المؤلفون: Vriend J; Department of Human Anatomy and Cell Science, University of Manitoba, Winnipeg, MB R3T 2N2, Canada., Liu XQ; Department of Obstetrics, Gynecology and Reproductive Sciences, University of Manitoba, Winnipeg, MB R3T 2N2, Canada.; Biochemistry and Medical Genetics, Rady Faculty of Health Sciences, University of Manitoba, Winnipeg, MB R3T 2N2, Canada.

المصدر: International journal of molecular sciences [Int J Mol Sci] 2024 Jul 09; Vol. 25 (14). Date of Electronic Publication: 2024 Jul 09.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: MDPI Country of Publication: Switzerland NLM ID: 101092791 Publication Model: Electronic Cited Medium: Internet ISSN: 1422-0067 (Electronic) Linking ISSN: 14220067 NLM ISO Abbreviation: Int J Mol Sci Subsets: MEDLINE

مواضيع طبية MeSH: Medulloblastoma*/genetics , Medulloblastoma*/mortality , Medulloblastoma*/pathology , Chromosomes, Human, Pair 17*/genetics , Chromosomes, Human, Pair 6*/genetics, Humans ; Cerebellar Neoplasms/genetics ; Cerebellar Neoplasms/mortality ; Cerebellar Neoplasms/pathology ; Gene Expression Regulation, Neoplastic ; DNA Copy Number Variations ; HMGA1a Protein/genetics ; HMGA1a Protein/metabolism ; Female ; Gene Expression Profiling

المؤلفون: Messaoudi M; Laboratory of Genetics, Immunology and Human Pathologies, Faculty of Sciences of Tunis, University of Tunis El Manar, 2092, Tunis, Tunisia. messaoudi.prof@gmail.com., Pakstis AJ; Department of Genetics, Yale University School of Medicine, New Haven, CT, 06520, USA., Ezzaher T; Laboratory of Genetics, Immunology and Human Pathologies, Faculty of Sciences of Tunis, University of Tunis El Manar, 2092, Tunis, Tunisia., Boussetta S; Laboratory of Genetics, Immunology and Human Pathologies, Faculty of Sciences of Tunis, University of Tunis El Manar, 2092, Tunis, Tunisia., Ben Ammar Elgaaied A; Laboratory of Genetics, Immunology and Human Pathologies, Faculty of Sciences of Tunis, University of Tunis El Manar, 2092, Tunis, Tunisia., Kidd KK; Department of Genetics, Yale University School of Medicine, New Haven, CT, 06520, USA., Cherni L; Laboratory of Genetics, Immunology and Human Pathologies, Faculty of Sciences of Tunis, University of Tunis El Manar, 2092, Tunis, Tunisia.; Higher Institute of Biotechnology of Monastir, Monastir University, 5000, Monastir, Tunisia.

المصدر: Mammalian genome : official journal of the International Mammalian Genome Society [Mamm Genome] 2024 Sep; Vol. 35 (3), pp. 445-460. Date of Electronic Publication: 2024 Jul 04.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: Springer-Verlag Country of Publication: United States NLM ID: 9100916 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1432-1777 (Electronic) Linking ISSN: 09388990 NLM ISO Abbreviation: Mamm Genome Subsets: MEDLINE

مواضيع طبية MeSH: Chromosomes, Human, Pair 17*/genetics , Polymorphism, Single Nucleotide* , Haplotypes* , Genetic Variation* , Genetics, Population*, Humans ; Africa, Northern ; Black People/genetics ; Tunisia ; Principal Component Analysis ; Libya ; Gene Frequency ; North African People

المؤلفون: Ak B; Ege University Hospital, Department of Medical Genetics, Izmir 35100, Turkey. Electronic address: bilgesuak22@gmail.com., Güngör Ö; Ege University Hospital, Department of Medical Genetics, Izmir 35100, Turkey., Karaca E; Ege University Hospital, Department of Medical Genetics, Izmir 35100, Turkey., Durmaz B; Ege University Hospital, Department of Medical Genetics, Izmir 35100, Turkey., Bozer DS; Ege University Hospital, Department of Hematology, Izmir 35100, Turkey., Töbü M; Ege University Hospital, Department of Hematology, Izmir 35100, Turkey., Akın H; Ege University Hospital, Department of Medical Genetics, Izmir 35100, Turkey.

