. Biol. Macromol.
New structural insights into the recognition of undamaged splayed-arm DNA with a single pair of non-complementary nucleotides by human nucleotide excision repair protein XPA.
Lian FM, Yang X, Jiang YL, Yang F, Li C, Yang W, Qian C
XPA (Xeroderma pigmentosum complementation group A) is a core scaffold protein that plays significant roles in DNA damage verification and recruiting ...
Read More
Source: PubMed
Pediatr Dermatol 2020 Jan 19
Basosquamous carcinoma and melanoma collision tumor in a child with xeroderma pigmentosum.
Bostanci S, Akay BN, Kirmizi A, Okcu Heper A, Farabi B
Xeroderma pigmentosum (XP) is a rare autosomal recessive genodermatosis associated with hypersensitivity to ultraviolet radiation (UVR), being due to ...
Read More
Source: PubMed
Pediatr Dermatol 2020 Jan 19
Basosquamous carcinoma and melanoma collision tumor in a child with xeroderma pigmentosum.
Bostanci S, Akay BN, Kirmizi A, Okcu Heper A, Farabi B
Xeroderma pigmentosum (XP) is a rare autosomal recessive genodermatosis associated with hypersensitivity to ultraviolet radiation (UVR), being due to ...
Read More
Source: PubMed
Br. J. Dermatol. 2020 Jan 20
Quality of life in the photodermatoses: the hidden toll of photosensitivity.
Walburn J, Sarkany RPE
Read More
Source: PubMed
Br. J. Dermatol. 2020 Jan 20
Quality of life in the photodermatoses: the hidden toll of photosensitivity.
Walburn J, Sarkany RPE
Read More
Source: PubMed
Sci Rep
Large deletions in immunoglobulin genes are associated with a sustained absence of DNA Polymerase ?.
Lerner LK, Nguyen TV, Castro LP, Vilar JB, Munford V, Le Guillou M, Mohammad MM, Vergé V, Rosselli F, Menck CFM, Sarasin A, Aoufouchi S
Somatic hypermutation of immunoglobulin genes is a highly mutagenic process that is B cell-specific and occurs during antigen-driven responses leading ...
Read More
Source: PubMed
Int J Mol Sci
Drosophila as a Model Organism to Understand the Effects during Development of TFIIH-Related Human Diseases.
Zurita M, Murillo-Maldonado JM
Human mutations in the transcription and nucleotide excision repair (NER) factor TFIIH are linked with three human syndromes: xeroderma pigmentosum (X ...
Read More
Source: PubMed
Int. J. Biol. Macromol.
New structural insights into the recognition of undamaged splayed-arm DNA with a single pair of non-complementary nucleotides by human nucleotide excision repair protein XPA.
Lian FM, Yang X, Jiang YL, Yang F, Li C, Yang W, Qian C
XPA (Xeroderma pigmentosum complementation group A) is a core scaffold protein that plays significant roles in DNA damage verification and recruiting ...
Read More
Source: PubMed
Pediatr Dermatol 2020 Jan 19
Basosquamous carcinoma and melanoma collision tumor in a child with xeroderma pigmentosum.
Bostanci S, Akay BN, Kirmizi A, Okcu Heper A, Farabi B
Xeroderma pigmentosum (XP) is a rare autosomal recessive genodermatosis associated with hypersensitivity to ultraviolet radiation (UVR), being due to ...
Read More
Source: PubMed
Br. J. Dermatol. 2020 Jan 20
Quality of life in the photodermatoses: the hidden toll of photosensitivity.
Walburn J, Sarkany RPE
Read More
Source: PubMed