المصدر: Cancer genetics [Cancer Genet] 2024 Aug; Vol. 286-287, pp. 48-51. Date of Electronic Publication: 2024 Jul 24.

نوع المنشور: Case Reports; Journal Article

بيانات الدورية: Publisher: Elsevier Country of Publication: United States NLM ID: 101539150 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 2210-7762 (Print) NLM ISO Abbreviation: Cancer Genet Subsets: MEDLINE

مواضيع طبية MeSH: Leukemia, Promyelocytic, Acute*/genetics , Leukemia, Promyelocytic, Acute*/drug therapy , Translocation, Genetic* , Chromosomes, Human, Pair 17*/genetics, Humans ; Male ; Aged ; Tretinoin/therapeutic use ; Chromosomes, Human, Pair 15/genetics ; Chromosomes, Human, Pair 22/genetics ; In Situ Hybridization, Fluorescence

المؤلفون: Regis E; National Heart and Lung Institute, Imperial College London, London, United Kingdom., Fontanella S; National Heart and Lung Institute, Imperial College London, London, United Kingdom., Curtin JA; Division of Infection, Immunity and Respiratory Medicine, Faculty of Biology, Medicine and Health, Manchester Academic Health Sciences Centre, University of Manchester and University Hospital of South Manchester NHS Foundation Trust, Manchester, United Kingdom., Pinot de Moira A; National Heart and Lung Institute, Imperial College London, London, United Kingdom., Edwards MR; National Heart and Lung Institute, Imperial College London, London, United Kingdom., Murray CS; Division of Infection, Immunity and Respiratory Medicine, Faculty of Biology, Medicine and Health, Manchester Academic Health Sciences Centre, University of Manchester and University Hospital of South Manchester NHS Foundation Trust, Manchester, United Kingdom., Simpson A; Division of Infection, Immunity and Respiratory Medicine, Faculty of Biology, Medicine and Health, Manchester Academic Health Sciences Centre, University of Manchester and University Hospital of South Manchester NHS Foundation Trust, Manchester, United Kingdom., Johnston SL; National Heart and Lung Institute, Imperial College London, London, United Kingdom., Custovic A; National Heart and Lung Institute, Imperial College London, London, United Kingdom. Electronic address: a.custovic@imperial.ac.uk.

المصدر: The Journal of allergy and clinical immunology [J Allergy Clin Immunol] 2024 Aug; Vol. 154 (2), pp. 308-315. Date of Electronic Publication: 2024 Mar 15.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: Mosby Country of Publication: United States NLM ID: 1275002 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1097-6825 (Electronic) Linking ISSN: 00916749 NLM ISO Abbreviation: J Allergy Clin Immunol Subsets: MEDLINE

مواضيع طبية MeSH: Chromosomes, Human, Pair 17*/genetics , Polymorphism, Single Nucleotide* , Rhinovirus*, Humans ; Male ; Female ; Asthma/genetics ; Asthma/immunology ; Interferons ; Child ; Respiratory Sounds/genetics ; Respiratory Sounds/immunology ; Picornaviridae Infections/immunology ; Picornaviridae Infections/genetics ; Genetic Predisposition to Disease ; Chemokine CXCL10/genetics ; Leukocytes, Mononuclear/immunology ; Child, Preschool

المؤلفون: Kiyozawa D; Department of Anatomic Pathology, Graduate School of Medical Sciences, Kyushu University, 3-1-1 Maidashi, Higashi-Ku, Fukuoka, 812-8582, Japan.; Department of Pathology and Laboratory Medicine, Cedars-Sinai Medical Center, Los Angeles, CA, USA., Iwasaki T; Department of Anatomic Pathology, Graduate School of Medical Sciences, Kyushu University, 3-1-1 Maidashi, Higashi-Ku, Fukuoka, 812-8582, Japan., Takamatsu D; Department of Urology, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan., Kohashi K; Department of Pathology, Graduate School of Medicine, Osaka Metropolitan University, Osaka, Japan., Miyamoto T; Department of Anatomic Pathology, Graduate School of Medical Sciences, Kyushu University, 3-1-1 Maidashi, Higashi-Ku, Fukuoka, 812-8582, Japan., Fukuchi G; Department of Anatomic Pathology, Graduate School of Medical Sciences, Kyushu University, 3-1-1 Maidashi, Higashi-Ku, Fukuoka, 812-8582, Japan.; Department of Urology, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan., Eto M; Department of Urology, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan., Yamashita M; Department of Pathology and Laboratory Medicine, Cedars-Sinai Medical Center, Los Angeles, CA, USA., Oda Y; Department of Anatomic Pathology, Graduate School of Medical Sciences, Kyushu University, 3-1-1 Maidashi, Higashi-Ku, Fukuoka, 812-8582, Japan. oda.yoshinao.389@m.kyushu-u.ac.jp.

المصدر: Virchows Archiv : an international journal of pathology [Virchows Arch] 2024 Aug; Vol. 485 (2), pp. 299-306. Date of Electronic Publication: 2024 Jun 14.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: Springer International Country of Publication: Germany NLM ID: 9423843 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1432-2307 (Electronic) Linking ISSN: 09456317 NLM ISO Abbreviation: Virchows Arch Subsets: MEDLINE

مواضيع طبية MeSH: Kidney Neoplasms*/genetics , Kidney Neoplasms*/pathology , In Situ Hybridization, Fluorescence* , Chromosomes, Human, Pair 7*/genetics , Chromosomes, Human, Pair 17*/genetics , Chromosomes, Human, Y*/genetics, Humans ; Male ; Middle Aged ; Female ; Aged ; Adult ; Comparative Genomic Hybridization ; Immunohistochemistry ; Chromosome Aberrations ; Carcinoma, Renal Cell/genetics ; Carcinoma, Renal Cell/pathology ; DNA Copy Number Variations

المؤلفون: Nguyen-Khac F; Unité de Cytogénétique, Hôpital Pitié-Salpêtrière, APHP, Sorbonne Université, Paris, France.; Cell Death and Drug Resistance in Lymphoproliferative Disorders Team, Centre de Recherche Des Cordeliers, INSERM, Sorbonne Université, Université Sorbonne Paris Cité, Université Paris Descartes, Université Paris Diderot, Paris, France., Baron M; Service d'Hématologie Clinique, Hôpital Pitié-Salpêtrière, APHP, Sorbonne Université, Paris, France., Guièze R; Hematology Department, Clermont-Ferrand University Hospital, Clermont Auvergne University, Clermont-Ferrand, France., Feugier P; Department of Hematology, University Hospital of Nancy, Nancy, France., Fayault A; FILO, Tours University Hospital, Tours, France., Raynaud S; Laboratory of Hematology, University Hospital of Nice, Nice, France., Troussard X; Laboratory of Hematology, CHU Caen Normandie, Caen, France., Droin N; Inserm U1287, Gustave Roussy, Université Paris-Saclay, Villejuif, France., Damm F; Department of Hematology, Oncology, and Cancer Immunology, Charité - Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin, Humboldt-Universität Zu Berlin, Berlin, Germany., Smagghe L; Unité de Cytogénétique, Hôpital Pitié-Salpêtrière, APHP, Sorbonne Université, Paris, France., Susin S; Cell Death and Drug Resistance in Lymphoproliferative Disorders Team, Centre de Recherche Des Cordeliers, INSERM, Sorbonne Université, Université Sorbonne Paris Cité, Université Paris Descartes, Université Paris Diderot, Paris, France., Leblond V; Service d'Hématologie Clinique, Hôpital Pitié-Salpêtrière, APHP, Sorbonne Université, Paris, France., Dartigeas C; Department of Hematology, CHU Tours, Hôpital Bretonneau, Tours, France., Van den Neste E; Department of Hematology, Cliniques Universitaires Université Catholique de Louvain Saint-Luc, Bruxelles, Belgium., Leprêtre S; Department of Clinical Hematology, Centre Henri Becquerel, Rouen, France., Bernard OA; Inserm U1170, Université Paris-Saclay, Gustave Roussy Cancer Campus, Villejuif, France., Roos-Weil D; Cell Death and Drug Resistance in Lymphoproliferative Disorders Team, Centre de Recherche Des Cordeliers, INSERM, Sorbonne Université, Université Sorbonne Paris Cité, Université Paris Descartes, Université Paris Diderot, Paris, France.; Service d'Hématologie Clinique, Hôpital Pitié-Salpêtrière, APHP, Sorbonne Université, Paris, France.

مؤلفون مشاركون: on behalf the FILO (French Innovative Leukaemia Organization) Group

المصدر: British journal of haematology [Br J Haematol] 2024 Aug; Vol. 205 (2), pp. 495-502. Date of Electronic Publication: 2024 Apr 23.

نوع المنشور: Journal Article; Multicenter Study

بيانات الدورية: Publisher: Wiley-Blackwell Country of Publication: England NLM ID: 0372544 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1365-2141 (Electronic) Linking ISSN: 00071048 NLM ISO Abbreviation: Br J Haematol Subsets: MEDLINE

مواضيع طبية MeSH: Leukemia, Lymphocytic, Chronic, B-Cell*/genetics , Leukemia, Lymphocytic, Chronic, B-Cell*/drug therapy , Leukemia, Lymphocytic, Chronic, B-Cell*/mortality , Mutation* , Immunoglobulin Heavy Chains*/genetics , Chromosomes, Human, Pair 17*/genetics, Humans ; Male ; Female ; Middle Aged ; Aged ; Prognosis ; Prospective Studies ; Chromosome Deletion ; Adult ; Aged, 80 and over ; Immunoglobulin Variable Region/genetics ; Immunotherapy/methods ; Antineoplastic Combined Chemotherapy Protocols/therapeutic use

المؤلفون: Wilcock D; From ARUP Laboratories, Salt Lake City, Utah (Wilcock)., Sirohi D; the Department of Pathology and Laboratory Medicine, Huntsman Cancer Institute, University of Utah Health, Salt Lake City (Sirohi, Albertson, Cleary, Coleman, Jedrzkiewicz, Mahlow, Ruano, Gulbahce)., Albertson D; the Department of Pathology and Laboratory Medicine, Huntsman Cancer Institute, University of Utah Health, Salt Lake City (Sirohi, Albertson, Cleary, Coleman, Jedrzkiewicz, Mahlow, Ruano, Gulbahce)., Cleary AS; the Department of Pathology and Laboratory Medicine, Huntsman Cancer Institute, University of Utah Health, Salt Lake City (Sirohi, Albertson, Cleary, Coleman, Jedrzkiewicz, Mahlow, Ruano, Gulbahce)., Coleman JF; the Department of Pathology and Laboratory Medicine, Huntsman Cancer Institute, University of Utah Health, Salt Lake City (Sirohi, Albertson, Cleary, Coleman, Jedrzkiewicz, Mahlow, Ruano, Gulbahce)., Jedrzkiewicz J; the Department of Pathology and Laboratory Medicine, Huntsman Cancer Institute, University of Utah Health, Salt Lake City (Sirohi, Albertson, Cleary, Coleman, Jedrzkiewicz, Mahlow, Ruano, Gulbahce)., Mahlow J; the Department of Pathology and Laboratory Medicine, Huntsman Cancer Institute, University of Utah Health, Salt Lake City (Sirohi, Albertson, Cleary, Coleman, Jedrzkiewicz, Mahlow, Ruano, Gulbahce)., Ruano AL; the Department of Pathology and Laboratory Medicine, Huntsman Cancer Institute, University of Utah Health, Salt Lake City (Sirohi, Albertson, Cleary, Coleman, Jedrzkiewicz, Mahlow, Ruano, Gulbahce)., Gulbahce HE; the Department of Pathology and Laboratory Medicine, Huntsman Cancer Institute, University of Utah Health, Salt Lake City (Sirohi, Albertson, Cleary, Coleman, Jedrzkiewicz, Mahlow, Ruano, Gulbahce).

المصدر: Archives of pathology & laboratory medicine [Arch Pathol Lab Med] 2024 Aug 01; Vol. 148 (8), pp. 890-897.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: College of American Pathologists Country of Publication: United States NLM ID: 7607091 Publication Model: Print Cited Medium: Internet ISSN: 1543-2165 (Electronic) Linking ISSN: 00039985 NLM ISO Abbreviation: Arch Pathol Lab Med Subsets: MEDLINE

مواضيع طبية MeSH: In Situ Hybridization, Fluorescence* , Receptor, ErbB-2*/genetics , Receptor, ErbB-2*/metabolism , Breast Neoplasms*/genetics , Breast Neoplasms*/pathology , Breast Neoplasms*/metabolism , Breast Neoplasms*/diagnosis , Chromosomes, Human, Pair 17*/genetics , Centromere*/genetics , Centromere*/metabolism, Humans ; Female ; Middle Aged ; Aged ; Adult ; Immunohistochemistry ; Aged, 80 and over ; Gene Dosage ; Biomarkers, Tumor/genetics ; Biomarkers, Tumor/metabolism ; Biomarkers, Tumor/analysis ; United States ; Pathologists

المؤلفون: Brakta S; Section of Reproductive Endocrine, Infertility, & Genetics, Department of Obstetrics & Gynecology, Medical College of Georgia at Augusta University, Augusta, GA, USA. Electronic address: sbrakta@augusta.edu., Du Q; Department of Neuroscience and Regenerative Medicine, Medical College of Georgia at Augusta University, Augusta, GA, USA., Chorich LP; Section of Reproductive Endocrine, Infertility, & Genetics, Department of Obstetrics & Gynecology, Medical College of Georgia at Augusta University, Augusta, GA, USA., Hawkins ZA; Section of Reproductive Endocrine, Infertility, & Genetics, Department of Obstetrics & Gynecology, Medical College of Georgia at Augusta University, Augusta, GA, USA., Sullivan ME; University of Pittsburgh, Pittsburgh, PA, USA., Ko EK; University of Pennsylvania, Philadelphia, PA, USA., Kim HG; Department of Neurosurgery, Robert Wood Johnson Medical School, Rutgers, The State University of New Jersey, Piscataway, NJ, USA., Knight J; Department of Genetics, Yale University School of Medicine, New Haven, CT, USA; Yale Center for Genome Analysis, Yale University, New Haven, CT, USA., Taylor HS; Department of Obstetrics, Gynecology and Reproductive Sciences, Yale University School of Medicine, New Haven, CT, USA., Friez M; Greenwood Genetics Center, Greenwood, SC, USA., Phillips JA 3rd; Division of Medical Genetics and Genomic Medicine, Department of Pediatrics, Vanderbilt University, Nashville, TN, USA., Layman LC; Section of Reproductive Endocrine, Infertility, & Genetics, Department of Obstetrics & Gynecology, Medical College of Georgia at Augusta University, Augusta, GA, USA; Department of Neuroscience and Regenerative Medicine, Medical College of Georgia at Augusta University, Augusta, GA, USA; Department of Physiology, Medical College of Georgia at Augusta University, Augusta, GA, USA.

المصدر: Molecular and cellular endocrinology [Mol Cell Endocrinol] 2024 Aug 01; Vol. 589, pp. 112237. Date of Electronic Publication: 2024 Apr 08.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: North Holland Publishing Country of Publication: Ireland NLM ID: 7500844 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1872-8057 (Electronic) Linking ISSN: 03037207 NLM ISO Abbreviation: Mol Cell Endocrinol Subsets: MEDLINE

مواضيع طبية MeSH: 46, XX Disorders of Sex Development*/genetics , Chromosomes, Human, Pair 17*/genetics , Congenital Abnormalities*/genetics , Heterozygote* , Mullerian Ducts*/abnormalities, Adolescent ; Adult ; Female ; Humans ; Pedigree

SCR Disease Name: Mullerian aplasia

المؤلفون: Li G; Department of Reproductive Genetics, International Peace Maternity and Child Health Hospital, School of Medicine, Shanghai Jiao Tong University, No.910, Hengshan Road, Shanghai, 200030, China.; Shanghai Key Laboratory of Embryo Original Diseases, Shanghai, 200030, China., Chen Y; Department of Reproductive Genetics, International Peace Maternity and Child Health Hospital, School of Medicine, Shanghai Jiao Tong University, No.910, Hengshan Road, Shanghai, 200030, China.; Shanghai Key Laboratory of Embryo Original Diseases, Shanghai, 200030, China., Han X; Department of Reproductive Genetics, International Peace Maternity and Child Health Hospital, School of Medicine, Shanghai Jiao Tong University, No.910, Hengshan Road, Shanghai, 200030, China.; Shanghai Key Laboratory of Embryo Original Diseases, Shanghai, 200030, China., Li N; Department of Reproductive Genetics, International Peace Maternity and Child Health Hospital, School of Medicine, Shanghai Jiao Tong University, No.910, Hengshan Road, Shanghai, 200030, China. liniu0509@163.com.; Shanghai Key Laboratory of Embryo Original Diseases, Shanghai, 200030, China. liniu0509@163.com.; Faculty of Medical Laboratory Science, College of Health Science and Technology, School of Medicine, Shanghai Jiao Tong University, Shanghai, 200025, China. liniu0509@163.com., Li S; Department of Reproductive Genetics, International Peace Maternity and Child Health Hospital, School of Medicine, Shanghai Jiao Tong University, No.910, Hengshan Road, Shanghai, 200030, China. shuyuanli816@163.com.; Shanghai Key Laboratory of Embryo Original Diseases, Shanghai, 200030, China. shuyuanli816@163.com.; Faculty of Medical Laboratory Science, College of Health Science and Technology, School of Medicine, Shanghai Jiao Tong University, Shanghai, 200025, China. shuyuanli816@163.com.

المصدر: BMC pregnancy and childbirth [BMC Pregnancy Childbirth] 2024 Jul 01; Vol. 24 (1), pp. 456. Date of Electronic Publication: 2024 Jul 01.

نوع المنشور: Journal Article; Case Reports

بيانات الدورية: Publisher: BioMed Central Country of Publication: England NLM ID: 100967799 Publication Model: Electronic Cited Medium: Internet ISSN: 1471-2393 (Electronic) Linking ISSN: 14712393 NLM ISO Abbreviation: BMC Pregnancy Childbirth Subsets: MEDLINE

مواضيع طبية MeSH: T-Box Domain Proteins*/genetics , Chromosomes, Human, Pair 17*/genetics , Haplotypes* , Heterozygote*, Humans ; Female ; Pregnancy ; Adult ; Chromosome Deletion ; Exome Sequencing ; Sequence Deletion ; Fetus/abnormalities ; Ultrasonography, Prenatal

المؤلفون: Graney PL; Department of Psychology & Center for Neuroscience Research, University at Albany, Albany, NY, USA. Electronic address: pgraney@albany.edu., Chen MY; Department of Integrative Anatomical Sciences, Keck School of Medicine of the University of Southern California, Los Angeles, CA, USA; Western University of Health Sciences, Pomona, CA, USA., Wood RI; Department of Integrative Anatomical Sciences, Keck School of Medicine of the University of Southern California, Los Angeles, CA, USA., Wagner CK; Department of Psychology & Center for Neuroscience Research, University at Albany, Albany, NY, USA.

المصدر: Hormones and behavior [Horm Behav] 2024 Jul; Vol. 163, pp. 105550. Date of Electronic Publication: 2024 Apr 25.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: Academic Press Country of Publication: United States NLM ID: 0217764 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1095-6867 (Electronic) Linking ISSN: 0018506X NLM ISO Abbreviation: Horm Behav Subsets: MEDLINE

مواضيع طبية MeSH: Decision Making*/drug effects , 17 alpha-Hydroxyprogesterone Caproate* , Dopamine*/metabolism , Delay Discounting*/drug effects, Animals ; Female ; Rats ; Pregnancy ; Impulsive Behavior/drug effects ; Rats, Sprague-Dawley ; Prefrontal Cortex/drug effects ; Animals, Newborn ; Reward